Tripodi Armando, Chantarangkul Veena, Primignani Massimo, Fabris Federica, Dell'Era Alessandra, Sei Cinzia, Mannucci Pier Mannuccio
Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Department of Internal Medicine and Medical Specialties, Milan, Italy.
Hepatology. 2007 Aug;46(2):520-7. doi: 10.1002/hep.21732.
The model for end-stage-liver-disease (MELD) is a mathematical score used to prioritize patients for liver transplantation and includes results for creatinine, bilirubin, and prothrombin time (PT) expressed as international normalized ratio (INR). The rationale of using the MELD rests on the assumption that the score would be the same across the country if the methods used to measure the variables yield the same numerical results regardless of the testing laboratory. Evidence was provided that specific methodologies may influence the MELD, and the PT-INR was identified as the most important. This study was designed to provide information on the between-thromboplastin variability and to explore alternatives to obviate such variability. Fifty-seven patients with cirrhosis were selected, and their PTs were measured with 7 thromboplastins. The thromboplastins were previously calibrated by testing plasmas from patients on vitamin K antagonists and healthy subjects to assign the international sensitivity index (ISI(vka)) needed to convert PT into INR. Each of the thromboplastins was also assigned an ISI(liver) by substituting in the calibration the plasmas from vitamin K antagonist patients with plasmas from patients with cirrhosis. INR and MELD values for individual patients were calculated by using the ISI(vka) or the ISI(liver). The mean INR(vka) obtained with the 7 thromboplastins were significantly different (P < 0.001). Conversely, the mean INR(liver) were not. Similarly, the mean MELD(vka) were significantly different (P < 0.001), but those differences were abrogated for the MELD(liver).
The alternative thromboplastin calibration using plasmas from patients with cirrhosis instead of from vitamin K antagonist patients is feasible and may resolve the variability of the MELD to prioritize patients for transplantation.
终末期肝病模型(MELD)是一种数学评分系统,用于确定肝移植患者的优先顺序,包括肌酐、胆红素和凝血酶原时间(PT)的结果,以国际标准化比值(INR)表示。使用MELD的基本原理基于这样一个假设:如果用于测量变量的方法产生相同的数值结果,无论检测实验室如何,该评分在全国范围内都将是相同的。有证据表明特定方法可能会影响MELD,并且PT-INR被确定为最重要的因素。本研究旨在提供有关凝血活酶之间变异性的信息,并探索消除这种变异性的替代方法。选择了57例肝硬化患者,用7种凝血活酶测量他们的PT。这些凝血活酶先前通过检测服用维生素K拮抗剂的患者和健康受试者的血浆进行校准,以确定将PT转换为INR所需的国际敏感指数(ISI(vka))。通过用肝硬化患者的血浆替代维生素K拮抗剂患者的血浆进行校准,每种凝血活酶还被赋予了一个ISI(liver)。使用ISI(vka)或ISI(liver)计算个体患者的INR和MELD值。用7种凝血活酶获得的平均INR(vka)有显著差异(P < 0.001)。相反,平均INR(liver)没有差异。同样,平均MELD(vka)有显著差异(P < 0.001),但对于MELD(liver),这些差异被消除了。
使用肝硬化患者的血浆而非维生素K拮抗剂患者的血浆进行替代凝血活酶校准是可行的,并且可能解决MELD的变异性问题,从而确定肝移植患者的优先顺序。