NATICK, Mass., and BARCELONA, Spain, Sept. 1 /PRNewswire/ -- Boston Scientific Corporation (NYSE: BSX) today announced final results from the landmark MADIT-CRT trial, which were published by the New England Journal of Medicine and presented during a Hot Line session at the annual European Society of Cardiology (ESC) Congress in Barcelona.
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Arthur Moss, M.D., Professor of Medicine at the University of Rochester Medical Center and Principal Investigator of the trial, presented the MADIT-CRT data. The primary endpoint showed that Boston Scientific's cardiac resynchronization therapy defibrillators (CRT-Ds) were associated with a 34 percent relative reduction in the risk of all-cause mortality or first heart failure event in asymptomatic and mild (NYHA Class I and II(1)) heart failure patients, when compared to standard implantable cardioverter defibrillators (ICDs) (p=0.001).
In addition, MADIT-CRT data showed that:
"The MADIT-CRT Executive Committee anticipated that the benefit for the CRT-D therapy group would be dominated by a reduction in heart failure events and the data overwhelmingly confirm that," said Dr. Moss. "Furthermore, CRT-D therapy showed an equal benefit in both ischemic and non-ischemic(3) patients. The MADIT-CRT data are compelling and help bridge a clinical gap in our understanding of heart failure in Class I and II patients."
"The publication of the manuscript by the New England Journal of Medicine and the presentation of MADIT-CRT data at ESC highlight the importance of this study, which clearly demonstrates that CRT-D therapy slows the progression of heart failure, further delaying the onset of more severe and life-limiting conditions," said Fred Colen, President, Boston Scientific Cardiac Rhythm Management. "We look forward to working with the FDA as we seek approval for an expanded indication for our CRT-D devices, based on these strong results."
MADIT-CRT is the world's largest randomized study of NYHA Class I and II patients, with more than 1,800 patients enrolled at 110 centers in 14 countries. Currently, heart failure patients must be defined as NYHA Class III or IV to be indicated for CRT-D therapy. However, approximately 70 percent of all heart failure patients in the U.S. fall into Class I or II. Nearly 22 million people worldwide, including more than 5.5 million Americans, suffer from some form of heart failure.
MADIT-CRT is an important continuation of Boston Scientific's exclusive sponsorship of landmark clinical trials that have broken new ground and helped improve outcomes for high-risk cardiac patients worldwide. More than 80 percent of U.S. patients who receive an ICD or CRT-D were first indicated for this life-saving therapy through clinical research(4) sponsored by Boston Scientific.
Boston Scientific is a worldwide developer, manufacturer and marketer of medical devices whose products are used in a broad range of interventional medical specialties. For more information, please visit: www.bostonscientific.com.
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(1) MADIT-CRT patients are high risk (asymptomatic or mildly symptomatic, New York Heart Association Class I and II). High-risk is defined as QRS width greater than or equal to 130 milliseconds and Left Ventricular Ejection Fraction less than or equal to 30%. The New York Heart Association clinical classifications of heart failure patients rank patients as Class I-II-III-IV, according to the degree of symptoms or functional limits, from asymptomatic to bed ridden.
(2) Left Ventricular Ejection Fraction (LVEF) is a measurement of how well the heart is pumping. People with healthy hearts usually have an LVEF of greater than or equal to 50%. Patients who were candidates for the MADIT-CRT study had an LVEF of less than or equal to 30%.
(3) Ischemic patients suffer from Coronary Artery Disease (CAD).
(4) Trials include MADIT, MADIT-II, CONTAK-CD, and COMPANION.
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|SOURCE Boston Scientific Corporation|
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