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首页> 外文期刊>Mediterranean Journal of Hematology and Infectious Diseases >DIRECT ACTING ANTIVIRAL TREATMENT FOR PATIENTS WITH END STAGE KIDNEY DISEASE WITH ACUTE HCV INFECTION
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DIRECT ACTING ANTIVIRAL TREATMENT FOR PATIENTS WITH END STAGE KIDNEY DISEASE WITH ACUTE HCV INFECTION

机译:急性HCV感染终末期肾脏疾病的患者直接进行抗病毒治疗

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Background: Hepatitis C virus (HCV) infection is a public health problem. Such an infection is prevalent and aggressive in patients with end-stage kidney disease (ESKD). The efficacy and the safety of direct acting antivirus (DAA) in patients with acute HCV and ESKD is under investigation. The aim of this study was to assess the safety and efficacy of sofosbuvir containing regimens in this difficult-to-treat population. Methods: A prospective and observational study was conducted to evaluate the efficacy and the safety of sofosbuvir containing regimen in patient with ESKD who were undergoing haemodialysis and were acutely infected with HCV. Subjects either received sofosbuvir 200 mg and daclatasvir 60 mg daily or sofosbuvir 400mg/ledipasvir 60mg daily for 12 weeks. Results: 19 Patients were recruited in this study who were infected with HCV genotype 1a. All subjects achieved sustained virologic response (SVR) twelve weeks after finishing the treatment course. No major adverse effects were reported and the treatment course was well tolerated. Conclusions: sofosbuvir containing regimens were effective and safe for the treatment of acute HCV in patients with ESKD who were on haemodialysis.
机译:背景:丙型肝炎病毒(HCV)感染是一个公共卫生问题。这种感染在患有终末期肾脏病(ESKD)的患者中普遍存在并且具有侵略性。正在研究直接作用抗病毒药物(DAA)在急性HCV和ESKD患者中的疗效和安全性。这项研究的目的是评估在这种难以治疗的人群中含索非布韦的方案的安全性和有效性。方法:进行一项前瞻性和观察性研究,以评估含索非布韦的方案在接受血液透析并急性感染HCV的ESKD患者中的疗效和安全性。受试者接受每天200 mg的索非布韦和60 mg的达卡他韦或每天索非布韦400mg / ledipasvir 60mg的治疗,持续12周。结果:本研究招募了19位感染了HCV基因型1a的患者。在完成治疗过程后十二周,所有受试者均达到了持续的病毒学应答(SVR)。没有重大不良反应的报道,并且治疗过程耐受良好。结论:含索非布韦的方案对于接受血液透析的ESKD患者,治疗急性HCV安全有效。

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