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新型 CoreValve(®) Evolut(™) 在退行性生物瓣主动脉瓣中的植入早期经验。

Early experience of implantation of the new CoreValve(®) Evolut(™) in degenerated bioprosthetic aortic valves.

机构信息

Cardiology and Cardiac Surgical Department, Royal Hospitals, Belfast Health & Social Care Trust, Belfast, BT12 6BJ.

出版信息

Catheter Cardiovasc Interv. 2014 Feb 15;83(3):485-92. doi: 10.1002/ccd.25125. Epub 2013 Aug 8.

Abstract

Transcatheter aortic valve implantation (TAVI) is an established treatment for severe aortic stenosis in high-risk patients. The PARTNER trial demonstrated equivalent 1-year survival rates between patients randomized to TAVI versus conventional surgery (Leon et al., N Engl J Med 2010;363:1597-1607), with sustained benefit up to 2 years (Makkar et al., NEJM 2012;366:1696-1704). Recently, the ADVANCE registry cited all-cause mortality rates of 4.5%, 12.8%, and 17.9% at 30-days, 6 months, and 1-year following TAVI in 1,015 high-risk patients (Linke, TCT 2012, 2012). In addition, TAVI was demonstrated to be a feasible treatment for severe native valve regurgitation in a series of 31 high-risk patients. The all-cause 30-day mortality rate was 6.4%, with a 30-day major stroke rate of 6.4%. At 1-year, the all-cause mortality rate was 12.5% (Roy et al., J Am Coll Cardiol 2012;60(17S):B264). We report the successful transcatheter implantation of the new CoreValve(®) Evolut(™) in two patients with regurgitant aortic bioprostheses.

摘要

经导管主动脉瓣植入术(TAVI)是一种治疗高危患者严重主动脉瓣狭窄的成熟方法。PARTNER 试验表明,随机分配至 TAVI 与传统手术的患者在 1 年时的生存率相当(Leon 等人,N Engl J Med 2010;363:1597-1607),并且在 2 年内持续获益(Makkar 等人,NEJM 2012;366:1696-1704)。最近,ADVANCE 注册研究报告称,在 1015 例高危患者中,TAVI 后 30 天、6 个月和 1 年的全因死亡率分别为 4.5%、12.8%和 17.9%(Linke,TCT 2012,2012)。此外,在一系列 31 例高危患者中,TAVI 被证明是一种可行的治疗严重原发性瓣膜反流的方法。全因 30 天死亡率为 6.4%,30 天主要卒中发生率为 6.4%。1 年时,全因死亡率为 12.5%(Roy 等人,J Am Coll Cardiol 2012;60(17S):B264)。我们报告了在 2 例有反流性主动脉生物瓣的患者中成功植入新的 CoreValve(®) Evolut(™)。

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