Liu Kun, Shen Jinglun, Wu Kaisheng, Meng Fei, Wang Shengxun, Zheng Shuai, Zhang Haibo
Department of Cardiac Surgery, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Department of Cardiac Surgery, Cardiac Center of Hennan Provincial People's Hospital, Fuwai Central China Cardiovascular Hospital, Zhengzhou, China.
Ann Transl Med. 2022 Jan;10(1):21. doi: 10.21037/atm-21-6513.
Prior to the approval of the Sapien valve in 2020, there were no commercially available short-frame valves for transapical mitral valve-in-valve (MVIV) implantation. In January 2019, we first attempted the reverse mounted J-valve for transapical MVIV implantation with good clinical results. The present study aimed to explore the safety and effectiveness of transapical MVIV implantation with the J-valve reversely mounted on the delivery system.
Patients who underwent transapical MVIV implantation using the J-valve were analyzed from January 2019 to December 2020 with a 1-year follow-up. Before the procedure, computed tomography (CT) angiography data were analyzed to determine the inner diameter, left ventricular outflow tract (LVOT), and coaxial angel. An oversize rate of 5-10% was used to select the J-valve depending on the scanned inner diameter of the original mitral bioprosthesis. During the procedure, the three U-shape graspers were one-to-one buckled with the three tissue valve struts with the assist of echo and fluoroscopy. The implant depth into the left atrium was a 0-20% part of the J-valve, and the valve was then released under rapid pacing. Post-balloon dilatation was used when needed.
Nineteen patients (mean age 70.05±11.19 years), with a mean Society of Thoracic Surgeons score of 8.01%±4.20%, were included. By transesophageal echocardiography, we found that the mean transvalvular gradient was 6.21±2.63 mmHg. The mean follow-up time was 20.31±7.23 months, and the survival rate was 94.74% at the last follow-up. The transvalvular gradient decreased from 15.06±3.00 mmHg at basal to 7.13±2.28 mmHg at the 1-year follow-up (P<0.001). The left ventricular ejection fractions (LVEF) increased from 60.31%±7.30% to 59.94%±7.72% at the 1-year follow-up (P=0.863). Thirteen (81.25%) patients had no or trace paravalvular leak (PVL), two (12.50%) patients had minor PVL, one (6.25%) patient had moderate PVL, and there were no cases of major regurgitation at the 1-year transthoracic echocardiography (TTE) examination results.
The J-valve reversely mounted on the delivery system can be used for transapical MVIV implantation with less operative morbidity and favourable outcomes.
在2020年Sapien瓣膜获批之前,尚无用于经心尖二尖瓣瓣中瓣(MVIV)植入的市售短框架瓣膜。2019年1月,我们首次尝试将J瓣膜反向安装用于经心尖MVIV植入,取得了良好的临床效果。本研究旨在探讨将J瓣膜反向安装在输送系统上进行经心尖MVIV植入的安全性和有效性。
对2019年1月至2020年12月期间接受使用J瓣膜经心尖MVIV植入的患者进行分析,并随访1年。术前,分析计算机断层扫描(CT)血管造影数据以确定内径、左心室流出道(LVOT)和同轴角度。根据原始二尖瓣生物瓣膜的扫描内径,采用5%-10%的过大率来选择J瓣膜。手术过程中,在超声心动图和荧光透视的辅助下,将三个U形抓持器与三个组织瓣膜支柱一对一扣合。植入左心房的深度为J瓣膜的0%-20%部分,然后在快速起搏下释放瓣膜。必要时使用球囊扩张。
纳入19例患者(平均年龄70.05±11.19岁),胸外科医师协会平均评分为8.01%±4.20%。经食管超声心动图检查发现,平均跨瓣压差为6.21±2.63 mmHg。平均随访时间为20.31±7.23个月,末次随访时生存率为94.74%。跨瓣压差从基线时的15.06±3.00 mmHg降至1年随访时的7.13±2.28 mmHg(P<0.001)。左心室射血分数(LVEF)在1年随访时从60.31%±7.30%增加至59.94%±7.72%(P=0.863)。13例(81.25%)患者无或微量瓣周漏(PVL),2例(12.50%)患者有轻度PVL,1例(6.25%)患者有中度PVL,1年经胸超声心动图(TTE)检查结果无严重反流病例。
反向安装在输送系统上的J瓣膜可用于经心尖MVIV植入,手术并发症较少,效果良好。