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经导管主动脉瓣置入术中自膨式瓣膜与球囊扩张式瓣膜的比较的荟萃分析。

Meta-analysis Comparing Valve-In-Valve Transcatheter Aortic Valve Implantation With Self-Expanding Versus Balloon-Expandable Valves.

机构信息

Department of Cardiology, Austin Health, Melbourne, Victoria, Australia.

Department of Cardiology, Austin Health, Melbourne, Victoria, Australia; Department of Medicine, The University of Melbourne, Victoria, Australia.

出版信息

Am J Cardiol. 2020 May 15;125(10):1558-1565. doi: 10.1016/j.amjcard.2020.02.021. Epub 2020 Mar 4.

Abstract

Valve-in-valve (ViV) transcatheter aortic valve implantation (TAVI) is an alternative to redo-surgery in patients with failed surgical bioprostheses. It remains unclear whether outcomes vary when using either self-expanding (SE) or balloon-expandable (BE) valves. The aim of this study was to compare outcomes between SE and BE transcatheter heart valves when used for ViV TAVI. A systematic review of PubMed, MEDLINE, and EMBASE was performed identifying studies reporting outcomes following ViV TAVI. Event rates were pooled for meta-analysis using a random-effects model. The primary outcome was all-cause mortality at 12 months. Secondary outcomes included 30-day and 3-year mortality in addition to standard safety outcomes after the procedure as per the Valve Academic Research Consortium criteria. Nineteen studies reporting outcomes for 1,772 patients were included: 924 in the SE group and 848 patients in the BE group. There was no significant difference in all-cause mortality at 12 months (SE 10.3% vs BE 12.6%, p = 0.165, I = 0%), or 3 years (SE 21.2% vs BE 31.2%, p = 0.407, I = 63.79). SE valves had lower transvalvular gradients after procedure and acute kidney injury, but higher rates of pacemaker insertion, moderate or severe paravalvular regurgitation and need for ≥2 valves (all p < 0.05). There were no differences in stroke, coronary obstruction, bleeding, or vascular complications. Despite significant differences in key procedural outcomes between SE and BE valves when used for ViV TAVI, we found no difference in 12-month mortality. Tailored device selection may further reduce the risk of adverse procedural outcomes, particularly over the longer term.

摘要

经导管主动脉瓣置换术(TAVI)是治疗外科生物瓣衰败患者的一种替代再手术的方法。在使用自膨式(SE)或球囊扩张式(BE)瓣膜时,结果是否存在差异尚不清楚。本研究旨在比较经导管心脏瓣膜 ViV TAVI 中使用 SE 和 BE 经导管心脏瓣膜的结果。通过系统检索 PubMed、MEDLINE 和 EMBASE 数据库,确定了报道 ViV TAVI 后结局的研究。使用随机效应模型对汇总事件率进行荟萃分析。主要结局是 12 个月时的全因死亡率。次要结局包括 30 天和 3 年死亡率,以及根据 Valve Academic Research Consortium 标准,术后标准安全性结局。共纳入 19 项研究,报告了 1772 例患者的结局:SE 组 924 例,BE 组 848 例。12 个月时的全因死亡率(SE 10.3%比 BE 12.6%,p=0.165,I=0%)或 3 年(SE 21.2%比 BE 31.2%,p=0.407,I=63.79%)无显著差异。SE 瓣膜术后跨瓣梯度较低,急性肾损伤发生率较高,但起搏器植入、中重度瓣周漏和需要≥2 个瓣膜的发生率较高(均 p<0.05)。在卒中、冠状动脉阻塞、出血或血管并发症方面无差异。尽管在使用 SE 和 BE 瓣膜进行 ViV TAVI 时,关键手术结局存在显著差异,但我们未发现 12 个月死亡率存在差异。选择量身定制的器械可能会进一步降低不良手术结局的风险,特别是在长期。

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