Medizinische Klinik und Poliklinik I, Ludwig-Maximilians University Klinikum, Ludwig-Maximilians University München, Munich, Germany; German Center for Cardiovascular Research (DZHK), Partner Site Munich Heart Alliance, Munich, Germany. Electronic address: https://twitter.com/stolz_l.
Centre for Cardiovascular Innovation, St Paul's and Vancouver General Hospital, Vancouver, British Columbia, Canada.
JACC Cardiovasc Interv. 2024 Aug 26;17(16):1936-1945. doi: 10.1016/j.jcin.2024.06.014.
Data on procedural and early outcomes after transjugular transcatheter tricuspid valve replacement (TTVR) are limited.
This study sought to evaluate first-in-man procedural and clinical outcomes after transjugular TTVR with a special focus on patients who received large device sizes in whom TTVR outcomes have been questioned.
The retrospective registry included patients who underwent TTVR using the LuX-Valve Plus system (Jenscare Biotechnology Co Ltd) for symptomatic tricuspid regurgitation (TR) from January 2022 until February 2024 at 15 international centers in a compassionate use setting. The endpoints were procedural TR reduction, in-hospital death, adverse events, and 1-month survival. We further stratified results according to the size of the implanted device (<55 vs ≥55 mm).
The registry included a total of 76 patients at a median age of 78 years (Q1-Q3: 72-83 years, 47.4% women). TR was reduced to ≤2+ and ≤1+ in 94.7% and 90.8% of patients (75.0% of patients received TTVR devices ≥55 mm) with well-sustained results at 1-month follow-up (TR ≤2+ in 95.0% and ≤1+ 86.8%). Residual TR was paravalvular in all cases. In-hospital death occurred in 4 patients (5.3%). Four patients (5.3%) underwent cardiac surgery during index hospitalization. Major in-hospital bleeding events occurred in 5 patients (6.6%). New in-hospital pacemaker implantation was required in 3.9% of patients in the overall cohort (5.7% in "pacemaker-naive" individuals). No cases of valve thrombosis, stroke, myocardial infarction, or pulmonary embolism were observed. At 1-month follow-up, survival was 94.4%, and NYHA functional class significantly improved. One further patient received a pacemaker, 1 further bleeding event occurred, and 2 patients underwent reintervention or surgery within the first 30 days after TTVR. No differences in procedural outcomes or adverse events were observed after stratification for valve size.
Transjugular TTVR appears to be a safe and effective treatment option for patients with severe TR with comparable outcomes in very large tricuspid anatomies.
经颈静脉经导管三尖瓣置换术(TTVR)后的程序和早期结果数据有限。
本研究旨在评估经颈静脉 TTVR 的首例患者的程序和临床结果,特别关注接受大器械尺寸的患者,这些患者的 TTVR 结果受到质疑。
回顾性登记包括 2022 年 1 月至 2024 年 2 月期间,在 15 个国际中心以同情使用的方式使用 LuX-Valve Plus 系统(Jenscare Biotechnology Co Ltd)治疗症状性三尖瓣反流(TR)的患者。终点是程序 TR 减少、住院期间死亡、不良事件和 1 个月生存率。我们还根据植入器械的大小(<55 vs ≥55 mm)进一步分层结果。
该登记册共包括 76 名患者,中位年龄为 78 岁(Q1-Q3:72-83 岁,47.4%为女性)。94.7%和 90.8%的患者 TR 减少至≤2+和≤1+(75.0%的患者接受≥55 mm 的 TTVR 器械),1 个月随访时结果持续(95.0%的患者 TR≤2+和 86.8%的患者 TR≤1+)。所有病例均存在瓣周 TR。4 例(5.3%)患者住院期间死亡。4 例(5.3%)患者在住院期间接受了心脏手术。5 例(6.6%)患者发生主要院内出血事件。总体队列中 3.9%的患者(无起搏器个体中 5.7%)需要植入新的起搏器。未观察到瓣膜血栓形成、中风、心肌梗死或肺栓塞。1 个月随访时,生存率为 94.4%,NYHA 心功能分级显著改善。另有 1 例患者植入起搏器,1 例发生进一步出血事件,2 例患者在 TTVR 后 30 天内再次介入或手术。根据瓣膜大小分层后,程序结果和不良事件无差异。
经颈静脉 TTVR 似乎是一种安全有效的治疗严重 TR 的方法,对于非常大的三尖瓣解剖结构,其结果相当。