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Nano Mask Launches Suite of Green Disinfectant Products for Hospital Market in the U.S. and Internationally

Posted on July 22, 2010 Written by Annalyn Frame

SOURCE: Nano Mask, Inc. (Emergency Filtration Products, Inc.)

FISHKILL, NY–(Marketwire – July 22, 2010) –  Nano Mask, Inc. (PINKSHEETS: NANM) today announced that it has entered into a manufacturing agreement with a well established Canadian company that will produce Nano Mask’s own proprietarily labeled multi amino acid enzyme cleaning products for the International and United States hospital markets. Nano Mask launched the distribution of this product suite on July 13, 2010 through a network of distributors and manufacturers’ representatives in the United States and internationally.

The Canadian manufacturer has developed a full line of enzyme based and chemical based medical specialty detergents for the demanding cleaning of medical instruments, laboratory glassware, endoscopes and hospital carts. These specialty detergents have become the preferred Multi-Enzyme Based Hospital instrument Pre-Soak and Cleaning Solution in the Canadian hospital market. Nano Mask’s initial products include:

  • Nano-Zyme, a Multi Enzyme Based Hospital Instrument Pre-Soak and Cleaning Solution that is a non foaming formulation that does not cause eye, nose, throat, skin or lung irritation as do the current products being used today.

  • Nano-Zyme Ortho Plus, a one step pre-soak enzymatic cleaning product specifically designed to emulsify and remove stubborn fats, oils, blood tissue, bone grease and lubricants on Orthopedic and Arthroscopic Instruments.

  • Nano-Med Care, a Multi Enzyme Based Pre Clean enzyme gel formulated as a transport gel to initiate the cleaning process at point of use in operating rooms, endoscopy suites, labs and central processing areas.

  • Nano-Odor Away, a Clear, Natural and Non Toxic liquid that eliminates odors from colostomy appliances and irrigation units, use of which eliminates the need to use masking agents and caustic chemicals.

“We are excited to launch this line of new green products for the hospital market in the U.S. and internationally,” said Edward J. Suydam, President and CEO, Nano Mask. “The reception from our distributors has been very strong and we expect to broaden our distribution capabilities — especially in international markets — over the coming months.”

Mr. Suydam added, “We entered this venture in an effort to create another source of revenues to complement the orders that we have generated from our distribution of Wein respirators while we continue to work on the completion of our own, proprietary NanoMask™ respirator.”

Separately, the company announced that it was continuing to make progress in bringing its S.E.C. filings up to date.

About Nano Mask, Inc.

http://nanomaskinc.com/

Nano Mask, Inc. is the inventor of the NanoMask, a disposable anti-microbial facemask currently under development and is a distributor of Wein Products’ line of disposable respirators and the new line of hospital detergent products.
Forward-looking Statement

This release may contain statements that are forward-looking. Such statements are made based upon current expectations that are subject to risk and uncertainty. Specifically, any unforeseen delays in distribution may affect the planned timeline for initiating actual sales of the product. NMI does not undertake to update forward-looking statements in this news release to reflect actual results of and changes in assumptions or changes in other factors affecting such forward-looking information. The actual future plans and results of the company could differ significantly from such forward-looking statements.

For further Information email:
Edward J. Suydam
President and CEO
Nano Mask, Inc.
[email protected]

Filed Under: Medical And Healthcare

FDA provides Complete Response Letter to NicOx’s New Drug Application for naproxcinod

Posted on July 22, 2010 Written by Annalyn Frame

SOURCE: NICOX

SOPHIA ANTIPOLIS, FRANCE–(Marketwire – July 22, 2010) – www.nicox.com

NicOx S.A. (NYSE Euronext Paris: COX) today announced the receipt of a
Complete Response Letter from the U.S. Food and Drug Administration (FDA)
related to the New Drug Application (NDA) for naproxcinod. Naproxcinod is
being developed for the relief of the signs and symptoms of osteoarthritis.

The FDA informed NicOx that its review of the NDA is complete and that it
does not approve the naproxcinod application. The FDA has recommended
conducting one or more long-term controlled studies to assess the
cardiovascular and gastrointestinal safety of naproxcinod. Additional
studies to demonstrate a clinically meaningful therapeutic benefit
attributable to the nitric oxide donation were also recommended. No
clinical efficacy studies were requested.

NicOx plans to discuss the Complete Response Letter and potential next
steps as early as possible with the FDA.

The naproxcinod Marketing Authorization Application (MAA) submitted by
NicOx in December 2009 is currently under review by the European Medicines
Agency (EMA).

NicOx remains well funded and had cash, cash equivalents and financial
instruments of ?138.5 million at the end of March 2010. The Company
will publish its financial results for the first half of 2010 on July 30,
2010. NicOx has no long-term debt and is constantly reviewing all aspects
of its cost base to ensure careful conservation of its funds.

NicOx has a broad pipeline of nitric oxide (NO)-donating New Molecular
Entities (NMEs) targeting the therapeutic areas of inflammatory,
cardiometabolic and ophthalmological diseases. NicOx has built a network of
strong partnerships for the development of some of its promising lead
compounds, including alliances with Merck & Co., Inc., Bausch + Lomb and
Ferrer.

Risks factors which are likely to have a material effect on NicOx’s
business are presented in the 4th chapter of the ” Document de
référence, rapport financier annuel et rapport de gestion 2009 ”
filed with the French Autorité des Marchés Financiers (AMF) on
March 5, 2010 and available on NicOx’s website (www.nicox.com) and on the
AMF’s website
(www.amf-france.org).

The Company notably draws the investors’ attention to the following risk
factors:

– Risques liés à la dépendance de la Société
à l’égard du naproxcinod (Risks related to the Company’s
dependence on the success of its lead product naproxcinod)

– Risques commerciaux et développements cliniques (Clinical
developments and commercial risk)

– Risques liés aux contraintes réglementaires et à la
lenteur des procédures d’approbation (Risks linked to regulatory
constraints and slow approval procedures)

– Manque de capacités dans les domaines de la vente et du marketing
(Lack of sales and marketing capabilities)

– Incertitude relative aux prix des médicaments et aux régimes de
remboursement, ainsi qu’en matière de réforme des régimes
d’assurance maladie (Uncertainty on drug pricing and reimbursement policies
and on the reforms of the health insurance systems)

NicOx (Bloomberg: COX:FP, Reuters: NCOX.PA) is a pharmaceutical company
focused on the research, development and future commercialization of drug
candidates. NicOx is applying its proprietary nitric oxide-donating R&D
platform to develop an internal portfolio of New Molecular Entities (NME)
for the potential treatment of inflammatory, cardio-metabolic and
ophthalmological diseases.

NicOx’s lead investigational compound is naproxcinod, an NME and a first-
in-class CINOD (Cyclooxygenase-Inhibiting Nitric Oxide-Donating) anti-
inflammatory drug candidate developed for the relief of the signs and
symptoms of osteoarthritis (OA). In July 2010, the FDA provided a Complete
Response Letter to the New Drug Application (NDA) for naproxcinod stating
that it does not approve the naproxcinod application. The naproxcinod
Marketing Authorization Application (MAA) submitted by NicOx in December
2009 is currently under review by the European Medicines Agency (EMA).

In addition to naproxcinod, NicOx’s pipeline includes several nitric oxide-
donating NMEs, which are in development internally and with partners,
including Merck & Co., Inc. and Bausch + Lomb, for the treatment of
hypertension, cardiometabolic diseases, eye diseases and dermatological
diseases.

NicOx S.A. is headquartered in France and is listed on Euronext Paris
(Compartment B: Mid Caps).

This press release contains certain forward-looking statements. Although
the Company believes its expectations are based on reasonable assumptions,
these forward-looking statements are subject to numerous risks and
uncertainties, which could cause actual results to differ materially from
those anticipated in the forward-looking statements. For a discussion of
risks and uncertainties which could cause actual results, financial
condition, performance or achievements of NicOx S.A. to differ from those
contained in the forward-looking statements, please refer to the Risk
Factors (“Facteurs de Risque”) section of the Document de Reference filed
with the AMF, which is available on the AMF website
(http://www.amf-france.org) or on NicOx S.A.’s website
(http://www.nicox.com).

CONTACTS

www.nicox.com

NicOx

Gavin Spencer – Vice President Business Development Tel +33 (0)4 97 24 53
00 – [email protected]

Media Relations Financial Dynamics

Europe

Guillaume Granier (France) – Tel: +33 (0)1 47 03 68 10 –
[email protected]

Stéphanie Bia (France) – Tel: +33 (0)1 47 03 68 10 –
[email protected]

Jonathan Birt (UK) – Tel +44 (0)20 7269 7205 – [email protected]

United States

Robert Stanislaro – Tel +1 212 850 5657 – [email protected]

Irma Gomez-Dib – Tel +1 212 850 5761 – [email protected]

NicOx S.A.,

Les Taissounières – Bât HB4 – 1681 route des Dolines – BP313,
06906 Sophia Antipolis cedex, France. Tel. +33 (0)4 97 24 53 00 – Fax +33
(0)4 97 24 53 99

This information is provided by HUGIN

Filed Under: Medical And Healthcare

MWI Veterinary Supply, Inc. Announces Its Third Quarter Fiscal 2010 Earnings Release Date and Conference Call Information

Posted on July 21, 2010 Written by Annalyn Frame

SOURCE: MWI Veterinary Supply

MERIDIAN, ID–(Marketwire – July 21, 2010) –  MWI Veterinary Supply, Inc. (NASDAQ: MWIV) announced today that the Company will release financial results for its fiscal year 2010 third quarter ended June 30, 2010 and update its business outlook for its fiscal year ending September 30, 2010 on Thursday, July 29, 2010. MWI will host a conference call the same day at 11:00 am eastern time to discuss these results and its business outlook.

For calls within the United States you can access the conference call by dialing (877) 638-4561 and international callers can access the conference by dialing (720) 545-0002. Participants will be required to register their name and company affiliation for the conference call. The conference call will also be carried live on the Company’s website at www.mwivet.com. Audio replay will be made available through August 12, 2010 by calling (800) 642-1687 for calls within the United States or (706) 645-9291 for international calls using the passcode 89688546 or by accessing the Company’s website.

About MWI Veterinary Supply, Inc.:
MWI Veterinary Supply, Inc. is a leading distributor of animal health products to veterinarians across the United States and United Kingdom. The products MWI sells include pharmaceuticals, vaccines, parasiticides, diagnostics, capital equipment, supplies, veterinary pet food and nutritional products. The Company markets these products to veterinarians in both the companion animal and production animal markets.

Contact:
Mary Pat Thompson
Senior Vice President of Finance and Administration and Chief Financial Officer
(208) 955-8930
Email Contact

Filed Under: Medical And Healthcare

Translational Medicine Alliance Announces 2010 Forum

Posted on July 21, 2010 Written by Annalyn Frame

SOURCE: Ewing Marion Kauffman Foundation

A Biomedical Industry Collaboration for Innovation

KANSAS CITY, MO–(Marketwire – July 21, 2010) –  The Translational Medicine Alliance Forum will convene October 13-14, 2010 at the Mandarin Oriental in Washington, DC. This year’s Forum will be hosted by three organizations with the common interest of accelerating translational research to the patient.

The Forum brings together leaders from academia, government agencies, and pharmaceutical, biotechnology and venture industries to work toward developing a deeper understanding of effective models to enable and accelerate the progress of translational medicine. Through focused, dynamic sessions and exclusive networking opportunities, attendees have the opportunity to learn about breakthrough approaches and progress on current best practices in translational medicine collaborations.

“Translational medicine holds some of the most promising advancements, and through this Forum, we are able to help facilitate and encourage a steady pathway to success for current and future research,” said Lesa Mitchell, vice president of Advancing Innovation, Ewing Marion Kauffman Foundation. The Kauffman Foundation helped found the Translational Medicine Alliance in 2007.

This Forum will focus on the following topics: regulatory science, lessons from the most experienced translational models, how and why rare disease and pediatric medicine are changing the landscape, transparency and access to data and reverse engineering translational science starting with the patient. 

The 2010 Forum is cosponsored by the Ewing Marion Kauffman Foundation, FasterCures and the Council for American Innovation. Registration for the Forum is now open. Early bird rates are available now through August 16, 2010, with a rate of $595 for corporate and $200 for academic and not-for-profit registrations. Space is limited. To register for the Forum, visit https://www.regonline.com/2010_translational_medicine_alliance_forum or call 866-831-3243.

Translational Medicine Alliance

The TransMed Partnership was formed in March 2007 to tap into the best ideas of thought leaders and develop an integrated strategy to support and advance the most promising technologies. The Alliance was founded by the Kauffman Foundation, Pfizer, Johnson and Johnson, Biogen Idec, FasterCures, Washington University, St. Louis (WUSTL) School of Medicine, BioVentures for Global Health, the Center for Emerging Technologies, BIOCOM, BIOTECanada, and LifeTech Innovations. For more information about the Alliance, please visit www.translationalmedicinealliance.org.

Contact
Jessica Cini
Translational Medicine Alliance
866-831-3243
[email protected]

Filed Under: Medical And Healthcare

VHA Study on Social Practices Reveals Manufacturers Can Help Lead Quality and Safety Efforts

Posted on July 21, 2010 Written by Annalyn Frame

SOURCE: Medline Industries, Inc.

Observational Study of Clinicians Revealed Opportunities to Redesign Products to Better Support Clinician-Patient Interaction

MUNDELEIN, IL–(Marketwire – July 21, 2010) –  A new VHA case study whitepaper released by Medline Industries, Inc. details how the company used observational studies and context-based design to build human factors and social behaviors into its redesigned Foley Catheter Management tray.

The whitepaper, Social Practice and Clinicians’ Meaning of Urinary Catheter Insertions, showed that the redesigned tray significantly influenced the clinician’s ability to provide high quality care by creating a greater focus on providing patient comfort, maintaining sterile technique and decreasing the time of the entire insertion process. The observational study was comprised of three separate three-day observations of clinicians conducting catheterizations in the emergency department, medical/surgical floors and operating rooms at Providence Sacred Heart Medical Center and Children’s Hospital, Spokane, WA.

“Health care manufacturers are often overlooked when clinicians redesign clinical practices. Yet, the design of a product can be key to helping clinicians improve clinical performance and patient education,” said Trent Haywood, MD, JD, Senior Vice President of Clinical Performance and Chief Medical Officer for VHA and lead investigator. “For example, Medline chose to redesign the urinary catheter tray based upon the observational data uncovered in the clinical setting. Such design emphasis shows how manufacturers can be a key partner in quality and safety.” 

The unique partnership between Medline and the VHA research team highlights how industry vendors can partner with healthcare providers to develop a comprehensive system that incorporates proper procedures and social behaviors that are easy to adopt in every day practice.

Medline launched its ERASE CAUTI program, which is based on the same criteria the CDC used in developing their new CAUTI prevention guidelines, last fall. Soon after the tray’s introduction, Medline met with the VHA Clinical Performance team to discuss studying the tray and how it’s used in actual clinical practice. Emphasis was put on understanding the objectives of catheter insertions from the clinician’s perspective, clarifying the actual practice that unfolds and identifying areas where the catheter management system aided the clinician or failed to aid the clinician based upon the clinician’s perspective on the practice.

Findings summarized in a case study whitepaper showed that clinicians preferred the benefits of the single layer tray which did not require steps related to maneuvering and positioning with a two layer tray. They also preferred the change to swab sticks that decreased the number of steps in the prepping and cleansing of the perineum. Clinicians retained the patent-pending patient education card for the patient or placed it in location where the patient might review it — a departure from previously observed behavior where the education was discarded without much attention. Clinicians also used the full-colored photography packaging to better explain the procedure to patients.

“Chief Nursing Officers (CNOs) want to help their staff reduce variability in the procedures that are done so that the potential to make an error decreases,” said Connie Yuska, Medline’s Vice President of Clinical Services and a former CNO. “We redesigned the tray taking into account the interaction between the patient and the clinician and facilitate learning — things that challenge nursing leaders every day.”

The VHA whitepaper, as well as additional information on the ERASE CAUTI program, is available for download on Medline’s website at www.medline.com/erase.

About Medline Industries, Inc. 
Medline, the nation’s largest privately held manufacturer and distributor of healthcare products, manufactures and distributes more than 100,000 products to hospitals, extended-care facilities, surgery centers, home care dealers and agencies. Headquartered in Mundelein, Ill., Medline has more than 900 dedicated sales representatives nationwide to support its broad product line and cost management services.

Over the past five years, Medline has been the fastest-growing distributor of medical and surgical supplies in the U.S., serving as the primary distributor to over 450 major hospitals and healthcare systems. As a leading distributor, Medline offers a comprehensive array of consulting and management services encompassing the supply chain and logistics, utilization and standardization, business tools and enhanced reporting capabilities and on-staff clinicians.

Media Contacts:
Jerreau Beaudoin
(847) 643-3011
John Marks
(847) 643-3309

Filed Under: Medical And Healthcare

AROK Purchasing Coalition Anticipates $25 Million Savings Through New Prime Vendor Supply Agreement With Medline Industries, Inc.

Posted on July 21, 2010 Written by Annalyn Frame

SOURCE: Medline Industries, Inc.

Medline Brand Products and Reduced Distribution Fees Drive Cost Savings

MUNDELEIN, IL–(Marketwire – July 21, 2010) –  Medline Industries Inc., the nation’s largest privately held manufacturer and distributor of healthcare supplies, announced today the signing of a cost management prime vendor agreement with the AROK Purchasing Coalition, a VHA supply network comprised of nearly 50 acute care facilities in Arkansas and Oklahoma. The five-year agreement is anticipated to save AROK an estimated $20-$25 million over the term of the contract.

Medline is expected to generate more than $500 million in medical and surgical product sales from the partnership over the term of the agreement. 

AROK was formed to help VHA member hospitals in Arkansas and Oklahoma increase efficiencies and reduce expenses by aggregating supply and services expenditures. 

As part of the agreement, Medline will provide its broad array of Medline brand medical and surgical products, including surgical procedure trays, patient care products, disposable protective gowns, exam gloves and bandages. Medline will drive cost savings to AROK members by delivering products direct to the healthcare facilities from two of Medline’s distribution centers located in Oklahoma City and Memphis, Tenn.

Medline will also deliver cost savings by reducing distribution fees on other national brand products and product standardization. In addition, Medline will provide enhanced reporting capabilities and offer comprehensive product utilization, education and practical solutions to help the facility control costs and improve patient care. 

About AROK
The AROK Purchasing Coalition is a VHA Supply Network. Twenty-one VHA health care organizations, representing nearly 50 hospitals in Arkansas and Oklahoma officially joined together in June 2008 to increase efficiencies and reduce expenses by aggregating supply and services expenditures. Combined annual supply purchases of the purchasing coalition represent in excess of $600 million. As a limited liability corporation, the AROK Purchasing Coalition is recognized as a single VHA member entity and as a large integrated delivery system by the supplier and distributor community. VHA operates the purchasing coalition at the direction of the members.

About Medline Industries, Inc. 
Medline, the nation’s largest privately held manufacturer and distributor of healthcare products, manufactures and distributes more than 100,000 products to hospitals, extended-care facilities, surgery centers, home care dealers and agencies. Headquartered in Mundelein, Ill., Medline has more than 900 dedicated sales representatives nationwide to support its broad product line and cost management services.

Over the past five years, Medline has been the fastest-growing distributor of medical and surgical supplies in the U.S., serving as the primary distributor to over 450 major hospitals and healthcare systems. As a leading distributor, Medline offers a comprehensive array of consulting and management services encompassing the supply chain and logistics, utilization and standardization, business tools and enhanced reporting capabilities and on-staff clinicians.

Medline has a growing network of 32 distribution centers around the country, as well as an expanding, dedicated transportation fleet with over 200 vehicles in a variety of sizes to fit customers’ specific delivery needs. The fleet is equipped with the latest navigation devices for enhanced order tracking and communication.

About VHA
VHA Inc., based in Irving, Texas, is a national network of not-for-profit health care organizations that work together to drive maximum savings in the supply chain arena, set new levels of clinical performance and identify and implement best practices to improve operational efficiency and clinical outcomes. Formed in 1977, through its 16 regional offices, VHA serves more than 1,400 hospitals and more than 25,500+ non-acute care providers nationwide. VHA was ranked by Modern Healthcare as the 7th best place to work in health care in 2009.

Media Contacts:
John Marks
(847) 643-3309
Jerreau Beaudoin
(847) 643-3011

Filed Under: Medical And Healthcare

www.healthoptionsworldwide.com: Medical Tourism Trends

Posted on July 21, 2010 Written by Annalyn Frame

SOURCE: Health Options Worldwide (HOW)

Employers Are Jumping on the Domestic Medical Travel Bandwagon

PRINCETON, NJ–(Marketwire – July 21, 2010) – In a recent USA Today article, medical tourism is getting a huge boost from American based employers and insurers who encourage employees to consider domestic medical travel. Therefore, instead of seeking out medical travel or affordable healthcare alternatives overseas such as Thailand or India, employees are being directed to regional facilities that offer high-quality care and lower prices. “The move is reducing healthcare costs by 20% to 40%, with the difference often covering travel expenses,” says David Goldstein, President of Health Options Worldwide (HOW), an online medical tourism company.

“When people hear the words ‘medical tourism,’ they automatically think overseas,” explained Goldstein, “But low-cost healthcare can be found in this country, even if it involves some travel.” Employers who offer domestic medical travel programs can save healthcare money by negotiating a single rate. This rate can include surgical and anesthesia fees and all medical care performed up until discharge.

Large corporations like Lowe’s, the home improvement retailer, already have such programs in place. A self-insured employer, Lowe’s struck a deal with a cardio care clinic where they send their employees for open-heart surgeries, valve repairs and pacemakers. In the future, they may add orthopedic surgeries to their program. Other large employers may soon follow suit with similar agreements with healthcare providers. Some companies provide financial incentives to medical travelers like waived deductions, copayment reductions and paid travel expenses.

“If this concept catches on, especially with large employers, it could help decrease healthcare costs and improve the quality of medical care by creating a competitive marketplace,” says Goldstein. Hospitals dictate costs and affect health insurance premiums. “However, it’s very sobering to see how much medical costs and quality can vary between hospitals and regions,” said Goldstein.

However, the focus should still be on quality along with financial balance, advises Goldstein. “With tempting financial incentives, employees may be forced to choose cost instead of quality, and the choice will be taken out of their hands,” explained Goldstein. Still the savings are hard to beat, especially when there are fewer complications from procedures that are done with high quality providers. Follow-up care, like physical therapy, is done locally and covered under the employee’s regular insurance plan.

Programs like these could spur the domestic healthcare marketplace to respond with even lower costs in order to lure patients to their centers. Insurance companies are hesitant to offer domestic medical travel incentives because it creates ill will with local healthcare providers, who then lower their costs in response. “This is why employers, healthcare providers and insurance companies will have no choice but to embrace this trend,” said Goldstein.

Contact:

David Goldstein
President
Health Options Worldwide
Domestic and International Healthcare Marketplace
Ph: 877-234-1345
www.healthoptionsworldwide.com

Click here to see all recent news from this company

Filed Under: Medical And Healthcare

Seegene Introduces First Real-time Molecular Diagnostic Test for Tuberculosis and Multi-drug Resistant Tuberculosis

Posted on July 21, 2010 Written by Annalyn Frame

SOURCE: Seegene

AnyplexTM MDR-TB Screening Test Identifies TB and Genetic Mutations Leading to TB Resistance to Isoniazid and Rifampicin

ROCKVILLE, MD and SEOUL, KOREA–(Marketwire – July 21, 2010) – The emergence and spread of drug-resistant mycobacterium tuberculosis (TB) threatens global TB control efforts, and there is an urgent need for new diagnostic tests that rapidly identify drug sensitivity profiles of TB strains. To help address these concerns, Seegene today introduced Anyplex™ MDR-TB Screening Test, the first real-time PCR molecular diagnostic capable of simultaneous detection of TB and genetic mutations leading to multi-drug resistant TB (MDR-TB) within four hours.

Seegene Anyplex™ MDR-TB Test will be introduced at the 2010 Annual Meeting and Clinical Lab Expo of the American Association for Clinical Chemistry (AACC), booth #1800.

According to the World Health Organization (WHO), TB strains that are resistant to all major anti-TB drugs have been documented in every country by the non-governmental organization recent survey. A particularly dangerous form of drug-resistant TB is multi-drug resistant TB (MDR-TB), which is defined as the disease caused by TB bacilli resistant to, among others, the two most powerful anti-TB drugs, isoniazid (INH) and rifampicin (Rif).The rate for successful MDR-TB treatment is extremely low and the progress of the disease is faster than normal TB, resulting in 40-50% of mortality rate. Rates of MDR-TB are troublingly high in some countries, especially in the former Soviet Union, and threaten TB infectious disease control efforts. WHO estimates that more than 440,000 people are infected with MDR-TB.

Using Anyplex™ MDR-TB Screening Test, healthcare workers will be able to quickly determine whether or not a patient is infected with a strain of TB that is resistant to INH and Rif. The Anyplex™ MDR-TB is a real-time detection test of M. tuberculosis that quickly and comprehensively determines the levels of targets in a patient’s various sample types, and identifies mutations of drug resistant genes to better inform a diagnosis.

Because genetic mutations that lead to antibiotic resistance are minute and sit close together, so far conventional PCR or conventional real-time PCR tests are not able to discriminate these mutations accurately within the same test procedure. In contrast, the Anyplex MDR-TB test can detect the mutations of drug resistant genes to Rif (rpoB: D516V/Y, H526D/Y, S531L) and INH (katG: S315T (2 cases); inhA promoter: -15(C/T)). The unprecedented speed and accuracy of the Anyplex MDR-TB Tests will enable doctors and clinicians to quickly provide an appropriate treatment to prevent the spread of MDR-TB.

Seegene’s new MDR-TB test takes TB diagnostics to a new level. Current TB test methods are hindered by speed (culture typically required 2-8 weeks for results), low sensitivity (acid-fast bacilli smear microscopy produced results in 24 hours but at the cost of missing a significant portion of TB cases) and low specificity (culture and microscopy methods not being able to efficiently differentiate between M. tuberculosis and non-tuberculosis mycobacteria). Furthermore, none of these approaches are able to rapidly and efficiently identify a patient’s resistance to the major drugs for treating TB — INH and Rif. Even if sequencing and Line Probe Assay are available to test drug resistance, the procedures are quite complicated and time-consuming.

“Making a fast and accurate diagnosis of the type of TB infection a patient may have is the most important step to curing a patient. Because MDR-TB is difficult to treat, preventing its spread throughout the population is essential. The Anyplex™ MDR-TB Test is a powerful new tool that healthcare workers can use to rapidly determine MDR-TB infections, which will both help stop it from spreading and allow health care professionals to set a course of alternative medications for infected patients,” said Jong-Yoon Chun, chief executive officer of Seegene.

Anyplex™ MDR-TB Test will not be available in the USA until regulatory clearance.

About Seegene

Seegene, Inc. is the leading biotechnology company developing, manufacturing and marketing innovative molecular diagnostic products. The company’s proprietary technologies in both PCR and Real-time PCR named ACP™, DPO™, and READ™, set a new solution for high-throughput and simultaneous multi-pathogen detection called “multiplex PCR”. The novel Real-time PCR technology, READ™, overcomes the limitations of conventional Real-time PCR, providing dramatic improvement in sensitivity and specificity. Seegene holds three novel Molecular diagnostic platforms: Seeplex®  system adapting DPO™ Technology, Anyplex™ and Magicplex™ systems that are Real-time PCR detection platforms adapting DPO™ and READ™ technologies. Seegene’s products detect multi-pathogens with great reliability and throughput, ultimately providing the most economical basis for saving time, labor and cost. Seegene’s mission is to maintain leadership in molecular diagnostics for infectious diseases, genetics, pharmacogenetics, and oncology using the innovative proprietary technologies.

For more information please visit www.seegene.com or call +301-762-9066.

Contacts:
Miyoun Lee, MSc
Seegene Inc.
301-762-9066
or
Constantine Theodoropulos
Base Pair Communications
617-816-4637

Filed Under: Medical And Healthcare

Medcor Recognized by Staples for Injury Triage Service

Posted on July 21, 2010 Written by Annalyn Frame

SOURCE: Medcor, Inc

MCHENRY, IL–(Marketwire – July 21, 2010) –  Medcor, Inc. announced its receipt of Staples’ Supplier of the Year award for Loss Prevention, recognizing Medcor’s contribution to improving health outcomes and controlling health costs. Medcor provides a 24/7 telephonic injury triage service for all Staples retail stores in North America. The service gives Staples employees immediate access to a registered nurse via a toll-free line to help determine the best course of action in the event of injury or illness at work. The service directs employees in first aid and self care, and makes referrals to appropriate off-site care for further treatment and diagnosis when necessary. More than 100 other vendors were considered in the selection process for this award. The award was presented to Medcor by Staples executives Wayne Jacobson and Dan Provost. Staples is the world’s largest office products company. 

“This is an important honor from an important client,” said Medcor President and CEO Philip Seeger, as he shared the award with nurses in Medcor’s call center in McHenry, Illinois. “Our nurses combine their experience and training with our software and clinical algorithms to deliver a very effective clinical intervention. The whole system is designed to work seamlessly within our client’s safety and risk management program.”

Medcor’s triage process is covered by three US patents, with additional patents pending. Medcor’s triage service is currently used by over 70,000 work locations from a variety of industries, including many national retailers. 

About Medcor

Medcor helps employers reduce costs of workers’ compensation and general health care. Medcor services include telephonic injury triage, on-site health and wellness clinics, outsourced safety staff, and employee screening. Medcor’s services are available 24/7 nationwide for worksites of any size in many industries. Headquartered in McHenry, IL, the company provides triage services to nearly 70,000 worksites in all 50 states and operates 163 on-site workplace clinics. Medcor’s triage methods are covered by U.S. & foreign patents, including U.S. No. 7,668,733; 7,716,070; & 7,720,692; other patents pending.

For more information, please contact: Kate Woldhuis at [email protected]

Contact:
Kate Woldhuis
[email protected]

Filed Under: Facilities And Providers

Datalliance VMI Customer, Bracco Diagnostics, Reviewed in Analyst Case Study on Healthcare Supply Chain

Posted on July 21, 2010 Written by Annalyn Frame

SOURCE: Datalliance

Datalliance Identified as Vendor Managed Inventory Platform and Partner for Program

CINCINNATI, OH–(Marketwire – July 21, 2010) –  The Vendor Managed Inventory (VMI) strategy being developed by Bracco Diagnostics, a leading provider of contrast media and related equipment to hospitals and imaging centers, was recently featured in a Gartner report on supply chain innovations in the healthcare industry titled “Case Study: Bracco Diagnostics Leverages Datalliance for Downstream Customer Alliances” published July 8, 2010. 

The case study discusses Bracco Diagnostics’ success with the first phase of their VMI program within its own distribution network, as well as the company’s strategy to offer VMI to key customers as a value-added service to manage inventory, prevent stock-outs, and optimize procure-to-pay processes. 

Addressing the challenges to collaborative supply chain processes such as VMI in the healthcare industry, the report lists the following as lessons learned:

  • “Trading partners must be willing to collaborate on the development of improved business processes, increasing the level of trust by establishing bidirectional goals and measures.

  • Both the hospital and upstream supplier must start by thinking from the patient back. They should then develop innovative solutions to age-old challenges, such as inefficient transactions, bloated network inventories and less-than-optimal customer satisfaction.

  • There are a host of ancillary benefits to establishing robust VMI capabilities between trading partners. For example, the cycle time required to renegotiate supply contracts can be greatly reduced when both parties have a clear line of sight to expected volumes, supplier performance and customer satisfaction.”

The full report is available to Gartner clients at www.gartner.com/resId=1397037.

“VMI continues to expand in the healthcare industry and we’re proud to be working with forward-thinking suppliers like Bracco Diagnostics and others to leverage it as one means of bringing down the cost of patient care,” said Bob Jennings, Datalliance VP of Sales & Marketing. “This is another example of the many successful VMI programs within our customer community.” 

Earlier, Datalliance VMI was positively referenced in the AMR Research report titled “The Resurgence of Vendor Managed Inventory: A Landscape” published in October 2009. Visit www.datalliance.com/2009_dec_pr1.html for more information about that report, which is also available on the Gartner web site for companies with appropriate subscriptions. AMR Research is now part of Gartner.

About Datalliance
Datalliance is a leading provider of collaborative commerce services, and the world’s largest independent VMI service provider. Delivered via the Internet using the ‘Software as a Service’ (SaaS) model, Datalliance solutions make it easy for suppliers and their customers to establish sales and inventory management relationships that fully align business objectives, improve collaboration, and streamline supply chain operations. Datalliance manages billions of dollars in orders, millions of SKUs, and thousands of locations for leading Fortune 1000 companies in a number of industries. For more information about Datalliance, visit www.datalliance.com

Contact:
Brian Lindner
Datalliance
513-791-7272

Filed Under: Facilities And Providers

Radient Pharmaceuticals Announces Exclusive Distribution Agreement With AMDL Australia Pty Ltd.

Posted on July 21, 2010 Written by Annalyn Frame

SOURCE: Radient Pharmaceuticals Corporation

Newest Commercialization Milestone Brings RPC’s Onko-SureTM IVD Cancer Test to Australia and New Zealand Markets

TUSTIN, CA–(Marketwire – July 21, 2010) – Radient Pharmaceuticals Corporation (NYSE Amex: RPC), a US-based pharmaceutical company specializing in the research, development and sales of In Vitro Diagnostic (IVD) cancer tests, announced today it has entered into an exclusive distribution agreement with AMDL Australia Pty Ltd. to market and commercialize RPC’s Onko-Sure™ in vitro diagnostic (IVD) cancer test in Australia and New Zealand.

Led by a strong management team of well-respected physicians and diagnostics professionals, AMDL Australia Pty Ltd. is an established, privately?owned distributor of healthcare products to laboratories, clinics, hospitals and other health care providers and research organizations throughout Australia and New Zealand. The company is the newest addition to Radient Pharmaceuticals’ portfolio of international distributors and under the terms of the agreement, will market, sell and distribute at minimum 3700 Onko?Sure IVD cancer test kits for use as a monitoring test for colorectal cancer (CRC) in Australia and New Zealand. AMDL Australia also holds responsibility for developing and executing a full-scale marketing strategy to drive product awareness and engage healthcare decision makers, thought?leaders, lab directors, physicians, patients and healthcare consumers in product purchases. Targeted distribution channels will include medical centers, hospitals, clinical laboratories, university labs.

According to Douglas MacLellan, Chairman and CEO of RPC, “We are extremely pleased to further expand the commercial availability of Onko-Sure through this partnership with AMDL Australia, a leading distributor in Australia and New Zealand. AMDL Australia has a well-established and significant sales force with a successful track record in these markets where we have not yet established a full commercial sales presence for Onko-Sure. Through this partnership, Onko-Sure will be available sooner and to more patients than otherwise possible in these selected markets.”

AMDL Australia’s Dr Chris Dirks remarked, “Epidemiological evidence estimates there are more than 13,000 new cases of CRC in Australia annually. CRC is a leading cause of cancer death in this country and through national cancer screening programs with the use of Onko-Sure we can enable health care providers with the ability to provide early detection, treatment and more vigilant monitoring, which in turn can lead to decreased mortality rates. We are pleased to be the exclusive distributor of Onko-Sure in the Australian and New Zealand markets.”

Onko?Sure is a simple, non?invasive, patent?pending and regulatory?approved in vitro diagnostic test that enables physicians and their patients to effectively monitor and/or detect certain types of cancers by measuring the accumulation of specific breakdown products in the blood called Fibrin and Fibrinogen Degradation Products (FDP). FDP levels rise dramatically with the progression of cancer. The test is approved for laboratory use in Australia and follows FDA clearance for the post treatment phase monitoring of patients with CRC. The test is a standard ELISA test can be requested for patients with CRC on regular pathology request forms by their physicians.

RPC Contact Information:
For additional information on Radient Pharmaceuticals, ADI and its portfolio of products visit the Company’s corporate website at www.Radient-Pharma.com. For Investor Relations information contact Kristine Szarkowitz at [email protected] or 1.206.310.5323.

About Radient Pharmaceuticals:
Headquartered in Tustin, California, Radient Pharmaceuticals is dedicated to saving lives and money for patients and global healthcare systems through the deployment of our Onko-Sure™ In Vitro Diagnostic cancer test. Our focus is on the discovery, development and commercialization of unique high-value diagnostic tests that help physicians answer important clinical questions related to early disease detection; treatment strategy; and the monitoring of disease progression, prognosis, and diagnosis to ultimately improve outcomes for patients. Radient Pharmaceutical’s current Onko-Sure™ cancer test is used to guide decisions regarding patient treatment, which may include decisions to refer patients to specialists, perform additional testing, or assist in the selection of therapy. To learn more about our company, people and potentially life-saving cancer test, visit www.radient-pharma.com.

Forward Looking Statements:
Safe Harbor Statement under the Private Securities Litigation Reform Act of 1995: The statements contained in this document include certain predictions and projections that may be considered forward-looking statements under securities law. These statements involve a number of important risks and uncertainties that could cause actual results to differ materially including, but not limited to, the performance of joint venture partners, as well as other economic, competitive and technological factors involving the Company’s operations, markets, services, products, and prices. With respect to Radient Pharmaceuticals Corporation, except for the historical information contained herein, the matters discussed in this document are forward-looking statements involving risks and uncertainties that could cause actual results to differ materially from those in such forward-looking statements.

RPC Contact:
Kristine Szarkowitz
Director-Investor Relations
Email Contact
Tel: 206.310.5323

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Filed Under: Facilities And Providers

Philips and Dako Join Forces in Digital Pathology

Posted on July 21, 2010 Written by Annalyn Frame

SOURCE: Dako

EINDHOVEN, THE NETHERLANDS and GLOSTRUP, DENMARK–(Marketwire – July 21, 2010) – Royal Philips Electronics (NYSE: PHG)(AEX: PHI) and Dako, a Danish company specializing in tissue-based cancer diagnostics, today announced that they have signed an agreement to integrate a selection of Dako’s image analysis applications into Philips’ future digital pathology solutions.

“Anatomic pathology is an essential element of virtually every cancer diagnosis and the demand for it is ever-increasing. Our goal is to develop integrated digital solutions that enhance the operational efficiency and productivity of pathology departments, as well as increasing diagnostic confidence,” says Bob van Gemen, General Manager of Philips Digital Pathology. “I am convinced that our partnership with Dako, with its leading market position and expert knowledge in detecting and quantifying specific biomarkers in cancer tissue, will significantly accelerate our clinical applications development program.”

“We are very pleased to announce this collaboration with Philips, a leading company in the healthcare industry that is committed to entering the digital pathology market,” says Lars Holmkvist, CEO of Dako. “By joining forces with Philips, we will be able to deliver highly competitive diagnostic tools based on Philips’ extensive clinical expertise and technology know-how and Dako’s expertise in advanced staining and image analysis in order to benefit pathology laboratories, pathologists and ultimately patients.”

Currently, anatomic pathology workflows to examine tissue samples are based on the microscope, through which pathologists examine tissue sections mounted on glass slides and treated with different stains. The staining enhances the contrast between, or reveals the presence of, cellular and molecular components such as cell nuclei or specific proteins. Accurate interpretation of the results is critical to the diagnosis and staging of each individual patient’s disease and requires a great deal of skill and experience. Digitizing the images that pathologists normally view through a microscope may enable the introduction of objective and quantitative image analysis tools.

Dr. Clive Taylor, MD, PhD, Professor at University of Southern California, USA, and a renowned expert in pathology, expresses about the collaboration: “Digital pathology has been long in gestation, in comparison to radiology, where images also are the currency of practice, and where image acquisition, transfer, interpretation and storage is almost entirely digital. In part, this lag is because acquisition of histopathology images is dependent upon a 100 year old technique of ’tissue fixation’, sectioning and staining. In part, it is because, somewhat surprisingly, fully digitized histopathology images are much larger than CT files, and difficult to manage and analyze. Progress has been slow because there has been no single institution, or company, that embraces both of these areas. It is exciting that collaborations like that between Dako and Philips are now bringing diverse but appropriate expertise to bear on implementing a full digital pathology program.”

A fast pathology slide scanner and an associated image management system form the basis of Philips’ proposed integrated solutions for digitizing pathology workflows. The Philips-Dako collaboration will initially focus on leveraging Dako’s image analysis software for tissue-based breast cancer diagnosis using its reagents for staining HER2, Estrogen Receptor (ER), Progesterone Receptor (PR), p53 and Ki-67 proteins. The detection and quantification of these proteins in biopsy tissue are highly relevant for the classification of breast cancers and the selection of appropriate therapy. Philips and Dako will also explore the possibility of extending the collaboration to include image analysis software for immunohistology-based prostate and colon cancer diagnostics.

About Royal Philips Electronics
Royal Philips Electronics of the Netherlands (NYSE: PHG)(AEX: PHI) is a diversified health and well-being company, focused on improving people’s lives through timely innovations. As a world leader in healthcare, lifestyle and lighting, Philips integrates technologies and design into people-centric solutions, based on fundamental customer insights and the brand promise of “sense and simplicity”. Headquartered in the Netherlands, Philips employs more than 116,000 employees in more than 60 countries worldwide. With sales of EUR 23 billion in 2009, the company is a market leader in cardiac care, acute care and home healthcare, energy efficient lighting solutions and new lighting applications, as well as lifestyle products for personal well-being and pleasure with strong leadership positions in flat TV, male shaving and grooming, portable entertainment and oral healthcare. News from Philips is located at www.philips.com/newscenter.

About Dako
Dako, based in Denmark, is a global leader in tissue-based cancer diagnostics. Hospital and research laboratories worldwide use Dako’s know-how, reagents, instruments and software to make precise diagnoses and determine the most effective treatment for patients suffering from cancer. Employing more than 1000 people and being present in more than 80 countries, Dako covers essentially all of the anatomic pathology markets globally. Dako is owned by a private equity fund, EQT. www.dako.com

For further information, please contact
Philips
Steve Klink
Tel.: +31 40 27 43703
Mobile: +31 6 10888824
E-mail: [email protected]

Dako
Maia Fredtoft Søchting
Tel.: +45 44859352
Mobile: +45 25461083
E-mail: [email protected]

Filed Under: Facilities And Providers

Allied Healthcare International Inc. to Host Fiscal 2010 Third Quarter Conference Call and Webcast

Posted on July 21, 2010 Written by Annalyn Frame

SOURCE: Allied Healthcare International Inc.

NEW YORK, NY–(Marketwire – July 21, 2010) –  Allied Healthcare International Inc. (NASDAQ: AHCI) (AIM: AHI) will host a conference call and webcast to discuss the financial and operating performance for its fiscal 2010 third quarter ended June 30, 2010 on Tuesday, August 3, 2010, at 10:00 AM Eastern Time / 3:00 PM UK Time. The call will be hosted by Sandy Young, Chief Executive Officer, and Paul Weston, Chief Financial Officer. The Company will issue its earnings press release prior to the call.

Dial-In Information
Allied invites all those interested in listening to management’s discussion of the results to join the call by dialing (877) 407-8031 for domestic participants and (201) 689-8031 for international participants. Participants may also access a live webcast of the conference call through the “Investors” section of Allied Healthcare’s Website: www.alliedhealthcare.com. 

A telephone replay will be available for one week following the call by dialing (877) 660-6853 for domestic participants and (201) 612-7415 for international participants. When prompted, please enter account number 286 and conference ID number 353906. A webcast replay will also be available and archived on the Company’s website for ninety days.

ABOUT ALLIED HEALTHCARE INTERNATIONAL INC.
Allied Healthcare International Inc. is a leading provider of flexible healthcare staffing services in the United Kingdom. Allied operates a community-based network of over 110 branches with the capacity to provide carers (known as home health aides in the U.S.), nurses, and specialized medical personnel to locations covering approximately 90% of the U.K. population. Allied meets the needs of private patients, community care, nursing and care homes, and hospitals. For more news and information please visit: www.alliedhealthcare.com.

