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

被引:15
作者
Blackman, Daniel J. [1 ]
Meredith, Ian T. [2 ,3 ,4 ]
Dumonteil, Nicolas [5 ]
Tchetche, Didier [5 ]
Hildick-Smith, David [6 ]
Spence, Mark S. [7 ]
Walters, Darren L. [8 ]
Harnek, Jan [9 ]
Worthley, Stephen G. [10 ]
Rioufol, Gilles [11 ,12 ]
Lefevre, Thierry [13 ]
Houle, Vicki M. [4 ]
Allocco, Dominic J. [4 ]
Dawkins, Keith D. [4 ]
机构
[1] Leeds Teaching Hosp, Dept Cardiol, Leeds, W Yorkshire, England
[2] Monash Med Ctr, Div Cardiol, MonashHeart, Melbourne, Vic, Australia
[3] Monash Univ, Melbourne, Vic, Australia
[4] Boston Sci Corp, Marlborough, MA USA
[5] Clin Pasteur, Dept Cardiol, Toulouse, France
[6] Brighton & Sussex Univ Hosp, Dept Cardiol, Sussex Cardiac Ctr, Brighton, E Sussex, England
[7] Royal Victoria Hosp, Dept Cardiol, Belfast, Antrim, North Ireland
[8] Prince Charles Hosp, Div Cardiol, Brisbane, Qld, Australia
[9] Univ Hosp Lund, Dept Cardiol, Lund, Sweden
[10] Royal Adelaide Hosp, Dept Cardiol, Adelaide, SA, Australia
[11] Hop Cardiol Lyon, Dept Cardiol, Lyon, France
[12] CARMEN, INSERM 1060, Lyon, France
[13] Inst Cardiovasc Paris Sud, Dept Cardiol, Massy, France
关键词
ACADEMIC RESEARCH CONSORTIUM; END-POINT DEFINITIONS; COREVALVE IMPLANTATION; CLINICAL-OUTCOMES; REPLACEMENT; IMPACT; CALCIFICATION; REGISTRY; METAANALYSIS; MORTALITY;
D O I
10.1016/j.amjcard.2017.04.026
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 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. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:292 / 299
页数:8
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