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  • Outcome of cardiac transplantation in patients requiring prolonged continuous-flow left ventricular assist device support.

Outcome of cardiac transplantation in patients requiring prolonged continuous-flow left ventricular assist device support.

The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation (2014-12-03)
Koji Takeda, Hiroo Takayama, Bindu Kalesan, Nir Uriel, Paolo C Colombo, Ulrich P Jorde, Melana Yuzefpolskaya, Donna M Mancini, Yoshifumi Naka
ABSTRACT

This study assessed the early and late outcomes after cardiac transplantation in patients receiving long-term continuous-flow left ventricular assist device (CF-LVAD) support. Between April 2004 and September 2013, 192 patients underwent HeartMate II (Thoratec, Pleasanton, CA) CF-LVAD placement as a bridge to transplant at our center. Of these, 122 (63%) successfully bridged patients were retrospectively reviewed. Patients were stratified into 2 groups according to their waiting time with CF-LVAD support of <1 year or ≥1 year. The study cohort was a mean age of 54 ± 13 years, 79% were male, and 35% had an ischemic etiology. The mean duration of CF-LVAD support before transplantation was 296 days (range, 27-1,413 days). The overall 30-day mortality was 4.1%. Overall post-transplant survival was 88%, 84%, 78% at 1, 3, and 5 years, respectively. The 32 patients (26%) with ≥1 year of CF-LVAD support (mean, 635 days) were more likely to have blood type O, a larger body size, and to have been readmitted due to recurrent heart failure and device failure requiring exchange than those with <1 year of CF-LVAD support. Patients who required prolonged support time also had worse in-hospital mortality (16% vs 6.7%, p = 0.12) and significantly lower survival at 3 years after transplantation (68% vs 88%, p = 0.049). The overall short-term and long-term cardiac transplant outcomes of patients supported with CF-LVAD are satisfactory. However, patients who require prolonged CF-LVAD support may have diminished post-transplant survival due to adverse events occurring during device support.

MATERIALS
Product Number
Brand
Product Description

Azathioprine, European Pharmacopoeia (EP) Reference Standard
USP
Azathioprine, United States Pharmacopeia (USP) Reference Standard
Supelco
Azathioprine, Pharmaceutical Secondary Standard; Certified Reference Material
Methylprednisolone, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
6α-Methylprednisolone, ≥98%
USP
Methylprednisolone, United States Pharmacopeia (USP) Reference Standard