Department of Cardiology, Gülhane Training and Research Hospital, Ankara, Turkey.
Department of Cardiology, University of Kyrenia, Kyrenia, Turkish Republic of Northern Cyprus.
Anatol J Cardiol. 2022 Jul;26(7):505-519. doi: 10.5152/AnatolJCardiol.2022.1440.
The present data aim to evaluate the feasibility of the orthotopic trans- catheter tricuspid valve replacement devices, echocardiographic, functional improve- ments, and mortality rates following replacement in patients with significant tricuspid valve regurgitation.
We systematically searched for the studies evaluating the efficacy and safety of transcatheter tricuspid valve replacement for significant tricuspid valve regurgitation. The efficacy and safety outcomes were the improvements in New York Heart Association functional class, 6-minute walking distance, all-cause death, and periprocedural andlong-term complications. In addition, a random-effect meta-analysis was performed comparing outcomes before and after transcatheter tricuspid valve replacement.
Nine studies with 321 patients were included. The mean age was 75.8 years, and the mean European System for Cardiac Operative Risk Evaluation II score was 8.2% (95% CI: 6.1 to 10.3). Severe, massive, and torrential tricuspid valve regurgitation was diagnosed in 95% of patients (95% CI: 89% to 98%), and 83% (95% CI: 73% to 90%) of patients were in New York Heart Association functional class III or IV. At a weighted mean follow-up of 122 days, New York Heart Association functional class (risk ratio = 0.20; 95% CI: 0.11 to 0.35; P < .001) and 6-minute walking distance (mean difference = 91.1 m; 95% CI: 37.3 to 144.9 m; P < .001) significantly improved, and similarly, the prevalence of severe or greater tri- cuspid valve regurgitation was significantly reduced after transcatheter tricuspid valve replacement (baseline risk ratio = 0.19; 95% CI: 0.10 to 0.36; P < .001). In total, 28 patients (10%; 95% CI: 6% to 17%) had died. Pooled analyses demonstrated non-significant differ- ences in hospital and 30-day mortality and >30-day mortality than predicted operative mortality (risk ratio = 1.03; 95% CI: 0.41 to 2.59; P = .95, risk ratio = 1.39; 95% CI: 0.69 to 2.81; P = .35, respectively).
Transcatheter tricuspid valve replacement could be an emerging treatment option for patients with severe tricuspid regurgitation who are not eligible for transcath-eter repair or surgical replacement because of high surgical risk and poor prognosis.
本研究旨在评估经导管三尖瓣置换术治疗重度三尖瓣反流患者的可行性,包括心脏超声、功能改善和死亡率。
我们系统地检索了评估经导管三尖瓣置换术治疗重度三尖瓣反流的疗效和安全性的研究。疗效和安全性指标包括纽约心脏协会(NYHA)心功能分级、6 分钟步行距离、全因死亡率以及围手术期和长期并发症。此外,还进行了随机效应荟萃分析,比较了经导管三尖瓣置换术前后的结果。
共纳入 9 项研究 321 例患者。患者平均年龄为 75.8 岁,欧洲心脏手术风险评估系统 II 评分平均为 8.2%(95%可信区间:6.1 至 10.3)。95%(95%可信区间:89%至 98%)的患者被诊断为重度、大量和 torrential 三尖瓣反流,83%(95%可信区间:73%至 90%)的患者处于 NYHA 心功能 III 或 IV 级。在平均 122 天的加权随访中,NYHA 心功能分级(风险比=0.20;95%可信区间:0.11 至 0.35;P<0.001)和 6 分钟步行距离(平均差值=91.1m;95%可信区间:37.3 至 144.9m;P<0.001)均显著改善,同样,经导管三尖瓣置换术后重度或以上三尖瓣反流的发生率也显著降低(基线风险比=0.19;95%可信区间:0.10 至 0.36;P<0.001)。共有 28 例患者(10%;95%可信区间:6%至 17%)死亡。汇总分析显示,住院死亡率、30 天死亡率和>30 天死亡率与预测手术死亡率相比无显著差异(风险比=1.03;95%可信区间:0.41 至 2.59;P=0.95)、风险比=1.39;95%可信区间:0.69 至 2.81;P=0.35)。
对于因手术风险高和预后差而不适合经导管修复或外科置换的重度三尖瓣反流患者,经导管三尖瓣置换术可能成为一种新的治疗选择。