...
首页> 外文期刊>Transplantation Proceedings >Levosimendan for primary graft failure after heart transplantation: a 3-year follow-up.
【24h】

Levosimendan for primary graft failure after heart transplantation: a 3-year follow-up.

机译:左西孟旦用于心脏移植后原发性移植失败:三年随访。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

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 mug/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.
机译:背景:原发性移植物衰竭(PGF)是一种严重的并发症,占心脏移植术后院内死亡率的42%。据推测,一旦达到30天生存期,PGF患者就不会增加死亡风险。左西孟旦可增加PGF患者的30天生存率。本文中,我们报道了在一个患者队列的单个中心进行的为期3年的随访,包括接受左西孟旦治疗的PGF病例。方法:自2005年9月至2006年12月,本院有53例患者接受了心脏移植手术,其中包括12例(22.6%)接受PGF治疗并接受左西孟旦24小时连续输注(0.10马克杯/千克/分钟)的患者。使用30天生存期以及1年和3年生存期对有或无PGF的患者进行比较,分析了1年和3年死亡率的危险因素(n = 41)。结果:两组之间的供体年龄,体重,身高和血清钠含量无显着差异。然而,缺血时间(259 +/- 53 vs 227 +/- 50 min; P = .06)和接受者年龄(51.6 +/- 15 vs 41.5 +/- 21岁; P = .07)更大。 PGF患者。两组的30天生存率均为92%。 1年和3年后,PGF组的生存率显着降低(50%比80.6%和41.7%对80.6%; P <.05),其中86.5%的PGF患者由于非心脏原因而死亡,主要是感染。结论:尽管左西孟旦治疗PGF可以提高30天生存率,但该组患者的1年和3年发病率却降低了。 PGF与不良的长期预后相关,这可能是移植后心脏低通量阶段系统性灌注不足的结果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号