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经导管三尖瓣临床试验:数据不完整与美国食品药品监督管理局批准的设备

Transcatheter Tricuspid Valve Clinical Trials: Incomplete Data and FDA-Approved Devices.

作者信息

Furman Deborah, Whisenant Brian

机构信息

Department of Internal Medicine, University of Utah, Salt Lake City, UT.

Department of Cardiovascular Medicine, Intermountain Medical Center, Murray, UT.

出版信息

Struct Heart. 2024 Jul 15;8(6):100335. doi: 10.1016/j.shj.2024.100335. eCollection 2024 Nov.

Abstract

Each reviewed trial of transcatheter tricuspid valve intervention demonstrated clinically meaningful improvement in Kansas City Cardiomyopathy Questionnaire (KCCQ)-defined quality of life and favorable right ventricular remodeling. KCCQ correlates with tricuspid regurgitation (TR) reduction, heart failure hospitalization, and mortality. Change in KCCQ is therefore meaningful both as a measure of quality of life and as a surrogate endpoint of the impact of TV interventions. TRILUMINATE, the first randomized trial to evaluate the safety and efficacy of tricuspid edge-to-edge repair, demonstrated clinically important benefits in KCCQ score and favorable right ventricular remodeling, which are appropriate endpoints for this symptomatic population. TRISCEND II, which evaluated the safety and effectiveness of the EVOQUE valve, enrolled patients with more New York Heart Association class III and IV heart failure and lower KCCQ scores than TRILUMINATE. EVOQUE tricuspid valve replacement in TRISCEND II reduced TR to mild or less in 94% of patients compared to 50% of patients treated with TriClip in TRILUMINATE. The higher-risk TRISCEND II population and the near elimination of TR with EVOQUE are consistent with the favorable trend in EVOQUE mortality. Patients with diminished left ventricular systolic function being considered for either of these tricuspid valve interventions should be optimized with guideline directed medical therapy. Significant left-side valve disease should be treated. Patients should be optimally diuresed and excluded with severe pulmonary hypertension. Patients with persistent severe TR and symptoms or right ventricular enlargement should be considered for intervention. Smaller coaptation gaps without significant pacemaker impingement may be well served with transcatheter tricuspid edge-to-edge repair, while larger coaptation gaps and leaflets pinned by right ventricular leads, particularly in patients tolerating oral anticoagulation, may be best served with transcatheter tricuspid valve replacement.

摘要

每项经导管三尖瓣介入治疗的回顾性试验均显示,堪萨斯城心肌病问卷(KCCQ)定义的生活质量有了具有临床意义的改善,且右心室重塑良好。KCCQ与三尖瓣反流(TR)减少、心力衰竭住院率和死亡率相关。因此,KCCQ的变化作为生活质量的衡量指标以及三尖瓣介入治疗效果的替代终点均具有意义。TRILUMINATE是首个评估三尖瓣缘对缘修复安全性和有效性的随机试验,该试验显示KCCQ评分有重要临床益处且右心室重塑良好,这些对于有症状的人群而言是合适的终点。TRISCEND II评估了EVOQUE瓣膜的安全性和有效性,该试验纳入的纽约心脏协会III级和IV级心力衰竭患者比TRILUMINATE更多,KCCQ评分更低。与TRILUMINATE中接受TriClip治疗的患者的50%相比,TRISCEND II中接受EVOQUE三尖瓣置换的患者中有94%的TR降至轻度或更低。TRISCEND II中风险更高的人群以及EVOQUE几乎消除TR的情况与EVOQUE死亡率的有利趋势一致。考虑接受这两种三尖瓣介入治疗的左心室收缩功能减退患者应接受指南指导的药物治疗进行优化。严重的左侧瓣膜疾病应予以治疗。患者应进行最佳利尿治疗,并排除严重肺动脉高压患者。对于持续存在严重TR且有症状或右心室扩大的患者,应考虑进行干预。对于较小的瓣叶对合间隙且无明显起搏器干扰的患者,经导管三尖瓣缘对缘修复可能效果良好,而对于较大的瓣叶对合间隙以及被右心室导线固定的瓣叶,特别是对于耐受口服抗凝治疗的患者,经导管三尖瓣置换可能是最佳选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d51/11632808/3b797d98c8a5/gr1.jpg

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