首页> 美国卫生研究院文献>Gastroenterology Research and Practice >The Comparative Efficacy and Safety of Entecavir and Lamivudine in Patients with HBV-Associated Acute-on-Chronic Liver Failure: A Systematic Review and Meta-Analysis
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The Comparative Efficacy and Safety of Entecavir and Lamivudine in Patients with HBV-Associated Acute-on-Chronic Liver Failure: A Systematic Review and Meta-Analysis

机译:恩替卡韦和拉米夫定在乙肝相关性慢性慢性肝衰竭患者中的​​比较疗效和安全性:系统评价和荟萃分析

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摘要

Background. Currently, both of entecavir and lamivudine are effective for patients with HBV-associated acute-on-chronic liver failure (ACLF). However, there is no consensus on the efficacy of entecavir versus lamivudine for patients with HBV-associated ACLF. The aim of the study was to compare the efficacy and safety of entecavir with that of lamivudine for HBV-associated ACLF patients. Methods. Publications on entecavir versus lamivudine in HBV-associated ACLF patients were comprehensively identified. Odds ratio and mean difference were used to measure the effect. Results. Ten studies, totaling 1254 patients, were eligible. No significant differences between the two drugs presented in the 1-, 2-, 3-, or 6-month survival rates. However, after 12 months of treatment, patients prescribed entecavir had a statistically higher survival rate (p = 0.008) and lower total bilirubin (p < 0.0001) and alanine aminotransferase (p = 0.04) levels compared to patients prescribed lamivudine. More patients achieved HBV negative levels when taking entecavir as measured at 1-, 3-, and 12-month time points and had a lower rate of HBV recurrence. Conclusion. While entecavir and lamivudine are both relatively safe and well tolerated, entecavir was more efficacious in terms of survival rate and clinical improvement in long-term treatment. Further prospective randomized controlled trials are needed to validate these results.
机译:背景。目前,恩替卡韦和拉米夫定对乙肝相关的慢性慢性肝衰竭(ACLF)患者均有效。然而,对于恩替卡韦和拉米夫定在HBV相关ACLF患者中的疗效尚无共识。该研究的目的是比较恩替卡韦和拉米夫定对HBV相关ACLF患者的疗效和安全性。方法。全面鉴定了恩替卡韦与拉米夫定在HBV相关ACLF患者中的出版物。使用赔率和平均差来衡量效果。结果。共有10项研究(共1254名患者)入选。两种药物在1、2、3或6个月的生存率方面无显着差异。但是,在治疗12个月后,与拉米夫定患者相比,开具恩替卡韦的患者在统计学上具有更高的存活率(p = 0.008),总胆红素(p <0.0001)和丙氨酸转氨酶(p = 0.04)水平。在1、3和12个月的时间点服用恩替卡韦时,有更多的患者达到HBV阴性水平,并且HBV复发率较低。结论。尽管恩替卡韦和拉米夫定相对安全且耐受性良好,但就长期治疗的存活率和临床改善而言,恩替卡韦更有效。需要进一步的前瞻性随机对照试验来验证这些结果。

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