Skip to the main content

Review article

https://doi.org/10.2478/acph-2018-0010

Efficacy of nucleoside analogues on hepatitis B virus-related liver failure: A network meta-analysis

JIAN WU ; Digestion Internal Medicine Department, Xijing Hospital, The First Affiliated Hospital of the Fourth Military Medical University, 127 West Changle Road, Xi’an, Shaanxi 710000, China
FANG YIN ; Digestion Internal Medicine Department, Xijing Hospital, The First Affiliated Hospital of the Fourth Military Medical University, 127 West Changle Road, Xi’an, Shaanxi 710000, China
XINMIN ZHOU ; Digestion Internal Medicine Department, Xijing Hospital, The First Affiliated Hospital of the Fourth Military Medical University, 127 West Changle Road, Xi’an, Shaanxi 710000, China


Full text: english pdf 671 Kb

page 19-30

downloads: 664

cite


Abstract

The purpose of this study was to compare the efficacy of nucleoside analogues (NAs) in the treatment of HBV-related liver failure. The data of patients with HBV-related liver failure treated with nucleoside analogues were used to conduct a network meta-analysis. A total of 1660 patients from 12 articles about the efficacy of lamivudine, entecavir, telbivudine and tenofovir for HBV-related liver failure treatment were recruited in the study. The highest two- and three-month survival rate was recorded for patients using tenofovir. The end-stage liver disease (MELD) score and mortality in patients undergoing tenofovir treatment were the lowest. Patients treated with telbivudine had the highest one-month survival rate. Patients receiving enticavir therapy showed the lowest HBV DNA level. Our results indicate that tenofovir may be the best therapy for the treatment of HBV-related liver failure compared to other nucleoside analogues (including lamivudine, entecavir and telbivudine) and non-NAs treatment.

Keywords

liver failure; hepatitis B virus; nucleoside analogue; tenofovir; network meta-analysis

Hrčak ID:

190214

URI

https://hrcak.srce.hr/190214

Publication date:

31.3.2018.

Visits: 1.690 *