CONTACT
Allied Healthcare International Inc.
Sandy Young
Chief Executive Officer
Paul Weston
Chief Financial Officer
+44 1785 810600

Or

Piper Jaffray Ltd. (Nominated Advisor)
Matthew Flower
Rupert Winckler
+44 20 3142 8700

Or

ICR Inc.
Sherry Bertner
Managing Director
+1 646 277 1200
[email protected]

Filed Under: Facilities And Providers

Breakthrough Publication (July 2010): FONAR UPRIGHT MRI Detects Injuries in Symptomatic Motor Vehicle Whiplash Patients Missed by Conventional…

Posted on July 21, 2010 Written by Annalyn Frame

SOURCE: FONAR Corporation

MELVILLE, NY–(Marketwire – July 21, 2010) –  FONAR Corporation (NASDAQ: FONR), The Inventor of MR Scanning™ announces new breakthrough results for the FONAR UPRIGHT® Multi-Position™ MRI. The medical journal “Brain Injury” (July 2010:24(7-8):988-994) has just released the exciting results of a study of 1200 neck pain patients. The study was published by 10 authors from distinguished universities in the U.S. and around the world (University of Oregon, University of Aarhus, Denmark, University of Aberdeen, Scotland, Columbia University, Portland State University) of their results from the scans of 1200 patients. Their study reported that 150% more whiplash patients (Table II – % CTE Trauma Patients) had demonstrable radiographic pathology when scanned upright than when they were scanned lying down (recumbent). Their investigation also reported that “patients with a history of motor vehicle crash-associated neck pain have a substantially higher frequency of cerebellar tonsillar ectopia (CTE)* of 1mm or more than non-traumatic subjects” when examined by the FONAR UPRIGHT® MRI. The authors were Michael D. Freeman, Scott Rosa, David Harshfield, Francis Smith, Robert Bennett, Christopher J. Centeno, Ezriel Kornel, Ake Nystrom, Dan Heffez and Sean S. Kohles.

As the authors reported, the frequency of these fallen cerebellar tonsils (CTE)* was found “4 times more often” in neck pain patients who had experienced whiplash trauma versus neck pain patients that had not experienced recent trauma, when the FONAR UPRIGHT® MRI scanner was used.

The authors further reported, “CTE (tonsil ectopia) was found 2.5 times more often in the upright trauma vs. the recumbent group” if the patients were scanned in the FONAR UPRIGHT® Multi-Position™ MRI. In sum the anatomic origin of the patient’s whiplash symptoms was successfully visualized 2.5 times more frequently when the patient was scanned upright in the FONAR UPRIGHT® Multi-Position™ MRI than when he/she was scanned lying down in the conventional recumbent-only MRI.

The upright MRI examination, therefore, now makes it possible to provide definitive radiographic evidence and image characterization of the pathology giving rise to a patient’s whiplash symptoms so that it can be medically treated. For the first time, definitive anatomic evidence of the injuries sustained by whiplash victims in a motor vehicle accident can be provided. Currently, as the authors point out, some claim that patient whiplash pain is “non-pathologic chronic pain” engendered by “psychosocial factors such as litigation.” The newly published results from the FONAR UPRIGHT® Multi-Position™ MRI establish that this is not correct.

The July 2010 published report of 1200 neck pain patients that were examined in both the recumbent position in a conventional MRI and upright in the FONAR UPRIGHT® Multi-Position™ MRI establishes a “new standard of care” for victims of automotive whiplash injuries wherein the patients’ injuries can now be anatomically visualized and specifically defined so that the most expedient medical treatment can be provided.

Overall, the pathologic anatomy responsible for the patient’s whiplash symptoms was successfully identified in 23.3% of whiplash trauma patients (Table II, Brain Injury, July 2010: 24 (7-8):998) when the patient was scanned upright in the FONAR UPRIGHT® Multi-Position™ MRI. The cause of the patient’s symptoms was identified after a whiplash injury only 9.3% of the time (Table II) when the patient was lying down in a conventional recumbent-only MRI, a difference of 2 1/2 times or 150%.

Raymond V. Damadian, M.D., president and founder of FONAR said, “it has been published(1) that there are approximately 3,000,000 REAR IMPACT(2) crash related (or CAD(3)) INJURIES(2) in the U.S. annually. Accordingly, the publication by M.D. Freeman and co-authors in the July 2010 issue of “Brain Injury” has established that of the 3,000,000 motor vehicle CAD injuries occurring annually in the U.S. 700,000 (23.3%) would exhibit cranio-cervical anatomic changes associated with their symptoms when examined upright in the FONAR UPRIGHT® Multi-Position™ MRI, while only 279,000 would have their pathology detected by a conventional lie-down MRI. At the rate of 3,000,000 CAD whiplash injuries per year, 420,000 patients each year would have the pathology responsible for their symptoms go undetected if they were examined solely in a conventional recumbent-only MRI.”

Dr. Damadian further stressed, “the sudden rise in the incidence of patients suffering from the Chiari syndrome (cerebellar tonsil ectopia) is a fairly recent occurrence that needs to be addressed by both the medical and automotive professions. As Galasko et. al. from the University of Manchester, Salford, U.K., reported regarding the change in the incidence of whiplash disorders following the 1982 enactment of seat-belt legislation in the U.K. (J. Musculoskeletal Pain, Vol 8. (1/2) pgs 15-27), the incidence of whiplash associated disorders (WAD) rose “far in excess of general road traffic accident cases,” and as they also reported, “rose at an alarming rate”.

“Consequently,” Dr. Damadian stated, “it is very important that the approximately 3,000,000 people per year in the U.S. involved in the rear end auto collisions that give rise to whiplash injuries, receive an UPRIGHT® MRI examination soon after the accident. This will assure that a cerebellar tonsil ectopia has not resulted from the accident so that they can be protected going forward, and protected before they become symptomatic. If found to have CTE, they can then be warned by their physicians to exercise especial caution whenever driving and to have devices like the head restraint impact suppressor cushions installed (add On Head Rest, www.addonheadrest.com) to prevent the whiplash reaction from occurring again in the event of a collision. 

“A real concern,” added Dr. Damadian, ” is that a subsequent auto-accident for a patient who had developed tonsil ectopia from a prior auto accident, but did not develop symptoms from the ectopia, can subsequently develop symptoms from even a MINOR subsequent accident. Wan, et. al. (Wan, M. J., Nomura, H., Tator, C. H. Neurosurg. 2008; 63: 748-753.), described a symptomatic “conversion” of previously asymptomatic Chiari Type 1 following MINOR(2) head and neck trauma” (Freeman, M. D. et. al. Brain Injury, July 2010: 24 (7-8):989.

Considering that long term studies have shown that some patients suffered frequent residual symptoms 17 years after the accident, mostly comprising neck pain, radiating pain and headaches, (Eur. Spine J. 2002; 11:227-34), this publication in “Brain Injury” clearly demonstrates the need and the superiority of the FONAR UPRIGHT® Multi-Position™ MRI for imaging patients involved in motor vehicle crashes that sustain whiplash injuries.

* Cerebellar tonsillar ectopia (CTE) constitutes downward displacement of the cerebellum of the brain into the opening in the bottom of the skull, the foramen magnum, through which the spinal cord exits the skull. The downward displacement can result in compression of the medulla of the brain, fourth ventricle and cerebellar vermis, giving rise to neck pain, chronic recurrent occipital headaches, upper extremity weakness and “drop attacks”. While afflicting a low percentage of Chiari 1 patients, such patients can be subject to instantaneous unpredictable losses of consciousness known as “drop attacks” in which the standing patient, without warning, suddenly collapses to the floor.

(1) Foreman, S. M., Croft, A. C. (eds) third edition. Whiplash injuries: The cervical acceleration/deceleration syndrome. Baltimore: Lippincott, Williams & Wilkins, 2001, Pg. 359.

(2) Capitalization added.

(3) Cervical Acceleration/Deceleration syndrome aka “whiplash”.

To obtain a copy of the article published in the peer-reviewed journal, “Brain Injury,” please contact FONAR at 631-694-2929×451 or by email at [email protected]. You may also use a search engine such as Google and search for the journal article entitled “A case-control study of cerebellar tonsillar ectopia (Chiari) and head/neck trauma (whiplash).

For investor and other information visit: www.fonar.com.

UPRIGHT® and STAND-UP® are registered trademarks and The Inventor of MR Scanning™, Full Range of Motion™, pMRI™, Dynamic™, Multi-Position™, True Flow™, The Proof is in the Picture™, Spondylography™ Spondylometry™ and Upright Radiology™ are trademarks of FONAR Corporation.

This release may include forward-looking statements from the company that may or may not materialize. Additional information on factors that could potentially affect the company’s financial results may be found in the company’s filings with the Securities and Exchange Commission.

Filed Under: Facilities And Providers

This Week on ORLive: Live Thoracoscopic Maze Procedure to Cure Atrial Fibrillation

Posted on July 20, 2010 Written by Annalyn Frame

SOURCE: OR-Live, Inc.

New On-Demand and Live Surgery Video for the Week of July 19, 2010

WEST HARTFORD, CT–(Marketwire – July 20, 2010) –  ORLive, the vision of improving health, presents a live thoracoscopic maze procedure to cure atrial fibrillation from PinnacleHealth. In addition to this live procedure, ORLive invites you to take part in the latest installment of the Virtual Brain Tumor Board, and to watch and learn from this month’s featured channel of no-visible-scar surgeries.

NEW ON ORLIVE

LIVE SURGERY VIDEO – Total Thoracoscopic Maze
Live Wednesday July 21, 2010, 7:00 PM EDT

The total thoracoscopic maze is a surgical procedure intended to permanently cure atrial fibrillation. This minimally invasive, beating heart procedure will be performed by Dr. Mubashir Mumtaz, Chief of Cardiothoracic Surgery at PinnacleHealth. 

Viewers are invited to interact with the surgical team by submitting questions via the ORLive website. To learn more about this broadcast and to sign up for an e-mail reminder go to ORLive.com.

ORLIVE REFERRALS – Week of July 19, 2010
Each week ORLive highlights on-demand videos for our membership and visitors. 

No Visible Scar Surgery Referral: Laparo-Endoscopic Single-Site (LESS) Procedure from Tampa General Hospital

CME Referral: Minimally Invasive Endoscopic Pituitary Surgery from Thomas Jefferson University Hospital

Viewer’s Referral: Whipple Procedure for Pancreatic Cancer from University of Maryland Medical Center

HIGHLIGHTS

NOW ON-DEMAND – The Anterior Supine Approach to Total Hip Arthroplasty
Now Available On-Demand

ORLive and Zimmer present a Total Hip Arthroplasty featuring the Continuum Acetabular System and the Fitmore Hip Stem. The surgery was originally presented live and was performed by Dr. Jonathan Yerasimides, University of Louisville Department of Orthopaedics, Louisville, KY and is moderated by Dr. Hari Bezwada, University of Pennsylvania School of Medicine Department of Orthopaedic Surgery, Philadelphia, PA. This video presents the entire surgical procedure, and provides an opportunity for firsthand insight of the safe and effective implantation and surgical procedure involved with the Continuum Acetabular System and the Fitmore Hip Stem.

This surgery video is available to members of the ORLive community, and members are still able to interact and ask questions via the ORLive website. Learn more about this broadcast at ORLive.com, and be ready to view this exciting procedure by activating your free membership to ORLive today.

PREVIEW – Prenatal Pediatrics
Premieres Tuesday, July 27, 12 PM EDT

Managing a high risk pregnancy can be difficult. NewYork-Presbyterian Morgan Stanley Children’s Hospital provides the maternal, fetal and pediatric expertise to care for high-risk pregnancies. NewYork-Presbyterian Morgan Stanley Children’s Hospital was one of only eight hospitals in the country ranked in each medical specialty measured by U.S. News & World Report, with distinct leadership in neonatology and pediatric cardiac surgery.

Watch the best in Prenatal Pediatrics July 27th at Noon.

Viewers of this video are invited to interact with the team via the ORLive website, and to join the community and receive regular updates from the NewYork-Presbyterian Morgan Stanley Children’s Hospital Center for Neonatal Pediatrics.

SUPPLEMENTAL CONTENT – VOX ORLive
Explore robotic assisted mitral valve surgery with cardiac surgeon Dr. Lynn Seto in the current episode of VOX ORLive, an audio podcast featuring the latest advancements in medicine, surgery, and medical technology.

About ORLive
ORLive is the leading provider of video communication channels to the healthcare community. Working collaboratively with hospitals and device manufacturers, ORLive produces and distributes customized, interactive, video programs that demonstrate the latest advances in medicine, surgical techniques and product innovations. The ORLive broadcasting network provides an intimate look at over 650 live and on-demand surgeries to a global audience, streaming over 50,000 hours of programming each month. The ORLive network can be found on-line at www.ORLive.com.

Contact:

Bonnie Gergely
Communications Manager
(860) 953-2900
Email Contact

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Filed Under: Medical And Healthcare

Nation’s Most Influential Eating Disorders Professionals Gather in Denver to Collaborate on Innovative Treatment Strategies

Posted on July 20, 2010 Written by Annalyn Frame

SOURCE: Eating Recovery Center

Treating Eating Disorders in Adolescents and Men Are Among Topics to Be Addressed at Rocky Mountain Eating Disorders Conference, August 13-14

DENVER, CO–(Marketwire – July 20, 2010) – Though statistics vary, most clinicians and dietitians agree — eating disorders are on the rise. To address this growing epidemic and discuss innovative treatment strategies, leading eating disorders professionals will gather in Denver August 13-14, 2010, at the 2nd Annual Rocky Mountain Eating Disorders Conference. 

Held at the Denver Marriott City Center in Denver, Colo., the conference is hosted by Eating Recovery Center, a national center for eating disorders recovery providing comprehensive treatment for anorexia and bulimia. CEUs are now available for several disciplines.

For the second consecutive year, the conference will focus on new treatment trends for anorexia nervosa, bulimia nervosa and EDNOS; as well as innovative strategies for addressing the complexities of these disorders. 

“Collaboration within the eating disorders community ultimately leads to better outcomes for our patients,” said Kenneth L. Weiner, MD, CEDS, founding partner and medical director of Eating Recovery Center. “At the Rocky Mountain Eating Disorders Conference, individuals have the opportunity to learn best practices and treatment innovations from some of the leading minds in the field.”

Here is a brief sampling of sessions and speakers:

  • Key Ingredients for Creating a Center of Excellence: A Primer for Building a Successful Program, Kenneth L. Weiner, MD, CEDS
  • Escaping the Wilderness: Recovery from Anorexia, Emmett R. Bishop, Jr., MD, CEDS
  • Medical Complications of Anorexia Nervosa and Bulimia, Philip Mehler, MD, FACP, CEDS
  • The Willing and Able: Understanding the Adolescent Brain in the Treatment of Eating Disorders, Ovidio Bermudez, MD, FAAP, FSAM, FAED, CEDS
  • New Models of Family Therapy in the Treatment of Eating Disorders, Craig Johnson, PhD, FAED, CEDS
  • The Mindful Therapist, Carolyn Costin, MA, Med, MFT, CEDS

Registration is $150 and includes all sessions, dinner on Friday night, continental breakfast and lunch on Saturday, as well as refreshment breaks. Single-day registration is $75. Student-discounted registration is $100 and $50 for single-day attendance. Space is limited and registration prior to the event is recommended.

For more information or to register for the 2nd Annual Rocky Mountain Eating Disorders Conference, visit Eating Recovery Center’s website or call 877-218-1344.

About Eating Recovery Center
Eating Recovery Center is a national center for eating disorders recovery, providing comprehensive treatment for anorexia and bulimia at the foot of the Rockies in beautiful Denver, Colorado. Facilities include a licensed behavioral hospital treating adults, an outpatient office, and an adolescent facility scheduled to open in November 2010. Our integrated program offers patients from across the country a continuum of care that includes inpatient, residential, partial hospitalization, intensive outpatient and outpatient services. Our compassionate team of professionals collaborates with treating professionals and loved ones to cultivate lasting behavioral change. For more information please contact us at 877-218-1344 or [email protected] or confidentially chat live on our website at www.EatingRecoveryCenter.com.

Contact:
Shannon Fern
CSG|PR
303-433-7020
Email Contact

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Filed Under: Medical And Healthcare

Medical Tourism Association Announces Strategic Initiatives for Much Awaiting Global Healthcare & Medical Tourism Congress 2010

Posted on July 20, 2010 Written by Annalyn Frame

LOS ANGELES, CALIFORNIA–(Marketwire – July 20, 2010) – The Medical Tourism Association, known for setting trends in the industry, announces new strategic initiatives under the theme progress in motion for global healthcare stakeholders, allowing them to discover & learn about intense topics of medical tourism, extending networking opportunities enhanced by dedicated sessions and creating knowledge sharing possibilities between government, insurance, healthcare and tourism professionals during THE World Medical Tourism & Global Healthcare Congress, taking place in LA from September 22nd – 24th. http://www.medicaltourismcongress.com.

“We recently announced our extensive agenda, today we are announcing the list of incredible speakers, coming exclusively with the sole purpose of providing a learning platform for industry stakeholders. We are particularly encouraged at the number of high level government officials who are attending the ministerial summit which indicates growing support from all sectors for medical tourism initiatives, especially ministers of health, tourism and economic development,” said Jonathan Edelheit, CEO of the Medical Tourism Association.

MTA team worked relentlessly this year to identify and invite top government officials from across the world, eminent professionals from US & International Insurance Companies, alongside some of the largest US and International Employers, on another hand, leading medical tourism experts and top global healthcare providers are revisiting the congress.

“Though we have received tremendous responses, we are receptive to have more top-notch experts and professionals to utilize the platform to share their knowledge, experience and expertise,” added Edelheit, inviting leading speakers to join congress by submitting white papers at http://www.medicaltourismcongress.com/en/speakers.html .

The congress is the biggest networking opportunity platform in the world for medical tourism and global healthcare related affairs. The addition of the “Buyers of Healthcare VIP Program” is also a unique feature which was added to create more interesting and one on one business meetings for all delegates and sponsors, bringing up to 200 employers, insurance companies, agents and medical tourism facilitators who are involved in or interested in patients traveling across borders for healthcare. 

“Networking is the spirit of our congress. We realize that social media and electronic channels can’t replace one-on-one meetings. Last year we got incredible responses and many delegates mentioned networking alone provided ROI, while learning & sharing experience was nothing but overwhelmingly a delightful experience,” says senior meeting manager Silvana Maldonado, working exclusively for networking and meeting sessions.

While extensive agenda, green healthcare initiative, learning opportunities, networking possibilities and knowledge sharing are base of the congress, seasoned speakers are the main focus which makes this a comprehensive Medical Tourism Mecca gathering.

  • Karen Beyer – Director of Global Benefits, General Electric

  • Mr. Jose M. Loaiza – Senior Network Manager, Blue Shield of California

  • Premier W. McKeeva Bush – Premier, Cayman Islands

  • Joanne Armenio – Director, International Benefits, Kraft Foods

  • Bob Ihrie – Senior VP of Employee Rewards and Services, Lowe’s Companies, Inc.

  • Luis Fernando Moreas – Secretary of Tourism, Porto Alegre Brazil

  • Kathy Clark – Compensation & Benefits Analyst, Blackbaud, Inc.

  • Anthony Amato – VP Compensation & Benefits, Discovery Communications

  • Kevin M. Fickenscher, M.D., CPE, FACPE, FAAFP – Chief Strategy and Development Officer, Dell Services

  • H. E. Mr. Nasser Al Budoor – Director, Ministry of Health, UAE, International Relations & Health Affairs and Director of Health Minister’s Office

  • Cheryl Matheis – Senior Vice President for Health Strategy, AARP

  • Laila Al Jassmi – CEO, Clinical Support Services Sector, Dubai Health Authority

  • David M. Cheek – Vice President of Sales, Pan American Life Insurance Group

  • Dr. Shetty – Heart Surgeon of India & Founder of Hospital Investment Project, Cayman Islands

  • Michael Bertaut – Senior Healthcare Intelligence Analyst, Blue Cross and Blue Shield of Louisiana

  • Jeff A. Argotsinger – Director, Business Leader Medical Expense Group, Swiss Reinsurance Company

  • Dr. Hisham Diwani – General Manager, Health Insurance, Ministry of Health Syria

  • Bavdeep Singh – CEO, Fortis Healthcare India

  • Emilio M. Williams – Managing Director, Johns Hopkins Medicine International

  • Dr. Rick van Pelt – Director Global Programs, Partners Harvard Medical International

  • Mark Scotland – Minister of Health, Cayman Islands

  • Jonathan Hart – Chief Medical Officer, International Medical Group

  • Pamela Frank – International Health Services Coordinator, Children’s Hospital of Boston

  • Fred Hagigi – Director, Executive Education Programs Professor of Health Services, UCLA School of Public Health

  • MaryBeth Kramer – Sr. Manager, Global Benefits and HR Services Compensation and Benefits, Verisign

  • Shady Fawzy Nawar – Assistant Vice President – Provider Management, Qatar Insurance Company-Doha

  • Arthur L. Diskin, MD, FACEP – Vice President and Global Chief Medical Officer, Royal Caribbean, Celebrity and Azamara Club Cruises

  • Martha Turnbull – Travel Health Insurance Association of Canada

  • Linda Cote – AGB Sales Director Pacific Region, Aetna

  • Dr. Jeannette Takemura – Dean of School of Social Work, Columbia University

  • Alexander Sander Domaszewicz – Principal and Senior Consultant, Mercer Health & Benefits Services

  • Robert S. Shestack – WBC, Managing Director, National Sales Leader, Employer Benefits Business, Marsh U.S. Consumer, a service of Seabury & Smith, Inc.

  • Brad Cook – International Patient Department, Hospital Clinica Biblica, Costa Rica

  • Renee-Marie Stephano – President, Medical Tourism Association

  • Jonathan Edelheit – CEO, Medical Tourism Association

  • Ralph Lawson – Executive Vice President and Chief Financial Officer
    Baptist Health South Florida

  • Greg Carlson – Assistant Professor, University of Alabama, Department of Health Services

  • Jason B. Krouse – Executive Vice President, Univers Workplace Benefits

  • William Cook – International Patient Department, Hospital Clinica Biblica

  • Dr. Prem Jagyasi – MD & CEO, ExHealth Dubai

  • Tom O’Hara – President, Surgical Trip LLC

  • Dr. Antonia Arnaert –Vice-President, Debson Medical Tourism

  • Dr. Narottam Puri – President, Medical Strategy & Quality, Fortis Healthcare

  • Wouter Hoeberechts – CEO, WorldMed Assist

  • Doug Wojcieszak, Founder, Sorry Works!

  • Richard Polak, President & CEO, IBIS Advisors

  • Derrell Connor, Account Executive, M3 Insurance Solutions for Business (M3)

  • Tom Hamilton – President, Carolina Benefit Designs

  • Daniel Friedland – MD, Founder & CEO, SuperSmartHealth

  • Jason Woods – Fairmont Specialty Group

  • Sonia Roschnik – Operational Director, NHS Sustainable Development Unit, UK

  • C. Duane Dauner – President, California Hospital Association

  • Stephen Hartigan – Chief Executive Officer, InterGlobal Insurance Company Ltd. (IGIC)

  • Peter Lozier – Executive Vice President Sales, Marketing and Provider Relations, CMN Inc.

  • Dr. Myles Druckman – Vice President Medical Services, Americas Region
    International SOS Assistance, Inc

  • Dean Stone – Manager Workers Compensation and Governance, National Australian Bank

  • Stuart Rowley – CEO, Prince Court Medical Center, Malaysia

To view a full list of speakers please CLICK HERE or go to http://medicaltourismcongress.com/en/speakers.html.

Join us for the VIP After Party

The World Medical Tourism & Global Healthcare Congress is also known for its networking cocktail receptions following the general sessions. On Wednesday, September 22, 2010 all registered delegates will be invited to share in an entertainment filled networking session jointly held with the Employer Healthcare Congress where up to 1000 employers, insurance agents, brokers, consulting firms and healthcare leaders will finishing up their three day congress event on the Green Circle Terrace. For more information about the VIP After Party, please go see the video at http://www.medicaltourismcongress.com/en/vip-party.html .

Additional Giant Leaps for 2010

The World Medical Tourism and Global Healthcare Congress includes two additional conferences which are the Expatriate Healthcare, Travel Insurance and Global Health Insurance Conference, http://www.expatriateconference.com and the Sustainable Healthcare and Hospital Development Conference, http://www.healthcaredevelopmentconference.com . Speakers listed above are from all three conferences.

The Medical Tourism Association™ (Global Healthcare Association) is the international non-profit trade association for the medical tourism and global healthcare industry made up of the top international hospitals, healthcare providers, medical travel facilitators, insurance companies, and other affiliated companies and members with the common goal of promoting the highest level of quality of healthcare to patients in a global environment. http://www.medicaltourismassociation.com. 

Marketing & PR by ExHealth / www.ExHealth.com

Filed Under: Medical And Healthcare

APHL Assists Haiti to Rebuild Devastated Lab System

Posted on July 20, 2010 Written by Annalyn Frame

SOURCE: Association of Public Health Laboratories

SILVER SPRING, MD–(Marketwire – July 20, 2010) – A critically needed modular laboratory facility is en route to Port-au-Prince thanks to a collaboration between the Association of Public Health Laboratories (APHL) and International Relief Solutions, LLC (IRS). The APHL Haiti Field Laboratory Support Team provided technical assistance to International Relief Solutions, LLC (IRS) in planning and design of the new laboratory, which will replace the temporary tent facility that has served the nation’s largest hospital since the January earthquake. 

The 24′ by 36′ modular laboratory will be erected at L’Hôpital de l’Université d’État d’Haïti (HUEH). Since the earthquake, the number of patients being treated at HUEH has tripled from 14,000 per month to almost 42,000 thus increasing demands for laboratory testing. Due to extremely high temperatures and no air conditioning in the tent, automated testing requiring cooler temperatures, such as hematology and blood chemistry, are being run manually. The result is that the current testing capacity is only 25% of the daily demand. The modular lab facility is designed with infrastructure for work benches, heating, ventilation, plumbing and electrical services. With direct hookup to electrical and water supplies, the laboratory building will have the air conditioning necessary to meet the requirements of the many intricate and delicate tests that the laboratory technicians on scene perform routinely. The lab will arrive with the electrical system and plumbing pre-installed allowing for a quick start-to-finish set up of approximately four days.

APHL Senior Technical Consultant and Team Leader for the APHL Haiti Field Laboratory Support Team, Dave Doherty, coordinated this effort from start to finish. Following the earthquake, the Centers for Disease Control and Prevention requested and authorized Doherty and his team to assist all of the public health network laboratories in Haiti in getting testing services back up and running to support the enormous demands for medical care and treatment. 

Better lab facilities will improve testing services and also enable laboratory technologists to get back to work. According to Doherty, “Many well-trained technologists in Haiti are unable to work and provide testing services because of the loss of laboratory facilities to earthquake damage.”

It could be years before the permanent structures are rebuilt; the new modular lab serves as a long term solution. This initiative was a success due to the collaboration of willing and committed partners, each of whom brought essential resources and expertise to assure an effective solution for meeting a critical need in Haiti. Lives will be saved and illnesses treated effectively because of the efforts of APHL, IRS and CDC. Doherty modestly explains, “We were able to come through. APHL has always come through in Haiti.”

The Association of Public Health Laboratories is a national non-profit located in Silver Spring, MD, that is dedicated to working with members to strengthen governmental laboratories with a public health mandate. By promoting effective programs and public policy, APHL strives to provide public health laboratories with the resources and infrastructure needed to protect the health of US residents and to prevent and control disease globally.

Contact:
Michelle M. Forman
240.485.2793
Email Contact

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Filed Under: Medical And Healthcare

Amazing Charts Emerges as EHR of Choice for Small Practices

Posted on July 20, 2010 Written by Annalyn Frame

SOURCE: Amazing Charts

Used by 3,600+ Practices and Growing by 70+ Practices Monthly

SAUNDERSTOWN, RI–(Marketwire – July 20, 2010) – For the small practice healthcare provider, selecting an Electronic Health Record (EHR) system can be a daunting task, with more than 300 vendors, complicated pricing, and products that are impossible to evaluate for usability, effectiveness, and implementation times. Oftentimes this leads to buyer’s remorse and later switching to another EHR.

Due to its industry-leading user satisfaction ratings in multiple studies, $995 price tag, and three month risk-free trial offer, Amazing Charts has quickly emerged as the EHR-of-choice for small practices.

Founded and designed by physician Jonathan Bertman, MD, FAAFP, specifically for offices with three or fewer providers, Amazing Charts enables rapid documentation of patient encounters, with fewer errors, faster coding, and ePrescribing. In most cases, no training is required for first-time users. Amazing Charts is a CCHIT Certified® 2008 Ambulatory EHR additionally certified for Child Health.

Gordon Comstock, MD, practices family and geriatric medicine in Arcade, New York, a low-income area of the state. His medical practice has over 3,000 patients, many of who are elderly and on fixed incomes.

At his former practice, Dr. Comstock saw his colleagues “spend nearly $280,000 on an EHR system they found to be unwieldy and difficult to use.” He notes that there were way too many little pull-down menus and data fields, forcing him to “dictate notes anyway because [he] couldn’t document notes during a visit.” Additionally, the practice had to hire a full-time person just to scan paper documents like referral letters and lab reports into the EHR.

Today he uses Amazing Charts to run his entire office.

Says Dr. Comstock, “Amazing Charts is the closest an EHR can get to how a family doctor likes to generate a note. Many of the referral letters I see from specialists are indecipherable because they are generated by EHRs that don’t communicate what the specialist actually saw and thought. Amazing Charts always allows me to express myself in a way that captures not only the data points, but also the subjective narrative of my thoughts and observations.”

Another practice, Community Medical Group in Downey, California, had a different set of problems. After decades in operation, the three physician practice had amassed over 7,200 patients and their charts had become a significant obstacle to keeping the office running.

According to Dr. Martin Sechrist, “specific charts were hard to track down, the filing backlog was lengthy, and it was often difficult to match charts with filings.” 

With Amazing Charts, every patient has an electronic health record that can be accessed from any computer in the office, remotely, or via a simple iPhone app.

Says Dr. Sechrist, “Amazing Charts mirrors the way we conduct patient encounters, and makes immediately available all patient demographics, imported items, and a patient summary of current issues, medications, and prior encounters. Even outside laboratory results are imported directly into the electronic medical record!”

Amazing Charts automatically generates an electronic “super-bill” whenever a note is signed, and records are backed up daily in a secured database on-site.

Amazing Charts V5 can be downloaded for a free, three-month trial at http://www.amazingcharts.com.

About Amazing Charts
AmazingCharts.com provides Electronic Health Record (EMR) software and services to small and medium sized healthcare practices. Used by more than 3,600 practices in the U.S., Amazing Charts has been growing by over 70 new practices each month, based on its high ratings for quality, price, support, ease of use, and impact on productivity. For more information visit www.amazingcharts.com or call 1-866-382-5932.

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Filed Under: Medical And Healthcare

Pregnancy and Pre-Existing Diabetes

Posted on July 20, 2010 Written by Annalyn Frame

SOURCE: American Diabetes Association

Diabetes Forecast With Information for Mothers-to-Be

ALEXANDRIA, VA–(Marketwire – July 20, 2010) – Pregnancy is a time of wonder and amazement — and for women with pre-existing diabetes, it is also a time for very extremely careful (and sometimes baffling) disease management. How do you plan for this? What risks are involved? What can you expect? The August issue of Diabetes Forecast, the consumer magazine of the American Diabetes Association, features articles about pregnancy with pre-existing diabetes to help you. With good care and planning, says Diabetes Forecast, women with either type 1 or type 2 diabetes can have safe pregnancies — and healthy babies.

Planning starts now. If you have diabetes and want to become pregnant, the first step should be visiting your doctor — or several doctors. Depending on your diabetes management, you may want to see an endocrinologist in addition to your ob-gyn for a pre-conception visit. When choosing your doctors, keep in mind that you may have appointments as often as twice a week, so try to find a physician that you are comfortable with and whose office you are comfortable getting to.

While pre-existing diabetes automatically puts your pregnancy in the high-risk category, healthy habits can lower the chance of problems for both mother and child. First and foremost, keep your blood glucose in check — in general, your A1C should be below 7 percent before you conceive. Your health care team may also want to discuss your weight, use of prenatal vitamins and other supplements, the status of any diabetes-related complications, and your current medications (such as ACE inhibitors or statins, which are not considered safe for use in pregnancy). Polycystic ovary syndrome is associated with type 2 diabetes, so for some women with diabetes, asking about fertility treatments may also be in order.

Once you become pregnant, your body’s changes can make blood glucose levels go from one extreme to the other. “I spent the entire first trimester with my face buried in the fridge,” says Kerri Sparling, 31, who has type 1 diabetes and whose daughter was born in April. “I was low all the time. It wasn’t until probably the second trimester that the insulin resistance kicked in. Everything I ate, the insulin didn’t cover it.” As your body changes through your pregnancy, so will its reactions to the elements you normally use to manage your blood glucose, so be prepared to communicate with your health care team often and make any necessary adjustments.

From pre-conception planning to integrating diabetes management into your birth plan and facing post-partum depression, having a baby can seem like an overwhelming task for women with diabetes, and yet, many women with diabetes find they have the best glucose control of their life during pregnancy. “This was so, so important to me that I was willing to do whatever to make sure she came out right,” says Sparling. “It’s so worth it.” Find more advice, explanations and insight about what to expect in the August issue of Diabetes Forecast.

This issue of Diabetes Forecast also features:

  • A Birthday Challenge: Marking 40 years with 40 races for ADA’s Team Diabetes
  • Drinking Calories: How you hydrate yourself makes a difference
  • A Serious Subject: Dealing with erectile dysfunction

Diabetes Forecast has been America’s leading diabetes magazine for more than 60 years, offering the latest news on diabetes research and treatment to provide information, inspiration and support to people with diabetes. 

The American Diabetes Association is leading the fight to stop diabetes and its deadly consequences and fighting for those affected by diabetes. The Association funds research to prevent, cure, and manage diabetes; delivers services to hundreds of communities; provides objective and credible information; and gives voice to those denied their rights because of diabetes. Founded in 1940, its mission is to prevent and cure diabetes and to improve the lives of all people affected by diabetes. For more information, please call the American Diabetes Association at 1-800-DIABETES (1-800-342-2383) or visit www.diabetes.org. Information from both these sources is available in English and Spanish.

Contact:
Dayle Kern
[email protected]
(703)549-1500 x2290

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Filed Under: Medical And Healthcare

Patient Channel and Newborn Channel Further Expand Ad Sales Team With Addition of Pharmaceutical Ad Sales Pro, Dammand Cherry

Posted on July 20, 2010 Written by Annalyn Frame

SOURCE: Interactivation Health Networks

Formerly With USA Weekend Magazine, Dammand Cherry Joins Interactivation Health Networks as Account Executive, Ad Sales

NEW YORK, NY–(Marketwire – July 20, 2010) –  Interactivation Health Networks, parent company of the Newborn Channel and Patient Channel, the nation’s most comprehensive in-hospital TV networks, today announced that Dammand Cherry will serve as Account Executive, Ad Sales, for both channels.

Dammand’s extensive experience in pharmaceutical media sales and agency management will provide advertisers with an additional point of contact intimately familiar with the pharmaceutical industry’s advertising needs and expectations.

“The pharmaceutical industry has always been an important partner for the Patient and Newborn Channel,” said Suzanne Fleming, SVP of Sales at Interactivation Health Networks. “Dammand’s experience in the health media space shows our continued commitment to personally cater to this industry, making it even easier for them to achieve a focused and effective out-of-home advertising campaign. We are thrilled to have him on-board as demand for both networks continues to grow.”

Newborn Channel and Patient Channel provide marketers with unparalleled access to their target consumers in a highly trusted environment. 

About Interactivation Health Networks
The Patient Channel and The Newborn Channel are the most comprehensive in-hospital TV networks. Delivered directly to patient rooms and waiting areas, the Channels provide viewers with original, award-winning health programs and advertisers with the unique ability to integrate brand messaging with content that is compelling and endorsed by healthcare professionals. The Newborn Channel broadcasts baby care and postpartum programming for new parents, reaching 60% of new moms. The Patient Channel features both condition-specific and preventative health programming to empower and inform patients. The channels are currently available in over 2,700 hospitals nationwide. For more information, visit http://interactivation.com/news/index.php/interactivation-health-networks/.

Media Contact Information:
For more information or to speak with an executive of the company, please contact:

Wendy Simmons or Josh Kail
Vendeloo
Ph: 718.522.9873
E-mail: Email Contact or Email Contact

Filed Under: Medical And Healthcare

Seegene’s New Magicplex(TM) Sepsis Test Indentifies Over 90 Indicators for Deadly In-Hospital Disease

Posted on July 20, 2010 Written by Annalyn Frame

SOURCE: Seegene

Multiplex Real-Time PCR Test Simultaneously Screens for Gram (+), Gram (-), Fungi and Antibiotic Resistant Genes to Deliver Highly Accurate Results Within Three Hours

ROCKVILLE, MD and SEOUL, KOREA–(Marketwire – July 20, 2010) – Seegene today announced the availability of Magicplex™ Sepsis, a new multi-pathogen screening test capable of quick and accurate identification of over 90 leading sepsis-causing pathogens. Magicplex Sepsis provides a novel and fast-acting diagnostic technique for hospitals to simultaneously verify a complex range of targets that indicate sepsis, the leading cause of death in non-coronary intensive care units worldwide. Seegene’s Magicplex Sepsis will be introduced at the 2010 Annual Meeting and Clinical Lab Expo of the American Association for Clinical Chemistry (AACC), booth # 1800.

Sepsis is a deadly disease that leaves no clear track back to initial indications, which could include gram-positive bacteria, gram-negative bacteria or fungi. The results are devastating: the annual incidence rate of sepsis has increased 91.3 percent over the last 10 years, and every hour 25 people in the United States die from severe sepsis. One of every three patients who develop severe sepsis will die within a month. Severe sepsis, the leading cause of death in the non-coronary intensive care unit, takes more lives than breast, colorectal, pancreatic, and prostate cancers combined.

The medical challenge to be overcome is to determine the correct treatment of sepsis within the first hours of the onset of the disease. Currently physicians and clinicians have little option but to run several available molecular diagnostic tests that offer little confidence that the results will definitely identify the presence of sepsis in a patient. The alternative to these relatively quick tests is a multiple-phase blood culture test, which is a time-consuming process, or current multiplex PCR with limited range of pathogen targets and poor test specificity. 

Seegene’s Magicplex Sepsis Test is a sharp break from this mold. Magicplex Sepsis is a real-time detection test that quickly and comprehensively determines the levels of suspected targets in a patient’s blood sample, and identifies drug resistant genes to better inform a diagnosis. The speed, accuracy and price of the Magicplex Sepsis Test will enable doctors and clinicians to quickly provide an appropriate treatment to head off the deadly disease.

The Magicplex Sepsis Test simultaneously screens for over 90 sepsis-causing pathogens: over 70 Gram (+) (30 Staphylococcus, 40 Streptococcus, 3 Enterococcus); 12 Gram (-); 6 Fungi; and 3 antibiotic resistant genes (mecA, vanA, vanB) can also be discriminated. The Magicplex Sepsis Test requires less than 1ml of patient’s whole blood and provides test results within three hours (after extraction). The test’s unique performance is a function of separate screening and identification steps. For example, when screening for over 90 sepsis-causing pathogens, the identification of exact pathogens can be carried out without starting from blood collection. 30 different pathogens are organized in different panels for identification and it only takes 40 minutes to detect.

“The Magicplex Sepsis Test will be the new gold standard for performing accurate, rapid and cost-effective sepsis diagnosis,” said Jong-Yoon Chun, chief executive officer of Seegene. “In treating sepsis, time and accuracy are demanded. Every hour of delay in giving patients the correct antibiotics results in an 8% increase in the mortality rate.”

“For doctors and clinicians performing faster diagnosis than by blood culture is a dream come true. By enabling doctors to make accurate diagnosis faster, Magicplex Sepsis can lead to improved patient outcomes in health care settings worldwide,” said Hong-Soo Kim, MD, Department of Internal Medicine, Institute of Gastroenterology, Soonchunhyang University College of Medicine, Korea.

Magicplex tests are based on Seegene’s proprietary READ™ technology, which combines the advantages of multiplex in a real-time system. The result is a molecular diagnostic testing system that provides higher specificity and sensitivity over currently available PCR systems.

The READ technology of Magicplex tests is a departure from probe- and primer-based PCR methods to produce false-free detection. Magicplex test works in a simple two-step process: first specifically amplifying the DNA sequence of target pathogens, then simply reading those signals using any real-time PCR instrument.

Magicplex Sepsis Test will not be available in the USA until regulatory clearance.

About Seegene

Seegene, Inc. is the leading biotechnology company developing, manufacturing and marketing innovative molecular diagnostic products. The company’s proprietary technologies in both PCR and Real-time PCR named ACP™, DPO™, and READ™, set a new solution for high-throughput and simultaneous multi-pathogen detection called “multiplex PCR.” The novel Real-time PCR technology, READ™, overcomes the limitations of conventional Real-time PCR, providing dramatic improvement in sensitivity and specificity. Seegene holds three novel Molecular diagnostic platforms: Seeplex®  system adapting DPO™ Technology, Anyplex™ and Magicplex™ systems that are Real-time PCR detection platforms adapting DPO™ and READ™ technologies. Seegene’s products detect multi-pathogens with great reliability and throughput, ultimately providing the most economical basis for saving time, labor and cost. Seegene’s mission is to maintain leadership in molecular diagnostics for infectious diseases, genetics, pharmacogenetics, and oncology using the innovative proprietary technologies.

For more information please visit www.seegene.com or call +301-762-9066.

Contacts:
Miyoun Lee, MSc
Seegene Inc.
301-762-9066
or
Constantine Theodoropulos
Base Pair Communications
617-816-4637

Filed Under: Medical And Healthcare

American Health Expands Disease Management Offering by Targeting High-Risk Population and Addressing Chronic Pain

Posted on July 20, 2010 Written by Annalyn Frame

SOURCE: American Health Holding, Inc.

WORTHINGTON, OH–(Marketwire – July 20, 2010) –  American Health Holding, Inc., a multi-URAC accredited medical management service provider, today announced the expansion of its Disease Management (DM) program to provide more program options to help clients contain costs while assisting individuals managing a chronic condition.

“We heard our customers’ request for a DM program that addresses those most in need of health management intervention,” states Paul Lavin, American Health’s President. “We felt our new High Risk Disease Management program was a solution. While American Health’s Comprehensive DM program targets approximately 20% of a client’s population, the new High-Risk program reaches the 5.5% who are at the highest risk for incurring large health care claims.”

In March 2009, American Health launched its new Population Health Management (PHM) program. Comprised of both DM and Lifestyle/Wellness components, PHM takes aim at helping benefit providers address rapidly rising health care costs while assisting individuals in achieving optimal health. At the start of the program, DM addressed seven chronic conditions for which evidence-based guidelines are established to impact health and measure improvement: asthma, chronic obstructive pulmonary disease, congestive heart failure, coronary artery disease, diabetes, hyperlipidemia, and hypertension.

“In addition to introducing our high-risk program, we have added chronic pain as the eighth condition that we manage,” notes Anne Klie, Director of Product Development and Marketing. “We recognized that by using our proven behavioral assessment and modification tools we can make a difference in the lives of people suffering from low back pain and osteo- and rheumatoid arthritis.”

Earlier this year, American Health’s participant satisfaction survey revealed that 100% of first-year participants would be likely to recommend the program. “We are pleased with our preliminary outcomes, and we look forward to continue enhancing the program experience for our members,” adds Lavin.

