Department of Cardiology, Quebec Heart and Lung Institute, Laval University, Quebec City, Canada.
Department of Cardiology, St. Paul's Hospital, Vancouver, Canada; Department of Cardiology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
JACC Cardiovasc Interv. 2019 Aug 12;12(15):1438-1447. doi: 10.1016/j.jcin.2019.04.038.
To evaluate the long-term (≥2 years) outcomes following transcatheter tricuspid valve repair (TTVr) with the FORMA Transcatheter Tricuspid Valve Repair System (Edwards Lifesciences, Irvine, California).
Scarce data exist on long-term outcomes following TTVr.
This multicenter experience included patients with severe tricuspid regurgitation (TR) who underwent TTVr with the FORMA system at 4 centers under a compassionate clinical use program. Data were collected at baseline, 30 days, and 1 year, and yearly thereafter.
Nineteen patients (76 ± 9 years of age, 74% women, mean EuroSCORE II [European System for Cardiac Operative Risk Evaluation] 9.2 ± 5.6%) with functional TR were included. Procedural success was achieved in 17 (89%) patients and there were no cases of 30-day mortality. At a median follow-up of 32 (interquartile range: 24 to 36) months, 4 (24%) patients had died (3 from terminal heart failure, 1 from sepsis) and 3 (18%) patients required rehospitalization for heart failure. There was 1 device-related thrombosis and 1 pulmonary embolism, both in the setting of subtherapeutic oral anticoagulation. Less than severe TR was observed at echocardiography in 67% of patients at the 2- to 3-year follow-up. Among 15 successfully implanted patients with at least 24-month follow-up, significant improvements in New York Heart Association functional class (p < 0.001), 6-min walk test (+54 m; p = 0.016) and Kansas City Cardiomyopathy Questionnaire score (+16 points; p = 0.016) were observed, compared with baseline.
TTVr using the FORMA system showed favorable long-term safety profile in high-surgical-risk patients, with sustained functional improvement and acceptable TR reduction up to 3 years.
评估经导管三尖瓣修复术(TTVr)后≥2 年的长期结果,采用 FORMA 经导管三尖瓣修复系统(爱德华兹生命科学公司,加利福尼亚州欧文)。
关于 TTVr 后长期结果的数据很少。
这项多中心经验包括在 4 个中心进行的经导管三尖瓣修复术,使用 FORMA 系统,根据同情临床使用计划进行。数据在基线、30 天和 1 年时收集,并在随后每年收集。
19 名患者(76±9 岁,74%为女性,平均欧洲心脏手术风险评估系统 II 评分 [European System for Cardiac Operative Risk Evaluation] 9.2±5.6%)有功能性三尖瓣反流。17 例(89%)患者达到了手术成功,无 30 天死亡率。中位随访 32(四分位间距:24 至 36)个月时,4 例(24%)患者死亡(3 例死于终末期心力衰竭,1 例死于败血症),3 例(18%)患者因心力衰竭再次住院。有 1 例与器械相关的血栓形成和 1 例肺栓塞,均发生在低强度口服抗凝治疗的情况下。在 2 至 3 年的随访中,67%的患者在超声心动图上观察到三尖瓣反流小于中度。在 15 例至少有 24 个月随访的成功植入患者中,与基线相比,纽约心功能协会功能分级(p<0.001)、6 分钟步行试验(+54 米;p=0.016)和堪萨斯城心肌病问卷评分(+16 分;p=0.016)均有显著改善。
在高手术风险患者中,使用 FORMA 系统的 TTVr 显示出良好的长期安全性,功能改善持续,三尖瓣反流减少可接受,长达 3 年。