Department of Cardiology, University Medical Center Mainz, Mainz, Germany.
Heart Center Leipzig at University of Leipzig, Leipzig, Germany.
J Am Coll Cardiol. 2024 Aug 13;84(7):607-616. doi: 10.1016/j.jacc.2024.05.006. Epub 2024 May 15.
Severe tricuspid regurgitation (TR) is known to be associated with poor quality of life and increased risk of death when left untreated.
We sought to report the 1-year clinical outcomes of subjects treated by tricuspid transcatheter edge-to-edge repair (TEER) with the TriClip system (Abbott Cardiovascular) in a contemporary real-world setting.
The bRIGHT (An Observational Real-World Study Evaluating Severe Tricuspid Regurgitation Patients Treated With the Abbott TriClip Device) postapproval study is a prospective, single-arm, open-label, multicenter postmarket registry conducted at 26 sites in Europe, with central event adjudication and echocardiographic core-laboratory assessment.
Enrolled subjects (n = 511) were elderly (79 ± 7 years) with significant comorbidities. A total of 88% had baseline massive or torrential TR, and 80% of subjects were in NYHA functional class III/IV. TR was reduced to moderate or less in 81% at 1 year. Significant improvements in NYHA functional class (21% to 75% I/II, P < 0.0001) and Kansas City Cardiomyopathy Questionnaire (KCCQ) score (19 ± 26-point improvement, P <0.0001) were observed at 1 year. One-year mortality was significantly lower in subjects who achieved moderate or lower TR at 30 days; however, there was no difference in mortality among subjects who achieved moderate, mild, or trace TR at 30 days. In addition to TR reduction at 30 days, baseline serum creatinine and baseline right ventricular tricuspid annular plane systolic excursion (RV TAPSE) were independently associated with mortality at 1 year (OR: 2.169; 95% CI: 1.494-3.147; P < 0.0001; OR: 0.636; 95% CI: 0.415-0.974; P = 0.0375). Mortality was not associated with baseline TR grade or with center volume.
Tricuspid TEER using the TriClip system was safe and effective through 1 year for subjects with significant TR and advanced disease in a diverse real-world population. (An Observational Real-world Study Evaluating Severe Tricuspid Regurgitation Patients Treated With the Abbott TriClip Device [bRIGHT]; NCT04483089).
重度三尖瓣反流(TR)与生活质量下降和未经治疗时死亡风险增加有关。
我们旨在报告在当代真实世界环境中使用 TriClip 系统(雅培心血管)进行三尖瓣经导管缘对缘修复(TEER)治疗的患者的 1 年临床结局。
bRIGHT(经 Abbott TriClip 装置治疗严重三尖瓣反流患者的观察性真实世界研究)是一项前瞻性、单臂、开放标签、多中心上市后注册研究,在欧洲的 26 个地点进行,采用中心事件裁决和超声心动图核心实验室评估。
入组患者(n=511)年龄较大(79±7 岁),合并症显著。基线时 88%有大量或 torrential TR,80%的患者处于纽约心脏协会(NYHA)功能 III/IV 级。1 年时 TR 减少至中度或更低的比例为 81%。1 年时 NYHA 功能分级(21%至 75%I/II,P<0.0001)和堪萨斯城心肌病问卷(KCCQ)评分(19±26 分改善,P<0.0001)有显著改善。30 天时达到中度或更低 TR 的患者 1 年死亡率显著降低;然而,30 天时达到中度、轻度或微量 TR 的患者死亡率无差异。除了 30 天 TR 降低外,基线血清肌酐和基线右心室三尖瓣环平面收缩期位移(RV TAPSE)与 1 年死亡率独立相关(OR:2.169;95%CI:1.494-3.147;P<0.0001;OR:0.636;95%CI:0.415-0.974;P=0.0375)。死亡率与基线 TR 分级或中心容量无关。
在真实世界的不同人群中,使用 TriClip 系统进行三尖瓣 TEER 治疗严重 TR 和晚期疾病的患者,安全性和有效性可维持 1 年。(经 Abbott TriClip 装置治疗严重三尖瓣反流患者的观察性真实世界研究 [bRIGHT];NCT04483089)。