About American Health Holding, Inc.
American Health Holding is a single-source provider of medical management services that supports millions of members across the health care continuum. The multi-URAC accredited organization has been helping clients to maximize cost savings while ensuring the quality and appropriateness of care since 1993. American Health provides a level of flexibility that supports integrated solutions for creating healthy outcomes. For more information about American Health visit the Web site: www.AmericanHealthHolding.com.

Contact:
Joanna Callihan
Marketing Manager
American Health Holding, Inc.
(614) 818-3222 Ext. 1431
[email protected]

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Filed Under: Medical And Healthcare

CLSI Publishes Performance Standards for Antimicrobial Susceptibility Testing; June 2010 Update

Posted on July 20, 2010 Written by Annalyn Frame

SOURCE: Clinical and Laboratory Standards Institute

WAYNE, PA–(Marketwire – July 20, 2010) – Clinical and Laboratory Standards Institute (CLSI) recently published “Performance Standards for Antimicrobial Susceptibility Testing; Twentieth Informational Supplement (June 2010 Update)” (M100-S20-U).

This update includes:

  • New interpretive criteria for doripenem for Enterobacteriaceae
  • Revised interpretive criteria for ertapenem, imipenem, and meropenem for Enterobacteriaceae
  • Guidance for use of the modified Hodge test (MHT) with revised interpretive criteria for carbapenems

Jean B. Patel, PhD, D(ABMM), Deputy Director, Office of Antimicrobial Resistance, Centers for Disease Control and Prevention, and member of the subcommittee that developed the update, says, “Carbapenemase-producing Enterobacteriaceae are a significant infection control concern, and rapid laboratory detection of isolates that may carry these resistance mechanisms is an important step in preventing transmission. Since these isolates will test nonsusceptible (ie, intermediate or resistant) to one or more of the carbapenem agents using the revised breakpoints, it will be easier for laboratories to identify these isolates and to report their findings to hospital infection preventionists.”

Michael N. Dudley, PharmD, FCCP, FIDSA, Senior Vice President, Research & Development and Chief Scientific Officer, Mpex Pharmaceuticals, Inc., and member of the subcommittee that developed the update, agrees, “It was important to provide further direction to laboratories on detection of isolates with reduced susceptibility to carbapenems. Unfortunately, there are no reliable clinical studies that allow assessment of the clinical response to treatment of carbapenem-producing strains to carbapenem antimicrobial agents. However, studies in animal models indicate that the minimal inhibitory concentration (MIC) is the best predictor of antibacterial effects. The new MIC breakpoints, coupled with US Food and Drug Administration (FDA)-approved dosage regimens used frequently in the clinic, provide for a better probability of attaining pharmacokinetic/pharmacodynamic exposures associated with antibacterial effects in vivo. The new intermediate and resistant breakpoints for carbapenems also ‘capture’ a majority of isolates that produce carbapenemases that can be confirmed using the MHT, if needed.”

He adds, “This new update will help laboratories improve quality and provide timelier reporting of susceptibility results.”

Tracy Dooley, MLT(ASCP), CLSI Standards Administrator, explains the importance of publishing a midyear update to the well-known annual antimicrobial susceptibility testing (AST) breakpoints, saying, “In an effort to disseminate information to users in a timelier manner, the Subcommittee on AST decided to publish a midyear M100 supplement with the new/revised carbapenem interpretive criteria for Enterobactericeae. This midyear publication allows laboratories to begin to initiate the implementation of these changes. One of the benefits of the new interpretive criteria is that nearly all carbapenemase-producing isolates will test nonsusceptible to one or more carbapenems. This alleviates the need to perform initial screening and confirmatory testing (MHT) for routine patient testing. Historically, each complete blood count (CBC) instrument/reagent manufacturer developed its unique approaches to system validation and performance claims. This standard will help create better standardization among manufacturers, as well as assist practicing laboratories in developing consistent testing.”

The tables in this M100-S20 June 2010 Update are to replace Tables 2A and 2A-S2 in
Performance Standards for Antimicrobial Susceptibility Testing; Twentieth Informational Supplement (M100-S20) (January 2010). For other tables referenced in this update, please see M100-S20 (January 2010).

CLSI is a volunteer-driven, membership-supported, nonprofit organization dedicated to developing standards and guidelines for the health care and medical testing community through a consensus process that balances the perspectives of industry, government, and the health care professions. For additional information on CLSI, visit the CLSI website at www.clsi.org or call 610.688.0100.

Contact:
Amanda Holm
Senior Marketing Manager
Phone: 610.688.0100 ext. 129
E-mail: Email Contact

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Filed Under: Medical And Healthcare

iData Research: Rapid Growth of NuVasive’s XLIF(R) for the Treatment of Back Pain Fuels MIS Spinal Fusion Procedures to Triple by 2016

Posted on July 20, 2010 Written by Annalyn Frame

VANCOUVER, BRITISH COLUMBIA–(Marketwire – July 20, 2010) – According to new spinal implant reports by iData Research (www.idataresearch.net), the leading global authority in medical device and pharmaceutical market research, the U.S. market for spinal implants is estimated to exceed $8 billion by 2016, while the MIS spinal implant market is estimated to reach over $3 Billion. In addition, rapid growth in artificial disc use will fuel the spinal motion preservation market to increase six-fold by 2016.

While many have predicted the cannibalization of spinal fusion procedures by motion preservation, iData’s report reveals healthy growth in the fusion market driven by a consistent rise in minimally invasive surgical (MIS) interbody procedures, the market for which will triple by 2016.

“Lateral lumbar interbody fusion, such as NuVasive’s XLIF(R) (NASDAQ:NUVA), is the most rapidly increasing MIS interbody fusion procedure,” says Dr. Kamran Zamanian, CEO of iData.

Despite growth in spinal fusion, the competing spinal motion preservation market, which includes cervical artificial discs, is also expected to experience strong growth. Reimbursement policies for motion preservation devices are expected to continue to drive this market.

“The cervical artificial disc segment is aiding strong growth in the spinal motion preservation market,” says Dr. Zamanian. “Companies such as DePuy, Medtronic and Synthes are leading the market, while many competitors such as Cervitech, Globus, NuVasive, SpinalMotion, and Zimmer are expected to emerge into this segment in the next few years.”

iData’s global report series on the “Markets for Spinal Implants & VCF 2010” and the “Markets for Minimally Invasive Spinal Devices 2010” also covers VCF, spinous process fixation, facet fixation and MIS pedicle screws.

For more information, register free on iData’s website at: http://www.idataresearch.net/idata/registration.php

About iData Research

iData Research (www.idataresearch.net/idata/discoveridata.php) is an international market research and consulting group focused on providing market intelligence for medical device and pharmaceutical companies.

Filed Under: Medical And Healthcare

Seniors In Touch Announces Patent Award

Posted on July 20, 2010 Written by Annalyn Frame

SOURCE: TrinityCare Senior Living, Inc.

FRIENDSWOOD, TX–(Marketwire – July 20, 2010) – TrinityCare Senior Living, Inc. (OTCBB: TCSR), today announced they have been awarded a patent for the Company’s interactive family communication system, Seniors In Touch (SIT).

“Seniors In Touch allows senior adults to use a simple touch screen computer system to send and recieve video messages, email, pictures, and other digital media,” says Brian Lang, Chief Executive Officer of SIT. “Family and friends from across town or across the nation can share messages, memories, and daily activity using the Internet, hand held technology, and other creative media. The award of this patent recognizes SIT’s technical and social media innovation.” The Company previously announced the implementation of this technology together with CoVideo Systems, a leader in providing video emailing, conferencing and presentation tools.

About Seniors In Touch

Seniors In Touch is an interactive communication system for senior adults and their families. Utilizing the latest in touch screen computing combined with established communication tools, seniors will be able to send text and video messages to persons in their contacts via a secure, user-friendly, touch interface. A family member serves as the administrator of the Seniors In Touch account to provide approved and safe interaction for the senior adult. Seniors In Touch will also provide photo-sharing services and limited web access for news, weather and sports that is approved by the administrator. The platform will also provide executive directors of senior living facilities a platform in which to communicate with both the senior adults and their families. For more information please visit www.seniorsintouch.com.

About TrinityCare Senior Living, Inc.

TrinityCare Senior Living (“TrinityCare”) develops, owns, and manages quality senior living facilities that focus on enriching the faith of the residents and providing state-of-the-art independent living, assisted living, memory care and adult day care services in a single location. The Company partners with local churches and developers for each facility and offers a wide range of both community and personal services to residents. TrinityCare is a rapidly growing company with three successful facilities currently operating in Texas and Tennessee. Near-term expansion plans target the Southeastern part of the United States. For more information please visit www.trinitycare.com.

TrinityCare is headquartered in Friendswood, Texas (Houston metropolitan area) and its common stock trades on the OTC Bulletin Board under the symbol “TCSR.”

Forward-Looking Statements

The information in this news release includes certain forward-looking statements that are based upon assumptions that in the future may prove not to have been accurate and are subject to significant risks and uncertainties, including statements related to the future financial performance of the Company. Although the Company believes that the expectations reflected in the forward-looking statements are reasonable, it can give no assurance that such expectations or any of its forward-looking statements will prove to be correct. Factors that could cause results to differ include, but are not limited to, successful execution of growth strategies, product development and acceptance, the impact of competitive services and pricing, general economic conditions, and other risks and uncertainties described in the Company’s periodic filings with the Securities and Exchange Commission.

For Additional Information, Please Contact:
Brian Lang
CEO
[email protected]

Filed Under: Medical And Healthcare

Cystinosis Research Foundation Names Three Pre-Eminent Scientists to 2010 Scientific Panel Advising Foundation

Posted on July 20, 2010 Written by Annalyn Frame

SOURCE: Cystinosis Research Foundation

IRVINE, CA–(Marketwire – July 19, 2010) –  The Cystinosis Research Foundation has named three prominent researchers to its Scientific Review Board, which reviews and recommends applications for grants to study the rare and fatal metabolic disease and develop new treatments and a cure. Cystinosis afflicts about 2,000 persons, mostly children, worldwide.

Joining the CRF’s Scientific Review Board are: Drs. Stephanie Cherqui of The Scripps Research Institute, La Jolla, Calif.; Allison Eddy of the University of Washington, Seattle, Wash. and Francisco Emma of the Bambino Gesù Children’s Hospital in Rome.

Leaving the CRF’s Scientific Review Board and retiring from a historic career in metabolic disease research is Dr. Jerry Schneider, M.D., who was Professor of Pediatrics and Dean for Academic Affairs at the University of California, San Diego. He is a developer of the two breakthrough treatments for cystinosis, which he began studying in 1965.

“We are fortunate to have such pre-eminent scientists advising us on funding cystinosis research. Over the years, they have made valuable contributions to cystinosis research and are committed to finding improved treatments and a cure,” said Nancy Stack, President and co-founder of the CRF.

She added that the lifelong research on cystinosis by Dr. Schneider “has brought us to the threshold of a new treatment and a cure. He has encouraged and mentored new researchers who now, in turn, have dedicated their careers to cystinosis. Cystinosis patients and their families owe him eternal gratitude,” Stack said.

Dr. Cherqui, Ph. D., an assistant professor at The Scripps Research Institute, is credited with developing a breakthrough cell and gene therapy regimen that has improved cystinosis in mice. She is a member of the CRF Gene Therapy Consortium. Dr. Cherqui worked in Paris with a group led by Dr. Corinne Antignac that identified the cystinosis CTNS gene. Her 2002 doctoral thesis was on molecular studies of cystinosis and the generation of the mouse model for cystinosis. Dr. Cherqui is a member of the American Society of Gene and Cell Therapy. She has authored 12 publications on cystinosis, including a cover article in the October issue of the scientific journal “Blood.”

Dr. Eddy, M.D., professor of pediatrics at the University of Washington, is internationally recognized for her work on the cellular and molecular basis of kidney fibrosis and progressive kidney disease. She is the director of the Tissue and Cell Biology Research Center at Seattle Children’s Research Institute and in 2009 was elected to the Council of the International Society of Nephrology. Dr. Eddy holds the Robert O. Hickman Endowed Chair in Pediatric Nephrology at the University of Washington. She is a graduate of the McMaster University Medical School in Canada.

Dr. Emma, M.D., is head of Pediatric Nephrology at the Bambino Gesù Children’s Hospital in Rome, Italy, and president of the Italian Society of Pediatric Nephrology. Dr. Emma’s laboratory research on cystinosis has been focused on studying cell mechanisms that regulate the expression of the CTNS gene and different isoforms of the cystinosin protein. He recently began studying the therapeutic potentials of stem cells for treatment of cystinosis with the support of the CRF. Dr. Emma received his medical degree from the Catholic University of Louvain, Brussels, Belgium. He trained at Children’s Hospital, Harvard Medical School, Boston, Mass.

Cystinosis is a metabolic disease that slowly destroys every organ in the body, including the liver, kidneys, eyes, muscles, thyroid and brain. There is a medicine that prolongs the children’s lives, but there is no cure. Most cystinosis sufferers succumb to the disease or its complications by age 40.

In patients with cystinosis, the amino acid cystine accumulates in the tissue due to the inability of the body to transport cystine out of the cell. This causes development of crystals, resulting in early cell death. There is a medication but, as yet, no cure for the disease.

Twice a year the CRF announces worldwide calls to the scientific community for research proposals. Since 2003, the CRF’s Scientific Review Board has played a key advisory role for 78 research grants totaling $11.8 million to scientists studying cystinosis in North America and Europe. Currently, there are 48 CRF-funded studies underway along with 13 CRF research fellows in the United States, Canada, France, Italy, Belgium, Ireland, Germany and The Netherlands.

The CRF is the leading funding source for cystinosis research. The foundation recently approved requests totaling $988,759 for seven new grants. Every dollar raised by the CRF is committed for medical research. Administrative costs are privately underwritten.

Nancy Stack and her husband, Geoffrey, a managing director of the SARES REGIS Group, an Irvine real estate company, have a daughter, Natalie, 19, with cystinosis.

For more information about Cure Cystinosis International Registry and the Cystinosis Research Foundation of Irvine, Calif., call Zoe Solsby at (949) 223-7610 or visit www.cystinosisresearch.org.

Contact:
Art Barrett
(714) 309-3700
Zoe Solsby
(949) 223-7610

Filed Under: Facilities And Providers

Renowned Hand and Upper Extremity Specialist of the Texas Medical Center, Dr. Evan Collins, Among First in Houston to Offer New Non Surgical Treatment…

Posted on July 19, 2010 Written by Annalyn Frame

SOURCE: Dr. Evan Collins

The Published Author and Methodist Hospital Hand Specialist Performs New Injection Procedure, Offers Minimally Invasive XIAFLEX® to Dupuytren’s Patients

HOUSTON, TX–(Marketwire – July 19, 2010) – Leading the charge in minimally invasive treatments for common hand and upper extremity conditions and injuries plaguing both men and women in society today, hand and upper extremity specialist, Dr. Evan Collins approves the use of new minimally invasive XIAFLEX® in the treatment of his patients suffering from Dupuytren’s Contracture.

The new injectable treatment first introduced in Europe recently received FDA approval for use in the United States and is now offered by a small group of specially trained orthopedic specialists. Dr. Collins, who was among the first to introduce the Percutaneous Needle Fasciotomy, also known as needle aponeurotomy (NA), in the treatment of Dupuytren’s Contracture nearly two years ago will offer the new XIAFLEX® treatment at The Methodist Hospital – Texas Medical Center.

XIAFLEX® is the first FDA-approved non surgical treatment for Dupuytren’s Contracture, enzymatically disrupting collagen when injected directly into a Dupuytren’s cord. Collagen disruption results in improved range of motion.

“There has been a great deal of work done in recent years to address the debilitating effects of Dupuytren’s Disease. This is among the first non surgical injection procedures approved by the FDA in the United States. We hope to restore range of motion to patients suffering from severe Dupuytren’s contractures, without the risks and recovery time of even the most advanced surgical procedures currently used to address them,” said Dr. Collins.

“Many people choose to live with the condition, which can dramatically affect even the most basic daily activities, because they are not comfortable with the treatments we have had to date. This non surgical approach may be a more appealing option for them,” Collins added.

Dupuytren’s disease is a progressive condition which causes the fibrous tissue of the palmar fascia (cords) to shorten and thicken. Eventually this will result in nodules causing fingers to contract, distorting the hand and reducing hand function. 

A Weill Cornell assistant professor and former Chief of Hand & Upper Extremity at Baylor College of Medicine, Dr. Evan Collins is awarded some of the highest nationally recorded patient satisfaction scores. He is featured among H Texas and Texas Monthly magazines’ recognized doctor’s listings and internationally renowned for his research in common hand and wrist conditions, tendinopathies, carpal tunnel syndrome, osteoarthritis and other debilitating joint conditions. 

For more information, please contact:
Dr. Evan Collins
(713) 441-3535
http://www.drevancollins.com

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Filed Under: Facilities And Providers

WellTek Subsidiary Announces National Conference Call on July 22, 2010; Covering an Important Message From Company CEO

Posted on July 19, 2010 Written by Annalyn Frame

SOURCE: WellTek Incorporated

WellCity Issues a ‘Call to Arms’ for All Network Marketers

ORLANDO, FL–(Marketwire – July 19, 2010) –  WellCity, Inc. (http://www.WellCity.com), a wellness-related social network and subsidiary of WellTek, Inc. (OTCBB: WTKN), today announced it will host a national conference call on July 22, 2010 at 9:30 pm EDT to present an important message from David George, CEO of WellCity.

The Company is rallying all network marketers to listen in on why WellCity is the single most effective medium today for creating optimum health and long-term wealth.

Subject: Important Message from David George, CEO of WellCity
Date: Thursday, July 22, 2010
Time: 9:30 pm EDT
Telephone Dial In: 1-760-569-7676
Access Code: 239460#
Self Mute/Unmute: *6

Skype Dial In: Add freeconferencecallhd.7676 to your Skype contacts
Use the Skype Dial Pad to enter the Access Code: 239460# Self Mute/Unmute *6

Note: Using Skype for these calls has additional steps than a standard Skype call.
To locate the Skype keypad to enter your access code when calling the conference, select the contact first and then the green Dial button. In the same area as the Dial button, next to the volume to the right, you will see a round drop down icon. Click on the icon and select Display Keypad from the drop down menu. After the call is connected, wait for the prompt and enter your access code using the Skype keypad followed by the # key.

About WellCity Incorporated
WellCity is a social utility where health- and wellness-minded ‘residents’ can closely commune with one another; receive support, information and encouragement from their ‘neighbors’ and from a league of leading professional experts; shop for health and wellness-oriented product and services; compete in WellCity’s proprietary 90-Day Wellness Challenge; and even enjoy income opportunities by leveraging their personal network. For more information on the Company, please visit www.WellCity.com.

About WellTek Incorporated
WellTek is a global health, fitness and wellness company that provides proven solutions to help address some of the world’s most pressing and costly health and wellness challenges. The Company owns and operates WellCity, Inc., a premiere wellness-related social utility that helps ‘residents’ live longer, feel better, look younger and enjoy life more as they age. The Company’s subsidiary, MedX Limited, manufactures, markets and distributes the most advanced medical exercise equipment to the medical and fitness markets. Through its wholly owned subsidiary Pure HealthyBack, Inc., WellTek is redefining healthcare delivery by providing health plans, self-insured employer groups, and consumers with a viable non-surgical, lower cost treatment for patients who are seeking lasting relief from chronic neck and back pain. For more information on the Company, please visit www.WellTekinc.com. 

Certain statements contained in this press release, which are not based on historical facts, are forward-looking statements as the term is defined in the Private Securities Litigation Reform Act of 1995, and are subject to substantial uncertainties and risks in part detailed in the respective Company’s Securities and Exchange Commission filings, that may cause actual results to materially differ from projections. Although the Company believes that its expectations are reasonable assumptions within the bounds of its knowledge of its businesses, expectations, representations and operations, there can be no assurance that actual results will not differ materially from their expectations. Important factors currently known to management that could cause actual results to differ materially from those in forward-looking statements include the Company’s ability to execute properly its business model, to raise additional capital to implement its continuing business model, the ability to attract and retain personnel — including highly qualified executives, management and operational personnel, ability to negotiate favorable future debt facilities and capital raises, and the inherent risk associated with a diversified business to achieve and maintain positive cash flow and net profitability. In light of these risks and uncertainties, there can be no assurance that the forward-looking information contained in this press release will, in fact, occur. 

FOR MORE INFORMATION, PLEASE CONTACT:
Legacy Marketing Group
Roxie Mooney
President & CEO
(
Twitter: roxiemooney)
407-575-3220
via email at [email protected]

Filed Under: Facilities And Providers

Automatic Infection Control and Decontamination Leader Launches Zimek Global Health Foundation

Posted on July 19, 2010 Written by Annalyn Frame

SOURCE: Zimek Technologies

TAMPA, FL–(Marketwire – July 19, 2010) – Zimek Technologies (www.zimek.com) today announced the formation of the Zimek Global Health Foundation, a 501-C-3 non-profit organization, created to focus public awareness of increasing infection rates and bacteria becoming resistant to antibiotic drugs, according to Jen Grosman, President of the Board of Directors for the Foundation.

The Zimek Global Health Foundation will conduct infection control medical peer reviews on reducing infection rates utilizing Zimek’s automatic touchless decontamination systems, lab testing, pilot case studies, infection control technology research and development, as well as distribute Zimek decontamination systems to underprivileged population centers and disaster stricken areas across America and internationally. Zimek Global Health Foundation will seek out partnerships with key non-profit, emergency and charitable organizations to coordinate distribution of Zimek’s infection control technology.

“As President of the Board of Directors for Zimek’s Global Health Foundation, we are extremely excited to create meaningful public awareness for the need of life-saving infection control technology and to continue our important research and development capabilities to prevent the spread of infectious diseases,” said Jen Grosman.

Zimek Technologies (www.zimek.com), based in Tampa, Florida, has been developing and marketing its patented automatic Micro-Mist™ decontamination technologies for more than five years. Zimek’s industry-leading technologies are used by the U.S. Department of Homeland Security, Fire and EMS departments, healthcare facilities, public health agencies, transit systems, correctional facilities and local law enforcement agencies across America.

Media Contact:
Bob Mazza
Public Relations
Zimek Technologies
(310) 994-4847
Email Contact

Filed Under: Facilities And Providers

Center for Technology and Aging Awards Remote Patient Monitoring (RPM) Technology Diffusion Grants

Posted on July 19, 2010 Written by Annalyn Frame

SOURCE: Center for Technology and Aging

OAKLAND, CA–(Marketwire – July 19, 2010) –  The Center for Technology and Aging today announced grants to five organizations for remote patient monitoring (RPM) technology projects that will demonstrate how RPM improves the quality and efficiency of chronic disease management and post-acute care of older adults. Each project involves a coordinated effort among patients, families and caregivers.

“RPM technologies make a huge difference in the quality of life for those living with chronic conditions,” said David Lindeman, PhD, director of the Center for Technology and Aging. “These projects will underscore the need to reform reimbursement policies and make possible wider adoption of these technologies in public programs — Medicare and Medicaid — as well as among private insurers and health care systems.”

The U.S. health care system could reduce costs by nearly $200 billion during the next 25 years if RPM tools were utilized to care for patients with congestive heart failure (CHF), diabetes, chronic obstructive pulmonary disease (COPD), and chronic wounds or skin ulcers. Eight of 10 older Americans have one or more chronic diseases.

The Center’s RPM initiative goals are to demonstrate that these technologies can be used more widely because they reduce: the use of ER’s and hospitals by older adults, the need for those with chronic illness to move to intensive higher-cost care settings, and the burden on family and professional caregivers.

RPM includes a wide variety of technology, such as point-of-care monitoring devices — weight scales, glucometers, implantable cardioverter-defibrillators, and blood pressure monitors — which become part of a fully integrated health data collection, analysis, and reporting system between the devices, patients, and clinicians.

The grantees are:

  • Sharp HealthCare Foundation (www.sharp.com/sharp-foundation) — Working with senior and home health agencies, this project will monitor patients who have five or more chronic conditions — which may include CHF, peripheral artery disease, COPD, atherosclerosis, hypertension, diabetes, and chronic kidney disease — with the goal of reducing unplanned hospital readmission rates.

  • New England Healthcare Institute (www.nehi.net) — Using the Electronic House Call System (ExpressMD Solutions) and in collaboration with the Massachusetts Technology Collaborative, Atrius Health, and Blue Cross Blue Shield of Massachusetts, this Massachusetts-based project seeks to demonstrate clinical and financial benefits from the use of RPM technologies as evidenced by reducing hospital readmissions.

  • Centura Health At Home (www.centurahealthathome.org) — In collaboration with an internal physician group, telehealth video technologies (inLife and Life View, made by American TeleCare) will be used to enhance 24/7/365 call center response for Centura Health at Home patients in Denver, Colorado. The goal is to reduce re-hospitalizations and to improve quality of life for patients who have diabetes, COPD, or CHF.

  • AltaMed Health Services (www.altamed.org) and Stamford Hospital (www.stamfordhospital.org) — This project will expand use of RPM technology (HoneyWell’s HomMed device) with low-income seniors in East Los Angeles, California and Stamford, Connecticut who have CHF, diabetes, COPD, or hypertension. The goal is to promote better self-management habits and healthy behaviors while also establishing a new healthcare para-professional position, the “Telehealth Technician,” through community college training programs.

  • California Association for Health Services at Home Foundation (www.cahsah.org) — In collaboration with several home care agencies, this project will use Intel’s Health Guide to monitor patients with chronic disease conditions or those needing post-acute care follow-up. The goal is to reduce avoidable 30-day readmissions, hospitalizations, and emergency department visits for Medi-Cal patients; and to inform public policy concerning RPM technology and Medi-Cal programs operating under federal waivers.

“One of the Center’s goals is to assure that funded projects aren’t ‘one and done,’ but are designed to be replicated,” said Lindeman. “Each grantee has identified ways to make sure their project can continue beyond the one?year grant period, can be broadly adopted by others, and is integrated within our long?term care system.”

The five $100,000 grants will be supplemented with a total of over $1,746,000 in matching funds. Individual project details and the Center’s RPM Position Paper are available at the Web site, www.techandaging.org.

The Center for Technology and Aging (www.techandaging.org) supports the rapid adoption and diffusion of technologies that enhance independence and improve home and community-based care for older adults. Through grants, research, and development of practical tools and best practice guidelines, the Center serves as an independent, non-profit resource for improving the quality and cost-effectiveness of long-term care services. The Center was established with funding from The SCAN Foundation (www.thescanfoundation.org) and is affiliated with the Public Health Institute (www.phi.org) in Oakland, CA.

FOR MORE INFORMATION:
Daniel Danzig
925-254-6078
Email Contact

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Filed Under: Facilities And Providers

Neuronetrix Showcases New Cognitive Testing Device at the Alzheimer’s Association Annual Meeting

Posted on July 19, 2010 Written by Annalyn Frame

SOURCE: Neuronetrix, Inc.

LOUISVILLE, KY–(Marketwire – July 19, 2010) –  This week at ICAD 2010, Neuronetrix for the first time publicly demonstrated their COGNISION™ System, an innovative platform which enables objective assessment of cognitive function. The demonstration focused on the COGNISION™ System’s ability, using a non-invasive technology called event-related potentials (ERP), to accurately measure the cognitive performance of a patient’s brain.

The demonstration was particularly important in light of a report presented by a select group of Alzheimer’s specialists from the National Institute on Aging (NIA) and the Alzheimer’s Association which proposed new diagnostic guidelines for Alzheimer’s disease. The report titled, “Redefining Alzheimer’s Disease,” proposes a new understanding of the disease which more closely matches clinical progression with a range of disease biomarkers. It also includes patients who meet clinical and cognitive criteria but who are negative for certain genetic, molecular, or structural biomarkers. “This is a tremendous opportunity for Neuronetrix as our test directly measures the electrical activity associated with cognition and is independent of biochemical pathways,” said Mauktik Kulkarni, Director of Research and Clinical Studies for Neuronetrix.

The new criteria also facilitates the tremendous drug development effort for disease modifying therapies for Alzheimer’s. Drug companies will now have a more reliable way of identifying those Alzheimer’s sufferers who might benefit from new drug therapies. The criteria also lays the groundwork for using positive changes in certain biomarkers as measures of drug effectiveness. “Because the COGNISION™ System could be used to measure progressive cognitive as well as drug response, we had tremendous interest from several of the large pharmaceutical companies at the conference,” said K.C. Fadem, Chief Operating Officer for Neuronetrix.

Neuronetrix previously completed a pilot clinical study with Alzheimer’s patients and healthy controls at the Sanders-Brown Alzheimer’s Disease Center at the University of Kentucky. The study validated the high data quality and ease-of-use of the COGNISION™ System in a clinical setting. Neuronetrix will soon be initiating a large multi-center clinical study which will validate their ERP biomarkers as an accurate and reliable measure of cognitive impairment. The company is planning a longitudinal follow up study which will validate their ERP biomarkers as a measure of progressive cognitive decline. “Because of the low cost, ease of use, and measurement potential of the COGNISION™ test, ERP testing could become a standard of care for those patients who develop cognitive disorders such as Alzheimer’s disease,” said K.C. Fadem.

About Alzheimer’s Disease
Alzheimer’s disease is a chronic neurodegenerative disease of the brain which eventually leads to death. Today, Alzheimer’s disease affects over five million Americans with 500,000 new cases reported each year. Medicare/Medicaid spending exceeds $100 billion on beneficiaries with Alzheimer’s and other dementias.

About Neuronetrix
Neuronetrix is an emerging med-tech company focused on revolutionizing the diagnosis of patients with neurologic disorders by providing accurate and meaningful diagnostic information to physicians early in the disease process.

Information about Neuronetrix is available at http://www.neuronetrix.com or by contacting K.C. Fadem at [email protected] or (502) 561-9040.

Filed Under: Facilities And Providers

RDM Associates Appoints Cynthia Sikina as New CEO

Posted on July 19, 2010 Written by Annalyn Frame

SOURCE: RDM Associates

CLARKSTON, MI–(Marketwire – July 19, 2010) –  RDM Associates, a specialized accounting and business consulting firm based in Clarkston, Mich., has announced the appointment of Cynthia Sikina to the newly-created position of CEO, according to company president and founder Rick Miller.

“We’re thrilled to have Cindy joining RDM Associates,” said Miller. “She brings well-rounded senior management talent and experience which are an exceptional fit with our goals and strategies. We’ve had the opportunity to work with Cindy in the past and we’ve been very impressed with her executive skills. Our accounting services model is non-traditional and technology intensive — concepts she relates to. I know that she will be a great asset to our firm as we work together to manage the next phase of our growth and expand our range of client services.”

Ms. Sikina’s responsibilities encompass the overall management of the firm’s business, including overseeing strategic planning, client services, new business and staff development. 

Since 2007, Ms. Sikina served as senior vice president and chief financial officer for Detroit’s Karmanos Cancer Institute & Center, where she was responsible for all aspects of fiscal management. Previous management positions have included COO/CFO for Wayne State University’s Physician Group from 2001-2007; director of financial services for the University of Michigan Medical School and other positions since 1992; and prior various financial planning and accounting roles for industrial companies beginning in 1981.

Prior to her role as CFO at KCI, Ms. Sikina served as a member of the KCI Board of Directors and its Finance and Executive committees for 6 years. She has also served as a member of the Karmanos-Crittenton Health Services Board of Directors.

She received an MBA with distinction from the University of Michigan Graduate School Of Business Administration in 1989 and is a member of the Beta Gamma Sigma Honor Society for high scholastic achievement. She earned a BBA degree with distinction from U of M in 1981 and received the CPA Certificate of Examination.

Ms. Sikina lives with her husband, Mark Sikina, in Novi.

CONTACT:
Barrett Kalellis
Shazaaam! Public Relations
248-366-0388

Filed Under: Facilities And Providers

CORRECTION FROM SOURCE: Odyssey and VistaCare Hospice in Texas

Posted on July 19, 2010 Written by Annalyn Frame

DALLAS, TEXAS–(Marketwire – July 19, 2010) – The following corrects and replaces the release sent on July 19, 2010 at 6:00 am ET. The phone number stated in the contact information and last paragraph of the release should have read “(214) 613-3133” instead of “(806) 553-6166”.

Odyssey and VistaCare Hospice in Texas can help you learn more about the type of care required in the final stages of life. 

“People appreciate the care hospice provides,” said Dr. Luis Gonzales, M.D., a National Medical Director for Odyssey Hospice and VistaCare Hospice. “Over 98% of family members tell us they would recommend hospice in Texas to others, and oftentimes our patients and families tell us they wish they’d been told about hospice in Texas sooner. Despite this, there are a lot of misconceptions among people who have not experienced the support hospice in Texas provides.”

One of the major misconceptions is that hospice is a location where one goes to live out the very last days of their life.

But in fact, hospice in Texas is a philosophy of care, and not a specific location at which to receive it. According to the National Hospice and Palliative Care Organization (NHPCO), 69% of hospice patients receive care in what they consider their home. The remainder are cared for in a hospice inpatient facility or hospital. Odyssey Hospice and VistaCare Hospice in Texas provide care wherever the patient’s home may be – a house, assisted living community, nursing home, or even during a brief hospital stay.

“The reality is that most people – medical professionals or otherwise – often equate hospice with death, but the truth is that hospice in Texas is about life” said Dr. Gonzales. “This lack of understanding can lead to a large number of people who are served by hospice in Texas for only a few days. Unfortunately, in these cases the patient and their loved ones don’t receive all of the benefits hospice offers.” Hospice is designed by Medicare to be a 6 month benefit, with the ability to provide care beyond that time for persons who remain eligible. Hospice in Texas is about quality of life.

Hospice in Texas provides compassionate, patient-centered care that offers medical expertise, comfort and support for those nearing the end of life, while also offering assistance for their loved ones. Hospice in Texas is delivered by a team of professionals who are experienced and committed to providing specialized care to persons seeking comfort, relief from symptoms, and gentle guidance.

Odyssey Hospice and VistaCare Hospice provide personalized care based on the needs of each patient and family. As one of the most experienced providers of hospice in Texas and throughout the United States, Odyssey and VistaCare offers CareBeyond, clinical programs for persons coping with specific illnesses. Developed by multidisciplinary team members, Odyssey and VistaCare hospice in Texas recognizes that patients with lung disease, for example, are treated differently, and have very different needs from, dementia patients. Using evidence based clinical practices, CareBeyond offers additional, specialized care to meet unique needs. 

Those who are approaching the end of life typically fear dying in pain, dying alone and are concerned about their loved ones. Hospice in Texas helps with each of these concerns. At Odyssey Hospice and VistaCare Hospice in Texas, our team of professionals is committed to serving patient and caregiver needs, whether they are physical, emotional or spiritual. Hospice is there when care and support are needed most.

With the early involvement of hospice, pain and symptoms are managed quickly so that people are comfortable. Only then can they work on other important aspects of their life. When chosen earlier, hospice in Texas provides greater benefits that are received for a longer period of time, including the opportunity for reflection and closure.

Hospice in Texas also provides bereavement care for up to 13-months for surviving family members. Care may include phone calls, newsletters, memorial services, connection to community resources and support. 

If you would like to receive more detailed, local information about hospice in Texas, please click here for information pertaining to hospice in Houston, or here for more information regarding hospice in Dallas. Odyssey & VistaCare also have hospice locations, providing in-home and/or inpatient treatment, throughout Texas. 

To learn more about hospice in Texas, please visit http://local.odsyhealth.com, or call (214) 613-3133.

Filed Under: Facilities And Providers

Study on Social Practices Reveals Manufacturers Can Help Lead Quality and Safety Efforts

Posted on July 19, 2010 Written by Annalyn Frame

SOURCE: Medline Industries, Inc.

Observational Study of Clinicians Revealed Opportunities to Redesign Products to Better Support Clinician-Patient Interaction

MUNDELEIN, IL–(Marketwire – July 19, 2010) –  A new VHA case study whitepaper released today by Medline Industries, Inc. details how the company used observational studies and context-based design to build human factors and social behaviors into its redesigned Foley Catheter Management tray.

The whitepaper, Social Practice and Clinicians’ Meaning of Urinary Catheter Insertions, showed that the redesigned tray significantly influenced the clinician’s ability to provide high quality care by creating a greater focus on providing patient comfort, maintaining sterile technique and decreasing the time of the entire insertion process. The observational study was comprised of three separate three-day observations of clinicians conducting catheterizations in the emergency department, medical/surgical floors and operating rooms at Providence Sacred Heart Medical Center and Children’s Hospital, Spokane, WA.

“Health care manufacturers are often overlooked when clinicians redesign clinical practices. Yet, the design of a product can be key to helping clinicians improve clinical performance and patient education,” said Trent Haywood, MD, JD, Senior Vice President of Clinical Performance and Chief Medical Officer for VHA and lead investigator. “For example, Medline chose to redesign the urinary catheter tray based upon the observational data uncovered in the clinical setting. Such design emphasis shows how manufacturers can be a key partner in quality and safety.” 

The unique partnership between Medline and the VHA research team highlights how industry vendors can partner with healthcare providers to develop a comprehensive system that incorporates proper procedures and social behaviors that are easy to adopt in everyday practice.

Medline launched its ERASE CAUTI program, which is based on the same criteria the CDC used in developing their new CAUTI prevention guidelines, last fall. Soon after the tray’s introduction, Medline met with the VHA Clinical Performance team to discuss studying the tray and how it’s used in actual clinical practice. Emphasis was put on understanding the objectives of catheter insertions from the clinician’s perspective, clarifying the actual practice that unfolds and identifying areas where the catheter management system aided the clinician or failed to aid the clinician based upon the clinician’s perspective on the practice.

Findings summarized in a case study whitepaper showed that clinicians preferred the benefits of the single layer tray which did not require steps related to maneuvering and positioning with a two layer tray. They also preferred the change to swab sticks that decreased the number of steps in the prepping and cleansing of the perineum. Clinicians retained the patent-pending patient education card for the patient or placed it in location where the patient might review it — a departure from previously observed behavior where the education was discarded without much attention. Clinicians also used the full-colored photography packaging to better explain the procedure to patients.

“Chief Nursing Officers (CNOs) want to help their staff reduce variability in the procedures that are done so that the potential to make an error decreases,” said Connie Yuska, Medline’s Vice President of Clinical Services and a former CNO. “We redesigned the tray taking into account the interaction between the patient and the clinician and facilitate learning — things that challenge nursing leaders every day.”

The VHA whitepaper, as well as additional information on the ERASE CAUTI program, is available for download on Medline’s website at www.medline.com/erase.

About Medline Industries, Inc. 

Medline, the nation’s largest privately held manufacturer and distributor of healthcare products, manufactures and distributes more than 100,000 products to hospitals, extended-care facilities, surgery centers, home care dealers and agencies. Headquartered in Mundelein, Ill., Medline has more than 900 dedicated sales representatives nationwide to support its broad product line and cost management services.

Over the past five years, Medline has been the fastest-growing distributor of medical and surgical supplies in the U.S., serving as the primary distributor to over 450 major hospitals and healthcare systems. As a leading distributor, Medline offers a comprehensive array of consulting and management services encompassing the supply chain and logistics, utilization and standardization, business tools and enhanced reporting capabilities and on-staff clinicians.

Media Contacts:
Jerreau Beaudoin
(847) 643-3011
John Marks
(847) 643-3309

Filed Under: Facilities And Providers

Sage to Offer Guidance and Tools to Help Physicians and Practices Navigate Meaningful Use Rules

Posted on July 19, 2010 Written by Annalyn Frame

SOURCE: Sage

TAMPA, FL–(Marketwire – July 19, 2010) – Sage North America Healthcare Division, providing practice management software and services to more than 80,000 physicians in North America, today announced several tools it is providing to practices, clients and members of the healthcare community to help them navigate the final Stage 1 meaningful use rules recently announced under the 2009 HITECH Act.

The final rule details the requirements physicians must satisfy to be eligible for financial incentives for the adoption and meaningful use of healthcare information technology under the HITECH Act.

“With the Stage 1 finalized rules, time is of the essence as healthcare providers race against the clock to prepare for and comply with the criteria,” said Betty Otter-Nickerson, President of Sage Healthcare. “With more than three decades of experience in this industry, we continue to be a knowledgeable and trusted source of information for our clients.”

The Health Information Technology for Economic and Clinical Health (HITECH) Act was created to promote the adoption and meaningful use of health information technology and includes more than $20 billion to aid in the development of a robust IT infrastructure for healthcare and to assist providers and other entities in adopting and using health IT.

Along with the Stage 1 meaningful use rules, a separate final rule was published establishing comprehensive guidelines that vendors’ products must meet for functionality, interoperability and security. Along with a third final rule released in June establishing a temporary certification program for testing and certification of vendor systems, the critical pieces are all in place to implement Stage 1 of the three-stage federal EHR incentive program designed to improve healthcare outcomes and patient care.

Tools of Success: Sage Meaningful Use White Paper, e-Consults and Webinar
Otter-Nickerson said she and Sage are aware of the confusion and questions surrounding meaningful use, the financial incentives, and how EHRs will drive efficiency and cost savings in today’s healthcare economy. To that end, Sage has developed several tools to help physicians and practices navigate the meaningful use landscape.

“We are dedicated to serving physicians and their practices, and we remain true to our mission of helping small and midsized ambulatory physician practices fulfill their ambitions, both with regard to using technology and to succeeding in a changing healthcare economy,” said Otter-Nickerson.

For physicians and practices seeking information about meaningful use rules, Sage North America Healthcare Division will host a one-hour public webinar on meaningful use and the final rule, featuring a 30-minute question and answer session. This free event, “Understanding Meaningful Use,” will take place Aug. 10, 2010, from noon to 1 p.m. EST. For more information or to register, visit www.SageHealth.com/MUFinalRule.

Webinar speakers will include Betty Otter-Nickerson, President, Sage Healthcare Division; Michael Burger, Sage Senior Director of Clinical Product Management; and Brenda Pawlak, Senior Manager of Health Policy at Manatt Health Solutions.

In addition, Sage is making a free white paper available to anyone interested in meaningful use. The white paper details how meaningful use may or may not affect practices differently and includes information about incentives and what it means to meaningfully use EHRs in the current healthsphere. The white paper will be available at the Sage Meaningful Use webinar.

Sage will also host several “e-consults” — web-based informational sessions for practice managers and physicians interested in learning more about meaningful use, the rules, and technology and electronic records in the practice space. For more information, please visit www.sagenorthamerica.com

“Now that the final rule has been released, we will continue to support and offer guidance in response to the needs of our clients and physicians while offering the market’s most competitive products,” said Otter-Nickerson.

Meaningful Use Webinar details:
Date: Tuesday, August 10
Time: Noon to 1 pm EST
Title: Understanding the “Meaningful Use” Final Rule
Cost: Free of charge
Registration URL: www.SageHealth.com/MUFinalRule
Moderator: Elizabeth W. Woodcock, MBA, FACMPE, CPC
Speakers:
Betty Otter-Nickerson, President, Sage Healthcare Division
Michael Burger, Sage Senior Director of Clinical Product Management
Brenda Pawlak, Manatt Health Solutions, Senior Manager of Health Policy

View Sage Healthcare Division YouTube interviews.

View Sage Healthcare Division information.

About Sage North America
Sage North America is part of The Sage Group plc, a leading global supplier of business management software and services. Sage North America employs 4,000 people and supports 3.1 million small and midsized business customers including more than 80,000 physicians. The Sage Group plc, formed in 1981, was floated on the London Stock Exchange in 1989 and now employs 13,100 people and supports 6.2 million customers worldwide. For more information, please visit the website at www.sagenorthamerica.com.

© 2010 Sage Software, Inc. All rights reserved. Sage, Sage Software, Sage logos and the Sage product and service names mentioned herein are registered trademarks or trademarks of Sage Software, Inc. or its affiliated entities. All other trademarks are the property of their respective owners.

