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Transcatheter Valve Repair in Heart Failure with Moderate to Severe Mitral Regurgitation

医学 心力衰竭 二尖瓣反流 心脏病学 二尖瓣修补术 内科学 置信区间 随机对照试验 随机化 二尖瓣 外科
作者
Stefan D. Anker,Tim Friede,Ralph-Stephan von Bardeleben,Javed Butler,M M Khan,Monika Diek,Jutta Heinrich,Martin Geyer,Marius Placzek,Roberto Ferrari,William T. Abraham,Ottavio Alfieri,Angelo Auricchio,Antoni Bayés‐Genís,John G.F. Cleland,Gerasimos Filippatos,Finn Gustafsson,Wilhelm Haverkamp,Malte Kelm,Karl‐Heinz Kück,Ulf Landmesser,Aldo P. Maggioni,Marco Metra,Vlasis Ninios,Mark C. Petrie,Tienush Rassaf,Frank Ruschitzka,Ulrich Schäfer,P. Christian Schulze,Konstantinos Spargias,Alec Vahanian,Jose Luis Zamorano,Andreas M. Zeiher,Mahir Karakas,Friedrich Koehler,Mitja Lainščak,Alper Öner,Nikolaos Mezilis,Efstratios K. Theofilogiannakos,Ilias Ninios,Michael Chrissoheris,Panagiota Kourkoveli,Κωνσταντίνος Παπαδόπουλος,Grzegorz Smołka,Wojciech Wojakowski,Krzysztof Reczuch,Fausto J. Pinto,Łukasz Wiewiórka,Zbigniew Kalarus,Marianna Adamo,Evelyn Santiago‐Vacas,T. Ruf,M. Gross,Joern Tongers,Gerd Hasenfuß,Wolfgang Schillinger,Piotr Ponikowski
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
被引量:33
标识
DOI:10.1056/nejmoa2314328
摘要

BackgroundWhether transcatheter mitral-valve repair improves outcomes in patients with heart failure and functional mitral regurgitation is uncertain.MethodsWe conducted a randomized, controlled trial involving patients with heart failure and moderate to severe functional mitral regurgitation from 30 sites in nine countries. The patients were assigned in a 1:1 ratio to either transcatheter mitral-valve repair and guideline-recommended medical therapy (device group) or medical therapy alone (control group). The three primary end points were the rate of the composite of first or recurrent hospitalization for heart failure or cardiovascular death during 24 months; the rate of first or recurrent hospitalization for heart failure during 24 months; and the change from baseline to 12 months in the score on the Kansas City Cardiomyopathy Questionnaire–Overall Summary (KCCQ-OS; scores range from 0 to 100, with higher scores indicating better health status).ResultsA total of 505 patients underwent randomization: 250 were assigned to the device group and 255 to the control group. At 24 months, the rate of first or recurrent hospitalization for heart failure or cardiovascular death was 37.0 events per 100 patient-years in the device group and 58.9 events per 100 patient-years in the control group (rate ratio, 0.64; 95% confidence interval [CI], 0.48 to 0.85; P=0.002). The rate of first or recurrent hospitalization for heart failure was 26.9 events per 100 patient-years in the device group and 46.6 events per 100 patient-years in the control group (rate ratio, 0.59; 95% CI, 0.42 to 0.82; P=0.002). The KCCQ-OS score increased by a mean (±SD) of 21.6±26.9 points in the device group and 8.0±24.5 points in the control group (mean difference, 10.9 points; 95% CI, 6.8 to 15.0; P<0.001). Device-specific safety events occurred in 4 patients (1.6%).ConclusionsAmong patients with heart failure with moderate to severe functional mitral regurgitation who received medical therapy, the addition of transcatheter mitral-valve repair led to a lower rate of first or recurrent hospitalization for heart failure or cardiovascular death and a lower rate of first or recurrent hospitalization for heart failure at 24 months and better health status at 12 months than medical therapy alone. (Funded by Abbott Laboratories; RESHAPE-HF2 ClinicalTrials.gov number, NCT02444338.)
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