




Healthcare Industry News: ICD
News Release - March 31, 2009
Results from Medtronic-Supported Clinical Trial Assessing Use of Implantable Cardiac Devices in Certain Heart Attack Patients Show Reduction in Sudden Cardiac Death
MINNEAPOLIS & ORLANDO, Fla.--(HSMN NewsFeed)--Results from the IRIS (Immediate Risk Stratification Improves Survival) clinical trial, supported in part by Medtronic, Inc. (NYSE: MDT ) and presented today at the 58th Annual Scientific Session of the American College of Cardiology, showed that sudden cardiac death in a specific subset of immediate post-MI (myocardial infarction) patients was statistically significantly reduced with implantable cardioverter-defibrillator (ICD) therapy. However, in this narrowly defined patient population, ICDs did not reduce mortality from all causes, as all causes are not treatable by ICDs.ICDs are 98 percent effective at terminating the dangerous heart rhythms that can lead to sudden cardiac death, but are not currently indicated for use in immediate post-MI patients. The IRIS trial sought to determine if survival amongst a subset of post-MI patients who were at high risk for sudden cardiac death could be improved by ICD therapy received in the first 31 days after a heart attack.
“Medtronic is committed to developing an evolving base of clinical evidence critical to scientific advancement and medical practice,” said David Steinhaus, M.D., medical director of the Cardiac Rhythm Disease Management business at Medtronic. “The IRIS trial is another example of our efforts to identify the patients who will benefit most from our life-saving and life-improving therapies.”
Research has shown that a significant percentage of people who survive a heart attack, or MI, will ultimately die as the result of a dangerous heart rhythm originating in the lower chambers of the heart1. Approximately 15 percent of these people will die in the first weeks, and an additional 10 percent during the first year, following the heart attack2, 3.
The patients selected for the trial were in the immediate post-MI stage (days five - 30), and based on selective criteria, represent less than five percent of those who have suffered a heart attack. The trial involved 902 patients at 92 centers in seven countries in Europe.
The IRIS results do not conflict with previous data that informed current evidence-based treatment guidelines which showed that use of ICDs in a more broadly defined range of post-MI patients (those who received ICD therapy at least 40 days after experiencing a heart attack) reduced all-cause mortality by 31 percent. Current medical guidelines recommend ICD therapy for post-MI patients with an ejection fraction – a common measure of the heart’s pumping function – of 35 percent and below, and after at least 40 days have passed since their heart attack.
About Medtronic
Medtronic, Inc. (www.medtronic.com), headquartered in Minneapolis, is the global leader in medical technology – alleviating pain, restoring health, and extending life for millions of people around the world.
Any forward-looking statements are subject to risks and uncertainties such as those described in Medtronic’s Annual Report on Form 10-K for the year ended April 25, 2008. Actual results may differ materially from anticipated results.
1 Selcuk Adabag, A, et al. Sudden death after myocardial infarction. JAMA. 2008:300(17):2022-2029.
2 Rustige J, et al. The 60 minutes myocardial infarction project. Treatment and clinical outcome of patients with acute myocardial infarction in Germany. Eur Heart J 1997;18(9):1438-46.
3 Schuster S, et al. Impact of Early Risk Stratification on the Length of Hospitalization in Patients with Acute Q-Wave Myocardial Infarction. The 60-minutes myocardial infarction project. Cardiology 1998;90(3):212-219.
Source: Medtronic
Issuer of this News Release is solely responsible for its
content.
Please address inquiries directly to the issuing company.
Related News Items
Medtronic appoints Thierry Piéton as Chief Financial OfficerMedtronic Achieves CE Mark Approval for BrainSense Adaptive Deep Brain Stimulation and Electrode Identifier, a Groundbreaking Advance In Personalized, Sensing-Enabled Care for People with Parkinson's Through Innovative Brain-Computer Interface Technology
Medtronic Receives FDA Clearance for New InPen(TM) App, Paving the Way for its Smart MDI System Launch with Simplera(TM) CGM