Silberhumer Gerd R, Pokorny Herwig, Hetz Hubert, Herkner Harald, Rasoul-Rockenschaub Susanne, Soliman Thomas, Wekerle Thomas, Berlakovich Gabriela A, Steininger Rudolf, Muehlbacher Ferdinand
Department of Transplant Surgery, Medical University Vienna, Vienna, Austria.
Transplantation. 2007 Mar 15;83(5):588-92. doi: 10.1097/01.tp.0000255319.07499.b7.
The purpose of this study was to analyze the impact of extended donor criteria (EDC) and of changes in the Model for End-Stage Liver Disease (MELD) score while waiting for liver-transplantation (Delta-MELD) on patient survival and initial graft function.
We included 386 consecutive patients with end-stage liver disease who underwent orthotopic liver transplantation at the Medical University Vienna between 1997 and 2003. Primary outcome was patient survival and secondary outcome was initial graft function. EDC included: age >60 years, >4 days intensive medical care, cold ischemia time >10 hr, need for noradrenalin >0.2 microg/kg/min or doputamin >6 microg/kg/min, a donor peak serum sodium >155 mEq/L, a donor serum creatinine >1.2 mg/100 mL, and a body mass index >30.
Delta-MELD was significantly higher in the nonsurvivor population (P=0.01) and EDC showed a significant influence on initial graft function (P=0.01). Worsening in either Delta-MELD or the presence of at least two EDC was not associated with an increased risk of primary graft dysfunction and death. Worsening in Delta-MELD and the presence of at least two EDC was significantly associated with primary graft dysfunction (P=0.01) and death (P=0.008).
The combination of a liver recipient with worsening Delta-MELD and a potential donor with at least two EDC should be avoided.
本研究旨在分析扩大供体标准(EDC)以及等待肝移植期间终末期肝病模型(MELD)评分的变化(Delta-MELD)对患者生存及初始移植物功能的影响。
我们纳入了1997年至2003年间在维也纳医科大学接受原位肝移植的386例连续性终末期肝病患者。主要结局为患者生存,次要结局为初始移植物功能。EDC包括:年龄>60岁、强化医疗护理>4天、冷缺血时间>10小时、去甲肾上腺素需求>0.2微克/千克/分钟或多巴胺需求>6微克/千克/分钟、供体血清钠峰值>155毫当量/升、供体血清肌酐>1.2毫克/100毫升以及体重指数>30。
非存活患者群体的Delta-MELD显著更高(P=0.01),且EDC对初始移植物功能有显著影响(P=0.01)。Delta-MELD恶化或至少存在两项EDC与原发性移植物功能障碍及死亡风险增加无关。Delta-MELD恶化且至少存在两项EDC与原发性移植物功能障碍(P=0.01)及死亡(P=0.008)显著相关。
应避免肝受体Delta-MELD恶化且潜在供体至少存在两项EDC的组合情况。