Tohidinezhad Fariba, Eslami Saeid, Abu-Hanna Ameen, Aliakbarian Mohsen
The Student Research Committee, Department of Medical Informatics, Faculty of Medicine, Mashhad, Iran.
Exp Clin Transplant. 2018 Dec;16(6):721-729. doi: 10.6002/ect.2017.0149. Epub 2018 Feb 16.
Under the present liver transplant policy, patients with the highest risk of death receive preference for organ placement. The aim of this study was to evaluate the Model for End-stage Liver Disease (MELD) and seven prognostic derivatives of this test for outcome prediction in cirrhotic patients on liver transplant wait lists.
The study included 416 patients (65.9% male; age 49 ± 13.9 years) who were entered to liver transplant wait lists from January 2013 to October 2016. Study endpoints were 3-month, 6-month, and 1-year mortality.
All prognostic models had acceptable overall performances (0.12 < Brier score < 0.21). The MELD-to-serum sodium ratio test outperformed its counterparts at all 3 endpoints. Estimated C statistics ranged from 0.77 to 0.83. The largest value at 3 months was for the 5-variable MELD score (0.83), and the largest value at 6 months (0.82) and 1 year (0.83) was for the MELD-albumin score. The Hosmer-Lemeshow goodness-of-fit test and calibration plots revealed underestimation for the entire range of predicted risk (P < .001). With decision curve analysis, the MELD-to-serum sodium ratio and United Kingdom Model for End-Stage Liver Disease scoring tests covered the most extensive range of optimal threshold probabilities.
Although some derivations, including sodium and albumin, showed effective prioritization of liver transplant candidates, poor calibration statistics highlighted the need for a recalibration process as an inevitable prerequisite before daily clinical use of these tests at the individual level.
在现行肝移植政策下,死亡风险最高的患者在器官分配上享有优先权。本研究的目的是评估终末期肝病模型(MELD)及其七个预后衍生指标对肝移植等待名单上肝硬化患者的预后预测能力。
本研究纳入了2013年1月至2016年10月进入肝移植等待名单的416例患者(男性占65.9%;年龄49±13.9岁)。研究终点为3个月、6个月和1年死亡率。
所有预后模型的总体表现均可接受(Brier评分0.12<Brier评分<0.21)。MELD与血清钠比值试验在所有3个终点的表现均优于其他指标。估计的C统计量范围为0.77至0.83。3个月时最大值为5变量MELD评分(0.83),6个月(0.82)和1年(0.83)时最大值为MELD - 白蛋白评分。Hosmer - Lemeshow拟合优度检验和校准图显示在预测风险的整个范围内存在低估(P<0.001)。通过决策曲线分析,MELD与血清钠比值和英国终末期肝病模型评分试验涵盖了最广泛的最佳阈值概率范围。
尽管包括钠和白蛋白在内的一些衍生指标显示出对肝移植候选者的有效优先排序,但校准统计不佳突出表明,在个体层面日常临床使用这些试验之前,重新校准过程是必不可少的先决条件。