Angellotti Domenico, Mattig Isabel, Samim Daryoush, Goebel Björn, Jantsch Charlotte, Rubinic Barbara, Ruf Tobias, Geisler Tobias, Kessler Mirjam, Adam Matti, Stolz Lukas, Dannenberg Varius, Kassar Mohammad, Stathogiannis Konstantinos, Cesario Vincenzo, Dumonteil Nicolas, Chrissoheris Michael, Spargias Konstantinos, Baldus Stephan, Rottbauer Wolfgang, Gerçek Muhammed, Bartko Philippe M, Lapp Harald, Dreger Henryk, Hausleiter Jörg, Lurz Philipp, Windecker Stephan, Rudolph Volker, Praz Fabien
Department of Cardiology, Bern University Hospital, University of Bern, Bern, Switzerland; Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy.
Deutsches Herzzentrum der Charité, Berlin, Germany.
JACC Cardiovasc Interv. 2025 Jun 21. doi: 10.1016/j.jcin.2025.06.002.
Transcatheter tricuspid valve replacement (TTVR) has been recently approved for the treatment of patients with severe tricuspid regurgitation (TR). Real-world evidence regarding the commercial use of TTVR is lacking.
The aim of this study was to investigate the real-world safety and efficacy of the EVOQUE TTVR system in patients with severe TR treated at 12 experienced heart valve centers in 5 European countries.
Consecutive patients treated with the EVOQUE system since approval in Europe (October 2023 to February 2025) were included in this retrospective analysis. Clinical outcomes were assessed at 30-day follow-up.
The study included 176 patients (mean age 77.8 years, 72.0% women, median TRI-SCORE 5 points [IQR: 2 points]). At a median follow-up time of 30 days (IQR: 2 days), severe or greater TR was reduced to mild or none in 126 of 128 patients (98.4%; P < 0.001). NYHA functional class improved from 20.2% (28 of 138) class I or II at baseline to 79.7% (110 of 138; P) at 1 month (P < 0.001), with signs of improved hepatorenal function (estimated glomerular filtration rate 47.0 ± 19.9 mL/min/1.73 m vs 53.7 ± 23.3 mL/min/1.73 m [P < 0.001]; bilirubin 14.2 ± 8.8 μmol/L vs 11.0 ± 9.8 μmol/L [P < 0.001]). Massive or torrential TR at baseline was more common among patients who improved compared with those with stable or worsening NYHA functional class (75 of 98 [76.5%] vs 20 of 40 [50.0%]; P = 0.004). Permanent pacemaker implantation was required in 21 of 111 pacemaker-naive patients (18.9%), in particular those with conduction disturbances at baseline (OR: 4.53; 95% CI: 1.73-11.82; P = 0.002). Moderate or severe right ventricular dysfunction was an independent predictor of clinical failure at 1-month follow-up (OR: 3.60; 95% CI: 1.39-9.32, P = 0.008).
TR elimination following TTVR in a real-world setting was associated with significant symptom and end-organ functional improvement. Patients with massive or torrential TR were more likely to experience functional improvement. Pre-existing conduction disturbances are associated with increased risk for pacemaker implantation, while baseline right ventricular dysfunction is a strong predictor of adverse clinical outcomes.
经导管三尖瓣置换术(TTVR)最近已被批准用于治疗严重三尖瓣反流(TR)患者。目前缺乏关于TTVR商业应用的真实世界证据。
本研究的目的是调查EVOQUE TTVR系统在欧洲5个国家12个经验丰富的心脏瓣膜中心治疗的严重TR患者中的真实世界安全性和有效性。
本回顾性分析纳入了自欧洲批准(2023年10月至2025年2月)以来接受EVOQUE系统治疗的连续患者。在30天随访时评估临床结局。
该研究纳入了176例患者(平均年龄77.8岁,72.0%为女性,TRI-SCORE中位数为5分[四分位间距:2分])。在中位随访时间30天(四分位间距:2天)时,128例患者中有126例(98.4%)的严重或更严重TR降至轻度或无(P<0.001)。纽约心脏协会(NYHA)心功能分级从基线时的20.2%(138例中的28例)为I级或II级改善至1个月时的79.7%(138例中的110例;P)(P<0.001),同时有肝肾功改善迹象(估计肾小球滤过率47.0±19.9ml/min/1.73m²对比53.7±23.3ml/min/1.73m²[P<0.001];胆红素14.2±8.8μmol/L对比11.0±9.8μmol/L[P<0.001])。与NYHA心功能分级稳定或恶化的患者相比,基线时存在大量或重度TR的患者改善更为常见(98例中的75例[76.5%]对比40例中的20例[50.0%];P=0.004)。111例无起搏器植入史的患者中有21例(18.9%)需要植入永久性起搏器,尤其是那些基线时有传导障碍的患者(比值比:4.53;95%置信区间:1.73 - 11.82;P=0.002)。中度或重度右心室功能障碍是1个月随访时临床失败的独立预测因素(比值比:3.60;95%置信区间:1.39 - 9.32,P=0.008)。
在真实世界中,TTVR后TR消除与症状和终末器官功能显著改善相关。存在大量或重度TR的患者更有可能出现功能改善。既往存在的传导障碍与起搏器植入风险增加相关,而基线右心室功能障碍是不良临床结局的有力预测因素。