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

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 pati...

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Published inJournal of gastroenterology and hepatology Vol. 29; no. 4; pp. 800 - 806
Main Authors Chen, Jun-Feng, Wang, Ke-Wei, Zhang, Shao-Quan, Lei, Zi-Ying, Xie, Jun-Qiang, Zhu, Jian-Yun, Weng, Wei-Zhen, Gao, Zhi-Liang, Lin, Bing-Liang
Format Journal Article
LanguageEnglish
Published Australia Blackwell Publishing Ltd 01.04.2014
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Summary: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 January 2009 to December 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 Group and DMT Group, 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 Group SMT and Group 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.
Bibliography:National Science and Technology Major Project - No. 2012ZX 10002004; No. 2012ZX10002007
Guangdong Province Government for the Science and Technology Projects - No. 2007B060401001; No. 2006B36005004
The Natural Science Foundation of Guangdong Province - No. 9151040701000019
istex:6F882089CB750EA2E3CD251A136B431163033EEE
ArticleID:JGH12454
Sun Yat-Sen University Clinical Research 5010 Program - No. 2007029
ark:/67375/WNG-RTR8T147-F
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0815-9319
1440-1746
1440-1746
DOI:10.1111/jgh.12454