聚乙二醇干扰素α-2a联合利巴韦林治疗慢性丙型肝炎的临床观察
Clinical observation of pegylated interferon alpha-2a combined with ribavirin in the treatment of chronic hepatitis C
摘要目的 观察聚乙二醇干扰素α-2a联合利巴韦林治疗慢性丙型肝炎的疗效和安全性.方法 将60例慢性丙型肝炎患者随机分为两组,给予抗病毒治疗,实验组给予皮下注射聚乙二醇干扰素α-2a 180ug,每周1次;对照组给予皮下注射干扰素α-2b 5MIU,隔日一次,两组均按体重同时服用联合利巴韦林900 ~ 1200mg,每天一次,疗程48周.分别在治疗前、治疗第4周、12周、24周、治疗结束时、治疗结束后24周测定患者血清HCV-RNA水平,同时观察不良反应.结果 实验组的快速病毒学应答率(RVR)为65.6%,完全早期病毒学应答率(cEVR)为81.2%,治疗结束应答率(ETVR)为90.6%,治疗结束后随访24周持续应答率(SVR)为84.4%,明显优于对照组.结论 聚乙二醇干扰素α-2a联合利巴韦林治疗慢性丙型肝炎具有良好的抗病毒疗效,安全性较好.
更多相关知识
abstractsObjective To observe the efficacy and safety of pegylated interferon alpha-2a combined with ribavirin in the treatment of chronic hepatitis C.Methods Sixty patients with chronic hepatitis C were divided into 2 groups randomly.The observation group was treated with pegylated interferon alpha-2a,and the control group was treated with interferon alpha-2b.All patients were given ribavirin according to the weight,and the treatment course was 48 weeks.HCV-RNA was tested before treatment,4 weeks,12weeks and 24 weeks after the start of treatment,end of treatment,24 weeks after the end of treatment.The adverse reactions were also observed.Results In the observation group,the rapid virological response (RVR) was 65.6%,the complete early virological response (cEVR) was 81.2%,the end treatment virological response (ETVR) was 90.6%,the sustained virological response (SVR) of 24 weeks after the end of treatment was 84.4%,and these rates were significantly higher than the control group.All patients received the whole course of treatment.Conclusions Treatment of chronic hepatitis C with pegylated interferon alpha-2a combined ribavirin was effective and safe.
More相关知识
- 浏览290
- 被引15
- 下载20

相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文