首页> 外文期刊>The Journal of Clinical Pharmacology: Official Journal of the American College of Clinical Pharmacology >Efficacy of lamivudine combined with adefovir dipivoxil versus entecavir monotherapy in patients with hepatitis B-associated decompensated cirrhosis: A meta-analysis
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Efficacy of lamivudine combined with adefovir dipivoxil versus entecavir monotherapy in patients with hepatitis B-associated decompensated cirrhosis: A meta-analysis

机译:拉米夫定结合Adefovir Dipivoxil与孕产病患者对乙型肝炎相关解偿性肝硬化患者的疗效:META分析

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Whether the combination of lamivudine (LAM) plus adefovir (ADV) de novo is more effective than entecavir (ETV) monotherapy in patients with HBV-associated decompensated cirrhosis is still controversial. We searched seven randomized controlled trials that included 411 patients in this meta-analysis. There are 205 and 206 patients in these two groups separately. The pooled risk ratio (RR) and mean difference (MD) were used to assess the treatment effects. ETV monotherapy significantly improved Child-Turcotte-Pugh (CTP) scores (MD=0.33, 95%CI [0.21-0.44], P<.00001), and was associated with lower rates of serum creatinine increase compared LAM-ADV combination therapy (RR=4.76, 95%CI [1.11-20.33], P=.04) at 48 weeks. The reduction of alanine aminotransferase (ALT) levels, HBV DNA levels, the rate of ALT normalization, undetectable HBV DNA, HBV e antigen (HBeAg) loss, HBeAg seroconversion and mortality were similar between the two groups. ETV is more effective than LAM-ADV in improving CTP scores at 48 weeks. Both of the LAM-ADVand ETV had similar efficacy in improving virological and biochemical parameters at 48 weeks of followup. Furthermore, use of these agents in decompensated HBV patients was generally safe and well tolerated at 48 weeks. However, the nephrotoxicity of ADV, and the potential adverse effects of ETV should be considered and monitored during prolonged therapy.
机译:无论是拉米夫定(林)加adefovir(adv)de novo的组合比entecavir(etv)单药治疗更有效,HBV相关的失代偿的肝硬化仍然存在争议。我们搜索了七项随机对照试验,其中包括411名患者在该荟萃分析中。这些两组分别有205和206名患者。汇总风险比(RR)和平均差异(MD)用于评估治疗效果。 ETV单一疗法显着改善了儿童扁桃 - PUGH(CTP)评分(MD = 0.33,95%CI [0.21-0.44],P <.00001),并与LAM-AV-AV组合疗法相比较低的血清肌酸酐率较低相关( RR = 4.76,95%CI [1.11-20.33],p = .04)在48周时。两组间,还原丙氨酸氨基转移酶(ALT)水平,HBV DNA水平,ALT归一化率,可损失的HBV DNA,HBV e抗原(HBEAG)损失,HBeAg血清转化和死亡率。 ETV比LAM-ADV在48周内改善CTP分数更有效。林-Avand ETV都在改善病毒学和生物化学参数在后续48周的情况下具有相似的功效。此外,在失代偿化的HBV患者中使用这些药剂通常在48周的48周内普遍安全且耐受良好。然而,在长时间治疗期间,应考虑和监测ETV的肾毒性和ETV的潜在不利影响。

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