A prospective, single-center, single-arm, and open-design study was performed to evaluate the feasibility and safety of transseptal transcatheter mitral valve replacement in the treatment of severe mitral regurgitation. Patients with symptomatic moderate-severe or severe mitral regurgitation at high-surgical risk and anatomically appropriate for the HighLife transseptal mitral valve replacement (TSMVR) system in West China Hospital, Sichuan University from December 2021 to August 2022 were enrolled. Four patients (1 male and 3 females) with severe mitral regurgitation were included, with a median age of 68.5 (64.0-77.0) years and a median Society of Thoracic Surgeons (STS) score of 8.1% (6.4%-8.9%). Technical success was achieved in all the patients. There was no residual mitral regurgitation, paravalvular leakage, or left ventricular outflow tract obstruction. Three major cardiovascular and cerebrovascular adverse events occurred within 30 days after the procedure, including ventricular tachycardia, iatrogenic atrial septal defect closure, and heart failure readmission. The current study preliminarily demonstrates that transcatheter mitral valve replacement using the HighLife system via the transseptal approach for severe mitral regurgitation is feasible and relatively safe.
前瞻性纳入2021年12月至2022年8月于四川大学华西医院就诊的外科手术风险高危且解剖结构适合使用HighLife系统行经房间隔途径经导管二尖瓣置换术(TSMVR)的症状性严重二尖瓣反流(3+或4+)患者4例。其中男1例,女3例,中位年龄68.5岁(64.0~77.0岁),中位美国胸外科医师协会(STS)评分8.1%(6.4%~8.9%)。所有患者均成功接受TSMVR,术后均无人工瓣膜瓣口反流、瓣周漏、左心室流出道梗阻。术后30 d内发生3例次主要心脑血管不良事件,包括室性心动过速、医源性房间隔缺损封堵及心力衰竭再入院。本研究初步表明,使用HighLife系统行TSMVR治疗严重二尖瓣反流是可行的,能有效消除反流,微创且相对安全。.