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Corrigendum to 'EASL recommendations on treatment of hepatitis C: Final update of the series [J Hepatol 73 (2020) 1170-1218].《欧洲肝脏研究学会丙型肝炎治疗推荐:系列最终更新版》勘误 [《肝脏病学杂志》73卷(2020年)1170 - 1218页]
J Hepatol. 2023 Feb;78(2):452. doi: 10.1016/j.jhep.2022.10.006. Epub 2022 Dec 1.
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One-Year Outcomes of the Multi-Center StudY to Transplant Hepatitis C-InfeCted kidneys (MYTHIC) Trial.多中心丙型肝炎感染肾脏移植研究(MYTHIC)试验的一年期结果。
Kidney Int Rep. 2021 Dec 1;7(2):241-250. doi: 10.1016/j.ekir.2021.11.022. eCollection 2022 Feb.
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Trends of treated hepatitis B, hepatitis C, and tuberculosis infection in long-term hemodialysis patients in Taiwan: A nationwide survey in 2010-2018.台湾地区长期血液透析患者乙型肝炎、丙型肝炎和结核病感染治疗趋势:2010-2018 年全国性调查。
J Formos Med Assoc. 2022 Feb;121 Suppl 1:S73-S81. doi: 10.1016/j.jfma.2021.12.019. Epub 2022 Jan 5.
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Hepatitis C virus reinfection in patients on haemodialysis after achieving sustained virologic response with antiviral treatment.接受抗病毒治疗实现持续病毒学应答后行血液透析患者丙型肝炎病毒再感染。
Aliment Pharmacol Ther. 2022 Feb;55(4):434-445. doi: 10.1111/apt.16697. Epub 2021 Nov 13.
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Sofosbuvir/Velpatasvir Prophylaxis for 12 Weeks in Hepatitis C Virus (HCV)-Negative Recipients Receiving Kidney Transplantation from HCV-Positive Donors.索磷布韦/维帕他韦预防方案用于接受 HCV 阳性供者肾移植的 HCV 阴性受者 12 周。
Ann Transplant. 2021 Sep 7;26:e933313. doi: 10.12659/AOT.933313.
6
Sofosbuvir plus velpatasvir combination for the treatment of chronic hepatitis C in patients with end stage renal disease on renal replacement therapy: A systematic review and meta-analysis.索磷布韦联合维帕他韦治疗接受肾脏替代治疗的终末期肾病患者慢性丙型肝炎病毒感染:系统评价和荟萃分析。
Nephrology (Carlton). 2022 Jan;27(1):82-89. doi: 10.1111/nep.13968. Epub 2021 Sep 14.
7
Renal function trajectories in hepatitis C infection: differences between renal healthy and chronic kidney disease individuals.丙型肝炎感染中的肾功能轨迹:肾功能正常者和慢性肾脏病患者之间的差异。
Sci Rep. 2021 Aug 25;11(1):17197. doi: 10.1038/s41598-021-96782-x.
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Outcomes of short-duration antiviral prophylaxis for hepatitis C positive donor kidney transplants.丙型肝炎阳性供肾移植的短期抗病毒预防的结果。
Am J Transplant. 2021 Nov;21(11):3734-3742. doi: 10.1111/ajt.16747. Epub 2021 Jul 26.
9
Elimination of Hepatitis C Virus in a Dialysis Population: A Collaborative Care Model in Taiwan.台湾透析人群丙型肝炎病毒的清除:一种协作护理模式
Am J Kidney Dis. 2021 Oct;78(4):511-519.e1. doi: 10.1053/j.ajkd.2021.03.017. Epub 2021 May 1.
10
Extrahepatic Manifestations of Chronic HCV Infection.慢性丙型肝炎病毒感染的肝外表现
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泛基因型直接作用抗病毒药物治疗慢性肾脏病 4 或 5 期合并丙型肝炎病毒感染患者。

Pan-genotypic direct-acting antivirals for patients with hepatitis C virus infection and chronic kidney disease stage 4 or 5.

机构信息

Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.

Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan.

出版信息

Hepatol Int. 2022 Oct;16(5):1001-1019. doi: 10.1007/s12072-022-10390-z. Epub 2022 Jul 25.

DOI:10.1007/s12072-022-10390-z
PMID:35876967
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9309604/
Abstract

Hepatitis C virus (HCV) infection is a major health problem with significant clinical and economic burdens in patients with chronic kidney disease (CKD) stage 4 or 5. Current guidelines recommend pan-genotypic direct-acting antivirals (DAAs) to be the first-line treatment of choice for HCV. This review summarizes the updated knowledge regarding the epidemiology, natural history, public health perspectives of HCV in patients with CKD stage 4 or 5, including those on maintenance dialysis, and the performance of pan-genotypic DAAs in these patients. The prevalence and incidence of HCV are much higher in patients with CKD stage 4 or 5 than in the general population. The prognosis is compromised if HCV patients are left untreated regardless of kidney transplantation (KT). Following treatment-induced HCV eradication, patient can improve the health-related outcomes by maintaining a long-term aviremic state. The sustained virologic response (SVR) rates and safety profiles of pan-genotypic DAAs against HCV are excellent irrespective of KT. No dose adjustment of pan-genotypic DAAs is required across CKD stages. Assessing drug-drug interactions (DDIs) before HCV treatment is vital to secure on-treatment safety. The use of prophylactic or preemptive pan-genotypic DAAs in HCV-negative recipients who receive HCV-positive kidneys has shown promise in shortening KT waiting time, achieving excellent on-treatment efficacy and safety, and maintaining post-KT patient and graft survival. HCV elimination is highly feasible through multifaceted interventions, including mass screening, treatment scale-up, universal precautions, and post-SVR reinfection surveillance.

摘要

丙型肝炎病毒(HCV)感染是一个重大的健康问题,在慢性肾脏病(CKD)4 或 5 期患者中具有显著的临床和经济负担。目前的指南建议泛基因型直接作用抗病毒药物(DAA)作为 HCV 的一线治疗选择。这篇综述总结了有关 CKD 4 或 5 期患者(包括维持性透析患者)中 HCV 的流行病学、自然史、公共卫生观点以及泛基因型 DAA 在这些患者中的应用的最新知识。HCV 在 CKD 4 或 5 期患者中的流行率和发病率远高于普通人群。如果不进行治疗,无论是否进行肾移植(KT),HCV 患者的预后都会受到影响。在治疗诱导的 HCV 清除后,患者可以通过维持长期无病毒血症状态来改善与健康相关的结局。泛基因型 DAA 治疗 HCV 的持续病毒学应答(SVR)率和安全性无论 KT 情况如何都非常出色。在 CKD 各阶段均无需调整泛基因型 DAA 的剂量。在 HCV 治疗前评估药物相互作用(DDI)对于确保治疗期间的安全性至关重要。在接受 HCV 阳性供肾的 HCV 阴性受者中预防性或抢先使用泛基因型 DAA 已显示出缩短 KT 等待时间、实现优异的治疗效果和安全性以及维持术后患者和移植物存活率的潜力。通过多方面的干预措施,包括大规模筛查、治疗扩大、普遍预防和 SVR 后再感染监测,HCV 的消除是高度可行的。