直接抗病毒药物联合治疗慢性丙型肝炎病毒基因型感染血液透析患者的疗效观察

Tuba ERÜRKER ÖZTÜRK, Selim GÜREL, Ayşegül ORUÇ, Alparslan ERSOY
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 Material and Methods Twenty hemodialysis patients with chronic hepatitis C followed in the gastroenterology outpatient clinic between 2016 and 2018 were evaluated retrospectively.
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引用次数: 0

摘要

背景先前用于治疗慢性丙型肝炎病毒(HCV)感染的干扰素和利巴韦林治疗由于剂量调整和药物相关的副作用而不能有效地用于血液透析患者。据报道,直接作用抗病毒药物(DAAs)治疗对血液透析患者有效。本研究旨在评价DAAs在慢性丙型肝炎血液透析患者中的疗效。材料与方法回顾性分析2016 - 2018年消化科门诊血液透析合并慢性丙型肝炎患者20例。结果20例患者中男性12例,女性8例。患者平均年龄50.7±8.6岁。6例患者无治疗经验。14例患者先前曾接受干扰素和/或利巴韦林治疗,但未达到持续病毒学应答(SVR)。基因1b型14例,基因1a型4例,基因1型2例。患者接受ombitasvir/paritaprevir/利托那韦(OBV/PTV/r)和达沙布韦(DSV)或利巴韦林(RBV)治疗12周或24周。2例患者为肝硬化,Child-Pugh评分为a,其中2例患者在DAAs治疗的第一个月因动静脉瘘血栓形成而停止治疗。对18例患者中的14例进行了SVR12评估,发现其阳性率为100%。接受SVR24治疗的10例患者中有1例复发。SVR24的这一比例与普通人群相似。 结论OBV/PTV/r和DSV或RBV方案是一种安全有效的治疗慢性丙型肝炎病毒基因1型血液透析患者的方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The efficacy of the direct-acting antiviral combination in hemodialysis patients with chronic hepatitis C virus Genotype 1 infection
Background Interferon and ribavirin treatments previously used in treating chronic hepatitis C virus (HCV) infection cannot be used effectively in hemodialysis patients due to dose adjustment and drug-related side effects. Direct-acting antivirals (DAAs) therapies have been reported to be effective in hemodialysis patients. This study aimed to evaluate the effectiveness of DAAs in hemodialysis patients with chronic hepatitis C. Material and Methods Twenty hemodialysis patients with chronic hepatitis C followed in the gastroenterology outpatient clinic between 2016 and 2018 were evaluated retrospectively. Results Twelve of the 20 patients were male, and eight were female. The mean age of the patients was 50.7±8.6 years. Six patients had no treatment experience. Fourteen patients had been previously treated with interferon and/or ribavirin but did not achieve sustained virological response (SVR). Genotype 1b was detected in 14 patients, genotype 1a in 4 patients, and genotype 1 in 2 patients. Patients were treated with ombitasvir/paritaprevir/ritonavir (OBV/PTV/r) and dasabuvir (DSV) or ribavirin (RBV) for 12 or 24 weeks. Two patients were cirrhotic and had a Child-Pugh score of A. Treatment was discontinued in 2 patients due to thrombus formation in the arteriovenous fistula in the first month of DAAs treatment. SVR12 was evaluated in 14 of 18 patients and found to be 100%. One of the ten patients accepted as SVR24 had a relapse. This rate of SVR24 was similar to that in the general population. Conclusions Our results supported that the OBV/PTV/r and DSV or RBV regimen was a safe and effective therapy for hemodialysis patients with chronic hepatitis C virus genotype 1.
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