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首页> 外文期刊>Digestive Diseases and Sciences >Treatment of genotype 4 hepatitis C recurring after liver transplantation using a combination of pegylated interferon alfa-2a and ribavirin.
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Treatment of genotype 4 hepatitis C recurring after liver transplantation using a combination of pegylated interferon alfa-2a and ribavirin.

机译:使用聚乙二醇化干扰素α-2a和利巴韦林联合治疗肝移植后复发的基因型4型丙型肝炎。

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摘要

BACKGROUND: Hepatitis C virus (HCV) recurrence after liver transplantation (LT) is universal and tends to be more aggressive. Data on post-transplant HCV genotype 4 treatment is scarce. The aim of this study is to assess the safety and efficacy of pegylated interferon alpha-2a (PEG-IFN) in combination with ribavirin in the treatment of recurrent HCV genotype 4 after LT. METHODS: Twenty-five patients infected with HCV genotype 4 were treated with PEG-IFN alpha-2a at a dose of 180 mug/week in addition to 800 mg/day of ribavirin (the dose was adjusted within the tolerated range of 400-1,200 mg). Pretreatment liver biopsies were obtained from all patients. Biochemical and virological markers were assessed before, during, and after treatment. RESULTS: Twenty-two patients (88%) achieved an early virological response (EVR) (12 patients tested negative for HCV-RNA). Fifteen (60%) and 14 patients (56%) achieved an end of treatment virological response (ETVR) and a sustained virological response (SVR), respectively. Five patients had advanced pretreatment liver fibrosis. Pretreatment ALT was elevated in 24 patients (96%). The most common adverse effects were flu-like symptoms and cytopenia. Eighteen patients (72%) required erythropoietin alpha and/or granulocyte-colony stimulating factor as a supportive measure. One patient developed severe rejection complicated by sepsis, renal failure, and death. Other adverse effects included depression, mild rejection, impotence, itching, and vitiligo. CONCLUSIONS: Post-transplant treatment with pegylated interferon alpha-2a and ribavirin achieved SVR in 56% of liver transplant recipients with chronic HCV genotype 4 infection. The combination was relatively safe and exhibited a low rate of treatment withdrawal.
机译:背景:肝移植(LT)后的丙型肝炎病毒(HCV)复发是普遍的,并且往往更具侵略性。移植后HCV基因型4治疗的数据很少。这项研究的目的是评估聚乙二醇化干扰素α-2a(PEG-IFN)与利巴韦林联合治疗LT后复发性HCV基因型4的安全性和有效性。方法:除800 mg /天的利巴韦林外,还以180杯/周的剂量用PEG-IFNα-2a治疗25名感染了HCV基因型4的患者(每天的剂量在400-1,200的容许范围内调整)毫克)。从所有患者获得治疗前肝活检。在治疗之前,期间和之后评估生化和病毒学标记。结果:22例患者(88%)达到了早期病毒学应答(EVR)(12例HCV-RNA阴性)。分别有15例(60%)和14例患者(56%)达到了治疗病毒学应答(ETVR)和持续病毒学应答(SVR)。五例患者进行了晚期肝纤维化治疗。治疗前的ALT升高了24例(96%)。最常见的不良反应是流感样症状和血细胞减少症。 18名患者(72%)需要促红细胞生成素α和/或粒细胞集落刺激因子作为支持措施。一名患者出现严重排斥反应,并伴有败血症,肾衰竭和死亡。其他不良反应包括抑郁,轻度排斥,阳ot,瘙痒和白癜风。结论:聚乙二醇干扰素α-2a和利巴韦林的移植后治疗在56%的慢性HCV基因型4感染的肝移植受者中实现了SVR。该组合相对安全,并且撤药率低。

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