首页> 外文期刊>Hepatology research: the official journal of the Japan Society of Hepatology >Efficacy of ribavirin monotherapy following combination therapy with interferon alfa-2b and ribavirin for patients with chronic hepatitis C.
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Efficacy of ribavirin monotherapy following combination therapy with interferon alfa-2b and ribavirin for patients with chronic hepatitis C.

机译:干扰素α-2b和利巴韦林联合治疗后利巴韦林单药治疗慢性丙型肝炎的疗效。

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摘要

Reappearance of HCV-RNA followed by exacerbation of biochemical parameters after combination therapy consisting of interferon and ribavirin is an obstacle to achieve sustained response and improve long-term prognosis. We hypothesed that ribavirin monotherapy after 6 months of combination therapy may improve sustained viral and biochemical responses, and conducted a prospective, randomized and controlled study. Thirty-eight patients with chronic hepatitis C treated with combination therapy for 6 months and had no detectable serum HCV-RNA were enrolled, and allocated into two arms. Group I (n=19) was continuously administered oral ribavirin for additional 6 months, and group II (n=19) was followed up without any further treatment. At the end of trial, HCV-RNA negativity was 11/19 (58%) in group I, and 6/19 (32%) in group II (p=0.191). Multivariant analysis demonstrated that ribavirin monotherapy was not a predictor for the eradication of HCV-RNA. In cases without sustained viral responses, serum ALT levels at baseline and the end of 48 weeks' trial were 54.6 and 44.4 in group I (p=0.237), and significant reduction with ribavirin monotherapy was not observed. In conclusion, ribavirin monotherapy following combination therapy fails to improve sustained viral response as well as biochemical response.
机译:在由干扰素和利巴韦林组成的联合治疗后,HCV-RNA的重新出现以及随后生化指标的恶化是实现持续应答和改善长期预后的障碍。我们假设利巴韦林单药联合治疗6个月后可改善持续的病毒和生化反应,并进行了一项前瞻性,随机和对照研究。纳入38例接受联合治疗6个月且无可检测血清HCV-RNA的慢性丙型肝炎患者,分为两组。 I组(n = 19)连续口服利巴韦林另外6个月,而II组(n = 19)得到随访,无需任何进一步治疗。在试验结束时,I组的HCV-RNA阴性为11/19(58%),II组的为6/19(32%)(p = 0.191)。多变量分析表明,利巴韦林单一疗法不是根除HCV-RNA的预测因子。在没有持续病毒反应的情况下,I组在基线和48周试验结束时的血清ALT水平分别为54.6和44.4(p = 0.237),并且未观察到利巴韦林单药治疗显着降低。总之,联合治疗后的利巴韦林单药治疗不能改善持续的病毒反应以及生化反应。

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