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Treatment of acute HCV infection in HIV-positive patients: experience from a multicentre European cohort.

机译:HIV阳性患者急性HCV感染的治疗:来自多中心欧洲队列的经验。

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BACKGROUND: Early treatment of acute HCV infection has been shown to improve virological response rates in HIV-positive patients; however, details on when and how to best treat acute HCV infection remain unclear at present. METHODS: In this European multicentre cohort study, HIV-positive patients with acute HCV infection were offered immediate or delayed anti-HCV therapy, pegylated interferon or pegylated interferon plus ribavirin combination therapy for 24 or 48 weeks, depending on the local protocol. The main outcome measure was the rate of sustained virological response (SVR). RESULTS: A total of 150 HIV-infected men with acute HCV were enrolled between 2001 and 2006, 111 of whom received anti-HCV therapy. The predominant HCV genotype was type 1 and was present in 71 (64%) patients. Patients were treated with pegylated interferon (n=14) or pegylated interferon plus ribavirin (n=97), with a median duration of treatment of 25 weeks. SVR was obtained in 62% (95% confidence interval 52-71) of patients. There was no difference in SVR by genotype, CD4(+) T-cell count, HIV RNA, HCV RNA, alanine aminotransferase levels or use of ribavirin. Negative HCV RNA at weeks 4 and 12 were strong predictors of SVR. CONCLUSIONS: High rates of SVR (62%) were obtained in HIV-coinfected patients with acute HCV infection undergoing early anti-HCV treatment using pegylated interferon alone or in combination with ribavirin. Treatment response at weeks 4 and 12 might be of help to further guide treatment duration. Urgent prospective studies are needed to further determine the optimal treatment regimen and the duration of therapy.
机译:背景:急性HCV感染的早期治疗已显示可提高HIV阳性患者的病毒学应答率。然而,目前尚不清楚何时以及如何最好地治疗急性HCV感染的细节。方法:在这项欧洲多中心队列研究中,根据当地方案,立即或延迟抗HCV治疗,聚乙二醇干扰素或聚乙二醇干扰素加利巴韦林联合治疗的HIV阳性患者应接受立即或延迟的抗HCV治疗,疗程为24或48周。主要结局指标是持续病毒学应答率(SVR)。结果:2001年至2006年间,共有150例HIV感染的急性HCV男性入组,其中111例接受了抗HCV治疗。 HCV的主要基因型是1型,存在于71名(64%)患者中。患者接受了聚乙二醇干扰素(n = 14)或聚乙二醇干扰素加利巴韦林(n = 97)的治疗,中位治疗时间为25周。在62%(95%置信区间52-71)的患者中获得了SVR。 SVR在基因型,CD4(+)T细胞计数,HIV RNA,HCV RNA,丙氨酸氨基转移酶水平或利巴韦林的使用方面无差异。第4周和第12周的HCV RNA阴性是SVR的强预测指标。结论:单独使用聚乙二醇干扰素或与利巴韦林联用,HIV感染的急性HCV感染患者接受早期抗HCV治疗后,获得高SVR率(62%)。第4周和第12周的治疗反应可能有助于进一步指导治疗时间。需要紧急的前瞻性研究来进一步确定最佳治疗方案和治疗持续时间。

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