Dvir Danny, Assali Abid, Vaknin-Assa Hana, Sagie Alexander, Shapira Yaron, Porat Eyal, Kornowski Ran
Department of Cardiology, Rabin Medical Center, Petach Tikva, Israel.
J Invasive Cardiol. 2011 Sep;23(9):377-81.
Restoring degenerated bioprosthetic valves by transcatheter valve implantation may obviate the need for redo surgery in carefully selected patients. We present our initial experience with valve-in-valve (VIV) procedures for failed aortic and mitral bioprosthetic valves.
Data were collected for all patients who underwent VIV procedures at a tertiary medical center (n = 6). Findings were analyzed and compared with those for transcatheter valve implantation in native valves at the same center during the last 3 years (n = 84).
Six patients of mean age 78.3 ± 13.8 years (range, 51-87) underwent VIV procedures with the CoreValve (n = 4) or Edwards-SAPIEN device (n = 2). Four (66%) had a failed prosthetic aortic valve, and 2 (33%) had a failed prosthetic mitral valve. Regurgitation accounted for valve failure in 83.3% of the VIV group versus 1.2% of the comparison group (p < 0.001). Procedural success and 30-day survival rates were 100%. Patient functional class improved significantly from 0% class I/II, 50% class III, and 50% class IV before the procedure to 66% class I, 33% class II, and 0% class III/IV after (p < 0.001).
This preliminary experience demonstrates that in carefully selected cases, transcathether valve implants can be safely and effectively deployed in stenotic and/or regurgitant degenerated bioprosthetic valves. Further evaluations in larger series are needed.
通过经导管瓣膜植入术修复退化的生物瓣膜假体,可能避免在精心挑选的患者中进行再次手术。我们展示了我们在主动脉和二尖瓣生物瓣膜假体失效的瓣膜中置瓣膜(VIV)手术的初步经验。
收集了在一家三级医疗中心接受VIV手术的所有患者的数据(n = 6)。分析结果并与同一中心过去3年中天然瓣膜经导管瓣膜植入术的结果进行比较(n = 84)。
6例平均年龄为78.3±13.8岁(范围51 - 87岁)的患者接受了使用CoreValve(n = 4)或爱德华兹 - SAPIEN装置(n = 2)的VIV手术。4例(66%)有失效的人工主动脉瓣膜,2例(33%)有失效的人工二尖瓣瓣膜。反流导致VIV组83.3%的瓣膜失效,而对照组为1.2%(p < 0.001)。手术成功率和30天生存率均为100%。患者功能分级从术前0%为I/II级、50%为III级、50%为IV级显著改善为术后66%为I级、33%为II级、0%为III/IV级(p < 0.001)。
这一初步经验表明,在精心挑选的病例中,经导管瓣膜植入物可以安全有效地部署在狭窄和/或反流的退化生物瓣膜假体中。需要在更大系列中进行进一步评估。