Press Contact:
Scott Rupp
Sage
(813) 249-4264
[email protected]

Filed Under: Facilities And Providers

TRDX Announces Negotiations Progressing Well With Genesis Biopharma; Definitive Agreement and Closing Expected Shortly

Posted on July 19, 2010 Written by Annalyn Frame

SOURCE: Trend Exploration, Inc.

LONG ISLAND, NY–(Marketwire – July 19, 2010) –  SciMeDent Health, Corp. f/k/a Trend Exploration, Inc. (“TRDX” or the “Company”) (PINKSHEETS: TRDX) today announces to its shareholders that its negotiations are progressing well towards a definitive agreement with Genesis Biopharma, Inc. (“Genesis”) to acquire an exclusive worldwide sublicense for a new compound in development for the treatment of Painful Diabetic Neuropathy (PDN).

The Company expects the definitive agreement and subsequent closing to be finalized in a reasonably short period of time.

Dr. Jan Stahl, CEO of TRDX, commented: “We are pleased to be nearing completion of negotiations with Genesis. Additionally, plans for funding the development of Genesis’ PDN solution are progressing. We look forward to the successful completion of these key milestones in the near future.”

About Genesis Biopharma, Inc.

Genesis Biopharma, Inc. (www.genesisbiopharma.com) is a Canadian corporation founded in 2007 to exploit the commercial potential for the therapeutic use of peptidomimetic (modified amino acid peptides) compounds. Amino acids are the building blocks of proteins, which are found in every cell of every living thing on Earth. Proteins consist of extremely long and complex amino acid chains. In contrast, a peptide is a short string of amino acids, joined by chemical bonds (also called “amide bonds”).

About SCIMEDENT f/k/a Trend Exploration, Inc. (PINKSHEETS: TRDX)

SciMeDent (www.scimedenthealth.com) is a company focused on being a leading developer and marketer of products and services for medicine, dentistry and life sciences. SciMeDent plans to achieve growth initially through mergers and acquisitions.

Cautionary Statement Regarding Forward-Looking Statements

A number of statements contained in this press release are forward-looking statements. These forward-looking statements involve a number of risks and uncertainties, including the sufficiency of existing capital resources, technological or industry changes and uncertainties related to the development of the Company’s business model. The actual results the Company may achieve could differ materially from any forward-looking statements due to such risks and uncertainties.

Filed Under: Facilities And Providers

NovaVision’s FDA-Cleared Visual Restoration Therapy (VRT) System and Company Assets Now Available

Posted on July 19, 2010 Written by Annalyn Frame

SOURCE: The Magnum Group

Nearly Three Billion Dollar Market Opportunity Estimated for NovaVision’s Post-Stroke and Traumatic Brain Injury Visual Restoration Treatments with Promising Research Conducted in Age-Related Macular Degeneration and Glaucoma

TIBURON, CA–(Marketwire – July 19, 2010) –  NovaVision, Inc., headquartered in Boca Raton, Fla., filed for Chapter 7 Bankruptcy in the State of Florida (Case #10-21343-PGH) on April 28, 2010 after more than seven years of continuous operation. The bankruptcy trustee has engaged The Magnum Group, Inc., to solicit offers for NovaVision’s assets which include the NovaVision Visual Restoration Therapy (VRT) system, a neuroplacticity platform that has been cleared by the U.S. Food and Drug Administration (FDA) for the treatment of stroke, traumatic brain injury, amblyopia (“lazy eye”) and optic nerve damage. 

NovaVision has received a total investment of $49,200,000 since its founding in 2003 and has generated revenues of approximately $1,000,000 each year for the past three years. The company’s non-invasive computer-based neuroplacticity products have treated more than 3,000 patients worldwide. NovaVision estimates the total market opportunity for its portfolio of products to exceed 300,000 units in U.S. optometry, ophthalmology, neurology, and primary care practices as well as rehabilitation centers. 

“NovaVision was the first company to commercialize a non-invasive, computer-based therapeutic model to help the large population of patients that have lost visual functionality and independence due to stroke or brain injury,” said Holger Weis, former Chief Financial Officer for NovaVision. “While it is extremely unfortunate that NovaVision has fallen victim to the current economic environment, there remains huge market potential to keep these treatments alive in the marketplace while continuing to commercialize the numerous patents and discoveries that NovaVision has invested nearly fifty million dollars to advance.”

NovaVision was founded in 2003 by Bernhard Sabel, PhD, who led the original research team that published a double-blind placebo controlled clinical study in Nature Medicine in 1998. This landmark study, as well as many subsequent studies, has validated VRT as a clinically proven treatment to restore lost vision resulting from stroke, traumatic brain injury, or other acquired brain injuries. In 2003, NovaVison’s Visual Restoration Therapy was granted 510(k) clearance by the U.S. FDA for the diagnosis and treatment of these conditions.

VRT treatment has been offered at leading neurological, eye and rehabilitation centers throughout the U.S. and Europe and it can be prescribed by eye doctors, neurologists or physiatrists. Data from a recent retrospective study showed that more than 70 percent of U.S. patients who underwent a six-month treatment protocol with NovaVision VRT showed significant improvement in their vision. 

“Visual field defects are common after brain insults such as stroke and traumatic brain injury and they cause significant disability,” said neurologist Jose G. Romano, MD, FAHA, Associate Professor of Clinical Neurology, Director, Cerebrovascular Division, University of Miami Miller School of Medicine. “In my experience, VRT has positively impacted the majority of patients treated with improvements in reading, mobility and avoidance of injuries. Techniques such as VRT are an important addition to the limited rehabilitation options available to these patients.”

The Company has also developed devices that aid in the diagnosis of visual field deficits, including an Inpatient Device for assessment and therapeutic use in rehabilitation centers and the Head Mounted Perimeter, a portable and ADA-compliant instrument to aid in the assessment of visual field deficits. Additional indications for VRT include age-related macular degeneration, glaucoma, diabetic retinopathy and attention deficit disorder/attention deficit hyperactivity disorder. 

“VRT is the only restorative therapy available for patients suffering from visual field loss following stroke or trauma,” said Michael Rosenberg, MD, Director of Neurology and Neuro-ophthalmology, New Jersey Neuroscience Institute at JFK Medical Center in Edison, New Jersey. “I have been providing VRT to my patients for more than five years with results similar to published research in which 70 percent of patients achieved marked improvements in visual function. It is my sincere hope that I will again be able to offer VRT as a treatment option very soon.”

NovaVision maintains a strong and broad based portfolio of patent protection on its methods and apparatus in the form of issued patents and applications, both domestically and internationally. In the U.S., the Company has a total of five issued patents and 12 pending applications. The international patent portfolio includes one issued patent and more than 30 pending applications. NovaVision’s wholly-owned European subsidiary, NovaVision AG, located in Magdeburg, Germany is also available for sale. 

To learn more about NovaVison’s assets and patents, please contact Randy McDonald, Managing Director and President of The Magnum Group, Inc. at [email protected] or (415) 435-5550.

About The Magnum Group

Founded in the San Francisco Bay Area in 1980, The Magnum Group, Inc. is the largest business development firm serving the ophthalmic (vision care) industry. Specializing in acquisition and financing agreements, strategic alliances, joint venture, licensing and distribution contracts, The Magnum Group represents both Buyers and Sellers and has managed more than $250 million in transactions since 1995. For more information, please visit http://www.themagnumgroup.com/

Contact:
Randy McDonald
Managing Director and President
The Magnum Group, Inc.
Email Contact
(415) 435-5550

Click here to see all recent news from this company

Filed Under: Facilities And Providers

Extendicare REIT Announces Second Quarter 2010 News Release and Conference Call Information

Posted on July 19, 2010 Written by Annalyn Frame

MARKHAM, ONTARIO–(Marketwire – July 19, 2010) – Extendicare Real Estate Investment Trust (“Extendicare REIT” or “Extendicare”) (TSX:EXE.UN) today announced it will hold a conference call and live audio webcast on Friday, August 6, 2010, at 10:00 a.m. (ET) to discuss financial results for the second quarter ended June 30, 2010.

Following the issuance of the news release on August 5, 2010, Extendicare will post a copy, along with an update of the supplemental information package, on its website www.extendicare.com under the investors/financial reports section.

The call will be hosted by Tim Lukenda, President and Chief Executive Officer; Doug Harris, Senior Vice President and Chief Financial Officer, and Paul Tuttle, President of Canadian Operations. Following management’s presentation, there will be a question and answer session for analysts and institutional investors.

To participate in the August 6, 2010, conference call, please dial 1-888-789-9572 or 416-695-7806 followed by the passcode 7354234#. The conference call will also be accessible via webcast at www.extendicare.com under the investors/presentations & webcasts section. A replay of the call will be available approximately two hours after completion of the live call until midnight on August 20, 2010. To access the rebroadcast dial 1-800-408-3053 or 416-695-5800, followed by the passcode 3683111#.

About Us

Extendicare REIT is a leading North American provider of long-term and short-term senior care services through its network of owned and operated health care centers. We employ 37,700 qualified and experienced individuals dedicated to helping people live better through a commitment to quality service that includes post-acute care, rehabilitative therapies and home health care services. Our 258 senior care centers in North America have capacity for approximately 28,900 residents. Extendicare REIT is a specified investment flow-through trust (SIFT) that has been subject to the SIFT tax since January 1, 2007.

Filed Under: Facilities And Providers

Odyssey and VistaCare Hospice in Texas

Posted on July 19, 2010 Written by Annalyn Frame

DALLAS, TEXAS–(Marketwire – July 19, 2010) – Odyssey and VistaCare Hospice in Texas can help you learn more about the type of care required in the final stages of life. 

“People appreciate the care hospice provides,” said Dr. Luis Gonzales, M.D., a National Medical Director for Odyssey Hospice and VistaCare Hospice. “Over 98% of family members tell us they would recommend hospice in Texas to others, and oftentimes our patients and families tell us they wish they’d been told about hospice in Texas sooner. Despite this, there are a lot of misconceptions among people who have not experienced the support hospice in Texas provides.”

One of the major misconceptions is that hospice is a location where one goes to live out the very last days of their life.

But in fact, hospice in Texas is a philosophy of care, and not a specific location at which to receive it. According to the National Hospice and Palliative Care Organization (NHPCO), 69% of hospice patients receive care in what they consider their home. The remainder are cared for in a hospice inpatient facility or hospital. Odyssey Hospice and VistaCare Hospice in Texas provide care wherever the patient’s home may be – a house, assisted living community, nursing home, or even during a brief hospital stay.

“The reality is that most people – medical professionals or otherwise – often equate hospice with death, but the truth is that hospice in Texas is about life” said Dr. Gonzales. “This lack of understanding can lead to a large number of people who are served by hospice in Texas for only a few days. Unfortunately, in these cases the patient and their loved ones don’t receive all of the benefits hospice offers.” Hospice is designed by Medicare to be a 6 month benefit, with the ability to provide care beyond that time for persons who remain eligible. Hospice in Texas is about quality of life.

Hospice in Texas provides compassionate, patient-centered care that offers medical expertise, comfort and support for those nearing the end of life, while also offering assistance for their loved ones. Hospice in Texas is delivered by a team of professionals who are experienced and committed to providing specialized care to persons seeking comfort, relief from symptoms, and gentle guidance.

Odyssey Hospice and VistaCare Hospice provide personalized care based on the needs of each patient and family. As one of the most experienced providers of hospice in Texas and throughout the United States, Odyssey and VistaCare offers CareBeyond, clinical programs for persons coping with specific illnesses. Developed by multidisciplinary team members, Odyssey and VistaCare hospice in Texas recognizes that patients with lung disease, for example, are treated differently, and have very different needs from, dementia patients. Using evidence based clinical practices, CareBeyond offers additional, specialized care to meet unique needs. 

Those who are approaching the end of life typically fear dying in pain, dying alone and are concerned about their loved ones. Hospice in Texas helps with each of these concerns. At Odyssey Hospice and VistaCare Hospice in Texas, our team of professionals is committed to serving patient and caregiver needs, whether they are physical, emotional or spiritual. Hospice is there when care and support are needed most.

With the early involvement of hospice, pain and symptoms are managed quickly so that people are comfortable. Only then can they work on other important aspects of their life. When chosen earlier, hospice in Texas provides greater benefits that are received for a longer period of time, including the opportunity for reflection and closure.

Hospice in Texas also provides bereavement care for up to 13-months for surviving family members. Care may include phone calls, newsletters, memorial services, connection to community resources and support. 

If you would like to receive more detailed, local information about hospice in Texas, please click here for information pertaining to hospice in Houston, or here for more information regarding hospice in Dallas. Odyssey & VistaCare also have hospice locations, providing in-home and/or inpatient treatment, throughout Texas. 

To learn more about hospice in Texas, please visit http://local.odsyhealth.com, or call (806) 553-6166.

Filed Under: Medical And Healthcare

Vigil Health Solutions Announces $200,000 Loan Agreement and Proposes a Share Consolidation to Its Shareholders

Posted on July 16, 2010 Written by Annalyn Frame

VICTORIA, BRITISH COLUMBIA–(Marketwire – July 16, 2010) – Vigil Health Solutions Inc. (TSX VENTURE:VGL)(“Vigil”) today announced that it has entered into an aggregate $200,000 loan agreement with British Columbia Discovery Fund (VCC) Inc. and GrowthPoint Capital Corp. The loan is secured by all of Vigil’s property and is due and payable on December 31, 2010. The loan is convertible at the option of the lenders into Vigil’s common shares at a rate of one common share for each $0.10 of indebtedness ($0.20 if Vigil’s proposed consolidation announced below occurs). Any common shares issued on conversion of the loan will be subject to a four month hold period from today’s date. The obligations of Vigil and the lenders under the loan agreement are conditional upon receipt of acceptance by the TSX Venture Exchange of the loan.

Vigil will seek shareholder approval at its Annual General and Special Meeting of shareholders to be held on August 24, 2010, to consolidate its common shares at a ratio of one new share for each twenty outstanding common shares. In order to be effective, the consolidation resolution must be approved by at least three-quarters of the shareholder votes cast at the meeting and be accepted by the TSX Venture Exchange. The purpose of the share consolidation is to facilitate future financings and strategic initiatives by Vigil. Vigil currently has 100,046,135 common shares outstanding. If the consolidation is approved, Vigil will have approximately 5,002,306 common shares outstanding. Vigil’s name will not be changed in connection with the proposed consolidation.

Filed Under: Facilities And Providers

Casting Call: All Breast Cancer Survivors Who Want to Be Part of the Next Pink Glove Dance Video

Posted on July 16, 2010 Written by Annalyn Frame

SOURCE: Medline Industries, Inc.

Video Shoot Takes Place Saturday, July 24, 3:00 p.m., Just East of Fort Point Pier

MUNDELEIN, IL–(Marketwire – July 16, 2010) – Medline Industries, Inc., the company who produced the original Pink Glove Dance, is looking for breast cancer survivors in the San Francisco area who want to be part of the next Pink Glove Dance video. The original video has become an internet sensation, generating almost 11 million views on YouTube since its release last November. The video features healthcare workers at Providence St. Vincent Medical Center in Portland, Ore. dancing while wearing pink gloves.

When and where will it be?
Filming will take place Saturday, July 24th at 3:00 p.m. in the big field just east of Fort Point Pier, with the Golden Gate Bridge in the background.

What are the qualifications to participate?
Participants need to be breast cancer survivors and willing to dance wearing pink gloves. No special dancing skills required. A choreographer will be there to teach simple routines.

How long will it take?
Approximately two hours.

How do I sign up?
Details of the video shoot and registration can be found online at www.pinkglovedance.com/sign-up.
Although participants can just show up on the day of the event, participants are encouraged to register online. 

Details of the day, and any weather updates, will be posted on www.pinkglovedance.com.

Why is this video being made?
The first video was created to help spread the word about breast cancer awareness and the importance of the healthcare worker who takes care of breast cancer patients. It was so successful and generated so much positive attention that hospitals around the country called to see if they could be part of the next video. So the idea of a sequel was developed that not only included hospital workers but breast cancer survivors too. 

Why pink exam gloves?
As a way to extend Medline’s breast cancer awareness campaign, the company developed a pink glove called Generation Pink™. Gloves are also the first point of contact between the healthcare worker and the patient. And, the fact the glove is pink, Medline hoped would get people talking about breast cancer. When the gloves were launched in October, Medline committed to donating $1 of every case purchased to the National Breast Cancer Foundation to fund mammograms for individuals who cannot afford them. In the past five years, Medline has donated almost $500,000 to the National Breast Cancer Foundation. 

Media Contact:
John Marks
(847) 643-3309

Jerreau Beaudoin
(847) 643-3011

Filed Under: Facilities And Providers

James Cook University Hospital Introduces Advanced TomoTherapy(R) Radiation Therapy Treatments

Posted on July 16, 2010 Written by Annalyn Frame

SOURCE: TomoTherapy

MADISON, WI–(Marketwire – July 16, 2010) – TomoTherapy Incorporated (NASDAQ: TOMO) maker of advanced, integrated radiation therapy solutions for cancer care, today announced that James Cook University Hospital (JCUH) in Middlesbrough, England began treating cancer patients with the TomoTherapy® Hi·Art® treatment system last month. The TomoTherapy treatment system, which enables delivery of state-of-the-art CT image-guided intensity modulated radiotherapy (IG-IMRT), reinforces the hospital’s leadership in cancer care for the people of the North East of England. 

Among the first people to be treated was a 55-year-old female patient from Middlesbrough with breast cancer and an unusual chest anatomy. “We could not have treated this woman on a conventional linear accelerator treatment machine, nor with surgery, so it’s extremely satisfying to know we can now offer this quality of treatment to a wider range of patients,” said Karen Pilling, the superintendent radiographer in charge of the TomoTherapy system at JCUH. “The start-up from training through to treating our first patients has been very smooth and easy, and we are benefiting from the reduced set-up time required by the TomoTherapy treatment system. With integrated CT image guidance we are able to see the treatment plan with isodose contours overlaid onto the daily CT images, giving us extra reassurance that the treatment is the most accurate possible.” 

The TomoTherapy treatment system delivers radiation therapy in continuous helical rotations around the patient’s body. By enabling precise IMRT, the system allows clinicians to conform treatment to the shape of the tumor while helping to reduce radiation exposure to surrounding healthy tissue and critical structures. In addition, TomoTherapy technology allows the radiotherapy staff to directly CT image the soft tissues and tumour immediately prior to treatment, and make any necessary adjustments, thereby ensuring greater accuracy for high precision techniques where internal anatomy might change throughout the course of treatment.

Dr. Peter Dunlop, clinical oncologist and clinical director of the James Cook oncology service, outlining his reasons for choosing the TomoTherapy platform stated, “We felt it was extremely important to have fully integrated image guidance and intensity modulation, and we believe TomoTherapy provides that most effectively. It produces the best conformality available. The design of the system is such that there are no junctions, no matching fields, minimized risk of dose calculation mistakes, no uncontrolled hotspots, no gantry collisions and no more electron mode errors. For patients, the megavoltage CT (MVCT) set-ups ensure that we are accurately targeting their tumours. We have found the operation is smooth and treatments are comfortable for patients because they are often quicker than with conventional IMRT, especially in complex head and neck cases.”

Christopher Walker, head of Radiotherapy Physics at James Cook, responsible for all technical and medical physics aspects of this advanced technology, stated, “Procurement of the TomoTherapy system has provided Middlesbrough with an ‘off the shelf’ technical solution to the challenges faced in delivering high quality radiotherapy. The TomoTherapy solution has allowed us to leapfrog to a position of excellence in cancer care in the U.K. The system has a small physical footprint coupled with a reduced radiation shielding requirement compared to conventional machines. We were able to install it in a pre-existing treatment room, which was considered obsolete by present day conventional radiotherapy standards. As a result, TomoTherapy technology has allowed us to provide additional treatment capacity without the need for an expensive new build whilst maximising the efficiency of the existing facility. Installation and acceptance testing passed quickly and seamlessly allowing the physics team to concentrate on the clinical commissioning process. This process was reduced to a relatively simple validation exercise as all the beam data required for patient treatment planning was already pre-loaded in to the dedicated planning computer. The collaborative approach presented by TomoTherapy has allowed us to rapidly introduce advanced treatment methodologies in a safe and controlled way. The whole process was greatly enhanced by the support and training offered to us both by TomoTherapy and Oncology Systems Limited.”

James Cook University Hospital, as a publicly funded National Health Service hospital, has firmly embraced this radiotherapy technology as the most advanced treatment in its arsenal and as a cost-effective approach for treating technically complex cases.

“At an extremely difficult economic time, particularly within the public sector, James Cook has above all, upheld its belief in the unsurpassed quality of treatment brought by TomoTherapy,” says Julie Mead, director and clinical advisor at Oncology Systems Ltd. “The whole oncology team, with support from the Trust Management, has worked hard to secure this new technology for the people of the North East of England. Now with its TomoTherapy system in place, James Cook has become a leader in the UK NHS with the ability to offer world class radiotherapy for its patients.”

TomoTherapy technology is developed and manufactured by TomoTherapy Inc. and is supplied in the U.K. by Oncology Systems Limited, based in Shrewsbury, England.

About James Cook University Hospital 
Based in the north east of England, JCUH is an NHS Foundation Trust and large district general hospital. The hospital was opened in October 2003 and has a capacity of 1,007 beds. It incorporates the full range of all acute and elective medical and surgical specialties including cardiac surgery, cardiology, renal medicine / haemodialysis, neurosurgery, vascular surgery and the regional spinal injuries unit. The radiotherapy and oncology service delivers an integrated service to a population of approximately one million, extending through Teesside, South Durham and North Yorkshire.

About Oncology Systems Limited 
Oncology Systems Limited (OSL), is a privately owned limited company based in Shrewsbury, England. OSL is an exclusive supplier of radiation therapy technology to the UK and Ireland. It distributes TomoTherapy® cancer treatment technology to the UK’s NHS and private radiotherapy facilities, and to both public and private providers in the Republic of Ireland.

About TomoTherapy Incorporated 
TomoTherapy Incorporated develops, markets and sells advanced radiation therapy solutions that can be used to treat a wide variety of cancers, from the most common to the most complex. The ring gantry-based TomoTherapy® platform combines integrated CT imaging with conformal radiation therapy to deliver sophisticated radiation treatments with speed and precision while reducing radiation exposure to surrounding healthy tissue. TomoTherapy’s suite of solutions include its flagship Hi·Art® treatment system, which has been used to deliver more than three million CT-guided, helical intensity-modulated radiation therapy (IMRT) treatment fractions; the TomoHD™ treatment system, designed to enable cancer centers to treat a broader patient population with a single device; and the TomoMobile™ relocatable radiation therapy solution, designed to improve access and availability of state-of-the-art cancer care. TomoTherapy’s stock is traded on the NASDAQ Global Select Market under the symbol TOMO. To learn more about TomoTherapy, please visit TomoTherapy.com.

©2010 TomoTherapy Incorporated. All rights reserved. TomoTherapy, Tomo, TomoDirect, TQA, the TomoTherapy logo and Hi·Art are among trademarks, service marks or registered trademarks of TomoTherapy Incorporated in the United States and other countries.

Investor Contact:
Thomas E. Powell
Chief Financial Officer
608.824.2800
Email Contact

Media Contacts:
Kevin O’Malley
Director, Corporate Communications
608.824.3384
Email Contact

Susan Lehman
Rockpoint Public Relations
510.832.6006
Email Contact

Filed Under: Facilities And Providers

Therma-Med Inc.’s Revenue Generating Bella Vita Clinic Showing Positive Signs of Growth and Expansion

Posted on July 16, 2010 Written by Annalyn Frame

SOURCE: Therma-Med Inc.

BEVERLY HILLS, CA–(Marketwire – July 16, 2010) –  After the completion of one quarter since the acquisition of the Bella Vita Clinic in the Greater Toronto Area (GTA), Therma-Med Inc. (PINKSHEETS: THRA) is pleased with the steady progress that has been evident throughout the transition period and are optimistic about the continued growth of the clinic. The clinic is picking up steam as we move into the second quarter of ownership, it has been established that the Bella Vita clinic is a revenue generating acquisition, and is an active contributor to Therma-Med Inc.’s overall growth plan. The clinic is actively in the process of hiring an additional Chiropractor, Massage Therapist and Naturopathic Doctor to its existing staff, in order to position themselves at the forefront of wellness centers in the area. The additional support will allow the clinic to operate at extended hours, conveniently catering to all patients, and the added services available will certainly attract patients that are searching for a “1 stop wellness retreat.”

The Therma-Med Inc. business model of implementing support services and making key revenue producing acquisitions is without question showing results on a small scale as is demonstrated with the Bella Vita Clinic. While taking these steps to grow operations at this recently acquired clinic, plans continue to move forward in accordance with the company’s business plan of targeting, researching, and implementing Thermal Imaging, medical support services and nutraceutical sales at additional key revenue generating clinics across North America.

About Therma-Med Inc.:
Therma-Med Inc. provides alternative medicinal procedures, premium nutritional supplements, medicinal products and current medical support services by making them available to patients through their clinics and online through e-commerce purchasing applications. Therma-Med Inc., through highly specialized Thermal Imaging and breakthrough alternative procedure clinics, is poised to become a healthcare industry leading company, providing the alternative medicine approach to good health, as well as providing patients with an adjunctive diagnostic procedure that effectively pursues and exposes the benefits of early detection and prevention of various medical conditions. Therma-Med Inc. utilizes thermal imaging systems that incorporate state-of-the-art infrared technologies and proprietary software to accurately and cost-effectively measure physiological changes in the human body, allowing patients of all walks of life access to a proactive form of maintaining good health and quality of life through early detection and prevention.

Cautionary Statement Regarding Forward-Looking Information:
Except for statements of historical fact relating to the Corporation, certain information contained herein constitutes forward-looking statements. Forward-looking statements are frequently characterized by words such as “potential,” “estimate,” “plan,” “expect,” “project,” “intend,” “believe,” “anticipate” and other similar words, or statements that certain events or conditions “may” or “will” occur. Forward-looking statements are based on the opinions and estimates of management at the date the statements are made, and are subject to a variety of risks and uncertainties and other factors that could cause actual events or results to differ materially from those projected in the forward-looking statements. The Corporation undertakes no obligation to update forward-looking statements if circumstances or management’s estimates or opinions should change. The reader is cautioned not to place undue reliance on forward-looking statements.

Contact:
Therma-Med Inc.
Investor Relations: 1-888-323-0929

Filed Under: Facilities And Providers

Sun Healthcare Group, Inc. Schedules Conference Call to Announce Earnings for the Second Quarter of 2010

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: Sun Healthcare Group, Inc.

IRVINE, CA–(Marketwire – July 15, 2010) –  Sun Healthcare Group, Inc. (NASDAQ: SUNH) invites investors to listen to a conference call with Sun’s senior management on Thursday, July 29, 2010, at 10 a.m. Pacific / 1 p.m. Eastern to discuss the Company’s earnings for the second quarter of 2010.

To listen to the conference call, dial (888) 437-9315 and refer to Sun Healthcare Group. A recording of the call will be available from 4 p.m. Eastern on July 29, 2010, until midnight Eastern on Aug. 30, 2010, by calling (888) 203-1112 and using access code 1833674.

About Sun Healthcare Group, Inc.

Sun Healthcare Group, Inc.’s (NASDAQ: SUNH) subsidiaries provide nursing, rehabilitative and related specialty healthcare services principally to the senior population in the United States. Sun’s core business is providing inpatient services, primarily through 166 skilled nursing centers, 16 combined skilled nursing, assisted and independent living centers, 10 assisted living centers, two independent living centers and eight mental health centers. On a consolidated basis, Sun has annual revenues of $1.9 billion and approximately 30,000 employees in 46 states. At March 31, 2010, SunBridge centers had 23,205 licensed beds located in 25 states, of which 22,423 were available for occupancy. Sun also provides rehabilitation therapy services to affiliated and non-affiliated centers through its SunDance subsidiary, medical staffing services through its CareerStaff Unlimited subsidiary and hospice services through its SolAmor subsidiary.

Contact:
Investor Inquiries
(505) 468-2341
Media Inquiries
(505) 468-4582

Filed Under: Facilities And Providers

Sales Revenue Exceeds Projections, BDI Pharma Demonstrates Continued Growth

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: BDI Pharma, Inc.

COLUMBIA, SC–(Marketwire – July 15, 2010) –  BDI Pharma, Inc. (BDI), the nation’s fastest growing national distributor of biotech therapies, announced that, in spite of the uncertainty of the nation’s current economic climate, Sales Revenues continued to rise during the first two (2) fiscal quarters of 2010. This expansion of business represented an increase of fifteen percent (15%) above that for the same period in 2009 and exceeded the company’s forecasted growth for the first six (6) months of the year. The Specialty Biopharmaceutical class of products, primarily in the clinical areas of Oncology and Infectious Disease, served as the primary driver for Sales Revenue during this period. Also notable were gains within the Protein Biotherapeutics class, specific to the Hemophilia and Hyper-Immune product lines.

In addition, BDI Pharma realized significant growth in staffing through new hires during Q2 2010. Over the past ninety (90) days, the size of the company’s Biopharmaceutical Sales Staff grew by twenty percent (20%). The company also experienced growth within the BDI Promotions Division (the company’s Advertising and Promotional Division), as well as the Corporate Customer Service Division and established a new specialty sales division during the past quarter.

“Growth, at BDI Pharma, is not just an objective, it is an expectation and, as such, it is something for which we plan and prepare,” said William A. Shirey, III, Executive VP. “The key to BDI Pharma’s growth can be found in our commitment to incorporate a relatively simple matter — the strategic allocation of corporate resources — and to merge it with something far more difficult — the actual expense of those resources in a conscientious manner. Many companies adopt the former, but ultimately bend in response to market pressure and lose their will to integrate the latter. At BDI Pharma, we apply both with equal veracity as we strive to supply substantial, quantifiable value to our customers and manufacturing trade partners, alike.”

About BDI Pharma, Inc.

Since 1995, BDI Pharma, Inc. (formerly known as Blood Diagnostics, Inc.) has built an exceptional reputation as the industry trusted source for products and service. The company has exhibited an exemplary track record providing an unparalleled level of customer service, market data and product integrity to both its customer base and trade partners. Such commitment to the product channel has earned BDI recognition as “ADR,” or Authorized Distributor of Record, for the manufacturers it represents. BDI’s specialty pharmaceutical focus is evident in its commitment to biotherapeutics, chemotherapies, vaccines and plasma protein therapies, including albumin, IVIG, coagulation factors, high-titer immune globulins, and injectables. 

BDI Pharma defines its customer-centric approach to serving the nation’s healthcare community through innovative inventory supply solutions, unparalleled customer service, extensive product knowledge, 24/7 emergency availability and urgent need delivery. An open-access resource for reference material, educational literature, market data and online ordering, BDI Pharma’s home web page www.bdipharma.com has become an industry renowned point of reference. Proprietary programs for product consignment (www.consignadvantage.com), influenza vaccine pre-booking (www.securiflu.com), vaccine ordering (www.securivax.com) and purchasing/reward programs (www.qoreprogram.com and www.securigam.com) round out a family of solutions tailored to the needs of the healthcare community at large.

Contact:
Brad Davis
Director of Marketing
Email Contact
(800) 948-9834

Filed Under: Facilities And Providers

Eveo Gets Results at 2010 ASCO Trade Show

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: Eveo

SAN FRANCISCO, CA–(Marketwire – July 15, 2010) –  With the innovative use of several emerging technologies, San Francisco-based digital healthcare agency Eveo made a big impression at the 2010 ASCO trade show. The 46th Annual meeting of the American Society of Clinical Oncology (ASCO) was held in Chicago, June 4-8, 2010, where more than 30,000 oncology specialists from around the world gathered to discuss the latest innovations in research, quality, practice and technology in cancer. Eveo (www.eveo.com) partnered with marketers to create customized, engaging programs that improved the overall quality of customer interactions and led to a dramatic increase in booth traffic.

Eveo’s Stereoscopic 3D Animation Video was viewed by over 1,000 participants at ASCO. In addition, the multi-touch technology and “Build a Patient” program were showstoppers as they deepened customer engagement and improved retention. Eveo also released several new applications for the iPhone and iPad that enabled health care providers to stay connected with their customers in a whole new way. “We knew the technologies we had in place were going to be a hit at ASCO,” says Eveo CEO and founder Olivier Zitoun, “but we didn’t expect the reaction to be as big as it was. The traffic in the booths was remarkable.”

Ensuring success at trade shows is no easy task. To maximize the potential for success, Eveo recommends following these simple best practices:

  1. Start planning for the launch of new technologies early in the booth planning process. The more time you spend up front, the more smoothly everything will go.
  2. Perform live technology testing for new programs as part of the booth planning and set up process. This is often overlooked, but an important key to success.
  3. Train reps and booth personnel on new technologies prior to the show. Reps should be focused on demonstrating exciting new technologies, not learning them as they go.
  4. Optimize booth staffing by utilizing reporting and tracking for all show displays.
  5. Send post-conference surveys to customers and corporate participants to learn about what worked and what didn’t.
  6. Make sure there are clear signs and directions for each display, especially if it is a new technology.
  7. To maximize ROI, develop programs that reps can use in the field after the show or health care providers can access digitally and/or via mobile devices. 

To enlist Eveo’s help in your next tradeshow, contact [email protected]. For a full list of Eveo’s services, visit http://eveo.com/what-we-do/.

ABOUT EVEO
For innovative e-marketing strategies and powerful digital solutions, many of the world’s leading pharmaceutical, biotech and medical device companies depend on Eveo, a full-service independent digital healthcare agency headquartered in San Francisco. Founded in1999, Eveo is led by CEO Olivier Zitoun and a seasoned management team with extensive backgrounds in healthcare and interactive. Eveo’s core capabilities encompass all facets of digital marketing, as well as non-traditional web solutions, video production, 3D animation, tradeshow solutions, mobile applications, multi-touch experiences and more. The agency has a staff of over 150, with field offices in Chicago, New York, New Jersey and Philadelphia. Over the course of its ten years in business, Eveo has collected over 70 industry awards and in 2010 was named the #1 Independent Digital Healthcare Agency in the U.S. (based on 2010 Agency List ranking agencies by revenue). Eveo is redefining the e in e-marketing. Visit: www.eveo.com

Media Contact:
Sonya More’
Email Contact
415 749 6777 x171

Filed Under: Facilities And Providers

WellTek Subsidiary Forms Strategic Partnership With Global Network Marketing Company

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: WellTek Incorporated

WellCity Establishes Launch Pad for Rapid Expansion

ORLANDO, FL–(Marketwire – July 15, 2010) –  WellCity, Inc. (http://www.WellCity.com), a wellness-related social network and subsidiary of WellTek, Inc. (OTCBB: WTKN), today announced a strategic partnership with XOOMA Worldwide (http://www.XoomaWorldwide.com), a global network marketing company, in which the two companies have collaborated to bring more than 200,000 new users, cutting edge wellness products, a robust infrastructure and a major distribution system into WellCity. The agreement serves as a catalyst for both companies to carry out its rapid expansion plans.

As part of the relationship, XOOMA will provide exclusive support with product distribution and logistics, one of XOOMA’s strongest assets. The two companies also agreed to work on future product development together.

“Our collaboration with WellCity is about joining our global mission of Changing the Health of a Generation with a true innovator in social networking,” said Ron Howell, President and CEO of XOOMA Worldwide. “We believe that the combination of WellCity and XOOMA’s strengths will be incredibly attractive to our distributors as well as WellCity ‘residents.'”

Randy Lubinsky, Chairman and CEO of WellTek, noted, “XOOMA provides WellCity with an immediate global platform and 200,000 new ‘residents,’ exposing us to a much larger audience. It’s a global brand that people already recognize.” Lubinsky continued, “The superiority of XOOMA products is consistent with the Gold Standard of our other brands. Partnering with XOOMA is a natural progression to our tactical expansion initiative and integrates well into WellTek’s growing portfolio of trusted health, fitness and wellness brands.”

About XOOMA Worldwide
XOOMA Worldwide is a global network marketing company distributing cutting edge health and wellness products: including vitamins and minerals, functional health beverages and weight loss and skin care products to over 60 countries around the world. XOOMA’s Scientific Advisory Board provides education and guidance on health related topics and peer-reviewed scientifically supported nutritional applications for prevention and optimal health support.

About WellCity Incorporated
WellCity is a social utility where health- and wellness-minded ‘residents’ can closely commune with one another; receive support, information and encouragement from their ‘neighbors’ and from a league of leading professional experts; shop for health and wellness-oriented product and services; compete in WellCity’s proprietary 90-Day Wellness Challenge; and even enjoy income opportunities by leveraging their personal network. For more information on the Company, please visit www.WellCity.com.

About WellTek Incorporated
WellTek is a global health, fitness and wellness company that provides proven solutions to help address some of the world’s most pressing and costly health and wellness challenges. The Company owns and operates WellCity, Inc., a premiere wellness-related social utility that helps ‘residents’ live longer, feel better, look younger and enjoy life more as they age. The Company’s subsidiary, MedX Limited, manufactures, markets and distributes the most advanced medical exercise equipment to the medical and fitness markets. Through its wholly owned subsidiary Pure HealthyBack, Inc., WellTek is redefining healthcare delivery by providing health plans, self-insured employer groups, and consumers with a viable non-surgical, lower cost treatment for patients who are seeking lasting relief from chronic neck and back pain. For more information on the Company, please visit www.WellTekinc.com. 

Certain statements contained in this press release, which are not based on historical facts, are forward-looking statements as the term is defined in the Private Securities Litigation Reform Act of 1995, and are subject to substantial uncertainties and risks in part detailed in the respective Company’s Securities and Exchange Commission filings, that may cause actual results to materially differ from projections. Although the Company believes that its expectations are reasonable assumptions within the bounds of its knowledge of its businesses, expectations, representations and operations, there can be no assurance that actual results will not differ materially from their expectations. Important factors currently known to management that could cause actual results to differ materially from those in forward-looking statements include the Company’s ability to execute properly its business model, to raise additional capital to implement its continuing business model, the ability to attract and retain personnel — including highly qualified executives, management and operational personnel, ability to negotiate favorable future debt facilities and capital raises, and the inherent risk associated with a diversified business to achieve and maintain positive cash flow and net profitability. In light of these risks and uncertainties, there can be no assurance that the forward-looking information contained in this press release will, in fact, occur. 

FOR MORE INFORMATION, PLEASE CONTACT:
Legacy Marketing Group
Roxie Mooney
President & CEO
(
Twitter: roxiemooney)
407-575-3220
via email at [email protected]

Filed Under: Facilities And Providers

Media Alert: Electronic Health Care (EHR) Expert From Amazing Charts Available for Comment on Impact of New Government Standards for EHRs on Small…

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: Amazing Charts

SAUNDERSTOWN, RI–(Marketwire – July 15, 2010) –  The Federal government issued new rules Tuesday that will reward doctors and hospitals for the “meaningful use” of electronic health records, a top goal of President Obama. The rules significantly scale back proposed requirements that the health care industry had denounced as unrealistic.

What: subject matter expert: impact of new government standards for EHRs on small physician practices

Why: Doctors and hospitals could receive as much as $27 billion over the next 10 years to buy equipment to computerize patients’ medical records. A doctor can receive up to $44,000 under Medicare and $63,750 under Medicaid, while a hospital can receive millions of dollars, depending on its size

Who: Amazing Charts founder and CEO Dr. Jonathan Bertman, one of the nation’s leading experts on EHR/EMR systems and issues/trends impacting small and medium-sized physician practices.

Amazing Charts, due to its industry-leading usability and satisfaction ratings in multiple studies and $995 price tag is the EHR-of-choice for small practices (used by more than 3600 practices in the U.S. alone)

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Filed Under: Facilities And Providers

New Study Proves Care by Podiatrists Dramatically Decreases Lower Limb Amputation

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: American Podiatric Medical Association

Research Results to be Presented at APMA’s 98th Annual Scientific Meeting

BETHESDA, MD–(Marketwire – July 15, 2010) –  

*MEDIA NOTE: Study will be presented at the Washington State Convention Center on Saturday, July 17, at 7:30am.

Essential foot care by a podiatrist has now been statistically proven to reduce hospitalization and amputation in adults with diabetes, according to a first of its kind study conducted by Thomson Reuters. The study will be presented by Vickie R. Driver, MS, DPM, during the American Podiatric Medical Association’s (APMA) 98th Annual Scientific Meeting in Seattle, July 15-18, 2010. The presentation will highlight the dramatic impact that as few as one visit to a podiatrist can have on patients with diabetes.

The study, which was sponsored by APMA, examined records for more than 32,000 patients with diabetes, ages 18-64, and compared health and risk factors for those who had podiatry visits to those who did not. Researchers found that care by a podiatric physician (defined as at least one preventative, pre-ulcer visit) was associated with a nearly 29 percent lower risk of amputation and 24 percent lower risk of hospitalization. Diabetic foot complications are the leading cause of non-traumatic lower limb amputation in the U.S. 

“The results of this study undeniably support visits to a podiatrist being critical to a diabetes patient’s health and well being,” said APMA member Dr. Driver. “No longer can care by a podiatrist be considered optional for those with diabetes, and the earlier a podiatrist is included in the diabetes management team, the better quality of life for the patient and greater health-care cost savings for all involved. This study clearly allows us to understand both the clinical and economic value of a podiatrist, in the team approach to saving diabetic patients’ feet.”

The study was conducted using Thomson Reuters’ MarketScan Research Databases, which house fully integrated, de-identified health-care claims data extensively used by researchers to understand health economics and outcomes. Studies based on MarketScan data have been published in more than 130 peer-reviewed articles in the past five years.

Lead researcher Teresa Gibson, PhD, director of health outcomes research at Thomson Reuters said, “Using the MarketScan Databases, we statistically matched patients with diabetes and foot ulcers who had visited a podiatrist with like patients who had not. The analysis of the data indicates that patients who had seen a podiatrist in the year prior to the onset of a foot ulcer had significantly lower rates of any amputation and hospitalization than those who had not.”

For additional information on the study, visit www.apma.org/diabetesstudy.

Media interested in attending the presentation during the APMA 98th Annual Scientific Meeting should contact Angela Berard at [email protected] or 301-861-9342.

Founded in 1912, the American Podiatric Medical Association (APMA) is the nation’s leading and recognized professional organization for doctors of podiatric medicine (DPMs). DPMs are podiatric physicians and surgeons, also known as podiatrists, qualified by their education, training and experience to diagnose and treat conditions affecting the foot, ankle and structures of the leg. The medical education and training of a DPM includes four years of undergraduate education, four years of graduate education at an accredited podiatric medical college and two or three years of hospital residency training. APMA has 53 state component locations across the United States and its territories, with a membership of close to 12,000 podiatrists. All practicing APMA members are licensed by the state in which they practice podiatric medicine. For more information, visit www.apma.org.

Thomson Reuters is the world’s leading source of intelligent information for businesses and professionals. We combine industry expertise with innovative technology to deliver critical information to leading decision makers in the financial, legal, tax and accounting, healthcare and science and media markets, powered by the world’s most trusted news organization. With headquarters in New York and major operations in London and Eagan, Minnesota, Thomson Reuters employs 55,000 people and operates in over 100 countries. For more information, go to www.thomsonreuters.com.

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Filed Under: Facilities And Providers

Child Care Insurance Professionals Makes Pitch to Lead the Child Care Insurance Industry to New Heights

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: Child Care Insurance Professionals

SALT LAKE CITY, UT–(Marketwire – July 15, 2010) –   When Patrick Treend was a member of the Florida Marlins organization, he faced some pretty stiff competition as an up-and-coming pitcher. Now, he’s making a pitch to become the voice of our nation’s Child Care and Early Education insurance industry.

Treend, President of Security Planning & Insurance Corporation, which for more than 30 years has been one of the nation’s most-trusted insurance Agencies, has quickly become one of the most highly respected advocates in the child care industry. He oversees the day-to-day operations of the parent company’s two primary entities, Child Care Insurance Professionals and Charter School Insurance Professionals, the preferred choice for insurance in early education and child care.

