Hahn Rebecca T, Makkar Raj, Thourani Vinod H, Makar Moody, Sharma Rahul P, Haeffele Christiane, Davidson Charles J, Narang Akhil, O'Neill Brian, Lee James, Yadav Pradeep, Zahr Firas, Chadderdon Scott, Eleid Mackram, Pislaru Sorin, Smith Robert, Szerlip Molly, Whisenant Brian, Sekaran Nishant K, Garcia Santiago, Stewart-Dehner Terri, Thiele Holger, Kipperman Robert, Koulogiannis Konstantinos, Lim D Scott, Fowler Dale, Kapadia Samir, Harb Serge C, Grayburn Paul A, Sannino Anna, Mack Michael J, Leon Martin B, Lurz Philipp, Kodali Susheel K
From Columbia University Irving Medical Center, New York (R.T.H., M.B.L., S.K.K.); Cedars-Sinai Medical Center, Los Angeles (R.M., M.M.), and Stanford University, Stanford (R.P.S., C.H.) - both in California; Piedmont Heart Institute, Marcus Heart Valve Center, Atlanta (V.H.T., P.Y.); Northwestern University Feinberg School of Medicine, Chicago (C.J.D., A.N.); Henry Ford Hospital, Detroit (B.O., J.L.); Oregon Health and Science University, Portland (F.Z., S.C.); Mayo Clinic, Rochester, MN (M.E., S.P.); Baylor Scott and White Heart Hospital Plano (R.S., M.S., P.A.G., M.J.M.) and Baylor Scott and White Research Institute Cardiac Imaging Core Laboratory (P.A.G., A.S.) - both in Plano, TX; Intermountain Medical Center, Murray, UT (B.W., N.K.S.); Christ Hospital, Cincinnati (S.G., T.S.-D.), and the Cleveland Clinic Foundation, Cleveland (S.K., S.C.H.); Heart Center Leipzig at Leipzig University, Leipzig (H.T.), and University Medical Center Mainz, Mainz (P.L.) - both in Germany; Morristown Medical Center, Morristown, NJ (R.K., K.K.); and the University of Virginia, Charlottesville (D.S.L., D.F.).
N Engl J Med. 2025 Jan 9;392(2):115-126. doi: 10.1056/NEJMoa2401918. Epub 2024 Oct 30.
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.
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.
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).
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.).
严重三尖瓣反流与致残症状及死亡风险增加相关。需要有关经皮经导管三尖瓣置换术后结局的数据。
在这项国际多中心试验中,我们将400例有严重症状性三尖瓣反流的患者按2:1的比例随机分配,分别接受经导管三尖瓣置换术加药物治疗(瓣膜置换组)或单纯药物治疗(对照组)。分层综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、索引事件后三尖瓣干预、因心力衰竭住院、堪萨斯城心肌病问卷总体总结评分(KCCQ-OS)至少提高10分、纽约心脏协会(NYHA)功能分级至少改善一级以及6分钟步行距离至少增加30米。通过比较所有可能的患者对,从分层中的第一个事件开始计算主要结局的获胜率。
共267例患者被分配到瓣膜置换组,133例被分配到对照组。1年时,支持瓣膜置换的获胜率为2.02(95%置信区间[CI],1.56至2.62;P<0.001)。在患者对的比较中,瓣膜置换组在任何原因导致的死亡(14.8%对12.5%)、索引事件后三尖瓣干预(3.2%对0.6%)、KCCQ-OS评分改善(23.1%对6.0%)、NYHA分级改善(10.2%对0.8%)以及6分钟步行距离改善(1.1%对0.9%)方面比对照组获胜更多。瓣膜置换组在因心力衰竭住院的年化率方面比对照组获胜更少(9.7%对10.0%)。瓣膜置换组15.4%发生严重出血,对照组为5.3%(P = 0.003);分别有17.4%和2.3%植入了新的永久性起搏器(P<0.001)。
对于严重三尖瓣反流患者,经导管三尖瓣置换术在主要综合结局方面优于单纯药物治疗,主要是由症状和生活质量的改善所驱动。(由爱德华兹生命科学公司资助;TRISCEND II 临床试验注册号,NCT04482062。)