实用肝脏病杂志 ›› 2015, Vol. 18 ›› Issue (5): 496-499.doi: 10.3969/j.issn.1672-5069.2015.05.012

• 乙型和丙型肝炎 • 上一篇    下一篇

不同抗病毒治疗方案治疗慢性丙型肝炎患者疗效分析

关翠英,阿娜尔古丽?穆哈买尔,王亚楠,葛力菲,郭宇   

  1. 835000新疆维吾尔自治区伊犁市 伊犁州友谊医院感染内科
  • 收稿日期:2015-01-10 出版日期:2015-09-10 发布日期:2016-02-18
  • 作者简介:关翠英,女,50岁,副主任医师 Email:duy172@163.com

Antiviral strategies of standardized regimen in patients with chronic hepatitis C

Guan Cuiying, Anaerguli Muhamaier,Wang Yanan,et al.   

  1. Department of Infectious Diseases,Friendship Hospital,Yili City 835000,Xinjiang Uygur Autonomous Region,China
  • Received:2015-01-10 Online:2015-09-10 Published:2016-02-18

摘要: 目的 观察慢性丙型肝炎患者个体化抗病毒治疗方案的疗效。方法 选取我院2008年1月至2013年1月收治的179例慢性丙型肝炎患者,根据患者年龄、体质量、血清HCV载量和HCV基因型的不同,选择不同类型和不同剂量的干扰素联合利巴韦林治疗方案。在179例患者中,65例患者接受聚乙二醇干扰素α-2a(PegIFN α)治疗,114例接受普通干扰素(IFN α-1b)治疗。治疗48 w,随访24 w。比较两组在不同干扰素剂量、病毒载量和不同病毒基因型患者病毒学应答率的差异。结果 在随访时,65例接受PegIFN α治疗的慢性丙型肝炎患者快速病毒学应答率(RVR)、早期病毒学应答率(EVR)和持续病毒学应答率(SVR)分别为47.7%、92.3%、93.8%,与普通干扰素1b组的58.8%、76.3%、80.7%比较,差异有统计学意义(P<0.05); 43例接受常规剂量PegIFN α-2a治疗的患者RVR、EVR和SVR分别为46.5%、97.7%和100.0%,与22例接受小剂量组的50.0%、81.8%和81.8%比,无显著性统计学差异(P>0.05);69例接受常规剂量普通干扰素治疗的患者RVR、EVR和SVR分别为60.9%、76.8%和82.6%,与45例接受小剂量组的55.6%、75.6%和77.8%比,无显著性统计学差异(P>0.05);14例接受PegIFN α-2a治疗的血清病毒低载量患者RVR、EVR和SVR分别为64.3%、85.7%和85.7%,与51例高病毒载量组的43.1%、94.1%和96.1%比,无显著性统计学差异(P>0.05);24例接受普通干扰素治疗的血清低病毒载量患者的RVR、EVR和SVR分别为54.2%、66.7%和70.8%,与90例高病毒载量组的60.0%、78.9%和81.1%比,无显著性统计学差异(P>0.05);41例接受PegIFN α-2a治疗的基因1型患者的RVR、EVR和SVR分别为31.7%、97.6%和97.6%,与24例非基因1型患者的75.0%、87.5%和87.5%存在显著性统计学差异(P<0.05);81例接受普通干扰素治疗的基因1型患者的RVR、EVR和SVR分别为46.9%、82.7%和87.6%,与33例非基因1型的66.7%(P<0.05)、75.7%(P>0.05)和78.8%(P>0.05)也存在差异。结论 根据CHC患者的基线特征、耐受性、HCV基因型及病毒学应答出现的时间优化抗病毒治疗方案,有利于个体化治疗,以获得较高的病毒学应答率,改善预后。

关键词: 慢性丙型肝炎, 聚乙二醇干扰素α-2a, 利巴韦林, 病毒载量, 基因型

Abstract: Objective To observe the efficacy of individualized treatment strategy in patients with chronic hepatitis C. Methods A total of 179 patients with chronic hepatitis C were recruited in this study. 65 received pegylated interferon α-2a (PegIFN α) and ribavirin,and 114 received IFN α-1b. All patients were treated for 48 weeks and followed-up for 24 weeks. According to the patient's age,body weight,serum HCV load and HCV genotype,the dose of interferon was modulated. Results At the end of follow-up,rates of rapid virologic response (RVR),early virologic response(EVR) and sustained virologic response in 65 patients receiving pegIFN α were 47.7%,92.3%,93.8%,much higher than those in IFN α-1b-treated patients (58.8%,76.3%,80.7%, respectively,P<0.05);the RVR,EVR and SVR in 43 patients receiving normal doses of pegIFN α-2 were 46.5%,97.7% and 100.0%,without significant difference as compared to 50.0%,81.8% and 81.8% in 22 patients with decreased dose of pegIFN α-2(P>0.05);the RVR,EVR and SVR in 69 patients receiving normal dose of IFN α1b were 60.9%,76.8% and 82.6%,without significant difference compared to 55.6%,75.6% and 77.8% in 45 patients receiving decreased dose of IFN α1b(P>0.05);the RVR,EVR and SVR in 14 patients with low viral load receiving pegIFN α-2a were 64.3%,85.7% and 85.7%,without significant difference compared to 43.1%,94.1% and 96.1% in 51 patients with high viral load(P>0.05);the RVR,EVR and SVR in 24 patients with low viral load receiving IFN α1b were 54.2%,66.7% and 70.8%,without significant difference compared to 60.0%,78.9% and 81.1% in 90 patients with high viral load(P>0.05);the RVR,EVR and SVR in 41 patients with hepatitis C viral genotype 1 infection receiving pegIFN α-2a were 31.7%,97.6% and 97.6%,significantly different with 75.0%,87.5% and 87.5% in 24 patients with non-genotype 1 infection(P<0.05);the RVR,EVR and SVR in 81 patients with genotype 1 infection receiving IFN α1b were 46.9%,82.7% and 87.6%,significantly different with 66.7%(P<0.05),75.7%(P>0.05) and 78.8% (P>0.05) in 33 with non-genotype 1 infection. Conclusion According to baseline characteristics,tolerability and HCV genotype,the standardized antiviral regimen should be optimized, which might get a higher virologic response and improve the prognosis of patients with chronic hepatitis C.

Key words: Hepatitis C, Pegylated interferon α-2a, Ribavirin, Viral load, Genotype