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完全可重新定位和可回收的莲花经导管主动脉瓣植入术后瓣周反流的预测因素(来自REPRISE II试验扩展队列)

Predictors of Paravalvular Regurgitation After Implantation of the Fully Repositionable and Retrievable Lotus Transcatheter Aortic Valve (from the REPRISE II Trial Extended Cohort).

作者信息

Blackman Daniel J, Meredith Ian T, Dumonteil Nicolas, Tchétché Didier, Hildick-Smith David, Spence Mark S, Walters Darren L, Harnek Jan, Worthley Stephen G, Rioufol Gilles, Lefèvre Thierry, Houle Vicki M, Allocco Dominic J, Dawkins Keith D

机构信息

Department of Cardiology, Leeds Teaching Hospitals, Leeds, United Kingdom.

Division of Cardiology, MonashHeart, Monash Medical Centre and Monash University, Melbourne, Australia; Boston Scientific Corporation, Marlborough, Massachusetts.

出版信息

Am J Cardiol. 2017 Jul 15;120(2):292-299. doi: 10.1016/j.amjcard.2017.04.026. Epub 2017 Apr 27.

Abstract

Paravalvular leak (PVL) after transcatheter aortic valve replacement is associated with worse long-term outcomes. The Lotus Valve incorporates an innovative Adaptive Seal designed to minimize PVL. This analysis evaluated the incidence and predictors of PVL after implantation of the Lotus transcatheter aortic valve. The REPRISE II (REpositionable Percutaneous Replacement of Stenotic Aortic Valve through Implantation of Lotus Valve System - Evaluation of Safety and Performance) Study With Extended Cohort enrolled 250 high-surgical risk patients with severe symptomatic aortic stenosis. Aortic regurgitation was assessed by echocardiography pre-procedure, at discharge and 30 days, by an independent core laboratory. Baseline and procedural predictors of mild or greater PVL at 30 days (or at discharge if 30-day data were not available) were determined using a multivariate regression model (n = 229). Of the 229 patients, 197 (86%) had no/trace PVL, 30 had mild, and 2 had moderate PVL; no patient had severe PVL. Significant predictors of mild/moderate PVL included device:annulus area ratio (odds ratio [OR] 0.87; 95% CI 0.83 to 0.92; p <0.001), left ventricular outflow tract calcium volume (OR 2.85; 95% CI 1.44 to 5.63; p = 0.003), and annulus area (OR 0.89; 95% CI 0.82 to 0.96; p = 0.002). When the device:annulus area ratio was <1, the rate of mild/moderate PVL was 53.1% (17 of 32). The rates of mild/moderate PVL with 0% to 5%, 5% to 10%, and >10% annular oversizing by area were 17.5% (11 of 63), 2.9% (2 of 70), and 3.2% (2 of 63), respectively. Significant independent predictors of PVL included device:annulus area ratio and left ventricular outflow tract calcium volume. When the prosthetic valve was oversized by ≥5%, the rate of mild or greater PVL was only 3%. In conclusion, the overall rates of PVL with the Lotus Valve are low and predominantly related to device/annulus areas and calcium; these findings have implications for optimal device sizing.

摘要

经导管主动脉瓣置换术后瓣周漏(PVL)与更差的长期预后相关。Lotus瓣膜采用了一种创新的自适应密封设计,旨在将瓣周漏降至最低。本分析评估了Lotus经导管主动脉瓣植入术后瓣周漏的发生率及预测因素。REPRISE II(通过植入Lotus瓣膜系统对狭窄主动脉瓣进行可重新定位的经皮置换——安全性和性能评估)扩展队列研究纳入了250例具有严重症状性主动脉瓣狭窄且手术风险高的患者。术前、出院时及30天时由独立核心实验室通过超声心动图评估主动脉瓣反流情况。使用多变量回归模型(n = 229)确定30天时(若无法获取30天数据则为出院时)轻度或更严重瓣周漏的基线和手术预测因素。在这229例患者中,197例(86%)无/微量瓣周漏,30例有轻度瓣周漏,2例有中度瓣周漏;无患者有重度瓣周漏。轻度/中度瓣周漏的显著预测因素包括器械与瓣环面积比(比值比[OR] 0.87;95%置信区间0.83至0.92;p <0.001)、左心室流出道钙化体积(OR 2.85;95%置信区间1.44至5.63;p = 0.003)和瓣环面积(OR 0.89;95%置信区间0.82至0.96;p = 0.002)。当器械与瓣环面积比<1时,轻度/中度瓣周漏发生率为53.1%(32例中的17例)。瓣环面积过大0%至5%、5%至10%和>10%时,轻度/中度瓣周漏发生率分别为17.5%(63例中的11例)、2.9%(70例中的2例)和3.2%(63例中的2例)。瓣周漏的显著独立预测因素包括器械与瓣环面积比和左心室流出道钙化体积。当人工瓣膜过大≥5%时,轻度或更严重瓣周漏发生率仅为3%。总之,Lotus瓣膜的瓣周漏总体发生率较低,主要与器械/瓣环面积及钙化有关;这些发现对优化器械尺寸具有指导意义。

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