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Dexamethasone in outcome of patients with hepatitis B virus‐related acute‐on‐chronic liver failure

医学 肝肾综合征 内科学 肝性脑病 地塞米松 胃肠病学 终末期肝病模型 肝病 脑病 腹水 自发性细菌性腹膜炎 乙型肝炎病毒 肝功能 乙型肝炎 入射(几何) 肝硬化 免疫学 病毒 肝移植 移植 物理 光学
作者
Junfeng Chen,KeWei Wang,Shaoquan Zhang,Ziying Lei,Jun‐Qiang Xie,Jianyun Zhu,Weizhen Weng,Zhiliang Gao,Bing‐Liang Lin
出处
期刊:Journal of Gastroenterology and Hepatology [Wiley]
卷期号:29 (4): 800-806 被引量:26
标识
DOI:10.1111/jgh.12454
摘要

Abstract Background and Aim Acute‐on‐chronic liver failure ( ACLF ) caused by hepatitis B virus ( HBV ) is a severe disease with high mortality. Immune injury plays an important role during the early stage of the disease. Our research aimed to investigate the safety and efficacy of dexamethasone therapy for patients with HBV ‐related ACLF . Methods A total of 134 inpatients with HBV ‐induced ACLF were enrolled from J anuary 2009 to D ecember 2012. All the patients received the standard medicine treatment (SMT), among whom 31 cases underwent additional dexamethasone injection for three times (dexamethasone treatment [DMT] Group). A total of 35 patients ( SMT Group) matched for baseline characters served as controls. Both the groups were followed up for 12 weeks. The survival rates, liver functions, and complications were recorded. Results The 12‐week cumulative survival rates were 45.7% (16/35)and 48.4% (15/31) for SMT G roup and DMT G roup, respectively, and no significant differences were found ( P = 0.959). There were no dramatic differences in liver function and model for end‐stage liver disease ( MELD ) score at 1, 2, 4, 8, and 12 weeks between two groups. There were no significant differences in the incidence of complications (i.e. infection, gastrointestinal bleeding, encephalopathy, hepatorenal syndrome, and ascites) from 1 to 12 weeks between G roup SMT and G roup DMT . More than 40 ages, MELD score more than 28 and encephalopathy were independent risk factors for the mortality of patients. Conclusions Dexamethasone cannot improve liver functions and 12‐week survival rates of patients with HBV ‐related ACLF . Age, MELD score, and encephalopathy are independent risk factors.
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