“My general philosophy is to work as our client’s voice, their advocate,” says Treend. “We strive to get the most competitive rates and coverage without any allegiance to any one carrier. Generally speaking, child care and early education has very little competition, little to no national resources and no voice as it relates to insurance services. In most cases, people are taken advantage of because of the lack of competition and overall lack of insurance professionals that focus on this market.”

Due to his vast insight and expertise on the current trends within the child care industry, Treend is asked to speak at all of the regional conferences for the prestigious National Child Care Association (NCCA). He was recently in Atlanta to address his constituents on the state of the health care industry.

On the new legislation for Health Care Reform: “Under the new Health Care Reform Law, small businesses will find major changes to how they must provide health coverage and how much they must pay for it,” claims Treend. “I remain concerned that any advances under the new reform bill will be eroded by the unchecked rise of health care costs that were not adequately addressed in the legislation.”

Added Treend, “As it relates to Child Care and small businesses in general, it will have a huge impact for the smaller centers. The majority of the smaller centers cannot afford a traditional group plan and, if they could, the employee base cannot afford their employee portion. The only thing that the reform bill will do in the near future is make the process more confusing and costly.”

For Treend to be asked to voice his opinions has not been uncommon since making his pitch to the insurance industry in 2002. After quickly rising in ranks at Liberty Mutual Group and Zion’s Insurance Agency, Treend set his strike zone on child care and early education, revamping Security Planning & Insurance Corporation by making it the first insurance Agency of its kind to focus exclusively on providing packaged insurance to private and independent Charter Schools and Child Care Centers nationwide.

Child Care Insurance Professionals and, more recently, Charter School Insurance Professionals, are already considered ahead of their time and are the preferred choice for child care and charter schools looking for cost savings, favorable terms, targeted service and exceptional follow-through.

“Child Care and Charter Schools now have the convenience of dealing with one insurance Agency that handles all their policies, creating a significant cost savings. Our firm’s business model of targeted insurance programs and packages, particularly in the commercial child care industry, has taught us the value of market specificity. We believe focusing on a specific market niche enables us to provide targeted service and benefits that an individual school or an independent provider would not be able to access,” said Treend. 

For more information on Child Care Insurance Professionals and Charter School Insurance Professionals, visit their respective sites at www.ChildCareInsuranceProfessionals.com and www.CharterSchoolInsurancePros.com or call (888) 812-9992.

Contact:
Patrick Treend
Child Care Insurance Professionals
Email Contact
888-812-9992

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Filed Under: Facilities And Providers

Remedent Reports Fourth Quarter and Year End Results and Remedent to Host a Conference Call at 11:00 A.M. EST, Tuesday, July 20, 2010

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: Remedent, Inc.

DUERLE, BELGIUM–(Marketwire – July 15, 2010) – Remedent, Inc. (OTCBB: REMI), an
international company specializing in research, development, and
manufacturing of oral care and cosmetic dentistry products, reported
results for the final quarter and for the year ended March 31, 2010 (in US
Dollars).

Net sales in the fourth quarter decreased 27% to $2.5 million from $3.4
million in the same year ago quarter. The decrease in sales was due to non
recurring license fees of approx $1 million received from Denmat in the
fourth quarter ended March 31, 2009.

Loss from operations in the fourth quarter was a loss of $111,138 $(0.01)
per share as opposed to a loss of $1,079,063 $(0.05) in the same year-ago
quarter, based upon 20 million weighted average basic shares outstanding.

Net loss for the year ended March 31, 2010 was $2.4 million or $(0.12) per
share, as compared with a loss of $3.0 million or $(0.15) per share for the
year ended March 31, 2009.

Cash and cash equivalents totaled $614,000 at March 31, 2010 as opposed to
$1.8 million at March 31, 2009.

Management Commentary

“Our sales strategy of shifting from our previous wholesale sales (B2B)
model via a distributor to a direct retail model (B2C) is beginning to take
shape. Included in our net loss of $111,000 for the fourth and final
quarter ended March 31, 2010, was a loss of $550,000 directly attributable
to our subsidiary Sylphar. The improved results are attributable to the
inclusion for the first time of our Asian operations into our consolidated
financial statements together with the gain realized from the sale of First
Fit. Sales at all our Spa locations, namely in Beijing, Hong Kong, Taiwan
and in Europe continue to exceed our expectations as sales continue to
climb during the first quarter of the next financial year,” said Guy De
Vresse the CEO of Remedent.

Conference Call Information

Remedent will host a conference call on July 20, 2010 at 11:00 a.m. Eastern
Standard time (8:00 a.m. Pacific time) to discuss these results and its
strategic plans for the future. A question and answer session will follow
management’s presentation. To participate in the call, dial the appropriate
number 5-10 minutes prior to the start time.

Date: Tuesday,  July 20,2010
Time 11:00 a.m. Eastern time (8:00 a.m. Pacific time).
Dial in number: 1-888-677-8749
International: 1-913-312-1482

A simultaneous web cast and replay of the call will be available through
July 31, 2010. The replay pass code is 8101477.

About Remedent

Remedent, Inc. specializes in the research, development, manufacturing and
marketing of oral care and cosmetic dentistry products. The company serves
professional dental industry with breakthrough technology for dental
veneers. These products are supported by a line of professional veneer
whitening and teeth sensitivity solutions. Headquartered in Belgium,
Remedent distributes its products to more than 35 countries worldwide. For
more information, go to www.remedent.com.

Statement under the Private Securities Litigation Reform Act of 1995

Statements in this press release that are “forward-looking statements” are
based on current expectations and assumptions that are subject to risks and
uncertainties. Such forward-looking statements involve known and unknown
risks, uncertainties and other unknown factors that could cause Remedent’s
actual operating results to be materially different from any historical
results or from any future results expressed or implied by such
forward-looking statements. In addition to statements that explicitly
describe these risks and uncertainties, readers are urged to consider
statements that contain terms such as “believes,” “belief,” “expects,”
“expect,” “intends,” “intend,” “anticipate,” “anticipates,” “plans,”
“plan,” “projects,” “project,” to be uncertain and forward-looking. Actual
results could differ materially because of factors such as Remedent’s
ability to achieve the synergies and value creation contemplated by the
proposed transaction. For further information regarding risks and
uncertainties associated with Remedent’s business, please refer to the risk
factors described in Remedent’s filings with the Securities and Exchange
Commission, including, but not limited to, its annual report on Form 10-K
and quarterly reports on Form 10-Q.

                      REMEDENT, INC. AND SUBSIDIARIES
                  CONSOLIDATED STATEMENTS OF OPERATIONS
                                (unaudited)



                           Three months ended            Year ended
                                March 31,                 March 31,
                            2010         2009         2010         2009
                        -----------  -----------  -----------  -----------
Net sales               $ 2,472,815  $ 3,390,355  $ 8,247,940  $14,639,541
Cost of sales               952,189    1,650,315    4,322,680    6,614,723
                        -----------  -----------  -----------  -----------
  Gross profit            1,520,626    1,740,040    3,925,260    8,024,818
                        -----------  -----------  -----------  -----------
Operating Expenses
Research and development     39,850       24,273      271,195      248,652
Sales and marketing         461,078      370,042    1,352,260    2,793,970
General and
 administrative           1,313,812    1,639,656    4,524,324    5,312,192
Depreciation and
 amortization               168,218      173,903      726,499      615,674
                        -----------  -----------  -----------  -----------
TOTAL OPERATING
 EXPENSES                 1,982,958    2,207,874    6,874,278    8,970,488
                        -----------  -----------  -----------  -----------
  OPERATING LOSS           (462,332)    (467,834)  (2,949,018)    (945,670)
                        -----------  -----------  -----------  -----------
NON-OPERATING (EXPENSE)
 INCOME 
Warrants issued pursuant
 to Distribution Agreement       --           --     (168,238)  (4,323,207)
Gain on disposition of OTC       --           --           --    2,830,953
IMDS provision                   --     (300,000)          --     (300,000)
Interest expense/other
 deductions                 (50,596)    (166,972)    (171,364)    (417,147)
Interest income/other
 income                      54,907        1,884      170,244      348,997
Other income                     --           --     (169,358)          --
                        -----------  -----------  -----------  -----------
TOTAL OTHER INCOME
 (EXPENSES)                   4,311     (465,088)    (168,238)  (1,860,404)
                        -----------  -----------  -----------  -----------

LOSS FROM CONTINUING
 OPERATIONS BEFORE
 INCOME TAXES              (458,021)    (932,922)  (3,118,376)  (2,806,074)
Income tax expense          (14,242)     (32,633)     (14,242)     (32,633)
                        -----------  -----------  -----------  -----------

NET LOSS FROM CONTINUING
 OPERATIONS BEFORE
 MINORITY INTEREST         (472,263)    (965,555)  (3,132,618)  (2,838,707)
NET (LOSS) INCOME
 ATTRIBUTABLE TO
 NON-CONTROLLING
 INTERESTS                 (346,683)     114,208     (782,703)     114,208
                        -----------  -----------  -----------  -----------

NET LOSS FROM CONTINUING
 OPERATIONS, ATTRIBUTABLE
 TO REMEDENT INC. COMMON
 STOCKHOLDERS           $  (111,138) $(1,079,763) $(2,349,915) $(2,952,915)
                        ===========  ===========  ===========  ===========

LOSS PER SHARE
Basic and fully diluted $     (0.01) $     (0.06) $     (0.12) $     (0.15)
                        ===========  ===========  ===========  ===========
WEIGHTED AVERAGE
 SHARES OUTSTANDING
Basic and fully
 diluted                 19,995,969   19,995,969   19,995,969   19,559,653
                        ===========  ===========  ===========  ===========

OTHER COMPREHENSIVE
 INCOME (LOSS):
Net loss attributable
 to Remedent, Inc.
 common stockholders    $  (111,138) $(1,079,763) $(2,349,915) $(2,952,915)
Foreign currency
 translation adjustment    (102,949)     (45,371)      (9,464)    (668,245)
                        -----------  -----------  -----------  -----------
Total other comprehensive
 loss                      (214,287)  (1,125,134)  (2,359,379)  (3,621,160)
Less: comprehensive
 (loss) income
 attributable to
 non-controlling
 interest                   (42,623)     (54,700)       7,130      (54,700)
                        -----------  -----------  -----------  -----------
COMPREHENSIVE LOSS
 ATTRIBUTABLE TO
 REMEDENT INC.,
 COMMON STOCKHOLDERS    $  (171,664) $(1,070,434) $(2,366,509) $(3,566,460)
                        ===========  ===========  ===========  ===========




                      REMEDENT, INC. AND SUBSIDIARIES
                        CONSOLIDATED BALANCE SHEETS


                                              March 31,2010  March 31,2009
                                              -------------  -------------
ASSETS
CURRENT ASSETS:
Cash and cash equivalents                     $     613,466  $   1,807,271
Accounts receivable, net of allowance for
 doubtful accounts of $65,845 at March 31,
 2010 and $33,966 at March 31, 2009                 806,931      3,208,120
Inventories, net                                  2,161,692      1,937,946
Prepaid expense                                     920,487      1,310,900
                                              -------------  -------------
Total current assets                              4,502,576      8,264,237
                                              -------------  -------------
PROPERTY AND EQUIPMENT, NET                       1,735,719      1,024,999
OTHER ASSETS
Long term investments and advances                  750,000        750,000
Patents, net                                        246,992        163,106
Goodwill                                            699,635             --
                                              -------------  -------------
Total assets                                  $   7,934,922  $  10,202,342
                                              =============  =============
LIABILITIES AND STOCKHOLDERS' EQUITY
 (DEFICIT)
CURRENT LIABILITIES:
Current portion, long term debt               $     215,489  $      78,798
Line of Credit                                      674,600        660,200
Accounts payable                                  1,932,684      1,398,420
Accrued liabilities                                 491,536      1,590,360
Due to related parties                              268,484             --
Income taxes payable                                     --         39,339
                                              -------------  -------------
Total current liabilities                         3,582,793      3,767,117
  Long term debt less current portion               425,882        100,542
                                              -------------  -------------
Total liabilities                                 4,008,675      3,867,659
                                              -------------  -------------

EQUITY:
Preferred Stock $0.001 par value (10,000,000
 shares authorized, none issued and
 outstanding)                                           --            --
Common stock, $0.001 par value; (50,000,000
 shares authorized, 19,995,969 shares issued
 and outstanding at March 31, 2010 and
 19,995,969 shares issued and outstanding at
 March 31, 2009)                                     19,996         19,996
Treasury stock, at cost; 723,000 and 723,000
 shares at March 31, 2010 and March 31, 2009
 respectively                                      (831,450)      (831,450)
  Additional paid-in capital                     24,742,201     24,106,055
Accumulated deficit                             (19,565,943)   (17,216,028)
Accumulated other comprehensive income (loss)
 (foreign currency translation adjustment)         (650,059)      (640,595)
Obligation to issue shares                           97,500             --
                                              -------------  -------------
Total Remedent, Inc. stockholders' equity         3,812,245      5,437,978
                                              -------------  -------------
Non-controlling interest                            114,002        896,705
                                              -------------  -------------
Total stockholders' equity                        3,926,247      6,334,683
                                              -------------  -------------
Total liabilities and equity                  $   7,934,922  $  10,202,342
                                              =============  =============

Filed Under: Facilities And Providers

Third Time’s a Charm, The Lasalle Group, Inc. Breaks Ground on New Specialized Assisted Living Community in Houston

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: The LaSalle Group, Inc.

Leading Real Estate Developer Constructs State-of-the-Art Facility Dedicated Specifically to Alzheimer’s and Memory Care in Spring, TX

SPRING, TX–(Marketwire – July 15, 2010) –  Dallas-based developer The LaSalle Group, Inc. is breaking ground on its third specialized Alzheimer’s and Memory Care Assisted Living Community in the Houston area, Autumn Leaves of Cypresswood, in Spring, TX. Company leadership, principal investors and other key partners will gather to see the newest addition to the Autumn Leaves family at official ground breaking ceremonies Tuesday, July 20 beginning at 11:00 a.m. Ceremonies will take place at the Cypresswood site located at 6327 Cypresswood Drive in Spring, TX. Local media and Spring area officials are invited to attend as well. 

Research of the Houston area has continued to show a demand for dedicated Alzheimer’s beds that exceeds the current supply. “We will continue to develop in the Houston market,” said Mitchell Warren, President of The LaSalle Group. “Our partners and investors recognize the pent-up need for our dedicated services that cater to this specific population and based on our in-depth market research results, we are committed to continuing our growth pattern in this market.” Autumn Leaves of Cypresswood will be the 15th property developed by LaSalle over the past ten years. Currently, The LaSalle Group has nine Autumn Leaves communities operating successfully in the Dallas/Fort Worth market and three in the greater Chicago area. The first Houston property to open, Autumn Leaves of The Woodlands, is set to accept their first residents in August; construction on the second Houston property, Autumn Leaves of Riverstone, is underway in Missouri City and scheduled to be completed in early Spring 2011. The company plans to continue their current expansion into the Houston market opening new communities in the area over the next three years.

Autumn Leaves of Cypresswood is scheduled to be completed and accepting residents by late Spring 2011. The property will feature 38 units and accommodate approximately 46 residents. For more information on this or other LaSalle Group projects, contact the home office at (214) 239-8400.

Construction and Management
Lake Superior Contracting, LaSalle’s in-house, full-service construction division, will coordinate and manage the design and construction of the new property ensuring the distinctive, research-based structural design attributed to all of LaSalle’s Autumn Leaves communities is in place. Sister firm Constant Care Management Company will manage and oversee all of the day-to-day operations once the community opens.

About The LaSalle Group, Inc. 
Family-owned and operated, The LaSalle Group (with its subsidiaries and affiliates) develops, builds, manages and owns specialized assisted living residences for people with Alzheimer’s and other forms of memory impairment, as well as other specialized real estate properties throughout the United States. For more information about our business, companies and current projects visit http://www.LaSalleGroup.com or call 1-800-452-7255. “Our Family Caring For Your Family”

About Alzheimer’s Disease
Alzheimer’s disease is a fatal and progressive brain disease that affects over 5.3 million Americans. Currently there is no cure and medications do not stop or reverse the disease. As the most common form of dementia, it accounts for more than approximately 60% of dementia cases.

CONTACT:
Lori Gillen
Communications Associate
The LaSalle Group/Constant Care Management
(214) 239-8400 x130

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Filed Under: Facilities And Providers

Healthnostics Repurchases 150 Million Shares of Its Stock

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: Healthnostics, Inc.

NEW YORK, NY–(Marketwire – July 15, 2010) –  Healthnostics, Inc. (PINKSHEETS: HNSS), a medical manufacturing and biotechnology analytics company, has sold an interest in MedBioWeb, Corp., in exchange for 150 million shares of its common stock, thereby reducing the actual issued and outstanding shares of Healthnostics, Inc., to 155,857,509.

As the Company refocuses its business, it is contemplating the possibility of a sale of its remaining interest in MedBioWeb Corp. MedBioWeb Corp. may more readily achieve its profit goals as an independent company and Healthnostics, through its recent acquisition, may be more able to show a substantial increase in per share earnings due to the near halving of outstanding shares.

The Company will continue to pursue acquisitions that are both compatible and synergistic.

“The Company is witnessing dramatic changes, all of which we believe bode well for our stockholders. We are focusing on profitability and earnings per share, factors that will enhance our ability to thrive and grow,” said Alan Grofe, president.

About Healthnostics
Healthnostics, Inc. is a medical and biotechnology analytics company that provides comprehensive patient clinical monitoring and risk management systems to acute care hospitals and utilizes its Internet portals to deliver medical and biotechnology resource information to industry professionals as well as to the general public. Healthnostics’ major products include: Worldwide Wipes Co., a manufacturer and distributor of medical and other wipes, MedGuardian, a patient care monitoring and risk management system for hospitals that is fully Web-based; and through the MedBioWeb subsidiary, MedBioWorld™, one of the largest professional medical and biotechnology directory resource and reference portal sites on the Internet, and FamilyMedicalNet, a companion consumer healthcare information portal.
For further information please visit Healthnostics www.healthnostics.com, and Worldwide Wipes Co. www.wipesco.com, MedBioWorld www.medbioworld.com, and FamilyMedicalNet www.familymedicalnet.com.

And visit us on Facebook at www.facebook.com/Healthnostics.

This press release may contain certain statements that are not descriptions of historical information, but are forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Exchange Act of 1934. These forward-looking statements refer to matters that involve risks and uncertainties. Such statements reflect management’s current views and are based on certain assumptions. Actual results could differ materially from the assumptions currently anticipated.

Contact:
Alan Grofe
P. 703-754-7126
[email protected]

Filed Under: Facilities And Providers

Radient Pharmaceuticals Launches New Investor Video Channel

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: Radient Pharmaceuticals Corporation

TUSTIN, CA–(Marketwire – July 15, 2010) –   Radient Pharmaceuticals Corporation (RPC) (NYSE Amex: RPC) announced today it has launched a new investor video channel on its corporate website (www.radient-pharma.com) to deliver regularly scheduled, dynamic video content to Wall Street and the investing community. The videos are also available at: http://radient.investorcandy.com/radient/RD#videos.

Investor communications through RPC’s new investor video channel will be delivered on a regular basis and will cover a broad range of topics and information, including personalized messages from RPC’s executive team, breaking company news, and in-depth updates on the Company’s business and product commercialization strategy, execution, timeline and progress. RPC also plans to leverage its online video channel as a medium to communicate to other key audiences beginning in the third quarter of 2010. Targeted audiences include distributors, strategic partners, oncologists, general practice physicians and cancer patients who may have used or are considering using RPC’s Onko-Sure in vitro diagnostic cancer test. 

“Video is becoming increasingly important as a way of reaching investors and business partners with valuable information,” commented RPC’s Chairman and CEO Mr. Douglas MacLellan. “RPC’s new Investor Video Channel is an excellent complement to our just launched corporate website and an excellent channel to communicate business activities that are of material importance our investing community.”

Updates on the availability of new content will be broadly communicated through the issuance of press releases. For additional information on RPC visit the Company’s website located at www.radient-pharma.com or contact RPC Investor Relations at 206.310.5323 or [email protected].

About Radient Pharmaceuticals:
Headquartered in Tustin, California, Radient Pharmaceuticals is a pharmaceutical company devoted to the research, development, manufacturing, and marketing of diagnostic and therapeutic products, including the company’s Onko-Sure in vitro diagnostic (IVD) cancer test — a simple, non-invasive, patent-pending and regulatory-approved test used for the detection, screening, and monitoring of various types of cancer. Onko-Sure is approved by: the US FDA for the monitoring of colorectal cancer; Health Canada as a lung cancer screen and as a cancer monitoring tool; and as a cancer monitoring or cancer screening test in the European Union, India, Korea, and Taiwan. Visit www.Radient-Pharma.com for additional information.

Forward Looking Statements:
Safe Harbor Statement under the Private Securities Litigation Reform Act of 1995: The statements contained in this document include certain predictions and projections that may be considered forward-looking statements under securities law. These statements involve a number of important risks and uncertainties that could cause actual results to differ materially including, but not limited to, the performance of joint venture partners, as well as other economic, competitive and technological factors involving the Company’s operations, markets, services, products, and prices. With respect to Radient Pharmaceuticals Corporation, except for the historical information contained herein, the matters discussed in this document are forward-looking statements involving risks and uncertainties that could cause actual results to differ materially from those in such forward-looking statements.

Radient Pharma Contact:
Kristine Szarkowitz
Director-Investor Relations
Email Contact
(Tel : ) 206.310.5323

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Filed Under: Facilities And Providers

SREH Launches www.SREHoldings.com as Online Corporate Headquarters

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: Strategic Rare Earth Metals, Inc.

SRE Holdings Solidifies Home Base on the World Wide Web for Clients and Shareholders

NEW YORK, NY–(Marketwire – July 15, 2010) –  (PINKSHEETS: SREH) — SREH CEO, Tony Dibiase, announces the official launch of the company’s website, www.SREHoldings.com, “toward overall branding, marketability, transparency and developing a strong corporate identity as a publicly traded holdings company. The site has been designed to provide easy access to information about SREH’s subsidiary companies, Mobile2Earth (www.mobile2earth.com) and Scientific News International (www.scientificnewsroom.com) both with a rich base of intellectual property as well as IP development internally and for clients,” states Dibiase.

www.SREHoldings.com is a clean interface for a user-friendly experience featuring company overviews, news, progress and updates. “The new website exemplifies the dynamism and scope of SREH and its subsidiaries. Serving as a home base, the website provides both existing and prospective clients and shareholders timely, quality information about SREH and its subsidiaries with links to each individual company’s website therein. Mobile2Earth and SNI are not exactly sexy companies, per se,” states Dibiase. “But therein lies a trademarked and 13 year industry tested news service, subscription based social networking, exclusive non-biased content for medical professionals, iPhone and iPad apps as members of the Apple Developer Connection, to start. They both feature highly unique, marketable IP that can lead to sexy growth and corporate expansion. The SREH website helps exhibit all that we do in an easily digestible form, with the individual company sites available for customers, clients and the like with branding in place, accordingly. Both companies feature robust capabilities and the new holdings page simplifies this and strengthens our brand all the while.”

The company has submitted current disclosure and financial documents with OTCMarkets and will announce an update in tier status once reflected on the site.

CUTTING EDGE MEDICAL MEETING NEWS EXCLUSIVELY AT Scientific News International! (www.scientificnewsroom.com) is SREH’s premiere all-in-one platform for medical conference and news information focusing on Cardiology, Gastroenterology, Hematology, Nephrology, Oncology, Primary Care, Rheumatology and Urology. The site is the web’s only online resource for medical professionals with access to the latest, cutting edge data presented at major medical meetings worldwide. Staffed by global medical writers, SNI reports the most current research and therapy findings directly. The site’s profitability is IP and subscription based without bias from any medical or pharmaceutical provider. 

In the beginning, there was…Fishing, Manga, global tide reports and more! Get your iphoneMobile2Earth (www.mobile2earth.com) app now. Choose from the iphone King James Bible, fishing reports worldwide, Japanese e-books and comics and so much more as Mobile2Earth unleashes phase 1 of its iphone app releases for mass consumption. 

Safe Harbor: This release may contain forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Statements contained in this release that are not historical facts may be deemed to be forward-looking statements. Investors are cautioned that forward-looking statements are inherently uncertain. Actual performance and results may differ materially from that projected or suggested herein due to certain risks and uncertainties including, without limitation, ability to obtain financing and regulatory and shareholder approvals for anticipated actions.

Contact:
SRE Holdings
Dba Strategic Rare Earth Metals
[email protected]

Filed Under: Facilities And Providers

Extendicare REIT Declares July 2010 Distribution

Posted on July 15, 2010 Written by Annalyn Frame

MARKHAM, ONTARIO–(Marketwire – July 15, 2010) – Extendicare Real Estate Investment Trust (“Extendicare REIT” or the “REIT”) (TSX:EXE.UN) today announced that it has declared a cash distribution of C$0.07 per unit of the REIT (the “REIT Units”) for the month of July 2010, which is payable to unitholders of record at the close of business on July 30, 2010, and will be paid on August 16, 2010.

Extendicare Limited Partnership (the “Partnership”) also announced that it has declared a cash distribution of C$0.07 per Class B limited partnership unit (the “Exchangeable LP Units”) for the month of July 2010, which is payable to unitholders of record at the close of business on July 30, 2010, and will be paid on August 16, 2010.

The current annualized distribution rate of the REIT and Partnership is C$0.84 per unit, payable in monthly distributions of C$0.07 per unit. In accordance with the distribution policy of both the REIT and the Partnership, unitholders of record at the close of business on the last business day of each calendar month will be paid a distribution on or about the 15th day of the following month.

Management estimates that approximately 70% of the 2010 distributions of the REIT and Partnership will be characterized as tax-deferred returns of capital for Canadian residents. To the extent the remaining 30% of distributions of the REIT and Extendicare LP to be made in 2010 are taxed as dividends, those paid to Canadian residents are eligible dividends as per the Income Tax Act (Canada). The REIT is not required to, and does not, calculate its “earnings and profits” pursuant to the United States Internal Revenue Code of 1986, as amended, and therefore no portion of its distributions represent qualified dividend income for U.S. tax purposes.

The REIT has a Distribution Reinvestment Plan, which provides Canadian resident holders of REIT Units and Exchangeable LP Units with the opportunity to increase their respective investments at a 3% discount to the volume weighted average trading price of the REIT Units on the TSX for the five trading days immediately preceding the distribution payment date. A copy of the Plan package is available under the investors section of the REIT’s website.

About Us

Extendicare REIT is a leading North American provider of long-term and short-term senior care services through its network of owned and operated health care centers. We employ 37,700 qualified and experienced individuals dedicated to helping people live better through a commitment to quality service that includes post-acute care, rehabilitative therapies and home health care services. Our 258 senior care centers in North America have capacity for approximately 28,900 residents. Extendicare REIT is a specified investment flow-through trust (SIFT) that has been subject to the SIFT tax since January 1, 2007.

Forward-looking Statements

Information provided by Extendicare REIT from time to time, including this release, contains or may contain forward-looking statements concerning anticipated financial events, results, circumstances, economic performance or expectations with respect to the REIT and its subsidiaries, including its business operations, business strategy, and financial condition. Forward-looking statements can be identified because they generally contain the words “expect”, “intend”, “anticipate”, “believe”, “estimate”, “project”, “plan” or “objective” or other similar expressions or the negative thereof. Forward-looking statements reflect management’s beliefs and assumptions and are based on information currently available, and the REIT assumes no obligation to update or revise any forward- looking statement, except as required by applicable securities laws. These statements are not guarantees of future performance and involve known and unknown risks, uncertainties and other factors that may cause actual results, performance or achievements of the REIT to differ materially from those expressed or implied in the statements. Given these risks and uncertainties, readers are cautioned not to place undue reliance on the REIT’s forward-looking statements. Further information can be found in the disclosure documents filed by Extendicare REIT with the securities regulatory authorities, available at www.sedar.com and on the REIT’s website at www.extendicare.com.

Filed Under: Facilities And Providers

Medelis Selects PharmaPros’ eClinical OnDemand(TM) Solution

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: PharmaPros

PharmaPros to Provide Integrated Data and Technology Services

CAMBRIDGE, MA–(Marketwire – July 15, 2010) –  PharmaPros, a technical consulting and solutions provider specializing in data and workflow management for clinical trials, today announced that Medelis, a single-source provider for oncology drug development services, has selected PharmaPros’ recently launched eClinical OnDemand™ solution, a unique Software as a Service (SaaS) subscription model for data and technology management.

With eClinical OnDemand™, PharmaPros acts as an outsourced technology department providing all of the technology implementation, management, and support for an end-to-end eClinical suite, as a managed service accessible by the study, program, or as a functionally outsourced department. With this solution, small to mid-sized organizations gain the advantage of a seasoned technology team and best-in-class clinical technology suite delivered with the added value of Dataflow Manager, PharmaPros’ first-in-class study management solution. With Dataflow Manager as the solution’s central interface, study teams can collaborate on study management operations using real-time data intelligence, across systems, sources, and vendors.

“We are excited to have been selected by Medelis to provide this solution. PharmaPros has a unique domain expertise at the intersection of data and technology. This enables us to not only deliver the highest quality services, but to enable specialty service providers to focus on their core competencies and deliver innovative solutions,” said PharmaPros CEO, Peg Regan.

PharmaPros will provide additional services to support both EDC and paper based studies using their proprietary methodology: electronic Data Lifecycle Management (eDLM) in conjunction with Dataflow Manager. With the advantage of an integrated study workflow and access to in-stream study progress, Medelis and PharmaPros will work seamlessly throughout the trial to ensure the expected data lifecycle, trial milestones, and data availability are managed to expectation.

“We are pleased to have found this unique solution to extend our own service offerings. eClinical OnDemand™ has enabled us meet client requirements for progressive technology, in-stream study status and integrated data extracts on-demand, providing us a competitive advantage we would not have with other, more traditional outsourced solutions,” said Bob Bosserman, CEO of Medelis Inc.

PharmaPros’ eClinical OnDemand™ is the first solution of its kind in the industry. Providing small to midsize companies a fully integrated eClinical technology suite, supported by mission critical services to ensure data is managed and available on a continuum from start-up to analysis. Integrated data from all sources including sites, labs, and imaging centers are delivered through PharmaPros study management application Dataflow Manager, providing study teams an unparalleled view of study progress.

About PharmaPros Corporation
PharmaPros Corporation is a technical consulting and solutions provider specializing in data and technology for clinical trials. The company’s innovative approach and deep industry expertise, has resulted in the commercialization of a revolutionary solution that is redefining clinical trials management. The company’s premiere solution — Dataflow Manager™ — provides the ability to manage clinical trials using the most accurate and up-to-date information available, enabling trial sponsors and managers to make more rapid, and better-informed decisions during a trial. PharmaPros was formed in 1996, with headquarters in Cambridge, MA.

Contact:

Brion Regan
Email Contact
www.pharmapros.com

Filed Under: Facilities And Providers

Sunesis Issued European Patent Covering Voreloxin Combination

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: Sunesis Pharmaceuticals, Inc.

SOUTH SAN FRANCISCO, CA–(Marketwire – July 15, 2010) –   Sunesis Pharmaceuticals, Inc. (NASDAQ: SNSS) today announced that the European Patent Office (EPO) has granted a European patent covering combinations of the Company’s lead drug candidate, voreloxin, with cytarabine. Cytarabine is the standard-of-care treatment for Acute Myeloid Leukemia (AML), and the therapy used in combination with voreloxin in a fully enrolled Phase 2 trial in patients with relapsed and/or refractory AML. Sunesis has also announced plans to initiate a multinational, randomized, double-blind, placebo-controlled, pivotal Phase 3 clinical trial of voreloxin in combination with cytarabine in a relapsed/refractory AML patient population in the second half of this year. European Patent No. 1 729 770 B1, titled “SNS-595 [voreloxin] and Methods of Using the Same,” following completion of the patent validation process, will provide patent coverage for such combination products in 30 member states of the European Patent Convention, including the major European markets, through 2025. Corresponding patent applications are pending in major markets throughout the world including Australia, Canada, Japan and the United States. 

“This patent is an important new addition to our intellectual property estate, as it covers the combination of voreloxin and cytarabine, the contemplated initial market application,” stated Daniel Swisher, Chief Executive Officer of Sunesis. “We are pursuing a sophisticated and deliberate strategy to provide exclusive coverage in the voreloxin patent estate out to 2030. Beyond our granted patents, we have filed patent applications covering formulations, combination uses, dosing, manufacturing processes and composition of matter claims. We look forward to the successful prosecution of these patent applications in multiple territories around the world.”

About Voreloxin

Voreloxin is a first-in-class anticancer quinolone derivative, or AQD, a class of compounds that has not been used previously for the treatment of cancer. Voreloxin both intercalates DNA and inhibits topoisomerase II, resulting in replication-dependent, site-selective DNA damage, G2 arrest and apoptosis. Voreloxin is currently being evaluated in a fully enrolled single agent Phase 2 clinical trial (known as the REVEAL-1 trial) in previously untreated elderly AML patients and in a fully enrolled Phase 2 clinical trial combining voreloxin with cytarabine for the treatment of patients with relapsed/refractory AML. A Phase 2 single agent clinical trial in platinum-resistant ovarian cancer has also completed enrollment. Sunesis plans to initiate a multinational, randomized, double-blind, placebo-controlled, pivotal Phase 3 clinical trial of voreloxin in combination with cytarabine in a relapsed/refractory AML patient population in the second half of this year.

About Acute Myeloid Leukemia

AML is a rapidly progressing cancer of the blood characterized by the uncontrolled proliferation of immature blast cells in the bone marrow. The National Cancer Institute estimated that nearly 13,000 new cases of AML were diagnosed and approximately 9,000 deaths from AML occurred in the U.S. in 2009. Additionally, it is estimated that prevalence of AML is approximately 25,000 in the U.S. AML is generally a disease of older adults, and the median age of a patient diagnosed with AML is about 67 years. AML patients with relapsed or refractory disease and newly diagnosed AML patients over 60 years of age with poor prognostic risk factors typically die within one year, resulting in an acute need for new treatment options for these patients.

About Sunesis Pharmaceuticals

Sunesis is a biopharmaceutical company focused on the development and commercialization of new oncology therapeutics for the treatment of solid and hematologic cancers. Sunesis has built a highly experienced cancer drug development organization committed to advancing its lead product candidate, voreloxin, in multiple indications to improve the lives of people with cancer. For additional information on Sunesis Pharmaceuticals, please visit http://www.sunesis.com.

This press release contains forward-looking statements, including without limitation statements related to the prosecution of patent applications and Sunesis’ plans to initiate a pivotal Phase 3 clinical trial of voreloxin in the second half of this year. Words such as “evaluate,” “planned,” “will,” “look forward” and similar expressions are intended to identify forward-looking statements. These forward-looking statements are based upon Sunesis’ current expectations. Forward-looking statements involve risks and uncertainties. Sunesis’ actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of these risks and uncertainties, which include without limitation, risks related to Sunesis’ need for additional funding to fully finance the planned voreloxin pivotal trial, the risk that Sunesis’ development activities for voreloxin could be halted or significantly delayed for various reasons, the risk that Sunesis’ clinical studies for voreloxin may not demonstrate safety or efficacy or lead to regulatory approval, the risk that data to date and trends may not be predictive of future data or results, the risk that Sunesis’ nonclinical studies and clinical studies may not satisfy the requirements of the FDA or other regulatory agencies, risks related to the conduct of Sunesis’ clinical trials, risks related to the manufacturing of voreloxin, and the risk that Sunesis’ proprietary rights may not adequately protect voreloxin. These and other risk factors are discussed under “Risk Factors” and elsewhere in Sunesis’ Quarterly Report on Form 10-Q for the quarter ended March 31, 2010 and other filings with the Securities and Exchange Commission. Sunesis expressly disclaims any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in the company’s expectations with regard thereto or any change in events, conditions or circumstances on which any such statements are based.

SUNESIS and the logo are trademarks of Sunesis Pharmaceuticals, Inc.

Investor and Media Inquiries:
David Pitts
Argot Partners
212-600-1902

Eric Bjerkholt
Sunesis Pharmaceuticals Inc.
650-266-3717

Filed Under: Facilities And Providers

RightSmile(R) Adds Additional Revenue With SmileShoppes, and Will Reduce the Number of Shares Outstanding of Its Common Stock by Approximately 500…

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: RightSmile

PORT ST. LUCIE, FL–(Marketwire – July 15, 2010) –  RightSmile, Inc. (PINKSHEETS: RIGH) (www.RightSmile.com), the leader in Cosmetic Laser Teeth Whitening, continues to add more SmileShoppes across the country, while adding monthly reoccurring revenue at the same time. Furthermore, the Company will be reducing the current amount of shares outstanding by nearly 500 million shares within the coming days.

RIGH has been adding more SmileShoppes from the efforts of the independent rep groups recently signed up. Each SmileShoppe delivers monthly reoccurring revenue to the Company of approximately $500 per month, by just adding 10 new SmileShoppes per month at the end of a year the Company will have added $60,000 a month in additional revenue. The Company also has its first full time, in-house sales person, working from the corporate office in FL, and has been making good headway into the South Florida market.

The Officers of RIGH have decided to exchange their shares of Common stock for Preferred stock to ease investors’ minds that they may be selling their shares into the market. “Management is focused on building strong shareholder value and letting the shareholders know we are in it for the long haul,” stated Gene Caiazzo, President.

This reduction will reduce the Outstanding shares of the company’s Common stock to 550,000,000 from currently over 1 billion.

The Company has been working diligently on compiling and delivering all the information asked for by the audit team and looks forward to posting the audited financials on PinkSheets.

Once the financials are complete the company will hold its Annual Shareholders meeting this August in Fort Lauderdale, FL. As previously announced, all shareholders who attend the meeting can get their teeth whitened for free.

About RightSmile®:

Based in Port St. Lucie, Florida, RightSmile, Inc. engages in the distribution of branded and private label Cosmetic Laser Teeth Whitening products. Through Revodent, RIGH became a manufacturer of teeth whitening products. Revodent supplies numerous manufacturers/manu-packagers with components for teeth whitening solutions; in addition, they also supply final products designed for use in the dental, salon/retail and internet markets.

The Company believes all remarks made in the release to be accurate to the best of its knowledge.

The foregoing press announcement contains forward-looking statements that can be identified by terminology such as “believes,” “expects,” “potential,” “plans,” “suggests,” “may,” “should,” “could,” “intends,” or similar expressions. Such forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause the actual results to be materially different from any future results, performance or achievements expressed or implied by such statements. In particular, management’s expectations could be affected by, among other things, uncertainties relating to our success in completing acquisitions, financing our operations, entering into strategic partnerships, engaging management and other matters disclosed by us in our public filings from time to time. Forward-looking statements speak only as to the date they are made. The Company does not undertake to update forward-looking statements to reflect circumstances or events that occur after the date the forward-looking statements are made.

For additional information about this release please contact:

Wallstreet-Review
954-617-5663

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Filed Under: Facilities And Providers

Axxess Pharma, Inc. Nears Completion of Exclusive License Agreement to Manufacture and Market Anti-Inflammatory and Pain Relief Medication in Canada

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: Axxess Pharma, Inc.

Product to Be Prescribed by Orthopedic Surgeons, Rheumatologists, General Practitioners and Pharmacists Throughout Canada

ONTARIO, CA–(Marketwire – July 15, 2010) – Axxess Pharma, Inc. (PINKSHEETS: AXXE), a pharmaceutical company specializing in the marketing and distribution of both prescription and non-prescription medical products is pleased to announce they are in the process of adding an additional prescription drug to their product line. This drug known as Fortex is used for the relief of pain and inflammation of musculoskeletal conditions such as arthritis and muscle soreness.

Fortex will be prescribed by orthopedic surgeons, rheumatologists, general practitioners and pharmacists throughout Canada. Under the terms of the exclusive license agreement, Axxess Pharma will have sole rights to manufacture and market the prescription drug in Canada. The Company anticipates this prescription drug will provide a significant source of residual revenue due to the continued increase of senior citizens and overworked population.

For more information, please contact Investor Relations at (973) 351-3868.

About Axxess Pharma, Inc.:

Axxess Pharma, Inc. is a specialty pharmaceutical company that focuses on the marketing of dermatological, therapeutic nutritionals, pain management and diagnostic products in Canada and abroad since 1997. Axxess owns 22 established pharmaceutical prescription products that have proven sales in Canada and internationally. The company has an experienced management team and field sales force to market products nationally to hospitals and retail pharmacies as well as specialized practice areas including Dermatology and Nephrology, Neurology and Urology.

Safe Harbor

Statements about the Company’s future expectations and all other statements in this press release other than historical facts, are “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933, Section 21E of the Securities Exchange Act of 1934, and as that term is defined in the Private Securities Litigation Reform Act of 1995. The Company intends that such forward-looking statements be subject to the safe harbors created thereby.

The above information contains information relating to the Company that is based on the beliefs of the Company and/or its management, as well as assumptions made by any information currently available to the Company or its management. When used in this document, the words “anticipate,” “estimate,” “expect,” “intend,” “plans,” “projects,” and similar expressions, as they relate to the Company or its management, are intended to identify forward-looking statements. Such statements reflect the current view of the Company regarding future events and are subject to certain risks, uncertainties and assumptions, including the risks and uncertainties noted. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove to be incorrect, actual results may vary materially from those described herein as anticipated, believed, estimated, expected, intended or projected. In each instance, forward-looking information should be considered in light of the accompanying meaningful cautionary statements herein. Factors that could cause results to differ include, but are not limited to, successful performance of internal plans, the impact of competitive services and pricing and general economic risks and uncertainties.

Filed Under: Facilities And Providers

Implementation of the Affordable Care Act Must Lead to Adequate Diabetes Screening

Posted on July 15, 2010 Written by Annalyn Frame

SOURCE: American Diabetes Association

ALEXANDRIA, VA–(Marketwire – July 14, 2010) –  On Wednesday, July 14, the Obama Administration joined medical professionals and leaders from the health community to announce preventive health care coverage made available under the Affordable Care Act. Under this act, new insurance plans are required to provide preventive care without cost-sharing, which will remove financial barriers for many Americans for preventive services that can help alleviate disease and reduce costs. 

The American Diabetes Association believes that while this is laudatory, relying exclusively on the United States Preventive Services Task Force (USPSTF) “A and B” recommendations, will not lead to adequate screening of patients at risk for diabetes. Blood glucose screening is one of the most essential tools for detecting diabetes and something that should be part of a basic package of benefits and services. 

Under the new rule, asymptomatic adults with sustained high blood pressure will have access to diabetes screening and adults and children will have access to obesity screening and counseling through their clinician at no cost. Ensuring that patients with other risk factors, such as a family history of diabetes or who are obese, also have access to preventive screenings at low or no cost will allow for earlier diagnosis and subsequent prevention of dangerous and costly complications. 

Through implementation of the Affordable Care Act we must ensure that patients at high risk of diabetes are screened for the disease when they see their primary care physician. Nearly 6 million of the 24 million Americans living with diabetes have not been diagnosed. There is an additional 57 million Americans with pre-diabetes, and nearly 93 percent do not know it. If left untreated, diabetes leads to costly and dangerous complications such as blindness, amputation, heart disease, and kidney disease. Relying solely on the USPSTF recommendation, which gives an “I” statement to blood glucose screening for any asymptomatic patient not experiencing high blood pressure, will continue to leave millions of Americans undiagnosed and in danger of facing otherwise avoidable health complications such as blindness, amputation, heart disease, and kidney disease.

We are supportive of the provisions that cover obesity screening and other diabetes-related prevention services. We look forward to working with the Obama Administration and Congress to ensure that people have access to diabetes screenings, as well as to the preventive services that help to manage the disease and prevent complications following diagnosis.

