Kim Hwi Young, Chang Young, Park Jae Yong, Ahn Hongkeun, Cho Hyeki, Han Seung Jun, Oh Sohee, Kim Donghee, Jung Yong Jin, Kim Byeong Gwan, Lee Kook Lae, Kim Won
Departments of Internal Medicine, Seoul Metropolitan Government - Seoul National University Boramae Medical Center, Seoul, Korea.
Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
J Gastroenterol Hepatol. 2016 Feb;31(2):427-33. doi: 10.1111/jgh.13084.
Alcoholic liver diseases often evolve to acute-on-chronic liver failure (ACLF), which increases the risk of (multi-)organ failure and death. We investigated the development and characteristics of alcohol-related ACLF and evaluated prognostic scores for prediction of mortality in Asian patients with active alcoholism.
A total of 205 patients who were hospitalized with severe alcoholic liver disease were included in this retrospective cohort study, after excluding those with serious cardiovascular diseases, malignancy, or co-existing viral hepatitis. The Chronic Liver Failure (CLIF) Consortium Organ Failure score was used in the diagnosis and grading of ACLF, and the CLIF Consortium ACLF score (CLIF-C ACLFs) was used to predict mortality.
Patients with ACLF had higher Maddrey discriminant function, model for end-stage liver disease (MELD), and MELD-sodium scores than those without ACLF. Infections were more frequently documented in patients with ACLF (33.3% vs 53.0%; P = 0.004). Predictive factors for ACLF development were systemic inflammatory response syndrome (odds ratio [OR], 2.239; P < 0.001), serum sodium level (OR, 0.939; P = 0.029), and neutrophil count (OR, 1.000; P = 0.021). For prediction of mortality at predefined time points (28-day and 90-day) in patients with ACLF, areas under the receiver-operating characteristic were significantly greater for the CLIF-C ACLFs than for Child-Pugh, MELD, and MELD-sodium scores.
Infection and systemic inflammatory response syndrome play an important role in the development of alcohol-related ACLF in Asian patients with active alcoholism. The CLIF-C ACLFs may be more useful for predicting mortality in ACLF cases than liver-specific scoring systems.
酒精性肝病常进展为慢加急性肝衰竭(ACLF),这会增加(多)器官衰竭和死亡风险。我们研究了酒精相关ACLF的发生发展及特征,并评估了用于预测亚洲酒精依赖患者死亡率的预后评分。
本回顾性队列研究纳入了205例因严重酒精性肝病住院的患者,排除了患有严重心血管疾病、恶性肿瘤或合并病毒性肝炎的患者。采用慢性肝衰竭(CLIF)联盟器官衰竭评分对ACLF进行诊断和分级,并用CLIF联盟ACLF评分(CLIF-C ACLFs)预测死亡率。
与非ACLF患者相比,ACLF患者的Maddrey判别函数、终末期肝病模型(MELD)及MELD-钠评分更高。ACLF患者感染的记录更为频繁(33.3%对53.0%;P = 0.004)。ACLF发生的预测因素为全身炎症反应综合征(比值比[OR],2.239;P < 0.001)、血清钠水平(OR,0.939;P = 0.029)和中性粒细胞计数(OR,1.000;P = 0.021)。对于ACLF患者在预定时间点(28天和90天)死亡率的预测,CLIF-C ACLFs的受试者工作特征曲线下面积显著大于Child-Pugh、MELD及MELD-钠评分。
感染和全身炎症反应综合征在亚洲酒精依赖患者酒精相关ACLF的发生中起重要作用。与肝脏特异性评分系统相比,CLIF-C ACLFs在预测ACLF患者死亡率方面可能更有用。