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利巴韦林单药治疗慢性丙型肝炎感染:Cochrane肝胆组对随机试验的系统评价和荟萃分析。

Ribavirin monotherapy for chronic hepatitis C infection: a Cochrane Hepato-Biliary Group systematic review and meta-analysis of randomized trials.

作者信息

Brok Jesper, Gluud Lise L, Gluud Christian

机构信息

The Cochrane Hepato-Biliary Group, Copenhagen Trial Unit, Center for Clinical Intervention Research, Copenhagen University Hospital, Denmark.

出版信息

Am J Gastroenterol. 2006 Apr;101(4):842-7. doi: 10.1111/j.1572-0241.2006.00505.x. Epub 2006 Feb 22.

Abstract

OBJECTIVES

Adding ribavirin to interferon improves treatment response for patients with chronic hepatitis C, but the effects of ribavirin monotherapy are unclear. We conducted a systematic review to assess the benefits and harms of ribavirin monotherapy for patients with chronic hepatitis C.

METHODS

Randomized trials were identified through the Cochrane Hepato-Biliary Group Controlled Trials Register, The Cochrane Library, MEDLINE, and EMBASE (last search May 2005). The primary outcomes were sustained virological response (loss of HCV RNA) and liver-related morbidity plus all-cause mortality. Secondary outcomes included end-of-treatment virological response, biochemical response (normalization of transaminases), histological response, and adverse events.

RESULTS

We included 11 randomized trials with 521 patients. Ten trials had unclear control of bias. Ribavirin had no significant effect on sustained (risk difference (RD), 0%; 95% confidence intervals (CI), -2% to 3%) or end-of-treatment virological response (RD, 0%; 95% CI, -3% to 3%). Ribavirin had no significant effect on liver-related morbidity plus mortality (RD, 0%; 95% CI, -2% to 3%). Ribavirin significantly improved histological response and end-of-treatment biochemical response, but not sustained biochemical response. Ribavirin significantly increased the risk of anemia and treatment discontinuation.

CONCLUSIONS

We found no evidence to support ribavirin monotherapy for patients with chronic hepatitis C, but trials were small and type II errors cannot be excluded. Patients intolerant to interferon should not continue treatment with ribavirin alone outside randomized trials.

摘要

目的

对于慢性丙型肝炎患者,在干扰素治疗中加用利巴韦林可改善治疗反应,但利巴韦林单药治疗的效果尚不清楚。我们进行了一项系统评价,以评估利巴韦林单药治疗慢性丙型肝炎患者的获益与危害。

方法

通过Cochrane肝胆疾病组对照试验注册库、Cochrane图书馆、MEDLINE和EMBASE(最后检索时间为2005年5月)识别随机试验。主要结局为持续病毒学应答(HCV RNA消失)以及肝脏相关发病率加全因死亡率。次要结局包括治疗结束时的病毒学应答、生化应答(转氨酶正常化)、组织学应答和不良事件。

结果

我们纳入了11项随机试验,共521例患者。10项试验的偏倚控制情况不明。利巴韦林对持续病毒学应答(风险差(RD),0%;95%置信区间(CI),-2%至3%)或治疗结束时的病毒学应答(RD,0%;95%CI,-3%至3%)无显著影响。利巴韦林对肝脏相关发病率加死亡率无显著影响(RD,0%;95%CI,-2%至3%)。利巴韦林显著改善了组织学应答和治疗结束时的生化应答,但未改善持续生化应答。利巴韦林显著增加了贫血和治疗中断的风险。

结论

我们没有发现证据支持对慢性丙型肝炎患者采用利巴韦林单药治疗,但试验规模较小,不能排除Ⅱ类错误。不耐受干扰素的患者不应在随机试验之外继续单独使用利巴韦林治疗。

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