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Five-Year Follow-up after Transcatheter Repair of Secondary Mitral Regurgitation

医学 危险系数 二尖瓣反流 指南 置信区间 心脏病学 内科学 临床终点 二尖瓣夹子 外科 随机对照试验 心力衰竭 病理
作者
Gregg W. Stone,William T. Abraham,JoAnn Lindenfeld,Saibal Kar,Paul Grayburn,D. Scott Lim,Jacob M. Mishell,Brian Whisenant,Michael Rinaldi,Samir Kapadia,Vivek Rajagopal,Ian J. Sarembock,Andreas Brieke,Steven O. Marx,David J. Cohen,Federico M. Asch,Michael J. Mack
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
卷期号:388 (22): 2037-2048 被引量:198
标识
DOI:10.1056/nejmoa2300213
摘要

Data from a 5-year follow-up of outcomes after transcatheter edge-to-edge repair of severe mitral regurgitation, as compared with outcomes after maximal doses of guideline-directed medical therapy alone, in patients with heart failure are now available.We randomly assigned patients with heart failure and moderate-to-severe or severe secondary mitral regurgitation who remained symptomatic despite the use of maximal doses of guideline-directed medical therapy to undergo transcatheter edge-to-edge repair plus receive medical therapy (device group) or to receive medical therapy alone (control group) at 78 sites in the United States and Canada. The primary effectiveness end point was all hospitalizations for heart failure through 2 years of follow-up. The annualized rate of all hospitalizations for heart failure, all-cause mortality, the risk of death or hospitalization for heart failure, and safety, among other outcomes, were assessed through 5 years.Of the 614 patients enrolled in the trial, 302 were assigned to the device group and 312 to the control group. The annualized rate of hospitalization for heart failure through 5 years was 33.1% per year in the device group and 57.2% per year in the control group (hazard ratio, 0.53; 95% confidence interval [CI], 0.41 to 0.68). All-cause mortality through 5 years was 57.3% in the device group and 67.2% in the control group (hazard ratio, 0.72; 95% CI, 0.58 to 0.89). Death or hospitalization for heart failure within 5 years occurred in 73.6% of the patients in the device group and in 91.5% of those in the control group (hazard ratio, 0.53; 95% CI, 0.44 to 0.64). Device-specific safety events within 5 years occurred in 4 of 293 treated patients (1.4%), with all the events occurring within 30 days after the procedure.Among patients with heart failure and moderate-to-severe or severe secondary mitral regurgitation who remained symptomatic despite guideline-directed medical therapy, transcatheter edge-to-edge repair of the mitral valve was safe and led to a lower rate of hospitalization for heart failure and lower all-cause mortality through 5 years of follow-up than medical therapy alone. (Funded by Abbott; COAPT ClinicalTrials.gov number, NCT01626079.).
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