Healthcare Industry News: calcium channel blocker
News Release - March 11, 2009
St. Jude Medical Announces European CE Mark Approval of Neurostimulation System for Chronic AnginaST. PAUL, Minn.--(HSMN NewsFeed)--St. Jude Medical, Inc. (NYSE:STJ ) today announced European CE Mark approval of its Genesis® neurostimulation system for managing a form of chest pain known as chronic angina pectoris, or chronic angina.
“This approval is an important step forward in being able to provide pain solutions for people who have exhausted most other treatments,” said Chris Chavez, president of the St. Jude Medical Neuromodulation Division. “Our goal is to continue to develop new applications for our medical technologies and to provide physicians with more options in their choice of treatments.”
Angina is chest pain or discomfort that usually occurs as a result of decreased blood and oxygen supply to the heart, and it is the most prevalent symptom of coronary heart disease. It is often described as a squeezing pain in the chest, shoulders, arms, neck, jaw or back and is sometimes described as feeling like indigestion. Approximately 54 million people worldwide have angina according to the World Health Organization. An estimated 15 percent of all angina cases are considered chronic, equating to approximately 8.1 million people worldwide who live with chronic angina.
“While the stimulator will help mask the pain of angina, studies have shown that neurostimulation will not mask the pain of a heart attack,” said Mike J.L. DeJongste, M.D., department of cardiology, Thoraxcenter, University Medical Center, University of Groningen, Groningen, The Netherlands. “This therapy is designed to provide relief for those patients who suffer from chronic angina that does not respond sufficiently to optimal medication and revascularization treatments.”
Chronic angina persists despite medications such as nitroglycerin, beta blockers or calcium channel blockers, which are often used to treat coronary artery disease. For some of these patients, revascularization procedures such as coronary angioplasty or bypass surgery (which are intended to restore blood flow to the heart) may pose too much risk.
A study published in the journal Heart found that neurostimulation was effective at reducing angina and the need for nitrate medications to treat it. In the study, angina patients who used neurostimulation several times a day had 86 percent fewer episodes of angina and lowered their nitrate use by 89 percent compared to periods in which they received placebo treatment.
“People living with chronic angina often face a poor quality of life due to constant or recurring physical pain and loss of social function,” said Clas Mannheimer, professor, Multidisciplinary Pain Center, Östra Hospital, Gothenburg, Sweden. “Neurostimulation provides a minimally invasive treatment option for managing this painful condition.”
In addition to chronic angina, the Genesis neurostimulation system is approved for treating chronic neuropathic pain of the trunk and limbs and pain from back surgeries that have failed. More than 45,000 patients in 35 countries have been implanted with St. Jude Medical neurostimulation systems. Patients can obtain more information about neurostimulation pain therapies at www.PowerOverYourPain.com.
The Genesis neurostimulation system has not been approved in the U.S. for the treatment of chronic angina.
About St. Jude Medical
St. Jude Medical develops medical technology and services that focus on putting more control into the hands of those who treat cardiac, neurological and chronic pain patients worldwide. The company is dedicated to advancing the practice of medicine by reducing risk wherever possible and contributing to successful outcomes for every patient. Headquartered in St. Paul, Minn., St. Jude Medical employs approximately 14,000 people worldwide and has five major focus areas that include: cardiac rhythm management, atrial fibrillation, cardiac surgery, cardiology and neuromodulation. For more information, please visit www.sjm.com.
This news release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 that involve risks and uncertainties. Such forward-looking statements include the expectations, plans and prospects for the Company, including potential clinical successes, anticipated regulatory approvals and future product launches, and projected revenues, margins, earnings and market shares. The statements made by the Company are based upon management’s current expectations and are subject to certain risks and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements. These risks and uncertainties include market conditions and other factors beyond the Company’s control and the risk factors and other cautionary statements described in the Company’s filings with the SEC, including those described in the Risk Factors and Cautionary Statements sections of the Company’s Annual Report on Form 10-K for the fiscal year ended January 3, 2009. The Company does not intend to update these statements and undertakes no duty to any person to provide any such update under any circumstance.
Source: St. Jude Medical
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