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本文引用的文献

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Hepatology. 2020 Feb;71(2):686-721. doi: 10.1002/hep.31060.
2
Ledipasvir and sofosbuvir fixed-dose combination with and without ribavirin for 12 weeks in treatment-naive and previously treated Japanese patients with genotype 1 hepatitis C: an open-label, randomised, phase 3 trial.在未经治疗和先前经治的日本基因 1 型丙型肝炎患者中,使用利巴韦林联合或不联合利巴韦林的雷迪帕韦和索非布韦固定剂量复方制剂治疗 12 周:一项开放标签、随机、3 期临床试验。
Lancet Infect Dis. 2015 Jun;15(6):645-53. doi: 10.1016/S1473-3099(15)70099-X. Epub 2015 Apr 8.
3
Ledipasvir and sofosbuvir in patients with genotype 1 hepatitis C virus infection and compensated cirrhosis: An integrated safety and efficacy analysis.索磷布韦与利迪帕韦治疗基因 1 型丙型肝炎病毒感染合并代偿性肝硬化患者的安全性和疗效综合分析。
Hepatology. 2015 Jul;62(1):79-86. doi: 10.1002/hep.27826. Epub 2015 May 9.
4
Sofosbuvir for treatment of chronic hepatitis C.索磷布韦用于治疗慢性丙型肝炎。
Hepatol Int. 2015 Apr;9(2):161-73. doi: 10.1007/s12072-014-9606-9. Epub 2015 Jan 28.
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Treatment with ledipasvir and sofosbuvir improves patient-reported outcomes: Results from the ION-1, -2, and -3 clinical trials.用 ledipasvir 和 sofosbuvir 治疗可改善患者报告的结局:来自 ION-1、-2 和-3 临床试验的结果。
Hepatology. 2015 Jun;61(6):1798-808. doi: 10.1002/hep.27724. Epub 2015 Mar 18.
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Long-term effect of antiviral therapy on disease course after decompensation in patients with hepatitis B virus-related cirrhosis.抗病毒治疗对乙型肝炎病毒相关肝硬化失代偿后疾病进程的长期影响。
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Liver Int. 2015 Jan;35 Suppl 1:51-5. doi: 10.1111/liv.12721.
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Efficacy and safety of faldaprevir, deleobuvir, and ribavirin in treatment-naive patients with chronic hepatitis C virus infection and advanced liver fibrosis or cirrhosis.法达普韦、地洛布韦和利巴韦林用于初治慢性丙型肝炎病毒感染且伴有晚期肝纤维化或肝硬化患者的疗效与安全性。
Antimicrob Agents Chemother. 2015 Feb;59(2):1282-91. doi: 10.1128/AAC.04383-14. Epub 2014 Dec 15.

直接抗病毒药物治疗失代偿期丙型肝炎病毒诱导的肝硬化

Direct antiviral agent treatment of decompensated hepatitis C virus-induced liver cirrhosis.

作者信息

Ohkoshi Shogo, Hirono Haruka, Yamagiwa Satoshi

机构信息

Shogo Ohkoshi, Haruka Hirono, Department of Internal Medicine, School of Life Dentistry at Niigata, the Nippon Dental University, Niigata-city 951-8580, Japan.

出版信息

World J Gastrointest Pharmacol Ther. 2015 Nov 6;6(4):114-9. doi: 10.4292/wjgpt.v6.i4.114.

DOI:10.4292/wjgpt.v6.i4.114
PMID:26558145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4635151/
Abstract

Recently, direct antiviral agents (DAAs) have been increasingly used for the treatment of chronic hepatitis C virus (HCV) infections, replacing interferon-based regimens that have severe adverse effects and low tolerability. The constant supply of new DAAs makes shorter treatment periods with enhanced safety possible. The efficacy of DAAs for treatment of compensated liver cirrhosis (LC) is not less than that for treatment of non-cirrhotic conditions. These clinical advantages have been useful in pre- and post-liver transplantation (LT) settings. Moreover, DAAs can be used to treat decompensated HCV-induced LC in elderly patients or those with severe complications otherwise having poor prognosis. Although encouraging clinical data are beginning to appear, the actual efficacy of DAAs for suppressing disease progression, allowing delisting for LT and, most importantly, improving prognosis of patients with decompensated HCV-LC remains unknown. Case-control studies to examine the short- or long-term effects of DAAs for treatment of decompensated HCV-LC are urgently need.

摘要

近年来,直接抗病毒药物(DAAs)越来越多地用于治疗慢性丙型肝炎病毒(HCV)感染,取代了具有严重不良反应和低耐受性的基于干扰素的治疗方案。新DAAs的持续供应使得缩短治疗周期并提高安全性成为可能。DAAs治疗代偿期肝硬化(LC)的疗效不低于治疗非肝硬化情况的疗效。这些临床优势在肝移植(LT)前后的环境中很有用。此外,DAAs可用于治疗老年患者或有严重并发症、预后较差的失代偿性HCV诱导的LC。尽管令人鼓舞的临床数据开始出现,但DAAs在抑制疾病进展、允许LT除名以及最重要的是改善失代偿性HCV-LC患者预后方面的实际疗效仍然未知。迫切需要进行病例对照研究,以检验DAAs治疗失代偿性HCV-LC的短期或长期效果。