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ABBOTT PARK, Ill.,
Oct. 30, 2013 /PRNewswire/ -- Abbott today announced clinically meaningful changes to quality of life, a reduction in rehospitalization for heart failure, and functional improvements for patients treated with the company's first-in-class, catheter-based MitraClip
® therapy for patients with degenerative mitral regurgitation (MR) who are at prohibitive risk for mitral valve surgery. Findings were presented today at the 25
th annual Transcatheter Cardiovascular Therapeutics (TCT) scientific symposium in
San Francisco and simultaneously published in the
Journal of the American College of Cardiology.
The MitraClip device, which received U.S. Food and Drug Administration (FDA) approval last week, provides physicians with a breakthrough treatment option for patients suffering from MR. The MitraClip device is now available in
the United States for patients with significant symptomatic degenerative MR who are at prohibitive risk for mitral valve surgery. Degenerative MR is a type of MR caused by an anatomic defect of the mitral valve of the heart. Prohibitive risk is determined by the clinical judgment of a heart team due to the presence of one or more surgical risk factors.
"The results of this study show that, even for some of the most ill and debilitated patients, the MitraClip system is safe and results in good clinical outcomes," said
D. Scott Lim, M.D., associate professor of Cardiovascular Medicine at the
University of Virginia Health System in
Charlottesville, Va., and lead author of the publication. "These prohibitive-risk patients have had, until now, no approved therapies to improve the quality of their lives."
Data from 127 patients with degenerative MR at prohibitive surgical risk treated with the MitraClip device demonstrate:
Clinically meaningful changes to quality of life. Following MitraClip treatment, changes in SF-36 summary scales (a quality-of-life survey) were well above established thresholds showing minimum clinically important differences.
A reduction in rehospitalization for heart failure of 73 percent.
Functional improvements, with 76 percent of patients with baseline NYHA Functional Class III improving to NYHA Functional Class I or II, and 65 percent of patients with baseline NYHA Functional Class IV improving to NYHA Functional Class I or II.
Favorable ventricular remodeling, with left ventricular end-diastolic and end-systolic volume decreased significantly at one year compared with baseline.
A majority of patients discharged to home (87 percent), rather than to nursing care.
Findings were presented during the TCT conference by
Ted Feldman, M.D., FSCAI, director, Cardiac Catheterization Laboratory and The Mr. and Mrs. Charles R. Walgreen Chair in Interventional Cardiology, NorthShore University HealthSystem, Evanston, Ill.
"These positive results, which were reviewed as part of the totality of data from Abbott's FDA submission, along with clinical results from more than 2,200 patients treated with the device, confirm the benefit of the innovative MitraClip therapy for this very sick patient population," said
Chuck Foltz, senior vice president, vascular, Abbott. "This year's TCT conference has been particularly exciting for Abbott, with enormous enthusiasm about MitraClip from clinicians in
the United States and around the world, and more than 65 presentations highlighting data related to the therapy."
Multiple trials, published reports, and registries of patients treated with the MitraClip device consistently demonstrate a positive safety profile, reduction in mitral regurgitation, improvement in symptoms, and reduction in hospitalizations for heart failure, even in some of the most ill and debilitated patients.