American Diabetes Association guidelines (below) recommend screening for individuals who meet the common risk factors for diabetes. These criteria are consistent with those used in scientific studies of diabetes prevention.

  • All adults who are overweight and have additional risk factors:
    • Physical inactivity
    • First degree relative with diabetes
    • Women diagnosed with gestational diabetes or who delivered a baby weighing > 9 lb.
    • Hypertension (high blood pressure) or cholesterol abnormality
    • Other clinical conditions associated with resistance to the effects of insulin
  • In the absence of the above criteria, testing should begin at age 45 years
  • If results are normal, testing should be repeated at least at 3 year intervals, with consideration of more frequent testing depending on initial results and risk status.

The American Diabetes Association believes that targeted diabetes screening as outlined by the our recommendations and supported by the National Institute of Diabetes and Digestive and Kidney Diseases, and are in line with risk factors recommended by the Centers for Disease Control and Prevention must be considered a covered preventive service. Doing so will meet the dual goals of the Affordable Care Act, that is emphasizing prevention and reining in healthcare costs.

The American Diabetes Association is leading the fight to stop diabetes and its deadly consequences and fighting for those affected by diabetes. The Association funds research to prevent, cure and manage diabetes; delivers services to hundreds of communities; provides objective and credible information; and gives voice to those denied their rights because of diabetes. Founded in 1940, our mission is to prevent and cure diabetes and to improve the lives of all people affected by diabetes. For more information please call the American Diabetes Association at 1-800-DIABETES (1-800-342-2383) or visit www.diabetes.org. Information from both these sources is available in English and Spanish.

Contact:
Christine Feheley
703 253-4374

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Filed Under: Facilities And Providers

VHA Advisory Panel Will Help Hospitals Transition to Value-Based Purchasing Environment

Posted on July 14, 2010 Written by Annalyn Frame

SOURCE: VHA

IRVING, TX–(Marketwire – July 14, 2010) –  VHA Inc., the national health care network, announced the formation of a national Value Based Purchasing (VBP) Advisory Panel. The panel, which consists of nationally-recognized experts, will help hospitals and clinicians transition into this new environment, where reimbursements are linked to quality and safety outcomes. The panel members were selected because they represent a broad array of clinical, operational, and behavioral disciplines with knowledge and experience related to specific components of the government’s value-based purchasing initiative or the environment in which it will operate. Through the efforts of the advisory panel, hospitals and clinicians will gain better insights into the choices and issues that arise with value-based purchasing. 

“The value-based purchasing environment is not simply about looking at performance measures and tracking progress,” said Trent Haywood, MD, JD, chief medical officer at VHA and a former deputy chief medical officer at the Centers of Medicare and Medicaid Services. “Instead, it is a new focus on how we can collectively create more value for patients, clinicians, and providers. For value creation to occur, we need broader insights into the choices we have. The diverse background and expertise of the panel provides these insights.”

Beginning Oct. 1, 2012, through its value-based purchasing program, CMS will link hospital payments to clinical quality and patient experience scores. Hospitals that don’t perform well could lose millions of dollars in Medicare reimbursements. In May 2010, VHA announced the creation of its Value Insurance Program Services, precisely designed to help member organizations focus on specific VBP performance improvement needs. 

“Reimbursement from payers, both government and private insurers, has long been based on the volume of care delivered, but the reimbursement model of the future will be based almost exclusively on the value that’s provided, and hospitals will struggle to adapt to this shift,” said panel member David B. Nash, MD, MBA, dean of the Jefferson School of Population Health. “The panel will provide unbiased insight into the changes that must occur across health care for implementation of value-based purchasing. Without this sort of guidance, the industry may be delayed in developing positive momentum to adopting value-based purchasing.”

The members of the VHA VBP Advisory Panel include:

  1. Ann Scott Blouin, RN, PhD, Executive Vice President, The Joint Commission, Oakbrook Terrace, Ill.
  2. Dale Bratzler, DO, MPH, President/CEO, Oklahoma Foundation for Medical Quality, Oklahoma City, Okla.
  3. Eric A. Coleman, MD, MPH, Director, Care Transitions Program, Denver
  4. Helen Darling, President, National Business Group on Health, Washington, D.C.
  5. R. Adams Dudley, MD, MBA, Professor of Medicine and Health Policy, Associate Director for Research, Philip R. Lee Institute for Health Policy Studies, University of California, San Francisco
  6. Susan Edgman-Levitan, PA, Executive Director, John D. Stoeckle Center for Primary Care Innovation, Massachusetts General Hospital, Boston
  7. Nancy Foster, Vice President for Quality and Patient Safety Policy, American Hospital Association, Washington, DC.
  8. Judith Hibbard, DrPH, Senior Researcher, Institute for Policy Research and Innovation, Professor, Department of Planning, Public Policy and Management, University of Oregon, Eugene, Ore.
  9. David Hunt, MD, FACS, Medical Director, Office of Provider Adoption Support, Office of the National Coordinator for Health IT, Washington, D.C.
  10. Ann Jordan, PhD, Professor of Anthropology, University of North Texas, Denton, Texas
  11. Beverly Jordan, RN, Vice President of Nursing/Chief Nurse Executive, Baptist Memorial Health Care, Memphis, Tenn.
  12. Harlan M. Krumholz, MD, SM Harold H. Hines, Jr. Professor of Medicine and Epidemiology and Public Health, Yale University School of Medicine, New Haven, Conn.
  13. Rob Maurer, PhD, Associate Professor, Health Systems Management, Texas Woman’s University, Dallas
  14. David B. Nash, MD, MBA, Dean, Jefferson School of Population Health, Philadelphia
  15. Greg Pawlson, MD, MPH, Executive Vice President, National Committee for Quality Assurance, Washington, D.C.
  16. Michael Rapp, MD, JD, FACEP, Director of Quality Measurement & Health Assessment Group, Office of Clinical Standards and Quality, Centers for Medicare and Medicaid Services, Baltimore
  17. Victoria Rich, RN, PhD, Chief Nurse Executive, Hospital of the University of Pennsylvania, Philadelphia
  18. Meredith Rosenthal, PhD, Associate Professor, Health Economics and Policy, Harvard School of Public Health, Boston
  19. Thinh H. Tran, MD, Chief Medical and Quality Officer, Baptist Health South Florida, Miami
  20. John Vassall II, MD, FACP, Chief Medical Officer, Swedish Medical Center, Seattle
  21. Stephen Wallenhaupt, MD, Executive Vice President/Chief Medical Officer, Novant Health, Winston-Salem, N.C.

ABOUT VHA
VHA Inc., based in Irving, Texas, is a national network of not-for-profit health care organizations that work together to drive maximum savings in the supply chain arena, set new levels of clinical performance and identify and implement best practices to improve operational efficiency and clinical outcomes. Formed in 1977, through its 16 regional offices, VHA serves more than 1,400 hospitals and more than 25,500+ non-acute care providers nationwide. VHA was ranked by Modern Healthcare as the 7th best place to work in health care in 2009.

Media Contact:
Lynn Gentry
Email Contact

Filed Under: Medical And Healthcare

Relational Solutions Announces "BlueSky Excel Builder" for Excel Users

Posted on July 14, 2010 Written by Annalyn Frame

SOURCE: Relational Solutions, Inc.

CLEVELAND, OH–(Marketwire – July 14, 2010) –  Relational Solutions announces the release of their new BlueSky Excel Builder. Life just got easier for Excel users with the BlueSky Excel Builder. BlueSky Excel Builder lets you create powerful spreadsheets from database queries quickly and easily. Users can mix and match data from multiple data sources using the dataset Wizard. This allows users to create queries without having to know anything about databases or the SQL language.

Pivot Tables made easy: BlueSky Excel Builder automatically pulls in the data and creates the Pivot Tables for you! Once data is in Excel, you simply use all the built in Excel features. Thus, there is no learning curve!

Distribute Excel Workbooks with security and data transparency: You can share Excel reports and report templates with other users simply by emailing it to them. If the user has the Excel Builder plug-in, they can update the report with a single mouse click and it will repopulate it with data relevant to their business area. Thus, Excel reports are updated with built-in security so that users get only what they are allowed to see providing total transparency to the business user.

Create Standardized Excel presentations: BlueSky Excel Builder is great for creating standardized Excel templates for Account Teams and casual users. Account Team members only need to click the “Refresh Data” button and the report will contain only the data they are entitled to see. It doesn’t get any easier!

Do you have PowerPoint Presentations linked to your Excel reports? Reports and charts linked from Excel to PowerPoint are also, repopulated when you click the “Refresh” button.

Integrated with Wal-mart RetailLink: User who want to directly populate their Excel reports with data they download from Walmart’s RetailLink, can now update their pre-designed Excel reports without the need to recreate their reports each time. This is because we have built our RetailLinker application right into our BlueSky Excel Builder. Wal-mart analysts can now easily update Wal-mart reports in Excel. Our Wal-mart Compliance Report and Request for Routing report can also be updated in three easy steps.

About Relational Solutions, Inc.
Based in Westlake, Ohio since 1996, RSI is a software and service company specializing in data integration and demand signal repositories for consumer goods companies. POSmart expedites the integration, cleansing and harmonization of point of sale data with syndicated, third-party and internal data, to improve retailer relationships, support customers better, streamline internal efficiencies, decrease OOS’s, and maximize profits. Applications include POSmart, POS Data Manager, BlueSky Analytics, BlueSky Forecaster, Promotion & New Item Tracking, RetailLinker, BlueSky ExcelBuilder and BlueSky Integration Studio (BIS).

Contact:
Janet Dorenkott
440-899-3296 x25
Email Contact

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Filed Under: Medical And Healthcare

Robotic Surgery Expert Dr. Ramin Mirhashemi, MD of Gynecological Oncology Associates Introduces His Brand New Website, www.GYNLA.com

Posted on July 14, 2010 Written by Annalyn Frame

SOURCE: GYNLA.com

TORRANCE, CA–(Marketwire – July 14, 2010) –  Dr. Ramin Mirhashemi, MD, FACOG, of Gynecological Oncology Associates realized he needed to have an online presence and branding for his practice. With the help of Aurora Information Technology, his website GYNLA.com is the ultimate medical resource for his patients. Dr. Mirhashemi is an expert in robotic surgery, which he performs to treat gynecologic cancers including uterine, ovarian, cervical, and vaginal cancers, as well as fibroids, endometriosis, ovarian tumors and pelvic prolapse (robotic sacrocolpopexy, robotic hysterectomy and robotic myomectomy).

The domain name, GYNLA.com, was devised to encompass the practice and the region served. A fun and bright website design with an animated banner incorporating the fresh, new logo on the home page houses a wealth of information on topics in Dr. Mirhashemi’s overall gynecological expertise, including gynecologic oncology and robotic surgery. Mirhashemi developed techniques to perform these surgeries through robotic laparoscopic techniques. The robotic procedure is more accurate and minimally invasive, due to smaller incisions. Patients experience less pain and usually recover in about 1 week.

Dr. Mirhashemi, who has the largest experience in robotic surgery for gynecologic conditions “west of the Mississippi,” is a subject matter expert who has published over 60 journal articles, research articles and book chapters in regards to women’s health. Mirhashemi attended Medical School at the University of Southern California and completed his internship and residency at the Brigham and Women’s Hospital/Massachusetts General Hospital at Harvard Medical School. He received his fellowship in Gynecologic Oncology at the University of Miami. To his credit, he is a former Associate Professor of Obstetrics and Gynecology at the UCLA School of Medicine, and the University of Miami School of Medicine, as well as the Director of the Familial Breast and Ovarian Cancer Genetic Center at the University of Miami School of Medicine.

Because Dr. Mirhashemi is dedicated to improving women’s health via comprehensive gynecology, gynecologic oncology, and urogynecologic services, his mission for the website was to provide as much information as possible regarding the most common female medical conditions as well as treatment options. Mirhashemi believes in the efficiency of state-of-the-art robotic surgery in gynecology. “Because large abdominal incisions are not needed with the da Vinci robot that is used in robotic surgery, my patients recover much faster than with traditional open surgery, that requires these larger incisions,” explained Mirhashemi. “With robotic surgery, most of patients are discharged within 24 hours of their operations, with fewer complications.”

The site provides patient information such as physician/practice background, patient testimonials and hospital affiliations. In order to constantly improve the patient experience, the site features an online patient questionnaire that captures patient feedback on their experience with the practice. “My practice is patient-focused and their cure and satisfaction go hand-in-hand,” explained Dr. Mirhashemi. “If we’ve managed to do both successfully, and provide the value-add of medical information and education, then we’ve done our job well.”

Contact:

Ramin Mirhashemi, MD
Phone: 310-375-8446
www.gynla.com

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Filed Under: Medical And Healthcare

CLSI Publishes Standard for Validation, Verification, and Quality Assurance of Automated Hematology Analyzers

Posted on July 14, 2010 Written by Annalyn Frame

SOURCE: Clinical and Laboratory Standards Institute

WAYNE, PA–(Marketwire – July 14, 2010) – Clinical and Laboratory Standards Institute (CLSI) recently published “Validation, Verification, and Quality Assurance of Automated Hematology Analyzers; Approved Standard–Second Edition” (H26-A2). This document covers portions of the life cycle of an automated multichannel hematology system and provides guidance for manufacturers’ validation, end-user laboratory verification, calibration, quality assurance (QA), and quality control (QC) through standardized approaches to ensure good science and clinical relevance.

Albert Rabinovitch, MD, PhD, NovoMetrics, Inc., and chairholder of the subcommittee that developed the document, says, “This new document applies the most current scientific and medically relevant approaches to assessment of automated hematology systems, replacing the shortfalls created by disparate individual sources. Beyond scientific presentation of theory, H26-A2 provides very detailed practical information (including appendices) on method evaluation that all readers will find useful. It serves as a model for clinical laboratory test systems in general, not just hematology.”

Historically, each complete blood count (CBC) instrument/reagent manufacturer developed its unique approaches to system validation and performance claims. This standard will help create better standardization among manufacturers, as well as assist practicing laboratories in developing consistent testing.

The intended audience includes manufacturers of such devices, end-user clinical laboratories, accrediting organizations, and regulatory bodies. End-user clinical laboratories will also find guidance for establishment of clinically reportable intervals (CRIs) and for QA for preexamination and examination aspects of their systems.

CLSI is a volunteer-driven, membership-supported, nonprofit organization dedicated to developing standards and guidelines for the health care and medical testing community through a consensus process that balances the perspectives of industry, government, and the health care professions. For additional information on CLSI, visit the CLSI website at www.clsi.org or call 610.688.0100.

Contact:
Amanda Holm
Marketing Manager
Phone: 610.688.0100 ext. 129
E-mail: Email Contact

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Filed Under: Medical And Healthcare

Eating Recovery Center Opens Outpatient Facility

Posted on July 14, 2010 Written by Annalyn Frame

SOURCE: Eating Recovery Center

New Denver Location Offers Team Approach to Eating Disorder Treatment, Expands Center’s Outpatient Services

DENVER, CO–(Marketwire – July 14, 2010) –  Eating Recovery Center, a national eating disorders recovery program providing comprehensive treatment for anorexia and bulimia, today announced the opening of a new outpatient location. Enabling Eating Recovery Center to expand its outpatient recovery services, the new Denver, Colo. office will offer integrated care for eating disorders in a flexible outpatient setting. 

“This expansion allows Eating Recovery Center to offer patients a collaborative, team-based approach to outpatient eating disorder treatment,” said Kenneth L. Weiner, MD, CEDS, co-founder and medical director of Eating Recovery Center. “With access to a team of individual and family therapists, dietitians, and medical professionals, patients benefit from a well-rounded treatment experience that can help them achieve sustainable recovery.”

The outpatient clinical team works together to help individuals and families who are new to eating disorder treatment address disordered eating and body image issues before they have the chance to escalate. The clinicians are also committed to helping individuals who have been in a recovery program stay on track as they move into lower levels of care. The services offered include individual and family therapy, dietary counseling, psychiatric medical management, body image and aftercare eating disorder support groups, and an evening intensive outpatient program, which begins this month. 

The evening intensive outpatient program is an integrated option for individuals who require more structure than individual counseling provides. Participants meet Mondays, Wednesdays and Thursdays from 5 to 9 p.m. and take part in individual counseling, group therapy, nutrition education and multifamily therapy. They learn to break patterns that maintain their diseases and integrate sustainable changes into their lives. The timing of the program enables participants to integrate the skills learned in evening sessions into their daily lives.

“Eating disorders are complex conditions and every person’s experience with the disease is different,” explains Weiner. “The evening intensive outpatient program allows us to tailor treatment to the individual needs of each patient and promote successful recovery.” 

Eating Recovery Center also operates a licensed behavioral hospital for adults with severe eating disorders, and will open an adolescent treatment facility in the Denver Lowry neighborhood in October 2010. All services are guided by the leadership and clinical expertise of Weiner and Emmett R. Bishop, Jr., MD, CEDS, co-founders of Eating Recovery Center and nationally renowned experts who have separately founded numerous other eating disorder programs throughout the country.

The outpatient office is now open at 600 S. Cherry Street, Suite 600, in Denver, Colo. For more information or to make an appointment, please call 877-218-1344. 

About Eating Recovery Center
Eating Recovery Center is a national eating disorders recovery program, providing comprehensive treatment for anorexia and bulimia at the foot of the Rockies in beautiful downtown Denver, Colorado. Facilities include a licensed behavioral hospital treating adults, an outpatient office, and an adolescent facility scheduled to open in October 2010. Our integrated program offers patients from across the country a continuum of care that includes inpatient, residential, partial hospitalization, intensive outpatient and outpatient services. Our compassionate team of professionals collaborates with treating professionals and loved ones to cultivate lasting behavioral change. For more information please contact us at 877-218-1344 or [email protected] or confidentially chat live on our website.

Contact:
Shannon Fern
CSG|PR
303-433-7020
Email Contact

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Filed Under: Medical And Healthcare

Unity Management Group Announces Acquisition Update

Posted on July 14, 2010 Written by Annalyn Frame

SOURCE: Unity Management Group, Inc.

MIAMI, FL–(Marketwire – July 14, 2010) – Unity Management Group Inc. (PINKSHEETS: UYMG) is a Health Resource Company specializing in Physician and Hospital Practice Management, Medical Discount Plans, Business Services, Billing Software and Technologies.

UMGI is proud to announce that is has entered into a negotiation for an acquisition that will increase its revenue and assets.

Unity is in a due diligence stage of acquiring a healthcare related company. In the coming week we will be updating share holders with financials and corporate information of the target company.

UMGI management feel s that this can be a perfect fit and the company is fully funded.

The funding requirements for the acquisition have been obtained. Further information will be released in the next 7 business days.

Unity Management Group Inc. is also proud to announce that it has completed its disclosure statement, and legal opinion in respect that these are the listing documents that are necessary to obtain current status on the OTC markets. We foresee us receiving our PS status by Friday.

“We are proud to announce these extremely important current events. As previously mentioned this is a milestone for UMGI, and the company is working diligently to complete this acquisition, we will be announcing the outcome of these events within the next couple of business days. As always the company would like to thank its past present and future investors,” said Michael Oliver, Vice President.

For more information please goes to our website which can be found at www.unitymanagementgroup.com

Share structure:

100,000,000 million authorized

87,035,620 million issued and outstanding

43,439,460 million float

Unity Management Group, a health resource company, will continue to provide innovative physician practice management services that offer high value and significant return on investment for physicians’ practices and hospitals through its three subsidiary companies: United Healthcare Solutions Inc., Unity Technologies Inc., and United Business Services Inc.

The first subsidiary, Unity Business Services, is a full service management company offering solutions in practice management, billing, staffing, contracting, licensing, credentialing, and accounting. Unity Business Services also offers assistance in HIPPA compliance, marketing, and unique solutions for practice start-ups and new practices.

Unity Technologies Inc. is a complete software solutions company offering billing, electronic medical records, and electronic health records for physician’s offices and hospitals.

United Healthcare Solutions, a national company based in Nevada, is a healthcare company that will be providing medical, vision and dental discount plans, as well as PPO and HMO networks. 

The combination of these three subsidies provides unprecedented access to skilled leadership, managed care expertise, information systems, and economies of scale. Alex Berkovich, President of United Management Group, stated, “Through this merger, we are in a unique position to address the rapidly changing needs of the medical community. Business expertise is critical to the success of today’s physician offices and hospitals and we expect unpatrolled growth in the near future.”  

Certain information discussed in this press release may constitute forward-looking statements within the Private Securities Litigation Reform Act of 1995 and the federal securities laws. Although the Company believes that the expectations reflected in such forward-looking statements are based upon reasonable assumptions at the time made, it can give no assurance that its expectations will be achieved. Readers are cautioned not to place undue reliance on these forward-looking statements. Forward-looking statements are inherently subject to unpredictable and unanticipated risks, trends and uncertainties such as the Company’s inability to accurately forecast its operating results; the Company’s potential inability to achieve profitability or generate positive cash flow; the availability of financing; and other risks associated with the Company’s business. The Company assumes no obligation to update or supplement forward-looking statements that become untrue because of subsequent events.

For more information, please visit our website at (www.unitymanagementgroup.com) or contact our office at:
Unity Management Group Inc.
954-531-0387

Unity Management Group Locations:

15325 N.W. 60th Avenue
Suite #101
Miami Lakes, Florida 33014

1348 East Hillsboro Blvd.
Deerfield Beach, Florida 33441

Filed Under: Medical And Healthcare

Radient Pharmaceuticals Launches New Corporate Video and Website

Posted on July 14, 2010 Written by Annalyn Frame

SOURCE: Radient Pharmaceuticals Corporation

TUSTIN, CA–(Marketwire – July 14, 2010) –  Radient Pharmaceuticals Corporation (NYSE Amex: RPC), a US-based pharmaceutical company, has announced the launch of its newly designed website located at www.radient-pharma.com and new corporate video featured on RPC’s new corporate website and recently launched Onko-Sure™ product website located at www.onkosure.com.

RPC’s new corporate website offers visitors ease of use and informative, comprehensive in-depth information on RPC’s company, management, products, and strategic plans. This site also provides a more comprehensive and informative investor relations section that will be of great interest to existing shareholders, prospective investors, the investment community in general, and the Company’s customers and strategic partners. Additionally, site visitors can now access more in-depth information on RPC’s corporate and product commercialization strategy, timeline and progress through RPC’s new corporate video which is accessible via www.radient-pharma.com and www.onkosure.com.

According to Douglas MacLellan, Chairman and CEO of Radient Pharmaceuticals, “Radient Pharmaceuticals is committed to providing and maintaining strong communication with our existing shareholders and prospective investors; the medical and healthcare community at large; and partners, suppliers, and customers. It is our expectation that with this new , informative and highly user-friendly design, RPC’s refreshed website will provide a more effective platform for the dissemination of news, updates, webcasts and pertinent shareholder and investor relations information concerning the company. As our company grows, we will continue to update our website with features and content that help our key audiences learn about what we do and the value we provide through our strong portfolio of cancer products, vaccines and therapies.”

Highlights of the newly designed RPC website include the following:

  • Functional and Highly Intuitive Interface: RPC’s website was designed to provide ease of use, featuring a multi-level navigation that allows users to quickly access desired content.
  • In-depth Investor Relations Section: includes investor highlights, RPC’s company history, and operations overview. In addition, this section offers RPC’s quote and data SEC filings, news releases, webcasts, analyst reports and information on the company’s strategic plans.
  • Management: a listing of the company’s Directors and Executive Officers along with their respective bios and e-mail contacts.
  • Product Portfolio and Associated Materials: A detailed overview of RPC’s product portfolio that includes clinical data and resources, regulatory and patent information, research and development initiatives, product innovations and relevant product news as it relates to our strategic plans and industry developments.
  • Corporate Video: new video that provides in-depth details on RPC’s corporate and product commercialization strategy, timeline and progress.

Headquartered in Tustin, California, Radient Pharmaceuticals Corporation is a US-based pharmaceutical company specializing in the research, development and sales of In Vitro Diagnostic Cancer tests. The Company’s focus is on the discovery, development & commercialization of unique high?value diagnostic tests that help physicians answer important clinical questions related to early disease detection; treatment strategy; and the monitoring of disease progression, prognosis, and diagnosis to ultimately improve outcomes for patients. Our Onko?Sure™ IVD cancer test is used to guide decisions regarding patient treatment, which may include decisions to refer patients to specialists, perform additional testing, or assist in the selection of therapy. For additional information on RPC and its portfolio of cancer products visit the Company’s corporate website at www.Radient-Pharma.com. For Investor Relations information contact Kristine Szarkowitz at [email protected] or 1.206.310.5323.

About Radient Pharma:
Headquartered in Tustin, California, Radient Pharmaceuticals Corporation is an integrated pharmaceutical company devoted to the research, development, manufacturing, and marketing of diagnostic, and premium skin care products.

Forward Looking Statements:
Safe Harbor Statement under the Private Securities Litigation Reform Act of 1995: The statements contained in this document include certain predictions and projections that may be considered forward-looking statements under securities law. These statements involve a number of important risks and uncertainties that could cause actual results to differ materially including, but not limited to, the performance of joint venture partners, as well as other economic, competitive and technological factors involving the Company’s operations, markets, services, products, and prices. With respect to Radient Pharmaceuticals Corporation, except for the historical information contained herein, the matters discussed in this document are forward-looking statements involving risks and uncertainties that could cause actual results to differ materially from those in such forward-looking statements.

AMDL Contact:
Kristine Szarkowitz
Director-Investor Relations
Email Contact
Tel: 206.310.5323

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Filed Under: Medical And Healthcare

Health Providers Must Cut Costs by 14% per Case to Break Even If Paid at Medicare Rates

Posted on July 14, 2010 Written by Annalyn Frame

SOURCE: Sg2

New Legislation, Declining Insurance Reimbursement Rates and an Aging Population Will Force Health Care Organizations to Improve Cost Management of Medicare Patients

SKOKIE, IL–(Marketwire – July 14, 2010) –  According to Sg2, a future-focused health care information company, a hospital would need to reduce its direct costs by an average of $1,082 per case, or 14%, to sustain its current operating margins if average inpatient payments were paid at today’s Medicare rates. This finding comes on the heels of recent economic trends that indicate commercial payers may begin decreasing their reimbursement rates in the near term.

Sg2’s analysis suggests that providers must assume more accountability across the care continuum by improving clinical performance and significantly reducing costs to better manage to Medicare margins. With MedPAC projections of overall Medicare margins to be -5.9% in 2010 and performance-based penalties looming, the threat of commercial insurance reimbursement rates approaching Medicare levels in some markets adds tremendous financial pressure to health providers.

The number of Medicare patients will nearly double between 2005 and 2030 as the 78 million members of the Baby Boomer generation begin turning 65 in 2011. Additionally, tough economic conditions continue to make it increasingly difficult for employers to afford health insurance coverage, thereby placing more pressure on commercial payers to reduce premium costs. This, in turn, forces payers to reduce reimbursement rates to providers — rates that could eventually approach Medicare levels in some regions.

According to the Centers for Medicare & Medicaid Services (CMS), 40% of total Medicare spending is “waste” caused by issues including provider error, unnecessary care, avoidable admissions and lack of care coordination. This new playing field sets the stage for health providers to dramatically cut costs and improve clinical performance to meet market dynamics. One strategy that providers can implement is a disease-centered clinical approach that will help organizations identify the top Medicare severity diagnosis-related groups (MS-DRGs) with the highest cost reduction opportunities. Another effective measure is for hospitals to improve their level of clinical integration by assessing their performance across all inpatient and outpatient settings. This is effectively addressed through Sg2’s Systems of CARE™ (Clinical Alignment and Resource Effectiveness) methodology, which measures and monitors key health reform performance metrics such as potentially avoidable admissions and 30-day readmissions.

“This changing environment requires a radical shift in behavior. The onus firmly resides with the provider,” says Sg2 Chairman and CEO Michael Sachs. “The health care leader of the future must recognize incremental and long-term cost saving strategies today, while still delivering cost-effective, quality care. In order to survive and thrive, it is imperative for all organizations — regardless of size — to create a clinically integrated framework and understand financial implications of the growing Medicare population and performance-based incentives. Now is the time to implement a disease-centered approach that not only uncovers financial opportunities, but addresses clinical performance across both inpatient and outpatient settings.”

Sg2’s analysis is grounded in its Sg2 INSIGHT™ Clinical Performance Management System comparative database and the National Inpatient Sample (NIS). A hospital’s potential cost reduction exposure varies by market, provider type and size, with large community hospitals requiring the greatest percentage cost reduction at 17% to maintain overall operating margins at today’s Medicare reimbursement rates. For small- to medium-sized community hospitals, the average cost reduction is $849 per case and for academic medical centers it is $1,168 per case. Case mix, payer mix and relative payment levels drive the differences. For more information on this analysis, contact Sg2.

About Sg2
Sg2 is a health care information company that provides expert-led, future-focused systems for growth and clinical performance. Our advanced analytics, business intelligence, education and publications deliver measurable value across the full continuum of health care services. Sg2 works with more than 1,000 hospitals and health care organizations in the US and around the globe. For more information, visit www.sg2.com.

Media Contacts
Marty Gilbert
+1 847 779 5547
Email Contact

Michelle Dary
+1 847 779 5568
Email Contact

Filed Under: Medical And Healthcare

Bederra Corporation Submits Disclosure Information to Obtain Pink Sheets Current Information Status

Posted on July 14, 2010 Written by Annalyn Frame

SOURCE: Bederra Corporation

HOUSTON, TX–(Marketwire – July 14, 2010) –  Bederra Corporation (PINKSHEETS: BEDA) management has announced that it has submitted all necessary information to obtain Pink Sheets Current Information status and should obtain this status on otcmarkets.com within the next few days. This increased level of disclosure is intended to enhance shareholder transparency.

According to otcmarkets.com, “Companies that follow the International Reporting Standard or the Alternative Reporting Standard by making filings publicly available through the OTC Disclosure & News Service pursuant to Pink OTC Markets Guidelines for Providing Adequate Current Information are designated as Pink Sheets Current Information.” In its May 2010 OTC Market Snapshot, OTC Markets revealed that of 9,402 OTC companies, 1,237 were Pink Sheets Current Issuers. In May, trading in Pink Sheets Current Issuers accounted for more than 53% of the total trading dollar volume of OTC companies.

The company also announced that it has changed its Transfer Agent and has employed Transfer Online to streamline its securities management.

Management continues to seek additional acquisitions and diversification in an effort to bring long-term value to shareholders.

In the coming weeks the company will announce several actions that management believes will increase the long-term success of the company.

About Bederra Corp.
http://www.bederra.com
Bederra Corporation provides multiple modality diagnostic medical services to the greater Houston area and the world famous Texas Medical Center. The Company’s business strategy is to continue to expand its current operations and seek out additional acquisitions that will complement its core offerings.

Under The Private Securities Litigation Reform Act of 1995: The statements in the press release that relate to the company’s expectations with regard to the future impact on the company’s results from new products and services in development, including any planned acquisitions, are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. The results anticipated by any or all of these forward-looking statements might not occur. The Company undertakes no obligation to publicly release the result of any revisions to these forward-looking statements that may be made to reflect events or circumstances after the date hereof, or to reflect the occurrence of unanticipated events or changes in the Company’s plans or expectations.

Contact:
Bederra Corp.
Email Contact

Filed Under: Medical And Healthcare

Pulse Systems, Inc. Poised to Thrive in Meaningful Use Shakeup

Posted on July 14, 2010 Written by Annalyn Frame

SOURCE: Pulse Systems, Inc.

Pulse Clients Ready to Meet Requirements for ARRA Stimulus Fund Dispersal

WICHITA, KS–(Marketwire – July 14, 2010) – Pulse Systems, Inc., an industry-leading vendor of ambulatory healthcare software solutions, announced that today’s finalization of stage one Meaningful Use measures will remove uncertainty from the market and unleash widespread adoption of effective electronic health record technology — such as Pulse EHR — while displacing substandard systems. “With more than 300 solutions currently calling themselves EHRs, we anticipate these rules will quickly whittle that list down to a few critical players,” said Senior Vice President Bruce Rowley.

Though the finalized measures were released today, the Pulse solution has been allowing users to meet Meaningful Use for months. The Pulse Patient Relationship Management version 4.1.02 was the first solution to become a fully CCHIT Certified® 2011 Ambulatory EHR, proving it allowed users to meet the previously proposed Meaningful Use measures. “From the very beginning, our development strategy has been aligned with the HHS vision, while most of our competitors seem to have been hoping for watered-down measures that would allow their systems to qualify,” said Senior Vice President of Healthcare Information Systems Chris Gregg. 

Gregg continued, “Pulse is unique in the marketplace as a company that built every aspect of its solutions by drawing from a single patient record and database, creating one of the only end-to-end, organic systems in existence,” he said. “Most of the ‘solutions’ offered by larger companies have been stitched together through acquisitions of separate systems over the last decade leading to fragile internal interfaces and limited cross-module access to data.”

Gregg also acknowledged that fulfilling stage one Meaningful Use requirements is not enough to ensure the future of an EHR. “Interoperability is paramount to future relevancy in the medical industry,” he said. “We support the open transaction of information, and we have demonstrated this through our use of standardized language and codified data. This helps us to be prepared for the measures we expect to see in stages two and three of Meaningful Use.”

CEO and President of Pulse Basil Hourani reiterated, “Pulse has been ready for these measures to become finalized so our clients can receive the maximum allowable ARRA stimulus payments. Pulse provides an easier way to meet the Meaningful Use guidelines and we are proud to be among the few solutions truly prepared to lead the healthcare industry into the next chapter in EHR technology.”

About Pulse Systems, Inc.
Pulse offers Electronic Health Records (EHR), Practice Management, ePrescribing and Revenue Cycle Management (Billing Services) used nationwide in more than 26 medical specialties. Pulse Practice Management and EHR products have both earned five star ratings from AC Group. Since 1982 Pulse has focused on its mission to develop, market and support healthcare practice workflow solutions that are easier to purchase, implement, utilize and upgrade. This focus on making things easier for clients is the key to a remarkable 95% client renewal rate. For more information, visit www.pulseinc.com.

Bruce Rowley
Senior Vice President
[email protected]
(316) 636-5900 ext.1127

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Filed Under: Medical And Healthcare

Precision Dynamics Introduces New Securline(R) Bar Code Blood Band for Blood Recipient Identification

Posted on July 14, 2010 Written by Annalyn Frame

SOURCE: Precision Dynamics Corporation

Easy to Apply Bar Code Wristband ID System Matches the Right Patient to the Right Blood

SAN FERNANDO, CA–(Marketwire – July 14, 2010) – Precision Dynamics Corporation, the global leader in healthcare identification solutions, announced today the release of the new Securline® Bar Code Blood Band, a blood recipient ID wristband system that provides automated patient identification for blood transfusion, specimen collection, and tracking. As the only snap closure bar code blood band on the market, the product allows caregivers and phlebotomists to apply the band to patients quickly, correctly, and securely.

The Securline® Bar Code Blood Band uses serialized bar code ID and alpha-numeric codes to accurately match the right patient to the right blood. This improves patient safety by reducing identification related human errors that can occur during the blood transfusion process. The product’s 12 matching bar code labels (four on the wristband and eight on the detachable tail that is applied to blood tubes) can be applied to additional draw tubes, patient chart, transfusion requisition, and as a secondary label on blood bags. A clear, adhesive shield on the wristband’s information area protects the patient ID labels and bar code from moisture or solvents for accurate bar code scanning. Soft, latex-free material maximizes patient comfort and safety yet is also durable and strong.

In contrast to the other leading bar coded blood wristband on the market, the Securline® Bar Code Blood Band features an easy-to-use snap style closure and secure bar code labels, saving hospital staff valuable time and unnecessary frustration. Mary Ann Sharpe, Blood Bank Manager at Research Medical Center which belongs to HCA Midwest Health System, stated, “Securline® Bar Code Blood Bands are easy to apply because the bands snap closed just like our admission wristbands. The other bar code blood bands we were using before were complicated and our staff struggled with putting the bands on patients. Plus, the bar code labels on the Securline® product are very secure and don’t peel off accidentally like we experienced with the other band.”

“Bar coding continues to bring improvements in patient safety as hospitals adapt the technology to reduce human errors,” said Kim Canchola, Product Manager for Precision Dynamics. “The added bonus is the increase in productivity as hospitals use sheeted labels with bar codes instead of writing patient ID info by hand. The Securline® Bar Code Blood Band combines the sophistication and functionality of bar coding for blood transfusions with the simplicity and comfort of a high quality, non-transferable identification wristband. The positive response we’ve received from our customers about their experience with this product is rewarding because we know we’re helping solve their problems by doing what we do best — delivering first-class identification solutions.”

The Securline® Bar Code Blood Band meets current Joint Commission, AHA, and HIPAA requirements. For more information, please visit: www.pdcorp.com/healthcare or contact PDC’s Customer Care at 800-772-1122.

About Precision Dynamics Corporation:
The Leading Provider of Positive ID and Positive Outcomes™
With more than 50 years of experience, Precision Dynamics provides accurate, reliable, and easy-to-use healthcare ID solutions that empower the flawless delivery of care and enhance outcomes across all major hospital functions. Our products are used in all of the leading hospitals worldwide and comprise a comprehensive range of wristband and labeling systems that provide positive ID and positive clinical outcomes.

Precision Dynamics products meet important guidelines of The Joint Commission, World Healthcare Organization, FDA, AHA, and HIPAA. As the developer of the first single-piece patient wristband, the first bar code wristband system, and the first Smart Band® RFID wristband system, Precision Dynamics solutions are an integral part of some of the most successful patient safety initiatives. As an ISO 9001 certified company, Precision Dynamics follows a systematic, world-standard approach to ensure superior product design, manufacturing, and customer support services.

Media Contact:
Daniel Hobin
Precision Dynamics Corporation
818.897.1111 x1340
Email Contact

Filed Under: Medical And Healthcare

Trinity Biotech plc to Announce Second Quarter 2010 Financial Results

Posted on July 14, 2010 Written by Annalyn Frame

SOURCE: Trinity Biotech

Conference Call Scheduled for Thursday, July 29, 2010 at 11:00 am Eastern

DUBLIN, IRELAND–(Marketwire – July 14, 2010) –   Trinity Biotech plc (NASDAQ: TRIB), a leading developer and manufacturer of diagnostic products for the point-of-care and clinical laboratory markets, will report financial results for the second quarter of 2010 on Thursday, July 29, 2010. The Company has scheduled a conference call for that same day, Thursday, July 29, 2010 at 11:00am EDT (4:00pm BST) to discuss the results of the quarter.

Interested parties can access the call by dialing:

A simultaneous webcast of the call can be accessed at: http://www.videonewswire.com/event.asp?id=70724

A replay of the call can be accessed until August 3, 2010 by dialing:

The webcast of the call will be available for 30 days at: http://www.videonewswire.com/event.asp?id=70724

About Trinity Biotech plc
Trinity Biotech develops, acquires, manufactures and markets diagnostic systems, including both reagents and instrumentation, for the point-of-care and clinical laboratory segments of the diagnostic market. The products are used to detect infectious diseases and blood coagulation disorders, and to quantify the level of Hemoglobin A1c and other chemistry parameters in serum, plasma and whole blood. Trinity Biotech sells direct in the United States, Germany, France and the U.K. and through a network of international distributors and strategic partners in over 75 countries worldwide. For further information please see the company’s website: http://www.trinitybiotech.com. 

Forward-looking statements in this release are made pursuant to the “safe harbor” provision of the Private Securities Litigation Reform Act of 1995. Investors are cautioned that such forward-looking statements involve risks and uncertainties including, but not limited to, the results of research and development efforts, the effect of regulation by the United States Food and Drug Administration and other agencies, the impact of competitive products, product development commercialisation and technological difficulties, and other risks detailed in the Company’s periodic reports filed with the Securities and Exchange Commission.

Contact:
Trinity Biotech Plc
Kevin Tansley
(353)-1-2769800
E-mail: Email Contact

Lytham Partners LLC
Joe Diaz, Joe Dorame & Robert Blum
602-889-9700

Filed Under: Medical And Healthcare

HealthEast Care System Chief Operating Officer Recipient of Two Awards

Posted on July 14, 2010 Written by Annalyn Frame

SOURCE: HealthEast Care System

Ann Schrader Named 2010 Health Care Hero by Twin Cities Business Magazine and Medica, 2010 Jean Harris Award Winner by Women’s Healthcare Leadership Trust

ST. PAUL, MN–(Marketwire – July 14, 2010) –  HealthEast Care System is pleased to announce that Ann Schrader, Chief Operating Officer, has received two awards in the past two months for her significant contributions to Minnesota healthcare.

Schrader was named a 2010 Health Care Hero in Administrative Excellence by Twin Cities Business magazine and Medica. She was deemed one of eight of Minnesota’s outstanding contributors to the quality of health care in the state, selected from dozens of nominees for her time, focus, compassion, commitment, efforts, and imagination in delivering significant improvements in health care. Her drive to create a patient-centered experience, gold standard employee engagement, exceptional clinical outcomes, and dependable financial performance led to this honor.

Schrader, whose roots are as an RN caring for patients at the bedside, has spent the last 30 years as a senior leader at HealthEast. In 1986, she was instrumental in the merger of several St. Paul hospitals to create HealthEast Care System, the first successful unification of hospitals representing three Christian faiths in America. Schrader became HealthEast’s Chief Operating Officer in 1994. 

As operations leader, she was part of a team that brought about many firsts for HealthEast including:

  • St. Joseph’s, St. John’s and Woodwinds were the first hospitals in Minnesota to perform surgeries live on the Internet.
  • Bethesda Hospital became one of only two long-term acute care hospitals in the state.
  • HealthEast launched an online prenatal education program, the first of its kind in the United States.
  • HealthEast implemented a care navigation strategy that was the first of its kind in the Twin Cities.
  • Woodwinds Health Campus officially opened in Woodbury; it was the first hospital of its kind to offer a unique environment blending integrative medicine, technology, customer service, and a healing nature for patients and their families.

Tim Hanson, HealthEast Care System Chief Executive Officer, credits Schrader for being an essential driver of best practices at all levels of the organization. “Her sense of integrity, honesty, innovation, and accountability have been at the foundation of HealthEast’s success,” said Hanson. “Her vision and strategic planning acumen have helped us respond effectively to a constantly changing industry.”

Schrader has also been selected by the Women’s Healthcare Leadership Trust to receive its Jean Harris Award. The Trust is a 30-year-old organization whose primary purpose is to support, educate, and promote women leaders in healthcare. Established in 2001, this award reflects the vision, integrity, and public leadership of Jean Harris, a physician and former mayor of Eden Prairie, who was known for making a difference in the health care of our communities.

Over the years, Schrader has given her time and talent as a board member to many organizations reflecting a broad spectrum of interests (ranging from business leadership to social services). In addition, she has served as a coach and mentor for many aspiring leaders at HealthEast as well as MHA and MBA students from the University of Minnesota, University of St. Thomas, St. Catherine University, and Mentiumm 100.

These awards celebrate Schrader’s innovative service and program contributions to HealthEast as well as her lifetime commitment to helping young healthcare professionals grow and develop their talents and competencies.

HealthEast Care System is a community-focused, non-profit health care organization that provides innovative technology, compassionate care and a full spectrum of family health services. HealthEast includes Bethesda Hospital, St. John’s Hospital, St. Joseph’s Hospital, and Woodwinds Health Campus as well as outpatient services, clinics, home care, and medical transportation services. Practicing financial responsibility, HealthEast is the largest, locally-owned health care organization in the Twin Cities’ East Metro with 7,300 employees, 1,200 volunteers and 1,400 physicians on staff.

For more information, please contact:
Lynn Sadoff
Sr. Public Relations and Communications Specialist
(651) 326-3590 office
(651) 864-1023 pager – enter your 10-digit
number and press the # sign

Filed Under: Medical And Healthcare

Healthcare Services Group, Inc. Reports Results for the Three and Six Months Ended June 30, 2010 and Declares Increased Second Quarter 2010 Cash…

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: Healthcare Services Group, Inc.

