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中华消化病与影像杂志(电子版) ›› 2018, Vol. 08 ›› Issue (01) : 24 -28. doi: 10.3877/cma.j.issn.2095-2015.2018.01.006

所属专题: 文献

循证医学

替诺福韦酯与恩替卡韦在治疗慢性乙型肝炎的安全性与有效性的荟萃分析
尹丹萍1, 陈春明2,()   
  1. 1. 250031 济南军区总医院疾病预防控制科
    2. 250031 济南军区总医院医务部
  • 收稿日期:2017-12-06 出版日期:2018-02-01
  • 通信作者: 陈春明
  • 基金资助:
    2015年度济南军区总医院院长基金(2015QN02)

Safety and efficacy comparison between tenofovir and entecavir in treatment of chronic hepatitis B: a Meta-analysis

Danping Yin1, Chunming Chen2,()   

  1. 1. Department of Disease Prevention and Contrl, General Hospital of Jinan Military Command, Jinan 250031, China
    2. Department of Medical Administration, General Hospital of Jinan Military Command, Jinan 250031, China
  • Received:2017-12-06 Published:2018-02-01
  • Corresponding author: Chunming Chen
  • About author:
    Corresponding author: Chen Chunming, Email:
引用本文:

尹丹萍, 陈春明. 替诺福韦酯与恩替卡韦在治疗慢性乙型肝炎的安全性与有效性的荟萃分析[J/OL]. 中华消化病与影像杂志(电子版), 2018, 08(01): 24-28.

Danping Yin, Chunming Chen. Safety and efficacy comparison between tenofovir and entecavir in treatment of chronic hepatitis B: a Meta-analysis[J/OL]. Chinese Journal of Digestion and Medical Imageology(Electronic Edition), 2018, 08(01): 24-28.

目的

评估与比较恩替卡韦与替诺福韦酯在治疗慢性慢性乙型肝炎有效性及安全性。

方法

检索Pubmed/Medicine、Embase、Cochrane library数据库,恩替卡韦与替诺福韦酯治疗慢性乙型肝炎的研究,检索时间从数据库建立至2017年11月,由2名作者对检索数据进行提取与总结,运用Stata 12.0对数据进行统计学分析。

结果

共纳入此次荟萃分析共13篇,替诺福韦酯与恩替卡韦治疗HBV-DNA有效性方面,按照口服抗病毒药物时间,可分为2个亚组,24、48周其相对危险度与可信区间分别为:RR=1.00,95% CI(0.90~1.11),I2=30%,P=0.152;RR=1.08,95% CI(1.00~1.16),I2=53%,P=0.016。

结论

随访时间为24和48周时,在治疗慢性乙型肝炎HBV-DNA转阴率方面二者疗效相当。

Objective

To evaluate and compare the efficacy and safety of entecavir and tenofovir in treatment of chronic hepatitis B.

Methods

The researches on entecavir and tenofovir in treatment of chronic hepatitis B were searched in PubMed/Medicine, EMBase, Cochrane Library databases until November 2017.Two authors independently extracted and summarized the data.Stata 12.0 software was used to analyze the data.

Results

A total of 13 studies were included in this Meta-analysis.In the aspect of therapeutic effectiveness of tenofovir and entecavir for HBV-DNA, the research objects were divided into two subgroups according to the use time of oral antiviral drug, and the relative risk(RR)and confidence interval(CI)of 24 weeks and 48 weeks subgroup were as follows: RR=1.00, 95% CI(0.90-1.11), I2=30%, P=0.152; RR=1.08, 95% CI(1.00-1.16), I2=53%, P=0.016.

Conclusion

Tenofovir has a similar efficacy in HBV-DNA negative conversion ratio compared with entecavir in follow-up time 24 and 48 weeks.

图1 随访时间为24周二者在治疗HBV-DNA有效性方面对比
图2 随访时间为48周二者在治疗HBV-DNA有效性方面对比
图3 随访时间为48周二者在治疗HBV-DNA有效性方面敏感性分析
图4 随访时间为48周二者在治疗HBV-DNA有效性方面Begg′s检验
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