Experience With a Long-term Pulsatile Ventricular Assist Device as a Bridge to Heart Transplant in Adults

被引:0
|
作者
Gomez Bueno, Manuel [1 ,2 ]
Segovia Cubero, Javier [1 ,2 ]
Serrano Fiz, Santiago [3 ]
Ugarte Basterrechea, Juan [3 ]
Hernandez Perez, Francisco Jose [1 ]
Goirigolzarri Artaza, Josebe [1 ]
Castedo Mejuto, Evaristo [3 ]
Burgos Lazaro, Raul [3 ]
Garcia Montero, Carlos [3 ]
Monivas Palomero, Vanessa [1 ]
Mingo Santos, Susana [1 ]
Gonzalez Roman, Ana Isabel [4 ]
Alvarez Avello, Jose Manuel [4 ]
Vidal Fernandez, Mercedes [4 ]
Forteza Gil, Alberto [3 ]
Alonso-Pulpon, Luis [1 ,2 ]
机构
[1] Hosp Univ Puerta de Hierro, Serv Cardiol, Madrid, Spain
[2] CIBER Enfermedades Cardiovasc CIBERCV, Madrid, Spain
[3] Hosp Univ Puerta de Hierro, Serv Cirugia Cardiaca, Madrid, Spain
[4] Hosp Univ Puerta de Hierro, Serv Anestesia & Reanimac, Madrid, Spain
来源
REVISTA ESPANOLA DE CARDIOLOGIA | 2017年 / 70卷 / 09期
关键词
Heart failure; Ventricular assist device; Heart transplant; SUPPORT; FAILURE;
D O I
10.1016/j.recesp.2016.11.043
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction and objectives: Most long-term ventricular assist devices (VADs) that are currently implanted are intracorporeal continuous-flow devices. Their main limitations include their high cost and inability to provide biventricular support. The aim of this study was to describe the results of using paracorporeal pulsatile-flow VADs as a bridge to transplant (BTT) in adult patients. Methods: Retrospective analysis of the characteristics, complications, and outcomes of a single-center case series of consecutive patients treated with the EXCOR VAD as BTT between 2009 and 2015. Results: During the study period, 25 VADs were implanted, 6 of them biventricular. Ventricular assist devices were indicated directly as a BTT in 12 patients and as a bridge to decision in 13 due to the presence of potentially reversible contraindications or chance of heart function recovery. Twenty patients (80%) were successfully bridged to heart transplant after a median of 112 days (range, 8-239). The main complications included infectious (52% of patients), neurological events (32%, half of them fatal), bleeding (28%), and VAD malfunction requiring component replacement (28%). Conclusions: Eighty percent of patients with the EXCOR VAD as BIT achieved the goal after an average of almost 4 months of support. The most frequent complications were infectious, and the most severe were neurological. In our enivonment, the use of these pulsatile-flow VAD as BTT is a feasible strategy that obtains similar outcomes to those of intracorporeal continuous-flow devices. Full English text available from: www.revespcardiol.org/en (C) 2016 Sociedad Espanola de Cardiologla. Published by Elsevier Espana, S.L.U. All rights reserved.
引用
收藏
页码:727 / 735
页数:9
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