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Abbott's Minimally Invasive MitraClip? System for Mitral Regurgitation Demonstrates Positive Clinical and Quality-of-Life Results for Patients Too High Risk for Surgery
Publish date: Mar 10, 2013
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PR Newswire SAN FRANCISCO, March 10, 2013
SAN FRANCISCO, March 10, 2013 /PRNewswire/ -- Abbott (NYSE:
ABT) today announced data from the EVEREST II (Endovascular Valve Edge-to-Edge REpair STudy) High Surgical Risk cohort evaluating
the company's first-in-class catheter-based MitraClip® System for the treatment of mitral regurgitation (MR).
Findings were presented today at the 62nd Annual Scientific Session of the American College of Cardiology in San
Francisco. Abbott's MitraClip system, an investigational device in the United States, received CE
Mark in 2008 and is commercially available in approximately 30 countries, with more than 8,000 patients treated to date. The
device is delivered to the heart through the femoral vein, a blood vessel in the leg, and is designed to reduce MR by clipping
together the leaflets of the mitral valve to allow the heart to more efficiently pump blood. The EVEREST II High Surgical Risk cohort included data from patients enrolled in the multi-center EVEREST II High Risk
and REALISM continued access studies. Findings from 351 symptomatic U.S. patients deemed too high risk for open mitral valve
surgery demonstrated: "Patients with mitral regurgitation who are not candidates for mitral valve surgery due to risk of mortality have an unmet
need for a treatment option that will reduce symptoms and improve the quality of their lives," said D.
Scott Lim, M.D., associate professor of Cardiovascular Medicine at the University of Virginia
Health System in Charlottesville, Va. "The findings of the EVEREST II High Surgical Risk
cohort suggest that treatment with the MitraClip device represents a new option that could allow these high-risk patients
to return to activities they enjoy, and results in a reduction in hospitalizations for heart failure." "These results add to the large and growing body of data that show that the first-in-class percutaneous MitraClip therapy
can have positive results for high surgical risk patients suffering from the debilitating symptoms of significant mitral regurgitation,"
said Charles A. Simonton, M.D., FACC, FSCAI, divisional vice president, Medical Affairs, and
chief medical officer, Abbott Vascular. "We look forward to the March 20 FDA Advisory Committee
meeting to discuss the MitraClip system as a treatment option for this patient group in the United
States."
About Mitral Regurgitation
About the MitraClip System The device received CE Mark in 2008 and is commercially available in approximately 30 countries, with more than 8,000 patients
treated to date. The European Society of Cardiology (ESC) 2012 heart failure guidelines and the ESC/European Association for
Cardio-Thoracic Surgery 2012 guidelines for the management of valvular heart disease specify the MitraClip system as a treatment
option for high surgical risk patients with MR.
About Abbott Vascular
About Abbott
Visit Abbott at www.abbott.com and connect with us on Twitter at @AbbottNews. [1] Nkomo VT, Gardin JM, Skelton TN, Gottdiener JS, Scott CG, Enriquez-Sarano M. Burden of valvular heart diseases: a population-based study. Lancet. 2006 Sep 16; 368(9540):1005-11. SOURCE Abbott
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