Antunes Artur Gião, Teixeira Cristina, Vaz Ana Margarida, Martins Cláudio, Queirós Patrícia, Alves Ana, Velasco Francisco, Peixe Bruno, Oliveira Ana Paula, Guerreiro Horácio
Gastroenterology Department, Centro Hospitalar do Algarve, Rua Leão Penedo, 8000-386 Faro, Portugal.
Gastroenterology Department, Centro Hospitalar de Setúbal, Rua Camilo Castelo Branco, 2910-446 Setúbal, Portugal.
Gastroenterol Hepatol. 2017 Apr;40(4):276-285. doi: 10.1016/j.gastrohep.2017.01.001. Epub 2017 Feb 20.
Recently, the European Association for the Study of the Liver - Chronic Liver Failure (CLIF) Consortium defined two new prognostic scores, according to the presence or absence of acute-on-chronic liver failure (ACLF): the CLIF Consortium ACLF score (CLIF-C ACLFs) and the CLIF-C Acute Decompensation score (CLIF-C ADs). We sought to compare their accuracy in predicting 30- and 90-day mortality with some of the existing models: Child-Turcotte-Pugh (CTP), Model for End-Stage Liver Disease (MELD), MELD-Na, integrated MELD (iMELD), MELD to serum sodium ratio index (MESO), Refit MELD and Refit MELD-Na.
Retrospective cohort study that evaluated all admissions due to decompensated cirrhosis in 2 centers between 2011 and 2014. At admission each score was assessed, and the discrimination ability was compared by measuring the area under the ROC curve (AUROC).
A total of 779 hospitalizations were evaluated. Two hundred and twenty-two patients met criteria for ACLF (25.9%). The 30- and 90-day mortality were respectively 17.7 and 37.3%. CLIF-C ACLFs presented an AUROC for predicting 30- and 90-day mortality of 0.684 (95% CI: 0.599-0.770) and 0.666 (95% CI: 0.588-0.744) respectively. No statistically significant differences were found when compared to traditional models. For patients without ACLF, CLIF-C ADs had an AUROC for predicting 30- and 90-day mortality of 0.689 (95% CI: 0.614-0.763) and 0.672 (95% CI: 0.624-0.720) respectively. When compared to other scores, it was only statistically superior to MELD for predicting 30-day mortality (p=0.0296).
The new CLIF-C scores were not statistically superior to the traditional models, with the exception of CLIF-C ADs for predicting 30-day mortality.
最近,欧洲肝脏研究协会 - 慢性肝衰竭(CLIF)联盟根据慢性肝衰竭急性发作(ACLF)的有无定义了两个新的预后评分:CLIF联盟ACLF评分(CLIF-C ACLFs)和CLIF-C急性失代偿评分(CLIF-C ADs)。我们试图将它们预测30天和90天死亡率的准确性与一些现有模型进行比较:Child-Turcotte-Pugh(CTP)评分、终末期肝病模型(MELD)、MELD-Na、综合MELD(iMELD)、MELD与血清钠比值指数(MESO)、改良MELD和改良MELD-Na。
回顾性队列研究,评估了2011年至2014年间2个中心因失代偿性肝硬化入院的所有患者。入院时评估每个评分,并通过测量ROC曲线下面积(AUROC)比较其区分能力。
共评估了779例住院患者。222例患者符合ACLF标准(25.9%)。30天和90天死亡率分别为17.7%和37.3%。CLIF-C ACLFs预测30天和90天死亡率的AUROC分别为0.684(95%CI:0.599-0.770)和0.666(95%CI:0.588-0.744)。与传统模型相比,未发现统计学显著差异。对于无ACLF的患者,CLIF-C ADs预测30天和90天死亡率的AUROC分别为0.689(95%CI:0.614-0.763)和0.672(95%CI:0.624-0.720)。与其他评分相比,仅在预测30天死亡率方面在统计学上优于MELD(p=0.0296)。
新的CLIF-C评分在统计学上并不优于传统模型,但CLIF-C ADs在预测30天死亡率方面除外。