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

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-...

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Veröffentlicht in:Revista española de cardiología (English ed.) 2017-09, Vol.70 (9), p.727-735
Hauptverfasser: Gómez Bueno, Manuel, Segovia Cubero, Javier, Serrano Fiz, Santiago, Ugarte Basterrechea, Juan, Hernández Pérez, Francisco José, Goirigolzarri Artaza, Josebe, Castedo Mejuto, Evaristo, Burgos Lázaro, Raúl, García Montero, Carlos, Moñivas Palomero, Vanessa, Mingo Santos, Susana, González Román, Ana Isabel, Álvarez Avelló, José Manuel, Vidal Fernández, Mercedes, Forteza Gil, Alberto, Alonso-Pulpón, Luis
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Sprache:eng ; spa
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Zusammenfassung: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. 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. 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%). Eighty percent of patients with the EXCOR VAD as BTT 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.
ISSN:1885-5857
1885-5857
DOI:10.1016/j.rec.2017.03.004