BENSALEM, PA–(Marketwire – July 13, 2010) – Healthcare Services Group, Inc. (NASDAQ: HCSG)
reported that revenues for the three months ended June 30, 2010 increased
13% to $192,954,000 compared to $170,896,000 for the same 2009 period. Net
income for the three months ended June 30, 2010 increased 12% to $8,721,000
or $.20 per basic and per diluted common share, compared to the 2009 second
quarter net income of $7,815,000 or $.18 per basic and per diluted common
share.

Revenues for the six months ended June 30, 2010 increased 14% to
$376,755,000 compared to $331,305,000 for the same 2009 period. Net income
for the six months ended June 30, 2010 increased 4% to $16,149,000 or $.37
per basic and $.36 per diluted common share compared to the 2009 six month
period net income of $15,551,000 or $.36 per basic and $.35 per diluted
common share.

The Board of Directors has declared a second quarter 2010 regular quarterly
cash dividend of $.23 per common share, payable on August 6, 2010 to
shareholders of record at the close of business July 23, 2010. This
represents a 5% increase over the dividend declared for the 2010 first
quarter and a 21% increase over the 2009 same period payment. It is the
29th consecutive regular quarterly cash dividend payment, as well as the
28th consecutive increase since our initiation of regular quarterly cash
dividend payments in 2003.

The Company will host a conference call on July 14, 2010 at 8:30 AM Eastern
Time to discuss its results for the three and six month periods ended June
30, 2010. The call in numbers are 800-401-3551 and 913-312-0688 (passcode #
2084962).

Cautionary Statement Regarding Forward-Looking Statements

This release and any schedules incorporated by reference into this report
contain forward-looking statements within the meaning of Section 27A of the
Securities Act of 1933, as amended, and Section 21E of the Securities
Exchange Act of 1934 (the “Exchange Act”), as amended, are not historical
facts but rather based on current expectations, estimates and projections
about our business and industry, our beliefs and assumptions. Words such as
“believes,” “anticipates,” “plans,” “expects,” “will,” “goal,” and similar
expressions are intended to identify forward-looking statements. The
inclusion of forward-looking statements should not be regarded as a
representation by us that any of our plans will be achieved. We undertake
no obligation to publicly update or revise any forward-looking statements,
whether as a result of new information, future events or otherwise. Such
forward-looking information is also subject to various risks and
uncertainties. Such risks and uncertainties include, but are not limited
to, risks arising from our providing services exclusively to the health
care industry, primarily providers of long-term care; credit and collection
risks associated with this industry; one client accounting for
approximately 11% of revenues in the six month period ended June 30, 2010;
risks associated with our acquisition of Contract Environmental Services,
Inc. including integration risks and costs, or such business not achieving
expected financial results or synergies or failure to otherwise perform as
expected; our claims experience related to workers’ compensation and
general liability insurance; the effects of changes in, or interpretations
of laws and regulations governing the industry, our workforce and services
provided, including state and local regulations pertaining to the
taxability of our services; and the risk factors described in our Form 10-K
filed with the Securities and Exchange Commission for the year ended
December 31, 2009 in Part I thereof under “Government Regulation of
Clients,” “Competition” and “Service Agreements/Collections,” and under
Item IA “Risk Factors.” Many of our clients’ revenues are highly contingent
on Medicare and Medicaid reimbursement funding rates, which Congress has
affected through the enactment of a number of major laws during the past
decade, most recently the March 2010 enactment of the Patient Protection
and Affordable Care Act and the Health Care and Education Reconciliation
Act of 2010. Currently, the U.S. Congress is considering changes or
revising legislation to reform health care in the United States which,
among other initiatives, may impose cost containment measures impacting our
clients. These laws and proposed laws have significantly altered, or
threatened to alter, overall government reimbursement funding rates and
mechanisms. The overall effect of these laws and trends in the long-term
care industry have affected and could adversely affect the liquidity of our
clients, resulting in their inability to make payments to us on agreed upon
payment terms. These factors, in addition to delays in payments from
clients, have resulted in, and could continue to result in, significant
additional bad debts in the near future. Additionally, our operating
results would be adversely affected if unexpected increases in the costs
of labor and labor related costs, materials, supplies and equipment used in
performing services could not be passed on to our clients.

In addition, we believe that to improve our financial performance we must
continue to obtain service agreements with new clients, provide new
services to existing clients, achieve modest price increases on current
service agreements with existing clients and maintain internal cost
reduction strategies at our various operational levels. Furthermore, we
believe that our ability to sustain the internal development of managerial
personnel is an important factor impacting future operating results and
successfully executing projected growth strategies.

Healthcare Services Group, Inc. is the largest national provider of
professional housekeeping, laundry and dietary services to long-term care
and related facilities.

                     HEALTHCARE SERVICES GROUP, INC.
               CONDENSED CONSOLIDATED STATEMENTS OF INCOME
                               (Unaudited)

                                               For the Three Months Ended
                                                        June 30,
                                                  2010           2009
                                              -------------  --------------
Revenues                                      $ 192,954,000  $  170,896,000
Operating costs and expenses:
   Cost of services provided                    165,240,000     145,830,000
   Selling, general and administrative           13,150,000      13,516,000
                                              -------------  --------------
Income from operations                           14,564,000      11,550,000
Other income (loss):
    Investment and interest income (loss)          (383,000)      1,157,000
                                              -------------  --------------
Income before income taxes                       14,181,000      12,707,000
Income taxes                                      5,460,000       4,892,000
                                              -------------  --------------
Net income                                    $   8,721,000  $    7,815,000
                                              =============  ==============

Basic earnings per common share               $         .20  $          .18
                                              =============  ==============

Diluted earnings per common share             $         .20  $          .18
                                              =============  ==============

Cash dividends per common share               $         .22  $          .18
                                              =============  ==============
Basic weighted average number of common shares
 outstanding                                     43,965,000      43,537,000
                                              =============  ==============

Diluted weighted average number of common
 shares outstanding                              44,652,000      44,262,000
                                              =============  ==============




                     HEALTHCARE SERVICES GROUP, INC.
               CONDENSED CONSOLIDATED STATEMENTS OF INCOME
                               (Unaudited)

                                                 For the Six Months Ended
                                                         June 30,
                                                    2010          2009
                                                ------------- -------------
Revenues                                        $ 376,755,000 $ 331,305,000
Operating costs and expenses:
   Cost of services provided                      323,812,000   283,722,000
   Selling, general and administrative             27,051,000    24,392,000
                                                ------------- -------------
Income from operations                             25,892,000    23,191,000
Other income:
    Investment and interest income                    366,000     2,094,000
                                                ------------- -------------
Income before income taxes                         26,258,000    25,285,000
Income taxes                                       10,109,000     9,734,000
                                                ------------- -------------
Net income                                      $  16,149,000 $  15,551,000
                                                ============= =============

Basic earnings per common share                 $         .37 $         .36
                                                ============= =============

Diluted earnings per common share               $         .36 $         .35
                                                ============= =============

Cash dividends per common share                 $         .43 $         .35
                                                ============= =============
Basic weighted average number of common shares
 outstanding                                       43,932,000    43,497,000
                                                ============= =============

Diluted weighted average number of common shares
 outstanding                                       44,655,000    44,168,000
                                                ============= =============




                      HEALTHCARE SERVICES GROUP, INC.

                  CONDENSED CONSOLIDATED BALANCE SHEETS
                                (Unaudited)

                                                               December 31,
                                                June 30, 2010      2009
                                                ------------- -------------
Cash and cash equivalents                       $  34,968,000 $  31,301,000
Marketable securities, net                         44,099,000    52,648,000
Accounts receivable, net                          107,253,000   104,356,000
Other current assets                               23,715,000    23,865,000
                                                ------------- -------------
  Total current assets                            210,035,000   212,170,000

Property and equipment, net                         4,931,000     4,391,000
Notes receivable- long term, net                    6,165,000     4,623,000
Goodwill , net                                     16,955,000    17,087,000
Other Intangible Assets, net                        8,198,000     8,862,000
Deferred compensation funding                      11,238,000    10,783,000
Other assets                                        9,032,000     7,976,000
                                                ------------- -------------

Total Assets                                    $ 266,554,000 $ 265,892,000
                                                ============= =============


Accrued insurance claims- current               $   5,305,000 $   4,844,000
Other current liabilities                          27,237,000    29,873,000
                                                ------------- -------------
  Total current liabilities                        32,542,000    34,717,000

Accrued insurance claims- long term                12,377,000    11,302,000
Deferred compensation liability                    11,479,000    11,099,000
Stockholders' equity                              210,156,000   208,774,000
                                                ------------- -------------

Total Liabilities and Stockholders' Equity      $ 266,554,000 $ 265,892,000
                                                ============= =============

Company Contacts:
Daniel P. McCartney
Chairman and Chief Executive Officer
215-639-4274

Thomas Cook
President
215-639-4274

Filed Under: Medical And Healthcare

WellTek Subsidiary Unveils Platform for Integrating Network Marketing With Social Network

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: Welltek Incorporated

WellCity Monetizes the Use of Social Networking for ‘Residents’

ORLANDO, FL–(Marketwire – July 13, 2010) –  WellCity, Inc. (http://www.wellcity.com), a wellness-related social network and subsidiary of WellTek, Inc. (OTCBB: WTKN), today unveiled WellCity Market™, its network marketing platform, calling all consumers and network marketers to be one of the first to join this ground-breaking opportunity to create optimum health and long-term wealth by getting social inside WellCity.

“Until now, social network users have had no way to leverage their personal network as a direct income opportunity. Today, we’ve changed that,” said David George, CEO of WellCity. “We are the first social network to offer actual money to its users. With the integration of WellCity Market, our WellCity ‘residents’ have an unprecedented opportunity to help others achieve optimal health, while they earn income from the purchases made by their network of family and friends or ‘neighbors.’ It’s a simple idea: users get paid every time their ‘neighbors’ make a purchase inside WellCity Market.”

WellCity Market offers a breadth of natural products to help others live a more enriched life physically, spiritually and financially. The technology of online social networking provides the single most effective medium today for creating long-term wealth and for teaching people about new products and services that help people feel better, lose weight, prevent disease and become younger and stronger even as people grow older.

According to world-renowned economist Paul Zane Pilzer, the emerging Wellness Industry has quickly become the hottest trend in the world today and it is predicted to reach $1 trillion by 2012. Furthermore, according to Direct Selling News, well over $70 billion dollars in revenue was generated in 2009 by the top 100 network marketing companies. “The convergence of the Wellness Industry with Network Marketing and Social Networking provides an extraordinary opportunity for our residents in WellCity, as well our shareholders; we are creating the perfect storm of opportunity,” said Randy Lubinsky, Chairman and CEO of WellTek. “It’s comparable to merging Amway with Facebook.”

About WellCity Incorporated
WellCity is a social utility where health- and wellness-minded ‘residents’ can closely commune with one another; receive support, information and encouragement from their ‘neighbors’ and from a league of leading professional experts; shop for health and wellness-oriented product and services; compete in WellCity’s proprietary 90-Day Wellness Challenge; and even enjoy income opportunities by leveraging their personal network. For more information on the Company, please visit www.WellCity.com.

About WellTek Incorporated
WellTek is a global health, fitness and wellness company that provides proven solutions to help address some of the world’s most pressing and costly health and wellness challenges. The Company owns and operates WellCity, Inc., a premiere wellness-related social utility that helps ‘residents’ live happier, healthier, longer lives. The Company’s subsidiary, MedX Limited, manufactures, markets and distributes the most advanced medical exercise equipment to the medical and fitness markets. Through its wholly owned subsidiary Pure HealthyBack, Inc., WellTek is redefining healthcare delivery by providing health plans, self-insured employer groups, and consumers with a viable non-surgical, lower cost treatment for patients who are seeking lasting relief from chronic neck and back pain. For more information on the Company, please visit www.WellTekinc.com. 

Certain statements contained in this press release, which are not based on historical facts, are forward-looking statements as the term is defined in the Private Securities Litigation Reform Act of 1995, and are subject to substantial uncertainties and risks in part detailed in the respective Company’s Securities and Exchange Commission filings, that may cause actual results to materially differ from projections. Although the Company believes that its expectations are reasonable assumptions within the bounds of its knowledge of its businesses, expectations, representations and operations, there can be no assurance that actual results will not differ materially from their expectations. Important factors currently known to management that could cause actual results to differ materially from those in forward-looking statements include the Company’s ability to execute properly its business model, to raise additional capital to implement its continuing business model, the ability to attract and retain personnel — including highly qualified executives, management and operational personnel, ability to negotiate favorable future debt facilities and capital raises, and the inherent risk associated with a diversified business to achieve and maintain positive cash flow and net profitability. In light of these risks and uncertainties, there can be no assurance that the forward-looking information contained in this press release will, in fact, occur. 

FOR MORE INFORMATION, PLEASE CONTACT:
Legacy Marketing Group
Roxie Mooney
President & CEO
(
Twitter: roxiemooney)
407-575-3220
or via email at [email protected]

Filed Under: Medical And Healthcare

www.DrRidwan.com: Urologist Dr. Ridwan Shabsigh, MD Provides Action Tools for Men’s Health in His Online Medical Advice Talk Show

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: DrRidwan.com

NEW YORK, NY–(Marketwire – July 13, 2010) – Maimonides Medical Center Urologist Dr. Ridwan Shabsigh, director of the Division of Urology, created his “Ask The Doctor” medical advice talk show to help bridge the gap of men’s healthcare information in a simple-to-understand format. His online health talk show, “The Dr. Ridwan Show” delivers accurate and usable health information on common men’s health questions.

Along with an elite panel of experts, Drs. Harry Fisch, Michael Perelman and Richard Sadovsky, the group provides reliable health information to common men’s health questions. Ridwan and his medical panelists provide unique insights and advice that support the show’s tagline, “Health information you can use.” The panelists discuss a hot topic per episode in men’s health such as heart disease, prostate cancer, testosterone deficiency and erectile dysfunction.

Each episode of Dr. Ridwan’s unique online doctor consultation show concludes with helpful action tools that incite viewers to take positive actions for their health. The most helpful action tool is a men’s health calculator. This health risk calculator helps to raise awareness and motivate men to access health care services and pursue healthier lifestyles.

This men’s health calculator is not an absolute measure of risk or a substitute for professional health advice, but it helps men to assess their risk of having hypertension (high blood pressure), hyperlipidemia (high cholesterol), diabetes and/or coronary artery disease. The viewer can answer basic questions on health status, erectile dysfunction, relationships, and waist size to help determine health risk.

Other helpful tips provided on Dr. Ridwan’s doctor advice show:

  • Avoid abdominal obesity to prevent heart and vascular disease risk
  • Men’s health preventive ideas
  • Get annual checkup and prostate screenings
  • Ask for urologist referral if abnormal urinary symptoms exist
  • Men should work with partners to improve health
  • Review health risks and reduce these factors
  • Watch for sexual problems
  • Be aware of testosterone deficiency symptoms

By providing answers to medical questions online, Dr. Ridwan hopes to reduce the need for unnecessary procedures and tests. “In these times of healthcare reform, by educating my viewers, I hope to make them be more proactive in monitoring their health,” said Ridwan. “This way they won’t have to make unnecessary trips to the emergency room for something that can be taken care of in advance or prevented.”

Contact:

Dr. Ridwan Shabsigh
Ph: 718-283-7746
http://www.DrRidwan.com

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Filed Under: Medical And Healthcare

Redlands Community Hospital Joins VHA to Leverage Networking Opportunities

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: VHA

IRVING, TX–(Marketwire – July 13, 2010) –  Redlands Community Hospital, a 205-bed facility located in Southern California, has joined VHA Inc., the national health care network and business cooperative that serves 1,400 not-for-profit hospitals across the nation. Redlands wants to enhance its ability to network with other providers in the region to develop solutions to challenges they all face, such as how to enhance clinical quality in the face of dwindling resources. 

“Most hospitals and health systems are drawn to VHA because of its supply chain management services, but that wasn’t a primary motivator for us,” said Jim Holmes, president and chief executive officer at RCH, which purchases about $25 million in supplies annually. “The health care marketplace is an increasingly challenging environment, and we determined that it would be best for RCH to be part of a larger network of hospitals, without giving up our local control. VHA provides that opportunity.”

The CEO of another VHA member hospital in California, Jim West at Presbyterian Intercommunity Hospital in Whittier, actually sold Holmes on VHA. “I explained that being a member of VHA connects our organization to thought leaders and solutions that we need to improve performance. Being a member of VHA creates leverage and gives us clout we don’t have on our own. I think that discussion made the decision to join VHA easier for Redlands,” said West.

In addition to joining VHA’s national network, RCH is also joining VHA’s regional network, VHA West Coast, which links more than 90 hospitals in Arizona, California, Hawaii, Nevada and one hospital in both Oregon and Washington. Through VHA, these organizations leverage their knowledge, purchasing clout and other resources to help each other improve.

“VHA creates connections and energy that enable hospitals to accelerate their performance,” said Rick Barnett, senior vice president of VHA’s West Coast office, located in Pleasanton, Calif. “We’re excited about having RCH in the VHA family. We’ve pursued the organization for two years, and we believe RCH will benefit through its membership, and it will deliver benefits to other members as the RCH team interacts with VHA peers.” 

About VHA

Based in Irving, Texas, VHA is a national network of not-for-profit health care organizations that work together to drive maximum savings in the supply chain arena, set new levels of clinical performance and identify and implement best practices to improve operational efficiency and clinical outcomes. Formed in 1977, through its 16 regional offices, VHA serves more than 1,400 hospitals and more than 28,000 non-acute care providers nationwide. VHA was ranked by Modern Healthcare as the 7th best place to work in health care in 2009.

Media contact:
Lynn Gentry
Email Contact

Filed Under: Medical And Healthcare

International Stem Cell Institute Launches Customized Stem Cell Therapy Treatments for Cerebral Palsy

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: International Stem Cell Institute

Unprecedented Stem Cell Treatments Providing New Hope for Children With CP

SAN DIEGO, CA–(Marketwire – July 13, 2010) –  International Stem Cell Institute (ISCI, www.iStemCelli.com) announced today the launch of highly effective Stem Cell Therapy treatments aimed at providing a better quality of life for those suffering with Cerebral Palsy (CP).

Details are available at www.iStemCelli.com/cerebralpalsy.html or calling 800-609-7795.

ISCI Executive Director Rita Alexander maintains, “Every parent wants their child to live a happy, healthy life as a baby, as a toddler, as a first grader. CP is a tremendously overwhelming condition — it’s really hard to understand the daily frustrations parents go through when a child is diagnosed with CP. And while the condition can’t be completely cured, our stem cell treatment is dramatically improving the quality of life for many children, much beyond their parent’s expectations. The results are truly amazing.”

Cerebral Palsy is not a disease like chicken pox or measles. It is an umbrella term for a group of related disorders stemming from different causes. The condition seriously affects muscle movement, and is caused by abnormalities in the brain. One million children in the US are afflicted with CP, and more will be diagnosed as we see an increase in the survival of premature infants and multiple births.

According to Alexander, CP is often associated with injury in the womb or during birth, and especially evident in premature infants. Alexander notes, “The earlier we can treat an infant or child with Stem Cell Therapy the greater the positive impacts on their future development.” She continues, “We’re working with very young children and infants. Stem Cell Therapy is a very gentle treatment, it’s gentle enough for a six month old baby.”

The procedure — safely and comfortably administering placental stem cells into several key parts of the body — is a leading-edge alternative CP treatment proving highly effective for infants and even older children afflicted with CP. Alexander relates, “The good thing is parents don’t have to wait for the new developments in this field, the procedure is available right now and affordable for most families.”

Stem cell therapy has been shown to relieve a wide variety of CP symptoms. Alexander claims, “We’re treating children with a variety of symptoms, like the lack of muscle coordination, those who have stiff and tight muscles or floppy muscles, children with exaggerated reflexes and children dragging one foot or walking on their toes.”

ISCI’s Stem Cell Therapy treatments are also being hailed as a potent medical tool in treating the seizures, difficulty with vision, hearing and speech, incontinence, and recurring lung infections that children can often experience with CP.

ISCI’s CP patient advocate, LeiMomi Ferrill, has personally seen impressive results with stem cell therapy in CP patients. “You’re heart really goes out to these parents and children. When a parent tells us their child can now roll over, or talk or balance a bit, they’re walking through a door where they feel there is hope for the very first time. We have one child, William, who was practically comatose and unable to communicate. He’s now telling his Mother he loves her, knows and calls his brothers by name, and is talking with his family about what he likes to eat.”

Alternative treatments currently being explored for CP include electrical stimulation — pulsing electricity into the motor nerves — and hyperbaric oxygen therapy in which high concentrations of oxygen are forced into brain tissues under pressure. Researchers at the University of Georgia are conducting the first ever FDA approved stem cell clinical trials for brain injuries. Dr. James Carroll, chief of pediatric neurology at the MCG School of Medicine, claims, “Stem cell therapies using cord blood have been used successfully for more than 20 years, but here we have a study which is breaking new ground in advancing therapies for brain injury.”

ISCI strongly supports scientific research on CP, especially the work of the Cerebral Palsy International Research Foundation (CPIRF), the leading nongovernmental organization funding advanced research in CP.

Patients and families with Cerebral Palsy are encouraged to learn about treatments by calling the International Stem Cell Institute at 800-609-7795 or online at www.istemcelli.com/cerebralpalsy.html.

About ISCI (www.iStemCelli.com)
ISCI is an innovator in stem cell therapy and regenerative medicine dedicated to providing a pathway to treatments which may improve health and quality of life for thousands of people with degenerative diseases around the world. Over 3,000 patients have safely undergone stem cell treatments. The company accepts patients globally, and is dedicated to the highest medical and ethical standards.

Disclaimer: Stem Cell Therapies offered for consideration by International Stem Cell Institute are not currently approved by the FDA and the treatments and procedures mentioned take place outside the USA. Stem Cell Treatments are not a cure for any condition, disease or injury, nor a substitute for proper medical diagnosis and care. The information contained in this press release and ISCI’s written materials should not be considered medical advice. It is intended to be used for educational and information purposes only.

Contact:
Mark Russo
Global Marketing Director
International Stem Cell Institute
phone 858-609-7795

Filed Under: Medical And Healthcare

Four Healthcare Companies Receive Inaugural Medline Preferred Vendor Recognition Award

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: Medline Industries, Inc.

Award Recognizes Collaboration, Outstanding Operational and Sales Performance

MUNDELEIN, IL–(Marketwire – July 13, 2010) – Medline Industries, Inc., the nation’s largest privately held manufacturer and distributor of healthcare supplies, today announced the winners of its inaugural 2009 Preferred Vendor Recognition Awards. Selected by a panel of executives from Medline’s Preferred HealthCare Division, the Preferred Vendor Awards were given to four Medline partners who not only demonstrated outstanding performance in sales and operations but also have collaborated as a true partner in Medline’s initiatives and in achieving mutual goals.

The following companies were honored at Medline’s 2010 National Meeting and Sales Conference in Montgomery, TX:

  • Rookie Vendor of the Year: SunTech Medical (Morrisville, NC) was recognized for their support and sales growth of the SunTech 247 vital signs device since Medline launched the product in May 2009. 
  • Vendor of the Year: Abbott Diabetes Care (Alameda, CA) was honored as the Vendor of the year who demonstrated a strong commitment to sales and marketing, as well as operational and supply chain excellence.
  • Sales Merit Award: Abbott Nutritional (Columbus, OH), and Caltech Industries (Midland, MI) were both recognized for showing outstanding sales growth over the prior year while maintaining key economic initiatives.

“Our partnership with vendors is an essential element of our success with our customers,” said Maroun Abouzeid, president of Preferred HealthCare. “We thank all our partners for their contributions and congratulate our award-winning partners for their ongoing leadership.”

About Medline Industries, Inc.
Medline, the nation’s largest privately held manufacturer and distributor of healthcare products, manufactures and distributes more than 100,000 products to hospitals, extended-care facilities, surgery centers, home care dealers and agencies. Headquartered in Mundelein, Ill, Medline has more than 800 dedicated sales representatives nationwide to support its broad product line and cost management services.

Over the past five years, Medline has been the fastest-growing distributor of medical and surgical supplies in the U.S., serving as the primary distributor to over 450 major hospitals and healthcare systems. As a leading distributor, Medline offers a comprehensive array of consulting and management services encompassing the supply chain and logistics, utilization and standardization, business tools and enhanced reporting capabilities and on-staff clinicians.

Medline has a growing network of 34 distribution centers around the country, as well as an expanding, dedicated transportation fleet with over 180 vehicles in a variety of sizes to fit customers’ specific delivery needs. The fleet is equipped with the latest navigation devices for enhanced order tracking and communication. 

Media Contacts:
Jerreau Beaudoin
(847) 643-3011

John Marks
(847) 643-3309

Filed Under: Medical And Healthcare

New Study Shows Hospital-Based Out-of-Home Advertising Delivers Above Average ROI

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: Interactivation Health Networks

Proves ‘Fourth Screen’ Value of Interactivation Health Networks’ Channels

NEW YORK, NY–(Marketwire – July 13, 2010) –  The Patient Channel, a 24/7 in-hospital television network from Interactivation Health Networks, has conducted a study for one if its pharmaceutical advertisers that demonstrates above average ROI — a 5:1 ROI after six months and 8:1 ROI after a 12 month targeted advertising campaign — further evidence of the immense value of Digital Out-of-Home advertising, particularly as it relates to hospitals as a “fourth screen” location. 

“The reason why advertising is so effective at hospital bedside, and why the Patient Channel and Newborn Channel work is simple — we provide marketers with a unique and differentiated platform that offers compelling and essential health content delivered at the precise moment it is needed most,” said Suzanne Fleming, SVP of Sales at Interactivation Health Networks. “Our channels provide the ideal branding environment where consumers are highly attentive, highly motivated and ready to act. Connecting brands with our hyper-focused audience is an opportunity that is hard to replicate with traditional television advertising.”

Interactivation Health Networks engaged IMS Consulting to perform a quantitative ROI study based upon dispensed prescribing tied to participating physicians exposed to a specified pharmaceutical company’s program. The study found that when comparing post-exposure prescribing to a similar control group of physicians, identified by IMS, the pharmaceutical company saw a +2.1% incremental increase in prescribing, representing a positive return on the pharmaceutical company’s investment with Interactivation Health Networks.

Results from the IMS study corroborate findings from studies conducted by Nielsen* and Razorfish** that project the continued rise of Out-Of-Home advertising due to the unchallenged ability to pinpoint a targeted, and often captive, audience with relevant messaging. For brands within the health and wellness field, the Interactivation Health Networks are a documented means of successfully activating these consumers.

Advertisers who use The Patient and Newborn Channels will have the added opportunity of further engaging with their target audience via Interactivation’s propriety interactive technology. This would allow viewers of ads to directly and immediately interact with the brand with their mobile device to receive more information or coupons on the advertised product. For example, consumers can locate a nearby retailer by texting their zip code to the Interactivation-owned short code promoted in their on-air commercial.

About Interactivation Health Networks
The Patient Channel and The Newborn Channel are the most comprehensive in-hospital TV networks. Delivered directly to patient rooms and waiting areas, the Channels provide viewers with original, award-winning health programs and advertisers with the unique ability to integrate brand messaging with content that is compelling and endorsed by healthcare professionals. The Newborn Channel broadcasts baby care and postpartum programming for new parents, reaching 60% of new moms. The Patient Channel features both condition-specific and preventative health programming to empower and inform patients. The channels are currently available in over 2,700 hospitals nationwide.

IMS Health Consulting conducted the study with one of the Patient Channel’s long-standing advertisers.

*Nielsen Inaugural Fourth Screen Report – April 12, 2010
**Razorfish Outlook Report 2010

Filed Under: Medical And Healthcare

Healthnostics Completes Acquisition

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: Healthnostics, Inc.

NEW YORK, NY–(Marketwire – July 13, 2010) –  Healthnostics, Inc. (PINKSHEETS: HNSS), a medical and biotechnology analytics company, has completed its acquisition of Worldwide Wipes Co., “a U.S. manufacturer and distributor of wipes for medical, veterinary, disinfecting, and a variety of other uses, and the company’s market ranges from cartons for individuals to truckloads for corporations. The Company places a priority on price, quality, and convenience, providing prompt, free shipping.”

Terms of the acquisition include net profit benchmarks of $300,000 to $600,000 in the first year and $600,000 to $900,000 in the second year.

“We are pleased to announce the completion of the most important event in our Company’s history. The Worldwide Wipes price points are exceptionally competitive, and its customer base is nationwide. Following several years of base-building, this acquisition represents such a quantum leap for Healthnostics that we are contemplating a name and stock symbol change that reflects the diversified nature and direction of the Company,” said President Alan Grofe.

About Healthnostics

Healthnostics, Inc. is a medical and biotechnology analytics company that provides comprehensive patient clinical monitoring and risk management systems to acute care hospitals and utilizes its Internet portals to deliver medical and biotechnology resource information to industry professionals as well as to the general public. Healthnostics’ major products include: Worldwide Wipes Co., a manufacturer and distributor of medical and other wipes, MedGuardian, a patient care monitoring and risk management system for hospitals that is fully Web-based; and through the MedBioWeb subsidiary, MedBioWorld™, one of the largest professional medical and biotechnology directory resource and reference portal sites on the Internet, and FamilyMedicalNet, a companion consumer healthcare information portal.

For further information please visit Healthnostics www.healthnostics.com, and Worldwide Wipes Co. www.wipesco.com, MedBioWorld www.medbioworld.com, and FamilyMedicalNet www.familymedicalnet.com.

And visit us on Facebook at www.facebook.com/Healthnostics.

This press release may contain certain statements that are not descriptions of historical information, but are forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Exchange Act of 1934. These forward-looking statements refer to matters that involve risks and uncertainties. Such statements reflect management’s current views and are based on certain assumptions. Actual results could differ materially from the assumptions currently anticipated.

Contact:
Alan Grofe
P. 703-754-7126
[email protected]

Filed Under: Medical And Healthcare

CPI Announces New Look, Logo, and Website

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: CPI

MILWAUKEE, WI–(Marketwire – July 13, 2010) –  CPI has released a new company logo and website. The new crisisprevention.com consolidates all CPI websites, including preparetraining.com, dementiacarespecialists.com, and iancici.org, into a single enhanced and redesigned site.

Based on customer and Certified Instructor feedback, crisisprevention.com is completely revamped to include more intuitive navigation, improved account management, and an enhanced online shopping experience. It also includes a new documentation feature, which allows Certified Instructors to submit training documentation online.

The company logo has been redesigned to reflect the CPI mission and values. The logo shows people reaching out to each other with their hands, symbolizing the integral relationship between CPI and its Certified Instructors in their mission to educate, empower, and enrich the lives of others. Individual logos for each CPI specialized offering — Nonviolent Crisis Intervention® training, Prepare Training® program, and Dementia Care Specialists — have also been updated with a fresh, coordinated look.

According to Tony Jace, CPI chief executive officer, the new logos and website mirror the company’s commitments to expand the message of care and well-being.

“We value our commitment to increase the effectiveness of our Certified Instructors as they manage their day-to-day interactions and responsibilities. Through our new look and improved tools, we continue to provide individuals and organizations the resources they need to create safer, enriched environments,” he said.

CPI, headquartered in Milwaukee, WI, is the world’s leading training organization specializing in the safe management of disruptive and assaultive behavior. CPI’s cornerstone Nonviolent Crisis Intervention® training and Prepare Training® programs focus on workplace violence prevention and offer effective strategies for managing anxious, hostile, or violent behavior. Through Dementia Care Specialists, CPI also offers dementia care training to improve function, safety, and quality of life. Since 1980, more than 6 million professionals have participated in CPI training, and thousands of organizations worldwide have successfully implemented CPI’s unique behavior management techniques.

Contact:
Robert D. Rettmann
Research and Communications Services Coordinator
CPI
414.979.7075
[email protected]

Filed Under: Medical And Healthcare

Ryerson Counsels Clients in Improving Hospital Charge Capture

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: Ryerson Healthcare Consultants

AKRON, OH–(Marketwire – July 13, 2010) –  Hospitals can gain significant revenue by improving documentation of services and procedures and instituting better material management practices.

That’s the counsel from Ryerson Healthcare Consultants, medical revenue specialists and the nation’s leader in emergency department process improvement. The Ryerson organization serves clients with hospital charge capture experience gained through working with more than 540 hospitals in 40 states.

Whether they are working on clients’ surgical services or emergency department charge capture, Ryerson’s experts tailor improvement recommendations to fit each hospital’s specific challenges.

“OR and ED operations are uniquely complex, and staff in both areas tend to experience problems in properly documenting, coding and billing for all chargeable procedures and supplies,” said President Peter Ryerson. “Our team of hospital charge capture specialists includes people who have considerable experience as RNs in both areas, with track records of success in successfully improving their client hospitals’ revenues.”

Such experience and knowledge is invaluable for hospital charge capture improvement, the goal for the majority of Ryerson Healthcare Consultants’ clients. Ryerson said his team develops solutions that result in improvements to the charge protocol and hospital charge capture process.

“In many, if not most, cases, it comes down to strengthening our clients’ documentation and billing processes,” Ryerson said. “We find that many hospitals lack the tools and information necessary to properly document, code and bill. The obvious result is billing that fails to capture all of the services that are rendered.”

He said refining the documentation and charge processes and training managers and staff in the proper procedures can result in significant gains in both OR and ED charge capture. In many cases, such gains can transform a money-losing surgical services or emergency department into a reliable profit center. 

Ryerson’s team also works on strengthening material management procedures. Relying on time-proven protocols, Ryerson develops best-practice material management processes and helps its client hospitals institute them. Ryerson also guides training of staff and managers in the value of remaining in compliance with the procedures.

“We also find that improving communication between the financial managers and the clinical staff pays great dividends,” he said. “When the financial people and clinicians understand each other’s roles in achieving profitability, we see time after time that this enhances the hospital’s ability to effectively cost and bill for provided services.”

Contact:
Peter Ryerson
Ryerson Healthcare Consultants
330-670-6900
[email protected]

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Filed Under: Medical And Healthcare

Providence Willamette Falls Medical Center to Add OR Workflow Automation System

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: Patient Care Technology Systems

It Joins Providence Portland and Providence St. Vincent in Providing a Consistent Platform for Patient Care

CHARLOTTE, NC–(Marketwire – July 13, 2010) –  Patient Care Technology Systems (PCTS), a subsidiary of Consulier Engineering, Inc. (NASDAQ: CSLR), today announced that Providence Willamette Falls Medical Center will add Amelior ORTracker® — a web-based workflow visibility and automation solution built to streamline patient flow and improve efficiency — in their Oregon City, OR Surgical Services Department. 

Providence Willamette Falls Medical Center is a 143-bed healthcare facility serving the Portland area since 1954. In October 2009, Willamette Falls Hospital officially became Providence Willamette Falls Medical Center when it joined the Providence Health and Services family.

The installation, expected to be complete by the fourth quarter 2010, will include the solution Amelior ORTracker — part of the Amelior Enterprise Visibility and Workflow Automation Suite™ which comprises department to facility-wide software solutions and services designed to more efficiently and safely orchestrate patient care through the real-time visualization of patient flow. Hospitals can scale their implementations by the entities they wish to track (patients, staff, movable medical equipment), purpose (patient flow, temperature monitoring, asset management, infection control) and by the scope of hospital workflow (surgical services, acute care, inpatient floors, outpatient services, enterprise-wide).

With the Amelior ORTracker system, Providence Willamette Falls can monitor, in real-time, the status of patients as they travel through the perioperative process from pre-op, inter-op, PACU (post anesthesia care unit) and post-op. They will have access to computer watch lists that will provide a comprehensive view of the cases for the day, including real-time patient and staff status and location. 

Providence Willamette Falls will join its “sister” facilities Providence Portland Medical Center and Providence St. Vincent Medical Center, which have been using Amelior ORTracker since 2003. In the last seven years, these facilities have seen a reduced time waiting between stages of care in a perioperative visit, enabling them to add-on cases and effectively increase departmental capacity; provided a quieter, more healing environment by decreasing the need for overhead pages and phone calls; and improved safety through the automatic tracking of key intervals such as the administration of antibiotics.

“It’s Providence’s goal to continue to provide the best care possible in all the communities we serve. This includes providing a consistent platform for patient and staff satisfaction,” said Deborah Tuke Bahlman, Providence Health & Services – Oregon Regional IT Director of Surgical Services. 

Tony Marsico, president and chief executive officer for PCTS says, “We have a long history of partnering with Providence, and we welcome the opportunity to implement Amelior ORTracker in another PH&S facility. Providence again shows their continued dedication to their community.”

PCTS has expanded their Amelior Enterprise Visibility and Workflow Automation Suite into other departments within the Providence Health and Services community in Oregon, including the Providence Heart and Vascular Institute and the radiology department at Providence St. Vincent.

About Providence Willamette Falls Medical Center
Providence Willamette Falls Medical Center is a not-for-profit acute care hospital operated by Providence Health & Services in Oregon City, OR. Established in 1954 as Doctors’ Hospital, the hospital moved to its current location in 1961 and has 143 licensed beds at its 243,000-square-foot (22,600 m2) facility. Providence Willamette Falls also operates several medical offices and clinics outside of Oregon City in other parts of Clackamas County. Previously known as Willamette Falls Hospital, the hospital merged with Providence in 2009.

About Patient Care Technology Systems
Patient Care Technology Systems, a subsidiary of Consulier Engineering, Inc. (NASDAQ: CSLR), helps health care providers to improve patient flow, increase capacity and improve patient and staff safety by visualizing the real-time location and status of people and equipment throughout their facility. PCTS solutions have supported over 2 million patient visits annually and have shown a proven return on investment in high turnover, high-acuity units such as the emergency department and perioperative suites. The Amelior Enterprise Visibility and Workflow Automation Suite™ is interoperable with all leading locating technologies, including active-RFID, infrared, ultrasound, ultra-wideband, Wi-Fi and ZigBee. PCTS customers have been recognized nationally for improvements in efficiency and clinical excellence. For more information, visit www.pcts.com. 

This press release contains forward-looking statements within the meaning of federal securities laws. PCTS and CSLR caution you that any statements contained in this press release which are not strictly historical statements constitute forward-looking statements. Such forward-looking statements include, but are not limited to, those related to PCTS’s and CSLR’s expectations regarding continued business growth. These statements are neither promises nor guarantees, and involve risks and uncertainties that could cause actual results to differ materially from such forward-looking statements, (copies of which may be obtained at the SEC’s website at: http://www.sec.gov) — could impact the forward-looking statements contained in this press release. Readers should not place undue reliance on any such forward-looking statements, which speak only as of the date they are made. PCTS and CSLR disclaim any obligation to publicly update or revise any such statements to reflect any change in PCTS and CSLR’s expectations, or in events, conditions or circumstances on which any such statements may be based, or that may affect the likelihood that actual results will differ from those set forth in the forward-looking statements.

Contact:
Karen Beran
Marketing Manager, PCTS
714-642-1056
Email Contact

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Filed Under: Medical And Healthcare

Capsule Webinar Will Address How Device Integration Helps Meet Meaningful Use Criteria Such as CPOE

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: Capsule Tech, Inc.

ANDOVER, MA–(Marketwire – July 13, 2010) –  Capsule, the leading provider of medical device connectivity, announced that they will be hosting a webinar on July 21, 2010 at 1:00pm Eastern Time on a number of issues hospitals are facing in reaching meaningful use criteria outlined in the HITECH provision of the ARRA. Featured in the webinar will be how medical device integration improves patient care and safety and helps meet Phase I, II and III meaningful use criteria including CPOE.

Ann Farrell, Principal at Farrell Associates, and Kevin Phillips, Partner Development Manager at Capsule, will engage in an interactive discussion about medical device integration and meaningful use. They will discuss why it is critical that real time data be available when hospitals are implementing CPOE technology. They will also discuss how medical device integration can affect the entire enterprise and help meet a number of patient care and safety goals and why it therefore should be placed on a hospital’s short term priority list.

Key topics that will be discussed include: the real benefits of medical device integration, how device integration can recover nursing hours, how can it improve overall patient care and safety, how it addresses hospitals’ key issues surrounding clinical workflow and CPOE, and how device integration can help meet Phases 1, 2 and 3 meaningful use criteria as outlined in the HITECH provision of the ARRA. The speakers are also encouraging participants to submit individual questions prior to the webinar by filling out a form on the registration page. For more information and to register and submit your questions right away click here: https://www1.gotomeeting.com/register/614983312

About Capsule’s Enterprise Device Connectivity Solution™
Capsule’s Enterprise Device Connectivity Solution is the only solution that will truly adapt to the environment it operates in. Its design gives hospitals the option to deploy connectivity throughout the enterprise so that all departments, not just high acuity, can enjoy the value that device integration has to offer. And it completely integrates with existing or planned caregiver work processes and allows a facility to leverage existing technologies. For more information about Capsule’s Enterprise Device Connectivity Solution, visit http://www.capsuletech.com.

About the Capsule Neuron™ platform
The Capsule Neuron is Capsule’s Next Generation Bedside Platform for managing device connectivity. It is a touch screen device equipped with its own docking station that provides a universal view and status of connectivity for all devices connected to a patient, including devices that are connected locally to a Capsule Neuron docking station and devices that are networked via the hospitals’ wired or wireless LAN. And the Capsule Neuron provides the basis for an expanding set of solutions to enable positive patient association, improved bedside workflow and enhanced patient safety. For more information about the Capsule Neuron visit http://www.capsuletech.com/our-solution-capsule-neuron.htm.

About Capsule
For more than 12 years, Capsule has been the world’s leading, award-winning provider of solutions for medical device connectivity. The company has established market leadership through its FDA 510(k) cleared software and medical grade hardware products, its unique expertise in device protocols and firmware, and through its strong partnerships with major medical device manufacturers and HIS companies. Capsule’s solutions are proven, with over 617 installations at leading healthcare facilities worldwide and its technology is secure, with the largest installed device driver library. Furthermore, Capsule is continually recognized as the leader in the industry receiving the Frost & Sullivan Global Technology Leadership Award as well as the Deloitte Technology Fast 50 and Fast 500 EMEA Awards. And, with the introduction of the Capsule Neuron™ platform and Enterprise Connectivity Solution, Capsule will continue to be the leader, by working with our partners to develop and implement solutions that meet the short and long term patient safety needs of hospitals today. For more information about Capsule, visit the company’s Web site at http://www.capsuletech.com/ or contact the U.S. Marketing & Public Relations department at 978-482-2337.

Contact:
Amanda McAlpine
978-482-2322
Email Contact

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Filed Under: Medical And Healthcare

Global Surgical Equipment Market to Exceed $7 Billion by 2016

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: MarketResearch.com

ROCKVILLE, MD–(Marketwire – July 13, 2010) –  MarketResearch.com has announced the addition of GBI Research’s new report “Surgical Equipment Market to 2016 – Emerging Economies to Provide Future Growth Opportunities,” to their collection of Surgical Equipment market reports. For more information, visit http://www.marketresearch.com/product/display.asp?ProductID=2718784.

GBI Research’s medical equipment report, “Surgical Equipment Market to 2016 – Emerging Economies to Provide Future Growth Opportunities” provides key data, information and analysis on the global surgical equipment market. This report on medical technologies provides data on market landscape, competitive landscape and market trends information on three surgical equipment market categories — Electrosurgical Devices, Hand Instruments and Surgical Sutures. The report provides comprehensive information on the key trends affecting these categories, and key analytical content on the market dynamics. The report also reviews the competitive landscape, key pipeline products and technology offerings.

This report is built using data and information sourced from proprietary databases, primary and secondary research and in-house analysis by GBI Research’s team of industry experts.

