Department of Cardiology, University Medical Center of Mainz, Mainz, Germany.
University of Pittsburgh Medical Center Heart and Vascular Institute, Pittsburgh, Pennsylvania, USA.
JACC Cardiovasc Interv. 2023 Nov 13;16(21):2600-2610. doi: 10.1016/j.jcin.2023.09.029. Epub 2023 Oct 24.
The fourth-generation mitral transcatheter edge-to-edge repair (M-TEER) device introduced an improved clip deployment sequence, independent leaflet grasping, and 2 wider clip sizes to tailor the treatment of patients with mitral regurgitation (MR) for a broad range of anatomies. The 30-day safety and effectiveness of the fourth-generation M-TEER device were previously demonstrated.
The aim of this study was to evaluate 1-year outcomes in a contemporary, real-world cohort of subjects treated with the MitraClip G4 system.
EXPAND G4 is an ongoing prospective, multicenter, international, single-arm study that enrolled subjects with primary and secondary MR. One-year outcomes included MR severity (echocardiographic core laboratory assessed), heart failure hospitalization, all-cause mortality, functional capacity (NYHA functional class), and quality of life (Kansas City Cardiomyopathy Questionnaire).
A total of 1,164 subjects underwent M-TEER from 2020 to 2022. At 1 year, there was a durable reduction in MR to mild or less in 92.6% and to none or trace in 44.2% (P < 0.0001 vs baseline). Few subjects had major adverse events through 1 year (<2% for myocardial infarction, surgical reintervention, or single-leaflet device attachment). The 1-year Kaplan-Meier estimates for all-cause mortality and heart failure hospitalization were 12.3% and 16.9%. Significant improvements in functional capacity (NYHA functional class I or II in 82%; P < 0.0001 vs baseline) and quality of life (18.5-point Kansas City Cardiomyopathy Questionnaire overall summary score improvement; P < 0.0001) were observed.
M-TEER with the fourth-generation M-TEER device was safe and effective at 1 year, with durable reductions in MR severity to ≤1+ in more than 90% of patients and concomitant improvements in functional status and quality of life.
第四代二尖瓣经导管缘对缘修复(M-TEER)装置采用了改良的夹合器释放顺序、独立的瓣叶抓取和 2 个更宽的夹合器尺寸,以针对广泛的解剖结构为二尖瓣反流(MR)患者定制治疗方案。第四代 M-TEER 装置的 30 天安全性和有效性此前已得到证实。
本研究旨在评估第四代 M-TEER 装置在当代真实世界队列中的 1 年结果。
EXPAND G4 是一项正在进行的前瞻性、多中心、国际性、单臂研究,纳入了原发性和继发性 MR 患者。1 年的结果包括 MR 严重程度(超声心动图核心实验室评估)、心力衰竭住院、全因死亡率、心功能(纽约心脏协会心功能分级)和生活质量(堪萨斯城心肌病问卷)。
共有 1164 例患者在 2020 年至 2022 年间接受了 M-TEER 治疗。1 年后,MR 持久减轻至轻度或更轻的比例为 92.6%,无或微量的比例为 44.2%(与基线相比,P<0.0001)。通过 1 年,少数患者发生重大不良事件(心肌梗死、再次手术干预或单叶器械附着的发生率<2%)。1 年全因死亡率和心力衰竭住院率的 Kaplan-Meier 估计值分别为 12.3%和 16.9%。心功能(NYHA 心功能分级 I 或 II 的比例为 82%;P<0.0001 与基线相比)和生活质量(堪萨斯城心肌病问卷总体综合评分改善 18.5 分;P<0.0001)显著改善。
第四代 M-TEER 装置的 M-TEER 在 1 年时是安全有效的,MR 严重程度持久减轻至≤1+的患者比例超过 90%,同时功能状态和生活质量也得到改善。