首页> 外文期刊>The Journal of Clinical Pharmacology: Official Journal of the American College of Clinical Pharmacology >Entecavir plus adefovir combination therapy versus lamivudine add-on adefovir for lamivudine-resistant chronic hepatitis B: A meta-analysis
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Entecavir plus adefovir combination therapy versus lamivudine add-on adefovir for lamivudine-resistant chronic hepatitis B: A meta-analysis

机译:恩替卡韦联合阿德福韦联合拉米夫定联合阿德福韦治疗耐拉米夫定的慢性乙型肝炎:一项荟萃分析

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To determine whether adefovir (ADV) in combination with entecavir (ETV) is more effective than with lamivudine (LAM) in patients with lamivudine-resistant chronic HBV infection, electronic databases were searched through May 10th, 2013 to obtain relevant trials which met the inclusion criteria. Meta-analysis was performed on randomized controlled trials (RCTs) and non-randomized studies. Four trials containing a total of 323 patients were included. Serum HBV DNA reductions after 3 and 6 months of treatment in the ETV+ADV group were greater than that of LAM+ADV group (mean difference (MD)=0.90, 95% confidence interval (CI): 0.74-1.07, P<0.00001; MD=0.81, 95% CI: 0.57-1.06, P<0.00001). The rate of 6 months HBV DNA undetectability with ETV and ADV was higher than that of LAM and ADV (relative risk (RR)=1.63, 95% CI: 1.14-2.34, P<0.007). There were higher rates of serum ALT normalization than those in LAM+ADV group after 6 months of treatment (RR=1.40, 95% CI: 1.11-1.77, P<0.005). The ETV+ADV group had lower viral breakthrough and genotypic mutation rates than LAM+ADV group after 12 months of treatment (RR=0.24, 95% CI: 0.10-0.58, P=0.002). The combination of ETV plus ADV is a more effective rescue therapy than LAM add-on ADV in patients with LAM-resistant HBV.
机译:为了确定阿德福韦(ADV)与恩替卡韦(ETV)联合用药对拉米夫定耐药的慢性HBV感染患者是否比拉米夫定(LAM)更有效,在2013年5月10日之前搜索了电子数据库,以获得符合纳入标准的相关试验标准。荟萃分析是在随机对照试验(RCT)和非随机研究中进行的。包括总共323名患者的四项试验。 ETV + ADV组在治疗3个月和6个月后血清HBV DNA减少量大于LAM + ADV组(平均差异(MD)= 0.90,95%置信区间(CI):0.74-1.07,P <0.00001) ; MD = 0.81,95%CI:0.57-1.06,P <0.00001)。 ETV和ADV检测6个月HBV DNA的检出率高于LAM和ADV检测(相对风险(RR)= 1.63,95%CI:1.14-2.34,P <0.007)。治疗6个月后,血清ALT正常化率高于LAM + ADV组(RR = 1.40,95%CI:1.11-1.77,P <0.005)。治疗12个月后,ETV + ADV组的病毒穿透率和基因型突变率低于LAM + ADV组(RR = 0.24,95%CI:0.10-0.58,P = 0.002)。对于LAM耐药性HBV患者,ETV加ADV的联合治疗比LAM附加ADV更为有效。

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