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首页> 外文期刊>Alimentary pharmacology & therapeutics. >Systematic review and meta-analysis: D-Penicillamine vs. placeboo intervention in patients with primary biliary cirrhosis--Cochrane Hepato-Biliary Group.
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Systematic review and meta-analysis: D-Penicillamine vs. placeboo intervention in patients with primary biliary cirrhosis--Cochrane Hepato-Biliary Group.

机译:系统评价和荟萃分析:D-青霉胺与安慰剂/不干预原发性胆汁性肝硬化患者--Cochrane肝胆道疾病组。

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BACKGROUND: D-Penicillamine is used for patients with primary biliary cirrhosis due to its ability to decrease hepatic copper and modulate the immune response. The results on effects of D--penicillamine in randomized-clinical trials of primary biliary cirrhosis patients are inconsistent. AIM: To systematically evaluate the benefits and harms of D-penicillamine for patients with primary biliary cirrhosis. METHODS: We have performed a systematic review with meta-analyses of randomized-clinical trials to evaluate the effects of D-penicillamine for primary biliary cirrhosis. The primary outcomes are mortality and mortality or liver transplantation. We analysed the data by fixed-effect and random-effect models. RESULTS: Seven randomized trials including 706 patients were analysed. d-Penicillamine was without significant effects on mortality (RR 1.08, 95% CI: 0.82-1.43, P = 0.56), mortality or liver transplantation (RR 1.11, 95% CI: 0.74-1.68, P = 0.62), pruritus, liver complications, progression of liver histological stage and liver biochemical variables. D--Penicillamine significantly decreased serum alanine aminotransferase activity (weighted mean difference -45 IU/L, 95% CI: -75 to -15, P < 0.05) and led to significantly more adverse events (RR 4.18, 95% CI: 1.38-12.69, P = 0.01). CONCLUSION: D-Penicillamine did not appear to reduce the risk of mortality or morbidity, and led to more adverse events in patients with primary biliary cirrhosis.
机译:背景:D-青霉素胺可减少肝铜并调节免疫反应,因此可用于原发性胆汁性肝硬化患者。在原发性胆汁性肝硬化患者的随机临床试验中,D-青霉胺的疗效结果不一致。目的:系统评价D-青霉胺对原发性胆汁性肝硬化患者的利弊。方法:我们对随机临床试验的荟萃分析进行了系统评价,以评估D-青霉胺对原发性胆汁性肝硬化的影响。主要结果是死亡率和死亡率或肝移植。我们通过固定效应和随机效应模型分析了数据。结果:分析了7项随机试验,包括706例患者。 d-青霉素胺对死亡率(RR 1.08,95%CI:0.82-1.43,P = 0.56),死亡率或肝移植(RR 1.11,95%CI:0.74-1.68,P = 0.62),瘙痒,肝无明显影响并发症,肝脏组织学阶段进展和肝脏生化变量。 D--青霉素胺显着降低血清丙氨酸转氨酶活性(加权平均差异-45 IU / L,95%CI:-75至-15,P <0.05),并导致更多的不良事件(RR 4.18,95%CI:1.38) -12.69,P = 0.01)。结论:D-青霉胺似乎并未降低原发性胆汁性肝硬化患者的死亡或发病风险,并导致更多的不良事件。

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