Transcatheter Valve Replacement in Severe Tricuspid Regurgitation.

IF 96.2 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL New England Journal of Medicine Pub Date : 2025-01-09 Epub Date: 2024-10-30 DOI:10.1056/NEJMoa2401918
Rebecca T Hahn, Raj Makkar, Vinod H Thourani, Moody Makar, Rahul P Sharma, Christiane Haeffele, Charles J Davidson, Akhil Narang, Brian O'Neill, James Lee, Pradeep Yadav, Firas Zahr, Scott Chadderdon, Mackram Eleid, Sorin Pislaru, Robert Smith, Molly Szerlip, Brian Whisenant, Nishant K Sekaran, Santiago Garcia, Terri Stewart-Dehner, Holger Thiele, Robert Kipperman, Konstantinos Koulogiannis, D Scott Lim, Dale Fowler, Samir Kapadia, Serge C Harb, Paul A Grayburn, Anna Sannino, Michael J Mack, Martin B Leon, Philipp Lurz, Susheel K Kodali
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Abstract

Background: Severe tricuspid regurgitation is associated with disabling symptoms and an increased risk of death. Data regarding outcomes after percutaneous transcatheter tricuspid-valve replacement are needed.

Methods: In this international, multicenter trial, we randomly assigned 400 patients with severe symptomatic tricuspid regurgitation in a 2:1 ratio to undergo either transcatheter tricuspid-valve replacement and medical therapy (valve-replacement group) or medical therapy alone (control group). The hierarchical composite primary outcome was death from any cause, implantation of a right ventricular assist device or heart transplantation, postindex tricuspid-valve intervention, hospitalization for heart failure, an improvement of at least 10 points in the score on the Kansas City Cardiomyopathy Questionnaire overall summary (KCCQ-OS), an improvement of at least one New York Heart Association (NYHA) functional class, and an improvement of at least 30 m on the 6-minute walk distance. A win ratio was calculated for the primary outcome by comparing all possible patient pairs, starting with the first event in the hierarchy.

Results: A total of 267 patients were assigned to the valve-replacement group and 133 to the control group. At 1 year, the win ratio favoring valve replacement was 2.02 (95% confidence interval [CI], 1.56 to 2.62; P<0.001). In comparisons of patient pairs, those in the valve-replacement group had more wins than the control group with respect to death from any cause (14.8% vs. 12.5%), postindex tricuspid-valve intervention (3.2% vs. 0.6%), and improvement in the KCCQ-OS score (23.1% vs. 6.0%), NYHA class (10.2% vs. 0.8%), and 6-minute walk distance (1.1% vs. 0.9%). The valve-replacement group had fewer wins than the control group with respect to the annualized rate of hospitalization for heart failure (9.7% vs. 10.0%). Severe bleeding occurred in 15.4% of the valve-replacement group and in 5.3% of the control group (P = 0.003); new permanent pacemakers were implanted in 17.4% and 2.3%, respectively (P<0.001).

Conclusions: For patients with severe tricuspid regurgitation, transcatheter tricuspid-valve replacement was superior to medical therapy alone for the primary composite outcome, driven primarily by improvements in symptoms and quality of life. (Funded by Edwards Lifesciences; TRISCEND II ClinicalTrials.gov number, NCT04482062.).

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严重三尖瓣反流的经导管瓣膜置换术。
背景:严重的三尖瓣反流与致残症状和死亡风险增加有关。经皮经导管三尖瓣置换术后的疗效需要相关数据:在这项国际多中心试验中,我们按 2:1 的比例随机分配了 400 名有严重症状的三尖瓣反流患者,让他们接受经导管三尖瓣置换术和药物治疗(瓣膜置换组)或单纯药物治疗(对照组)。分层复合主要结局为任何原因导致的死亡、植入右心室辅助装置或心脏移植、三尖瓣指数后介入治疗、心力衰竭住院、堪萨斯城心肌病问卷总体总结(KCCQ-OS)得分至少提高10分、纽约心脏协会(NYHA)功能分级至少提高一级、6分钟步行距离至少提高30米。通过比较所有可能的患者配对,从分级中的第一个事件开始计算主要结果的胜出率:结果:共有267名患者被分配到瓣膜置换组,133名患者被分配到对照组。1年后,瓣膜置换术的获胜率为2.02(95%置信区间[CI],1.56至2.62;PC结论:对于严重三尖瓣反流患者,就主要的综合结果而言,经导管三尖瓣置换术优于单纯药物治疗,这主要归功于症状和生活质量的改善。(由Edwards Lifesciences资助;TRISCEND II ClinicalTrials.gov编号:NCT04482062)。
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来源期刊
New England Journal of Medicine
New England Journal of Medicine 医学-医学:内科
CiteScore
145.40
自引率
0.60%
发文量
1839
审稿时长
1 months
期刊介绍: The New England Journal of Medicine (NEJM) stands as the foremost medical journal and website worldwide. With an impressive history spanning over two centuries, NEJM boasts a consistent publication of superb, peer-reviewed research and engaging clinical content. Our primary objective revolves around delivering high-caliber information and findings at the juncture of biomedical science and clinical practice. We strive to present this knowledge in formats that are not only comprehensible but also hold practical value, effectively influencing healthcare practices and ultimately enhancing patient outcomes.
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