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丙型肝炎的治疗与管理。

Hepatitis C treatment & management.

作者信息

Andronescu D, Diaconu S, Tiuca N, Purcarea R M, Andronescu C I

机构信息

"Carol Davila" University of Medicine and Pharmacy, Gastroenterology Department, Emergency University Hospital, Bucharest.

"Carol Davila" University of Medicine and Pharmacy, "Dr. Carol Davila" Clinical Nephrology Hospital, Bucharest, Romania.

出版信息

J Med Life. 2014 Mar 15;7(1):31-6. Epub 2014 Mar 25.

PMID:24653754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3956092/
Abstract

Combination therapy with pegylated interferon alfa (PEG-IFN alfa) and the nucleoside analogue ribavirin is the current standard of care in patients infected with hepatitis C virus (HCV). Patients with HCV genotype 1 have a much less favorable response to therapy and are treated for 12 months, compared with patients infected with genotypes 2 and 3, in whom a 6-month course of therapy is sufficient. If viremia is present after 6 months, additional therapy has a negligible benefit, and treatment should be stopped in all patients regardless of the viral genotype. With HIV coinfection, all patients with a response to therapy at the end of 6 months should receive an additional 6 months of combination therapy regardless of the genotype. Patients with acute HCV infection should be treated for 6 months. The addition of protease inhibitors to the combination of PEG-IFN alfa and ribavirin is becoming the new standard of care for the treatment of chronic HCV infection. Regimens that include a protease inhibitor significantly improve sustained virologic response rates in patients with genotype 1 HCV infection.

摘要

聚乙二醇化干扰素α(PEG-IFNα)与核苷类似物利巴韦林联合治疗是目前丙型肝炎病毒(HCV)感染患者的标准治疗方案。与感染2型和3型HCV的患者相比,感染1型HCV的患者对治疗的反应较差,需接受12个月的治疗,而感染2型和3型HCV的患者6个月的疗程就足够了。如果6个月后仍存在病毒血症,额外治疗的获益微乎其微,所有患者均应停止治疗,无论病毒基因型如何。对于合并HIV感染的患者,所有在6个月末对治疗有反应的患者均应再接受6个月的联合治疗,无论基因型如何。急性HCV感染患者应接受6个月的治疗。在PEG-IFNα和利巴韦林联合治疗中添加蛋白酶抑制剂正成为慢性HCV感染治疗的新标准。包含蛋白酶抑制剂的治疗方案可显著提高1型HCV感染患者的持续病毒学应答率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65fa/3956092/90ed1aaf060b/JMedLife-07-31-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65fa/3956092/2919a2428c81/JMedLife-07-31-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65fa/3956092/a5b03a8abad1/JMedLife-07-31-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65fa/3956092/90ed1aaf060b/JMedLife-07-31-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65fa/3956092/2919a2428c81/JMedLife-07-31-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65fa/3956092/a5b03a8abad1/JMedLife-07-31-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65fa/3956092/90ed1aaf060b/JMedLife-07-31-g003.jpg

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本文引用的文献

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Sofosbuvir for hepatitis C genotype 2 or 3 in patients without treatment options.索磷布韦用于无治疗选择的 2 或 3 型丙型肝炎病毒感染患者。
N Engl J Med. 2013 May 16;368(20):1867-77. doi: 10.1056/NEJMoa1214854. Epub 2013 Apr 23.
2
Benefits from sustained virologic response to pegylated interferon plus ribavirin in HIV/hepatitis C virus-coinfected patients with compensated cirrhosis.聚乙二醇干扰素联合利巴韦林治疗代偿期肝硬化的 HIV/丙型肝炎病毒合并感染患者持续病毒学应答的获益。
Clin Infect Dis. 2013 Jun;56(11):1646-53. doi: 10.1093/cid/cit103. Epub 2013 Feb 19.
3
Nucleotide polymerase inhibitor sofosbuvir plus ribavirin for hepatitis C.
核苷酸聚合酶抑制剂索非布韦联合利巴韦林治疗丙型肝炎。
N Engl J Med. 2013 Jan 3;368(1):34-44. doi: 10.1056/NEJMoa1208953.
4
Boceprevir with peginterferon alfa-2a-ribavirin is effective for previously treated chronic hepatitis C genotype 1 infection.博赛泼维与聚乙二醇干扰素 alfa-2a-利巴韦林联合治疗对于既往治疗的慢性丙型肝炎基因型 1 感染有效。
Clin Gastroenterol Hepatol. 2013 Jan;11(1):81-87.e4; quiz e5. doi: 10.1016/j.cgh.2012.10.006. Epub 2012 Oct 10.
5
Fatigue before, during and after antiviral therapy of chronic hepatitis C: results from the Virahep-C study.慢性丙型肝炎抗病毒治疗前后的疲劳:来自 Virahep-C 研究的结果。
J Hepatol. 2012 Nov;57(5):946-52. doi: 10.1016/j.jhep.2012.06.030. Epub 2012 Jul 1.
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Preliminary study of two antiviral agents for hepatitis C genotype 1.慢性丙型肝炎病毒感染的抗病毒治疗进展
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Telaprevir alone or with peginterferon and ribavirin reduces HCV RNA in patients with chronic genotype 2 but not genotype 3 infections.特拉匹韦单药或与聚乙二醇干扰素和利巴韦林联合治疗可降低慢性基因型 2 但不能降低基因型 3 感染患者的 HCV RNA。
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Gastroenterology. 2010 Jan;138(1):116-22. doi: 10.1053/j.gastro.2009.10.005. Epub 2009 Oct 20.