Lee Chuanfang, Gong Yan, Brok Jesper, Boxall Elizabeth H, Gluud Christian
Cochrane Hepato-Biliary Group, Copenhagen Trial Unit, Copenhagen University Hospital, Denmark.
BMJ. 2006 Feb 11;332(7537):328-36. doi: 10.1136/bmj.38719.435833.7C. Epub 2006 Jan 27.
To evaluate the effects of hepatitis B vaccine and immunoglobulin in newborn infants of mothers positive for hepatitis B surface antigen.
Systematic review and meta-analysis of randomised clinical trials.
Electronic databases and hand searches.
Randomised clinical trials were assessed for methodological quality. Meta-analysis was undertaken on three outcomes: the relative risks of hepatitis B occurrence, antibody levels to hepatitis B surface antigen, and adverse events.
29 randomised clinical trials were identified, five of which were considered high quality. Only three trials reported inclusion of mothers negative for hepatitis B e antigen. Compared with placebo or no intervention, vaccination reduced the occurrence of hepatitis B (relative risk 0.28, 95% confidence interval 0.20 to 0.40; four trials). No significant difference in hepatitis B occurrence was found between recombinant vaccine and plasma derived vaccine (1.00, 0.71 to 1.42; four trials) and between high dose versus low dose vaccine (plasma derived vaccine 0.97, 0.55 to 1.68, three trials; recombinant vaccine 0.78, 0.31 to 1.94, one trial). Compared with placebo or no intervention, hepatitis B immunoglobulin or the combination of plasma derived vaccine and hepatitis B immunoglobulin reduced hepatitis B occurrence (immunoglobulin 0.50, 0.41 to 0.60, one trial; vaccine and immunoglobulin 0.08, 0.03 to 0.17, three trials). Compared with vaccine alone, vaccine plus hepatitis B immunoglobulin reduced hepatitis B occurrence (0.54, 0.41 to 0.73; 10 trials). Hepatitis B vaccine and hepatitis B immunoglobulin seem safe, but few trials reported adverse events.
Hepatitis B vaccine, hepatitis B immunoglobulin, and vaccine plus immunoglobulin prevent hepatitis B occurrence in newborn infants of mothers positive for hepatitis B surface antigen.
评估乙肝疫苗和免疫球蛋白对乙肝表面抗原阳性母亲所生新生儿的影响。
对随机临床试验进行系统评价和荟萃分析。
电子数据库和手工检索。
评估随机临床试验的方法学质量。对三个结局进行荟萃分析:乙肝发生的相对风险、乙肝表面抗原抗体水平及不良事件。
共纳入29项随机临床试验,其中5项被认为质量较高。仅有3项试验报告纳入了乙肝e抗原阴性的母亲。与安慰剂或不干预相比,接种疫苗可降低乙肝的发生(相对风险0.28,95%置信区间0.20至0.40;4项试验)。重组疫苗与血浆源性疫苗在乙肝发生方面无显著差异(1.00,0.71至1.42;4项试验),高剂量疫苗与低剂量疫苗之间也无显著差异(血浆源性疫苗0.97,0.55至1.68,3项试验;重组疫苗0.78,0.31至1.94,1项试验)。与安慰剂或不干预相比,乙肝免疫球蛋白或血浆源性疫苗与乙肝免疫球蛋白联合使用可降低乙肝的发生(免疫球蛋白0.50,0.41至0.60,1项试验;疫苗和免疫球蛋白0.08,0.03至0.17,3项试验)。与单独使用疫苗相比,疫苗加乙肝免疫球蛋白可降低乙肝的发生(0.54,0.41至0.73;10项试验)。乙肝疫苗和乙肝免疫球蛋白似乎是安全的,但很少有试验报告不良事件。
乙肝疫苗、乙肝免疫球蛋白以及疫苗加免疫球蛋白可预防乙肝表面抗原阳性母亲所生新生儿发生乙肝。