Levosimendan for Primary Graft Failure After Heart Transplantation: A 3-Year Follow-up

被引:11
作者
Beiras-Fernandez, A. [1 ]
Kur, F. [1 ]
Kaczmarek, I. [1 ]
Frisch, P. [1 ]
Weis, M. [2 ]
Reichart, B. [1 ]
Weis, F. [2 ]
机构
[1] Univ Munich, Klinikum Grosshadern, Dept Cardiac Surg, D-8000 Munich, Germany
[2] Univ Munich, Klinikum Grosshadern, Dept Anesthesiol, D-8000 Munich, Germany
关键词
CARDIAC ALLOGRAFT; MECHANICAL SUPPORT;
D O I
10.1016/j.transproceed.2011.05.021
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Primary graft failure (PGF) is a severe complication responsible for 42% of the in-hospital mortality after heart transplantation. It has been postulated that once 30-day survival is achieved, patients with PGF have no increased risk of death. Levosimendan increases the 30-day survival among patients with PGF. Herein we have reported a 3-year follow-up at a single center of a patient cohort including PGF cases treated with levosimendan. Methods. From September 2005 to December 2006 53 patients underwent heart transplantation at our institution, including 12 patients (22.6%) who presented with PGF and were treated with levosimendan using a 24-hour continuous infusion (0.10 mu g/kg/min). Risk factors for 1-year and three-year mortality were analyzed using 30-day as well as 1 and 3-year survivals comparing patients with versus without PGF (n = 41). Results. There were no significant differences in donor age, weight, height, and serum sodium between the groups. However, the ischemia time (259 +/- 53 vs 227 +/- 50 min; P = .06) and recipient age (51.6 +/- 15 vs 41.5 +/- 21 years; P = .07) were greater among the PGF patients. The 30-day survival rate was 92% in both groups. After 1 and 3 years, the survival rate was significantly lower among the PGF cohort (50% vs 80.6% and 41.7% vs 80.6%; P < .05) with 86.5% of PGF patients succunding due to non cardiac reasons, predominantly infections. Conclusions. Although treatment of PGF with levosimendan increased the 30-day survival, the 1 year and 3-year rates were reduced among this cohort of patients. PGF was associated with poor long-term outcomes, which may be a consequence of systemic malperfusion during the stage of cardiac low-output after transplantation.
引用
收藏
页码:2260 / 2262
页数:3
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