The global surgical equipment market has grown steadily during the last decade due to an increase in the number of hospitals and the rise in the number of surgical procedures performed both in the developed and emerging economies. In the future, the number of surgical procedures performed in the emerging economies is expected to grow at a faster rate than in developed economies, due to the higher economic growth forecasts for the emerging economies.

The surgical equipment market is highly competitive and fragmented with a healthy mix of international and local players. The addition of new hospitals and an increase in the number of operating rooms in existing hospitals in the emerging economies provide growth opportunities for both established players and new entrants.

Topics covered in the report include…

  • Key geographies covered include the US (United States), Canada, the UK (United Kingdom), Germany, France, Italy, Spain, Japan, China, India, Australia, and Brazil.
  • Market size and company share data for three surgical equipment market categories – Electrosurgical Devices, Hand Instruments and Surgical Sutures.
  • Annualized market revenues data from 2002 to 2009, forecast forward for 7 years to 2016. Company share data for 2009.
  • Qualitative analysis of key market trends, market drivers, and restraints by each category within the surgical equipment market.
  • The report also covers information on the leading market players, the competitive landscape, and the leading pipeline products and technologies.
  • Key players covered include Ethicon, Covidien, B. Braun, ERBE Elektromedizin, CONMED Corporation and Integra LifeSciences.

For more information, visit http://www.marketresearch.com/product/display.asp?ProductID=2718784.

Contact:
Sean Snyder
MarketResearch.com
[email protected]
240.747.3076

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Filed Under: Medical And Healthcare

Eat the Zucchini, Wear the Bikini

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: American Diabetes Association

American Diabetes Association Offers Completely Updated Personal Food Advisor to Help You Survive Summer and Beyond

ALEXANDRIA, VA–(Marketwire – July 13, 2010) –  Summer means gardening, grilling, and swimming at the pool. Summer’s produce and expanded cooking options also mean the season is an opportunity to improve your eating habits. The American Diabetes Association announced today a completely revised online nutrition tool in English and Spanish to help you get ready for the season: MyFoodAdvisor™ (www.diabetes.org/MyFoodAdvisor).

The award-winning MyFoodAdvisor has new and expanded features that allow people to track their daily meals, substitute healthier alternatives in recipes or on the plate, and browse recipes. People with diabetes, heart disease, kidney disease, high blood pressure, high cholesterol and those looking to lose weight can use MyFoodAdvisor to find nutrition information on calories, carbohydrates, sodium, fat and cholesterol.

“You would be surprised to see how small substitutions at meal time can make a real difference in your health,” commented Christine Tobin, CDE, President, Health Care & Education, American Diabetes Association. “MyFoodAdvisor can set you up for success by showing you healthy alternatives, tracking what you eat and helping create goals. Losing 10 or 15 pounds can help stop diabetes by preventing or delaying type 2 diabetes or diabetes complications.”

Join American Diabetes Association’s Director of Nutrition and Clinical Affairs Stephanie Dunbar, MPH, RD, and USA Today’s Medical Reporter Mary Brophy Marcus to discuss healthy eating and using the completely revised MyFoodAdvisor during a Twitter Chat on Thursday, July 15, at 2 p.m. ET, at @AmDiabetesChat and #ADA_USAT.

New features include:

  • Track It – You can create your own goals for calories, carbohydrate, sodium, saturated fat and fiber and compare what you currently are eating to what you want to be eating. This analysis allows you to make healthier options to lower sodium or saturated fat intake or to keep your carbohydrate intake consistent from day to day.
  • Spanish Version – The entire web site is now available in Spanish. The prevalence of diabetes is 2 to 4 times higher among Hispanics/Latinos.

Updated features include:

  • Healthy Alternative – This feature, unique to MyFoodAdvisor™, allows you to search for healthier foods. For example, searching for a healthier alternative to ground beef for your favorite burger recipe would provide choices for other ground meat products like turkey or even vegetable-based meat alternatives. The algorithm, based on recent research, takes into account 13 different nutrients to recommend the best alternatives based on your selections.
  • Recipe Analysis – Analyze your favorite recipes with our Create Dish functionality. You can request healthier options for all of your recipe ingredients to make your old favorite a healthier favorite. Your own recipes can be saved in your recipe box and imported into the tracking it tool, and ingredients added to a shopping list.
  • Create Dish – The portion sizes have been expanded to meet your preferences for using simple cooking measurements.
  • Simpler Navigation – The new version allows you to better search and compare food options.

“For people with diabetes and their caregivers, one of MyFoodAdvisor’s useful features remains that serving sizes are based on 15 grams of carbohydrate, which makes it easier to count carbs. There is also information on phosphorus and potassium, two important nutrients to watch for people with kidney disease,” commented Tobin. “But MyFoodAdvisor can help anyone looking to make smart food choices this summer.”

The American Diabetes Association is leading the fight to stop diabetes and its deadly consequences and fighting for those affected by diabetes. The Association funds research to prevent, cure and manage diabetes; delivers services to hundreds of communities; provides objective and credible information; and gives voice to those denied their rights because of diabetes. Founded in 1940, our mission is to prevent and cure diabetes and to improve the lives of all people affected by diabetes. For more information please call the American Diabetes Association at 1-800-DIABETES (1-800-342-2383) or visit www.diabetes.org. Information from both these sources is available in English and Spanish.

Contact:
Sarah Bradley
[email protected]
703-549-1500, ext. 2231

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Filed Under: Medical And Healthcare

Coma saludable para lucir bien este verano

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: American Diabetes Association

La Asociación Americana de la Diabetes ofrece un consejero de comida para ayudarle a prepararse para el verano y el futuro

ALEXANDRIA, VA–(Marketwire – July 13, 2010) – Prepararse para el verano significa sembrar
los jardines, limpiar el asador y salir a comprar trajes de baño. Los
productos del verano y las opciones para cocinar también significan que la
temporada es una oportunidad para mejorar sus hábitos alimenticios. La
Asociación Americana de la Diabetes anunció hoy sobre una herramienta en
línea de nutrición en español y en inglés que le ayudará a prepararse para
la temporada.: MiConsejerodeComida™ http://tracker.diabetes.org/es/.

MiConsejerodeComida tiene características nuevas y mejoradas que le
permitirán a las personas a mantener un registro de sus comidas diarias,
sustituir alternativas más saludables para recetas o en el plato. Las
personas con diabetes, enfermedades cardiacas, enfermedad renal, alta
presión arterial, alto colesterol y aquellas personas que quieren bajar de
peso pueden utilizar MiConsejerodeComida para encontrar información
nutricional sobre calorías, carbohidratos, sodio, grasa y colesterol.

“Hacer pequeños cambios al tiempo de la comida puede tener un impacto
positivo en su salud,” comentó Lorena Drago, RD, CDE, voluntaria de la
Asociación Americana de la Diabetes. “MiConsejerodeComida le puede enseñar
hacer alternativas saludables, crear metas y registrar lo que come. Si
pierde solamente 10 o 15 libras, usted puede ponerle alto a la diabetes al
prevenir o retrasar la diabetes tipo 2 o sus complicaciones…”

Las características nuevas incluyen:

  • Versión en español – Todo el sitio web está disponible ahora en
    español. La prevalencia de la diabetes es de 2 a 4 veces más alta entre
    los hispanos/latinos.
  • Regístrelo – Usted puede crear sus metas para calorías,
    carbohidratos, sodio, grasa saturada y fibra y compararlas con lo que
    actualmente está comiendo y lo que quisiera comer. Este análisis le permite
    hacer opciones más saludables para reducir el consume de sodio y grasa
    saturada o para mantener su consumo de carbohidratos consecuente en el día
    a día.

Las características actualizadas incluyen:

  • Alternativa saludable – Esta característica, exclusiva a
    MiConsejerodeComida™, le permite buscar comidas más saludables. Por
    ejemplo, si busca una alternativa más saludable para la carne de res
    molida para su receta favorita de hamburguesa, le proporcionaría otras
    opciones de carne molida tales como, pavo molido o alternativas
    vegetarianas. El algoritmo, que es basado en investigaciones recientes,
    toma en cuenta 13 nutrientes diferentes para recomendar la mejor
    alternativa basándose en sus selecciones.
  • Análisis de recetas – Analice sus recetas favoritas con nuestra
    función de Crear un plato. Usted puede solicitar opciones más saludables
    para los ingredientes de su receta para hacer que un viejo favorito sea un
    favorito saludable. Sus propias recetas pueden ser guardadas en su
    recetario e importadas a la herramienta de registro y los ingredientes
    pueden ser agregados a su lista de compras.
  • Crear un plato – Los tamaños de las porciones han sido
    incrementadas para reunir sus preferencias al utilizar medidas simples de
    cocina.
  • Navegación simple – Esto le permite buscar y comparar opciones
    de comidas con más facilidad.

“Los tamaños de las porciones en MiConsejerodeComida son basadas en 15
gramos de carbohidratos, lo cual hace que sea más fácil para las personas
con diabetes y sus cuidadores a contar carbohidratos. MiConsejerodeComida
también tiene información sobre fósforo y potasio, 2 nutrientes importantes
que se deben vigilar para las personas con enfermedad renal, comentó Lorena
Drago. “Sin importar para qué, MiConsejerodeComida puede ayudar a cualquier
persona a prepararse para el verano al enseñarle como hacer mejores
opciones de comida.”

La Asociación Americana de la Diabetes es líder en la lucha para ponerle
alto a la diabetes y sus consecuencias fatales y lucha por las personas
afectadas por esa enfermedad. La Asociación financia la investigación a fin
de prevenir, curar y controlar la diabetes; ofrece servicios para cientos
de comunidades; suministra información objetiva y verosímil; y da voz a
aquellas personas privadas de sus derechos como consecuencia de la
diabetes. La Asociación se fundó en 1940. Nuestra misión es prevenir y
curar la diabetes, así como mejorar la vida de todas las personas afectadas
por esa enfermedad. Para más información llamar al 1-800-DIABETES
(342-2383) o visitar www.portufamilia.org. Información sobre ambas fuentes
se encuentra disponible en inglés o en español.

Filed Under: Medical And Healthcare

Physicians Resource Network Achieves AdvancedMD AdvancedBiller Status in Four Months

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: AdvancedMD Software

Comprehensive Service Offering Ensures Efficiency and Compliance Among Client Base, While Reducing the Billing Staff Needed to Support a Single Client by 30 to 60 Percent

SALT LAKE CITY, UT–(Marketwire – July 13, 2010) –  AdvancedMD® Software, Inc., the leader in all-in-one, web-based practice management, Electronic Health Record (EHR), and billing applications for medical practices and medical billing services, today announced that Physicians Resource Network, Inc. (PRN) became an AdvancedMD billing partner in March, and achieved AdvancedBiller™ status in July, by adding 17 providers to the AdvancedMD platform within a four month period, with six of those providers on the AdvancedMD EHR clinical package.

PRN, using the automated, integrated AdvancedMD Software-as-a-Service (SaaS) platform, is able to eliminate manual processes between the client practice and the PRN billing center, enabling the company to reduce staff required to service a client practice by approximately 30 to 60 percent. “With AdvancedMD as our foundation,” said Frances Holinda, president of Physicians Resource Network, “we are able to offer our clients a complete solution to deliver everything they need to stay current under healthcare reform. It’s all there, whether it’s online charges, integrated EHR or automated reporting, we can accommodate virtually any need. AdvancedMD is our power tool, enabling me to consult with our clients and maximize their revenue.”

PRN, founded in 1993, is based in Ocean, N.J. The company supports 25 providers who practice primarily in nephrology, cardiology and various surgery practices. The firm offers a range of practice services, including demographics data entry, charge entry, charge submission, payment posting, secondary insurance claims submission, appeals follow up, patient statements and patient follow up. “We pretty much handle everything up to the point of sending out collection letters,” said Holinda, who has an MBA in Health Care Management and is a member of HBMA. “I had enough experience in billing to know what I needed and to know that what I saw in AdvancedMD was exactly what I needed.”

Previously Holinda ran her business on a Unix-based, client/server platform, located on her premises. Many of the processes she has been able to automate using AdvancedMD were manual processes under the older system. In order for her clients to link to the Unix system, they had to install complicated VPNs. Additionally, someone on her staff was responsible for managing regular data backups. “Comparing what my office could provide in terms of redundancy, automated backups and bandwidth into the data center, to what AdvancedMD can provide, my business simply could not make the kind of IT investments that AdvancedMD has made in its enterprise class data center,” she added.

Since her business is physician billing, the main concern Holinda had when selecting a new billing platform were the revenue cycle management tools. “The EHR capabilities were a bonus,” said Holinda. “The fact that the EHR is so good means I can offer that clinical product to my physicians with confidence. Plus, if they prefer a different EHR, AdvancedMD gives me the option of interfacing to external products. I have all the tools I need to do their billing. The physicians have choices!”

Bill Stone, vice president and general manager of the AdvancedMD Billing Services Program, said: “Physicians Resource Network is an excellent example of the kind of experienced, proven billing service company that the AdvancedBiller program is attracting. Not only does our technology enable these seasoned business managers to become more efficient in servicing their client base, the platform offers a range of clinical and front office tools that make the practice more efficient. As a vendor that does not compete with our billing services partners, AdvancedMD is wholly focused on helping our AdvancedBiller partners grow and become more profitable.”

Resources:

  • For additional background on Physicians Resource Network, read the case study.
  • For more information about the AdvancedBiller program, visit www.advancedbiller.com.

About Physicians Resource Network, Inc.

PRN, founded in 1993, is based in Ocean, N.J. The company supports 25 providers who practice primarily in nephrology, cardiology and various surgery practices. The firm offers a range of practice services, including demographics data entry, charge entry, charge submission, payment posting, secondary insurance claims submission, appeals follow up, patient statements and patient follow up. For more information, visit: http://www.saasmedicalbilling.com/

About AdvancedMD Software
AdvancedMD provides a market leading Software-as-a-Service (SaaS) electronic health record (EHR) and practice management (PM) software platform delivered to more than 10,000 providers and 300 medical billing service providers nationwide. As a complete Medical Practice Optimization solution, the product combines the clinical with the financial to improve workflow and revenue capture. The AdvancedMD solution includes a certified EHR, patient portal, scheduling, electronic eligibility verification, electronic prescribing, and mobile access capabilities for the practice, and sophisticated, efficient claims processing, denial tracking and revenue management for the billing professional. Processing more than 1M claims per month through its clearinghouse, the company is able to identify payer rule changes quickly and continuously adjust the software to reflect those changes, yielding first-pass claim acceptance rates of 95 percent or better, compared to the national average of 70 percent. For more information, please visit www.advancedmd.com.

Contact Information:

Media Contact:
Jan Wiedrick-Kozlowski
Activa PR
(585) 392-7878
Email Contact

General Contact:
Jim Elliot
VP Marketing
(801) 984-9500
Email Contact

Physicians Resource Network
Fran Holinda
President
(732) 695-8200 x117
Email Contact

Filed Under: Medical And Healthcare

AcuMedSpa Holdings, Inc. Announces It’s Entered Into Two Separate Acquisition Talks

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: AcuMedSpa Holdings Inc

TAMARAC, FL–(Marketwire – July 13, 2010) –  AcuMedSpa Holdings, Inc. (PINKSHEETS: AMSZ), a provider of Medical Aesthetic, Spa and Acupuncture services, announced it has entered into talks to make two separate acquisitions. One of the companies is domestic and the other international.

The domestic acquisition has a substantial nationwide footprint which when completed will open up several new markets for AcuMedSpa. The international acquisition is progressing well but is slightly behind the domestic one in terms of expected timeframe for finalization. When completed, it will provide AcuMedSpa with a global presence in the spa industry.

The company is also making headway with its project to open AcuMedSpa in Poland. Completion will take a little longer due to some of the legal aspects and complexities involved in dealing with the E.U.

The previous sale of the company’s “Spa within a Practice” subsidiary in the month of May, has cleared nearly half a million dollars in debt off the books and will allow AcuMedSpa to realize positive earnings in 2010. When originally stating its revenue and earnings expectations for the current year, the company took into consideration its pending acquisitions, incorporated with its current business activities. Upon completion of these two key acquisitions the company expects to meet and exceed its previously stated 2010 projections.

“Over the past few months we have been working very hard to successfully improve current operations while reducing our liabilities,” stated AcuMedSpa Holdings President Gregory Antoine. “Our objective all along has been to expand our business two ways. First through the successful acquisition of spa and aesthetic practices, and second by opening new facilities in key markets.” Mr. Antoine further commented, “Our progress so far this year together with these acquisitions nearing completion puts us on pace to exceed our $2,000,000 net income goal for 2010.”

The company also announced that its wholesale health and beauty division, Consumer Care of America LLC, is on pace to exceed expectations. The focus of this division is high volume sales. More detailed information on Consumer Care of America will be provided in a future update.

Please follow our progress on twitter: http://twitter.com/acumedinc

For additional info please visit our website: http://www.acumedspa.com/

This press release contains “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended and such forward-looking statements are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. You are cautioned that such statements are subject to a multitude of risks and uncertainties that could cause future circumstances, events, or results to differ materially from those projected in the forward-looking statements as a result of various factors, and other risks. You should consider these factors in evaluating the forward-looking statements included herein, and not place undue reliance on such statements. The forward-looking statements in this release are made as of the date hereof and AcuMedSpa Holdings, Inc. takes no obligation to update such statements.

Contacts:

Gregory Antoine
1-877-8-ACUMED

Filed Under: Medical And Healthcare

Scientific Leaders Urge Type 2 Diabetes Patients to Remain on Their Prescribed Medications Unless Instructed Otherwise by Their Health Care Provider

Posted on July 13, 2010 Written by Annalyn Frame

SOURCE: American Diabetes Association

American Association of Clinical Endocrinologists, American Diabetes Association and The Endocrine Society Issue Joint Statement in Response to Reports of Potential Cardiovascular Risks Associated With Rosiglitazone

ALEXANDRIA, VA–(Marketwire – July 12, 2010) –  Over the past several weeks reports have again surfaced regarding the cardiovascular safety of the diabetes drug rosiglitazone. While some analyses have suggested an increased cardiovascular risk with use of rosiglitazone, others have not provided any evidence of such an association. To help patients and physicians make informed decisions regarding use of rosiglitazone, the American Association of Clinical Endocrinologists (AACE), the American Diabetes Association and The Endocrine Society issued a joint statement with recommendations:
http://www.diabetes.org/for-media/2010/ada_aace_endo.html

The statement recommends that patients should continue taking all currently prescribed medications unless instructed otherwise by their health care provider. Stopping diabetes medications can result in higher levels of blood glucose that may cause serious short term health problems and could increase the risk of diabetes-related complications in the long term.

The joint statement also informs patients that regardless of the opinion and decisions on rosiglitazone, there are numerous drugs available to maintain glucose control in people with type 2 diabetes. Patients should discuss these options with their health care providers.

In the next few days (July 13-14) the U.S. Food and Drug Administration (FDA) is expected to complete the Joint Meeting of the Endocrinologic and Metabolic Drugs Advisory Committee and Drug Safety and Risk Management Advisory Committee. This committee was convened to evaluate the scientific research available on the safety of rosiglitazone and then issue its decision on how the drug should or should not be used. The joint statement recommends that until further clarification is provided by the FDA, the decision whether or not to use any medication must remain that of the treating provider in direct discussion with the individual patient.

Following any decision from the FDA, AACE, the American Diabetes Association and The Endocrine Society will provide detailed information interpreting FDA action for both health care professionals and patients with diabetes.

The American Diabetes Association is leading the fight to stop diabetes and its deadly consequences and fighting for those affected by diabetes. The Association funds research to prevent, cure and manage diabetes; delivers services to hundreds of communities; provides objective and credible information; and gives voice to those denied their rights because of diabetes. Founded in 1940, our mission is to prevent and cure diabetes and to improve the lives of all people affected by diabetes. For more information please call the American Diabetes Association at 1-800-DIABETES (1-800-342-2383) or visit www.diabetes.org. Information from both these sources is available in English and Spanish.

Founded in 1916, The Endocrine Society is the world’s oldest, largest and most active organization devoted to research on hormones and the clinical practice of endocrinology. Today, The Endocrine Society’s membership consists of over 14,000 scientists, physicians, educators, nurses and students in more than 100 countries. Society members represent all basic, applied, and clinical interests in endocrinology. The Endocrine Society is based in Chevy Chase, Maryland. To learn more about the Society and the field of endocrinology, visit our site at www.endo-society.org.

AACE is a professional medical organization with more than 6,000 members in the United States and 91 other countries. AACE members are physicians who specialize in endocrinology, diabetes, and metabolism. For more information about AACE, visit our Web site at www.aace.com, become a fan on Facebook at www.facebook.com/theaace or follow us on Twitter at www.twitter.com/theaace.

Contacts:

American Diabetes Association
Colleen Fogarty
(703) 549-1500, ext. 2146

The Endocrine Society
Aaron Lohr
(240) 482-1380

American Association of Clinical Endocrinologists
Bryan Campbell
(904) 353-7878, ext.122

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Filed Under: Medical And Healthcare

Help Hospitalized Veterans: Every Week Somebody’s Life Is Changed

Posted on July 12, 2010 Written by Annalyn Frame

SOURCE: Help Hospitalized Veterans

WINCHESTER, CA–(Marketwire – July 12, 2010) –  Michael Cooper is a Vietnam veteran from Tampa, Florida. Having served in the U.S. Army from 1970-73 as a helicopter flight engineer, Cooper saw more than his share of combat. “My father was a WWII Army veteran so the decision to serve my country came easily,” says Cooper. He also knows firsthand what it’s like to be hospitalized, adding, “It’s the boredom that’s the worst. All the free time you have between appointments is the hardest to deal with.” Cooper recalls coming out of surgery and the first thing he was asked was if he would like to assemble a craft kit. The individual offering the kit was a Craft Care Specialist (CCS), employed by national nonprofit Help Hospitalized Veterans (HHV) and stationed at the Tampa VA medical center.

As a patient, Cooper went on to enjoy working with many of the arts & crafts provided by HHV and later decided to volunteer in the craft clinic. His help with HHV craft kits has now come full-circle, as Cooper himself is now employed as the CCS at the Tampa VA Medical Center. “I never dreamed I’d have this job. It’s such a joy to be of service to other veterans. It’s particularly rewarding to help those who are feeling down. Every day I get to witness new sparks of life. For some veterans, work on the arts and crafts brings about improvement of fine and gross motor skills, while others enjoy increased attention spans. Cognitive improvements have even been seen in brain injury patients. Every week somebody’s life is changed,” adds Cooper. “We utilize the HHV kits throughout the hospital and favorites include model cars and motorcycles, leather and sun catchers.”

“Perhaps the most intriguing benefit the arts & crafts provide is the impact they’re having in the pain care clinic,” said Cooper. “You wouldn’t believe it, but people with significant pain find their tolerance level increases while working on the arts & crafts. It’s as if the diversion tricks the brain and for that period of time the patient is able to find relief and comfort.”

HHV is the largest supplier of free therapeutic arts and crafts kits to our nation’s VA and military hospitals. Since the organization was founded in 1971, over 25 million therapeutic arts and crafts kits have been donated to hospitalized veterans absolutely free of charge with over $3.5 million worth donated to the Tampa VA medical center since their inception to the program.

For more information on HHV programs and services please visit www.hhv.org or call toll-free 1-888-567-VETS.

Documents and/or Photos available for this release:
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To view supporting documents and/or photos, go to www.enr-corp.com/pressroom and enter Release ID: 263241

Filed Under: Medical And Healthcare

Survey Indicates Many Healthcare Facilities Are Not Fully Applying CDC CAUTI Prevention Guidelines

Posted on July 12, 2010 Written by Annalyn Frame

SOURCE: Medline Industries, Inc.

Almost Half Report Not Having an Annual Competency Validation Process for Staff on CAUTI Prevention Measure and Inserting Foley Catheters

MUNDELEIN, IL–(Marketwire – July 12, 2010) –  Only 40 percent of infection control professionals indicated that more than three-quarters of the nurses at their facility were applying the CDC’s CAUTI prevention guidelines, and less than half reported that their facilities were conducting annual education and training on alternatives to catheterization, according to a survey conducted today. The survey of infection control professionals was conducted at a breakfast forum on prevention of catheter-associated urinary tract infections (CAUTI), sponsored by Medline Industries, Inc. in conjunction with the Association for Professionals in Infection Control and Epidemiology (APIC) Annual Scientific Meeting being held in New Orleans, LA. 

Additionally, while nearly 80 percent of attendees cited CAUTI prevention as one of their facility’s top priorities this year, almost half reported that they do not have an annual competency validation process for staff to assure that they are competent in CAUTI prevention measures and inserting Foley catheters.

“These results reaffirm the need for industry vendors to partner with healthcare providers on a comprehensive system that incorporates proper procedures and social behaviors that are easy to adopt in everyday practice,” said Lorri Downs, R.N., B.S.N., M.S., C.I.C., vice president of Infection Prevention at Medline and a board certified infection preventionist. “Reducing CAUTI rates is not just about taking precautions. We must transfer knowledge to the bedside clinician in new ways such as through interactive learning and online competency validation courses to ensure industry guidelines become the standard course of care.”

That was the experience at Arkansas Methodist Medical Center, located in Paragould, AR. The organization did not have a formal education program in CAUTI prevention prior to implementing Medline’s ERASE CAUTI program, but has seen significant results since it began using the evidence-based program three months ago.

“Since we’ve been using the ERASE CAUTI program, our facility has experienced an almost 20 percent decrease in our CAUTI rate and a more than 10 percent decrease in the number of Foley catheters placed,” said Lisa Bridges, infection preventionist at Arkansas Methodist Medical Center. “I believe the decreases will be even more in the coming months. We are still in the process of educating our staff on following the guidelines. Having the checklist on the outer packaging helps us to make sure that catheterization is an appropriate option for the patient.”

Medline is highlighting evidence-based CAUTI prevention practices and products at this year’s APIC Congress (booth #1907). During the three-day exhibition, Medline is demonstrating its ERASE CAUTI program, a revolutionary new approach to managing catheters and reducing CAUTI. Based on the same criteria the CDC used in developing their new CAUTI prevention guidelines, the ground-breaking ERASE CAUTI program features a reengineered one-layered catheter tray coupled with an evidence-based clinical education program.

As part of its presentation, the Medline clinical team is conducting a series of live, multimedia overviews of its cutting edge competency validation tools for assessing and sustaining staff results. The interactive competency programs are available to staff anytime via Medline University, Medline’s online education resource, and can be easily incorporated into the annual skills competency program for a facility’s nursing staff.

CAUTI is one of the most common healthcare-associated infections, not only comprising 40 percent of all institutionally acquired infections, but also eight percent of infections in the home care setting. Studies show that one in four patients receives an indwelling urinary catheter at some point during their hospital stay and up to 50 percent of these catheters are placed unnecessarily.

Additional information on the ERASE CAUTI program is available on Medline’s website at www.medline.com/erase.

About Medline Industries, Inc. 
Medline, the nation’s largest privately held manufacturer and distributor of healthcare products, manufactures and distributes more than 100,000 products to hospitals, extended-care facilities, surgery centers, home care dealers and agencies. Headquartered in Mundelein, Ill., Medline has more than 900 dedicated sales representatives nationwide to support its broad product line and cost management services.

Over the past five years, Medline has been the fastest-growing distributor of medical and surgical supplies in the U.S., serving as the primary distributor to over 450 major hospitals and healthcare systems. As a leading distributor, Medline offers a comprehensive array of consulting and management services encompassing the supply chain and logistics, utilization and standardization, business tools and enhanced reporting capabilities and on-staff clinicians.

Media Contacts:
Jerreau Beaudoin
(847) 643-3011
John Marks
(847) 643-3309

Filed Under: Medical And Healthcare

CDC and APHL Partner to Enhance Public Health Labs in US and Abroad

Posted on July 12, 2010 Written by Annalyn Frame

SOURCE: Association of Public Health Laboratories

SILVER SPRING, MD–(Marketwire – July 12, 2010) –  The Association of Public Health Laboratories (APHL) has received an award for $16.3 million from the Centers for Disease Control and Prevention (CDC) to enhance the work of public health laboratories in the US and abroad. The award continues an APHL-CDC collaboration of over 20 years in support of governmental health laboratories.

Funded as a five-year cooperative agreement, the award will assist APHL to promote quality public health laboratory practice, strengthen the public health laboratory system and develop a well-trained workforce. 

“APHL is committed to improving health outcomes by strengthening the capacity of public health laboratories both nationally and globally,” said Dr. Patrick Luedtke, director of the Unified State Laboratories in Utah and APHL president. “Public health laboratories protect us against diseases, environmental hazards, natural disasters and other health threats. A stronger lab system means healthier people.”

APHL is a leader in development and implementation of public health laboratory practice, systems, policy and training. Members serve as laboratory first responders, protecting the public from diseases and environmental health hazards. 

The Association of Public Health Laboratories is a national non-profit located in Silver Spring, MD, that is dedicated to working with members to strengthen governmental laboratories with a public health mandate. By promoting effective programs and public policy, APHL strives to provide public health laboratories with the resources and infrastructure needed to protect the health of US residents and to prevent and control disease globally.

Contact:
Michelle M. Forman
Senior Media Specialist
240.485.2793
Email Contact

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Filed Under: Medical And Healthcare

This Week on ORLive: Live Anterior Supine Approach to Hip Arthroplasty and Updated Living Donor Liver Transplant Presentation

Posted on July 12, 2010 Written by Annalyn Frame

SOURCE: OR-Live, Inc.

New On-Demand and Live Surgery Video for the Week of July 12, 2010

WEST HARTFORD, CT–(Marketwire – July 12, 2010) –  ORLive, the vision of improving health, presents a live hip replacement surgery featuring the Continuum Acetabular System and the Fitmore Hip Stem from Zimmer. Earlier in the week ORLive will premiere an update to the Hepatocellular Carcinoma program presented by NewYork-Presbyterian, including information on living donor liver transplant options.

This week ORLive also invites you take part in the latest installment of the Virtual Brain Tumor Board, and to watch and learn from this month’s featured channel of no-visible-scar surgeries.

NEW ON ORLIVE

NEW VIDEO: Program Update: Hepatocellular Carcinoma – Living Donor Liver Transplant

Premieres Tuesday July 13 – In March of this year the Center for Liver Disease and Transplantation of NewYork-Presbyterian presented a special program that highlighted research findings on the diagnosis, treatment and survival rates of Hepatocellular Carcinoma (HCC), from. Now they’re updating this information with new segments on living donor kidney transplant.

HCC, the most common form of liver cancer, is diagnosed in about 24,100 people each year. Watch this webcast to learn more about the latest advances in the diagnosis and treatment of liver cancer.

Viewers will be able to interact and ask questions via the ORLive website. Learn more about this live video broadcast on ORLive.com.

LIVE SURGERY – The Anterior Supine Approach to Total Hip Arthroplasty

Live Wednesday, July 14, 2010, 7PM EDT

ORLive and Zimmer will present a live Total Hip Arthroplasty featuring the Continuum Acetabular System and the Fitmore Hip Stem. The surgery will be performed by Dr. Jonathan Yerasimides, University of Louisville Department of Orthopaedics, Louisville, KY and will be moderated by Dr. Hari Bezwada, University of Pennsylvania School of Medicine Department of Orthopaedic Surgery, Philadelphia, PA. The broadcast will last one hour and will show the entire surgical procedure. This opportunity allows for firsthand insight of the safe and effective implantation and surgical procedure involved with the Continuum Acetabular System and the Fitmore Hip Stem.

Viewers will be able to interact and ask questions via the ORLive website. Learn more about this program, and request a reminder on ORLive.com.

ORLIVE REFERRALS – Week of July 12, 2010

Each week ORLive highlights on-demand videos for our membership and visitors. 

No Visible Scar Surgery Referral: Advances in Laparoscopic Colorectal Surgery: Journey from HALS to NOTES from Covidien

CME Referral: Advances in Pancreatic Cancer Care from Thomas Jefferson University Hospital

Viewer’s Referral: Aortic Aneurysm Repair from Baptist Health Miami

HIGHLIGHTS

NOW ON-DEMAND – German Language Broadcast to Europe, Featuring ConforMIS iUni® G2 Patient Specific Partial Knee Replacement System

Now Available On-Demand

Originally broadcast live from the University of Wuerzburg Orthopedic Center for Musculoskeletal Research, this video features a partial knee replacement surgery using the ConforMIS iUni G2 system. The broadcast featured Dr. Wolfgang Fitz of Brigham and Women’s Hospital, Dr. Ulrich Nöth and Dr. Maximilian Rudert, both of the University of Wuerzburg Orthopedic Center for Musculoskeletal Research, presenting and performing the surgery. Learn more about this broadcast, presented entirely in German, at http://www.orlive.com/conformis-inc-/videos/n-chste-generation-patienten-spezifischer-knieoberfl-chenersatz-mit-conformis-iuni-sup-/sup-g2-17-00-uhr-mez-1

Viewers are still able to interact and ask questions via the ORLive website. Learn more about this program, and request a reminder on ORLive.com.

NOW ON-DEMAND – Advances in Treating Pediatric Epilepsy

Now Available On-Demand

If a child’s seizures can’t be controlled with medications, surgery may be the solution. See how the Neurosurgical team at NewYork-Presbyterian Phyllis & David Komansky Center for Children’s Health is making advancements in epilepsy. Hosted by Philip Stieg, MD, PhD, and featuring Jeffrey Greenfield, MD, PhD, Samual Weinstein, MD, and Theodore Schwartz, MD, this program goes in depth into the latest surgical advancements and options for patients. 

Viewers of this video are invited to interact with the surgeons via the ORLive website, and to join the community and receive regular updates from the NewYork-Presbyterian Phyllis & David Komansky Center for Children’s Health on pediatric epilepsy.

SUPPLEMENTAL CONTENT – VOX ORLive

Explore robotic assisted mitral valve surgery with cardiac surgeon Dr. Lynn Seto in the current episode of VOX ORLive, an audio podcast featuring the latest advancements in medicine, surgery, and medical technology.

About ORLive

ORLive is the leading provider of video communication channels to the healthcare community. Working collaboratively with hospitals and device manufacturers, ORLive produces and distributes customized, interactive, video programs that demonstrate the latest advances in medicine, surgical techniques and product innovations. The ORLive broadcasting network provides an intimate look at over 650 live and on-demand surgeries to a global audience, streaming over 50,000 hours of programming each month. The ORLive network can be found on-line at www.ORLive.com.

Contact:
Bonnie Gergely
Communications Manager
(860) 953-2900
Email Contact

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Filed Under: Medical And Healthcare

Pharma Benefits Executive Michael Darkoch Joins CNS Response

Posted on July 12, 2010 Written by Annalyn Frame

SOURCE: CNS Response

Darkoch to Lead Marketing and Commercialization Activities

ALISO VIEJO, CA–(Marketwire – July 12, 2010) –  CNS Response (OTCBB: CNSO) announces the appointment of Michael E. Darkoch as Executive Vice President and Chief Marketing Officer. In this role, Darkoch will assume all responsibility for the launch and commercialization of the Company’s flagship product, Referenced-EEG, including all marketing, business development and patient advocacy activities.

“Mike is a known quantity,” said CNS Response CEO George Carpenter. “In the world of pharmaceutical benefits, he understands what drives consumers, what payers pay for, and how to scale services around them. His industry expertise and payer relationships will be incredibly valuable as we introduce Referenced-EEG to a broader market. I’ve worked with Mike in three companies and his experience, skills and performance record will be crucial to our future success.”

Darkoch joins CNS Response with extensive executive experience at healthcare companies including Baxter International, CORE, Inc, and pharmaceutical benefits management firm Caremark Rx, where he grew sales from $100 million to $2.1 billion within five years, while achieving an industry record of 98 percent client retention for a two-year period. 

Prior to joining CNS Response, Darkoch held senior management positions with MedImpact Health Systems, a prescription benefit management firm in San Diego, where he successfully managed product development and increased new sales revenues 15 percent, market segment revenues by 40 percent and specialty products’ revenues by 35 percent. 

Darkoch commented, “One of the greatest challenges in the pharmaceutical arena is to understand how medications will impact patients differently, and mental disorders represent one of the largest opportunities where numerous medications have individualized outcomes.

“I believe Referenced-EEG may offer an important answer, helping physicians improve clinical outcomes for patients, and economic outcomes for us all. My goal is to establish the CNS Response brand and reputation quickly in this emerging area of personalized medicine.”

Darkoch holds a Bachelor of Science of Industrial Engineering from Lehigh University and Master of Science in Business from Southern Methodist University. He started his engineering and management career with Texas Instruments and Mobil Chemical Company, before moving into the healthcare and pharmaceutical sectors.

About CNS Response
Today, most physicians are able to base treatment on objective test data, such as EKGs, MRIs, blood tests, etc. Broadly speaking, such advances have not yet come to those physicians practicing psychiatry.

Referenced-EEG was developed by physicians to provide objective, personalized, statistical data on patient neurophysiology. In clinical trials, physicians using rEEG data have consistently achieved superior clinical results compared to physicians using trial and error pharmacotherapy.

The Company announced publication last week of results from its most recent clinical trial in The Journal of Psychiatric Research, in which physicians using Referenced-EEG (rEEG®) had success rates reaching 65 percent for patients with treatment-resistant depression.

To read more about the benefits this patented technology provides physicians, patients and insurers, please visit the CNS Response website, www.cnsresponse.com.

Safe Harbor Statement Under the Private Securities Litigation Reform Act of 1995
Except for the historical information contained herein, the matters discussed are forward-looking statements made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, as amended. These forward-looking statements involve risks and uncertainties as set forth in the Company’s filings with the Securities and Exchange Commission. These risks and uncertainties could cause actual results to differ materially from any forward-looking statements made herein.

Investors:
Marty Tullio
Managing Partner
McCloud Communications, LLC
949.553.9748
Email Contact

Media:
Chris Stern
Washington Media Group
202.628.1280
Email Contact

Click here to see all recent news from this company

Filed Under: Medical And Healthcare

New ‘Always On’ Air Sanitizer Fills Critical Gap in Infection Control

Posted on July 12, 2010 Written by Annalyn Frame

SOURCE: Prolitec

Prolitec’s ariaTM System Targets Airborne Bacteria

NEW ORLEANS, LA–(Marketwire – July 12, 2010) –  Hand washing and frequent wiping of surfaces like counters and handrails are necessary elements in institutional infection-control protocols. Effective as these techniques are, however, they are labor intensive, not automated, and do nothing to counter airborne bacteria — one of the primary mechanisms for the spread of disease. With the introduction of Prolitec, Inc.’s aria™ air-sanitizing agent, assisted-living facilities, hospitals, medical offices, and other enclosed spaces finally have a means of addressing this critical gap in infection control.

Prolitec’s Aerobiology and Infection Control division unveiled the new aria™ system today at the annual conference of the Washington, D.C.-based Association for Professionals in Infection Control and Epidemiology, in New Orleans.

The aria™ air-sanitizing system, which won EPA registration in November 2009, uses newly patented Prolitec technology to generate an invisible “dry” vapor of a safe and effective air sanitizing agent. The vapor can be distributed within a space directly from a small wall-mounted appliance or indirectly through an air handler. The result is a uniformly distributed vapor compliant with OSHA air-contaminant restrictions for workplace inhalation — one that is non-damaging to materials and electronics, yet significantly decreases the numbers of viable airborne bacteria under relatively wide conditions of relative humidity and temperature.

“Bacteria and other microorganisms are frequently introduced into the air by actions such as sneezing and coughing. Once microorganisms are airborne they can be inhaled or can settle and contaminate surfaces,” noted Dr. Craig A. Kelly, a veteran Johns Hopkins University scientist and chief of Prolitec’s Aerobiology and Infection-Control unit. “The function of the aria™ system is to reduce the concentration of airborne bacteria in a continuous and automated manner, thereby reducing the likelihood of inhalation or surface-settling of viable microorganisms.”

“An important feature of aria™ is that it is fully automated and works 24 hours a day, seven days a week without any human intervention,” noted Richard Weening, CEO of Milwaukee-based Prolitec. “The aria™ system can safely and effectively reduce background levels of airborne bacteria to establish the foundation of a successful infection-control protocol. It is the one part of the program that will always be 100% compliant.”

Dr. Kelly added: “Amid heightened awareness of disease transmission by airborne microorganisms, aria™ provides a critical tool for the infection-control professional to address airborne bacteria in a way that was not previously available. That can translate into a greater sense of safety and well-being for patients, residents, caregivers and visitors alike.”

About Prolitec
Prolitec (www.prolitec.com) develops and deploys air-treatment and air care technologies, including odor control, ambient scenting, aromatherapy and the use of scent as a medium of communication. Clients include assisted-living facilities, hotels, casinos, retailers and other commercial organizations in the United States and around the world. Prolitec’s Aerobiology and Infection Control Unit is developing interior air and surface systems to inhibit disease transmission.

NOTE TO EDITORS: Photos are available from Parness & Associates

Filed Under: Medical And Healthcare

New Report Forecasts HIV/AIDS Market to Reach $13.7 Billion by 2016

Posted on July 12, 2010 Written by Annalyn Frame

SOURCE: MarketResearch.com

ROCKVILLE, MD–(Marketwire – July 12, 2010) –  MarketResearch.com has announced the addition of GlobalData’s new report “HIV-AIDS – Pipeline Assessment and Market Forecasts to 2016,” to their collection of Diseases & Conditions market reports. For more information, visit http://www.marketresearch.com/product/display.asp?ProductID=2709528.

GlobalData’s report, “HIV/AIDS – Pipeline Assessment and Market Forecasts to 2016” provides an essential source of information and analysis on the global HIV/AIDS market. The report identifies the key trends shaping and driving the global HIV/AIDS market. The report also provides insights on the prevalent competitive landscape and the companies expected to significantly alter the market landscape. Most importantly, the report provides valuable insights on the pipeline products within the global HIV/AIDS sector. GlobalData estimated the HIV/AIDS market was worth $12 billion in 2009. It is forecast to grow at a Compound Annual Growth Rate (CAGR) of 2% for the next seven years to reach $13.7 billion by 2016. The global Human Immunodeficiency Virus (HIV) infection market will continue to grow between 2009 and 2016 at a slower rate due to a series of patent expiries during this period. The growth rate is likely to decline from 2012 onwards due to the impact of the patent expiry of key drugs. The market is characterized by a high unmet need of drugs which can cure the disease. Highly Active Antiretroviral Therapy (HAART) which requires patients to take different classes of drugs has however succeeded in achieving near zero levels of HIV in infected people. Increased uptake of HAART and increasing awareness (which leads to increased treatment seeking) will drive the market. The pipeline for HIV is strong and consists of more than 261 molecules currently in development for various disease segments.

Topics covered in the report include…

  • Annualized global HIV/AIDS market revenues data from 2001 to 2009, forecast for seven years to 2016.
  • Pipeline analysis data providing a split across phases by mechanism of action, and the emerging trends. The key classes of mechanism of action include HIV vaccines, Nonnucleoside Reverse Transcriptase Inhibitors (NNRTIs), Protease Inhibitors (PIs), Multi-class Combination Products, Nucleoside Reverse Transcriptase Inhibitors (NRTIs), CCR5 receptor antagonists, HIV integrase inhibitors, Nucleoside analogues, Viral entry inhibitors, Maturation inhibitors and Fusion Inhibitors.
  • Analysis of the current and future market competition in the global HIV/AIDS market. The key market players covered Boehring Ingelheim, Achillion Pharmaceuticals, GlaxoSmithKline, Incyte and Pharmasset, Shire Pharmaceuticals and Tibotec Virco
  • Insightful review of the key industry drivers, restraints and challenges. Each trend is independently researched to provide qualitative analysis of its implications.
  • A strategic competitor assessment, market characterization, unmet needs and implications for the future HIV/AIDS market.

For more information visit http://www.marketresearch.com/product/display.asp?ProductID=2709528.

Contact:
Sean Snyder
MarketResearch.com
[email protected]
240.747.3076

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Filed Under: Medical And Healthcare

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