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达卡他韦-阿舒瑞韦联合疗法治疗血液透析的慢性丙型肝炎病毒1b型感染患者的疗效与安全性

Effect and Safety of Daclatasvir-Asunaprevir Combination Therapy for Chronic Hepatitis C Virus Genotype 1b -Infected Patients on Hemodialysis.

作者信息

Miyazaki Ryoichi, Miyagi Kyoko

机构信息

Fujita Memorial Hospital, Internal Medicine, Fukui, Japan.

出版信息

Ther Apher Dial. 2016 Oct;20(5):462-467. doi: 10.1111/1744-9987.12407. Epub 2016 Apr 21.

Abstract

The prevalence of anti-hepatitis C virus (HCV)antibodies is higher in hemodialysis patients than in the general population, and several studies have reported poor vital prognosis in HCV-infected dialysis patients because infection with HCV is not only the cause of cirrhosis and hepatocellular carcinoma, but also a risk factor for cardiovascular disease. Although sustained virologic response (SVR) is achievable with interferon and ribavirin in dialysis patients, SVR rates are lower, and the use of ribavirin is challenging because of the risk of hemolytic anemia. Recently, interferon-ribavirin free direct acting antivirals (DAAs) treatment has shown strong efficacy and fewer adverse events for chronic HCV infection patients without using dialysis, but there are few reports about DAAs for such patients. Thus, we conducted a study to examine the effect and safety of daclatasvir and asunaprevir in chronic hepatitis C virus genotype 1b-infected hemodialysis patients. We treated 10 patients: seven males and three females. Before treatment, we detected resistance-associated variants on the NS5A region, which is the L31M site variant, in two patients. Although two patients showed resistance-associated variant, all the patients showed quick disappearance of HCV RNA in the serum and achieved a SVR12. During this therapy, no patients displayed abnormal liver function during treatment. Two patients experienced diarrhea and another one patient complained of nausea soon after treatment but these were relieved by symptomatic therapy. We report good results of treatment for chronic hepatitis C virus genotype 1b -infected patients on hemodialysis with all oral DAAs (daclatasvir and asunaprevir).

摘要

血液透析患者中抗丙型肝炎病毒(HCV)抗体的流行率高于普通人群,多项研究报告称,HCV感染的透析患者的生命预后较差,因为感染HCV不仅是肝硬化和肝细胞癌的病因,也是心血管疾病的危险因素。虽然透析患者使用干扰素和利巴韦林可实现持续病毒学应答(SVR),但SVR率较低,且由于存在溶血性贫血风险,使用利巴韦林具有挑战性。最近,不含干扰素 - 利巴韦林的直接作用抗病毒药物(DAA)治疗已显示出对未接受透析的慢性HCV感染患者具有强效且不良事件较少,但关于此类患者使用DAA的报道很少。因此,我们进行了一项研究,以检查达拉他韦和阿舒瑞韦在慢性丙型肝炎病毒1b型感染的血液透析患者中的疗效和安全性。我们治疗了10名患者:7名男性和3名女性。治疗前,我们在两名患者的NS5A区域检测到与耐药相关的变异,即L31M位点变异。虽然两名患者显示出与耐药相关的变异,但所有患者血清中的HCV RNA均迅速消失,并实现了SVR12。在该治疗过程中,没有患者在治疗期间出现肝功能异常。两名患者出现腹泻,另一名患者在治疗后不久抱怨恶心,但通过对症治疗得到缓解。我们报告了使用全口服DAA(达拉他韦和阿舒瑞韦)治疗慢性丙型肝炎病毒1b型感染的血液透析患者的良好结果。

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