Treatment of children with HBeAg-positive chronic hepatitis B: A systematic review and meta-analysis

被引:14
|
作者
El Sherbini, Azza [1 ]
Omar, Asmaa [2 ]
机构
[1] Tanta Fever Hosp, Res Unit, Tanta 3111, Egypt
[2] Tanta Univ, Fac Med, Publ Hlth Prevent & Social Med Dept, Tanta, Egypt
关键词
Children; Chronic hepatitis B; Meta-analysis; Treatment; INTERFERON-ALPHA THERAPY; CONTROLLED-TRIAL; RECOMBINANT INTERFERON-ALPHA-2B; COMBINATION TREATMENT; LAMIVUDINE TREATMENT; ENTECAVIR TREATMENT; ANTIVIRAL THERAPY; VIRUS-INFECTION; VITAMIN-E; ADOLESCENTS;
D O I
10.1016/j.dld.2014.08.032
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Effective management of children with chronic hepatitis B is still an unresolved issue. Aim: To assess the outcome of different therapeutic regimens among children with HBeAg-positive chronic hepatitis B. Methods: Electronic database searches identified clinical trials that completed specific periods of treatment and follow-up. Sustained response rates were defined by the loss of HBV DNA and HBeAg, and by the normalization of liver enzymes. The loss of HBsAg and seroconversion to anti-HBs were also listed. Results: Our searches found 20 eligible articles (1112 enrolled patients, 2-18 years old). Interferon-alpha therapy showed significantly higher sustained response rate and loss of HBsAg than no therapy (Odd's ratio 3.0, 95% confidence interval 1.6-5.4; and 2.3, 1.1-11.3, respectively). The sustained response rate was not significantly different between interferon and interferon plus lamivudine, or plus prednisone, or plus hepatitis B vaccine; this rate was significantly higher for interferon compared with combined interferon plus levamisole or vitamin E. Conclusion: Interferon-alpha is still the most effective treatment option for children with HBeAg-positive chronic hepatitis B. Randomized trials are warranted for further comparing interferon to newer antiviral agents in terms of efficacy, safety, emergence of mutant variants, and cost/benefit ratio. (C) 2014 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1103 / 1110
页数:8
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