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Pegylated interferon plus ribavirin combination therapy for chronic hepatitis C in patients with congenital coagulation disorders.

机译:聚乙二醇干扰素加利巴韦林联合治疗先天性凝血功能异常的慢性丙型肝炎。

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Chronic hepatitis C (CHC) and end-stage liver disease are becoming an increasingly common cause of mortality in patients with congenital bleeding disorders, especially in the HIV-coinfected group. Combination of pegylated interferon (Peg-IFN) and ribavirin has recently become the treatment of choice for CHC. In this study, we evaluated the safety and efficacy of combination therapy with Peg-IFN plus ribavirin for the treatment of CHC in human immunodeficiency virus (HIV)- and HIV+ patients with congenital bleeding disorders. Between 2000 and 2004, 50 (18-68 years old) patients with CHC (19 HIV+) from two hemophilia centers were included in the study. They were treated with weekly subcutaneous administration of Peg-INF-alpha combined with 800-1,200 mg ribavirin daily, for 24-48 weeks depending on viral genotype. Response was evaluated at weeks 12, 24, 48 (end of treatment response) and 72 had sustained virological response). Overall, 22/50 patients (43.8%) had end of treatment response and 20/50 (40%) sustained virological response. HIV- patients responded similarly to the general population (58.1%), while HIV+ patients had very low response rates (10.5%). The high rate of discontinuation (36.9%) as a result of side effects contributed to the observed low response rate in the HIV+ group. The only factor strongly associated with sustained virological response in the HIV- patients was the reduction of HCV RNA at 12 weeks (p = 0.001). Patients with viral genotypes other than 1 had higher SVR rates, but this was not found to be statistically significant. Peg-INF plus ribavirin is safe for the treatment of CHC monoinfected patients with inherited bleeding disorders, with similar response rates to nonhemophiliacs. On the contrary, in HIV coinfected hemophilic patients under highly active antiretroviral therapy it is associated with severe toxicity and very poor sustained virological response rates. Careful evaluation and several considerations are needed before starting treatment in this population.
机译:慢性丙型肝炎(CHC)和终末期肝病正成为先天性出血性疾病(尤其是HIV合并感染组)患者越来越常见的死亡原因。聚乙二醇化干扰素(Peg-IFN)和利巴韦林的组合最近已成为CHC的首选治疗方法。在这项研究中,我们评估了Peg-IFN加利巴韦林联合疗法治疗先天性出血性疾病的人类免疫缺陷病毒(HIV)-和HIV +患者的CHC的安全性和有效性。在2000年至2004年之间,来自两个血友病中心的50例(18-68岁)CHC(19 HIV +)患者被纳入研究。根据病毒基因型,每周皮下注射Peg-INF-alpha与800-1,200 mg病毒唑联合治疗,治疗时间为24-48周。在第12、24、48周(治疗反应结束)评估反应,并且72例持续病毒学反应)。总体而言,有22/50名患者(43.8%)的治疗终止反应和20/50名患者(40%)的持续病毒学应答。 HIV患者的反应与普通人群相似(58.1%),而HIV +患者的反应率非常低(10.5%)。由于副作用而导致的高停用率(36.9%)导致了在HIV +组中观察到的低应答率。与HIV患者持续病毒学应答密切相关的唯一因素是HCV RNA在12周时减少(p = 0.001)。病毒基因型不是1的患者具有较高的SVR率,但是在统计学上未发现有此意义。 Peg-INF加利巴韦林可安全治疗患有遗传性出血性疾病的CHC单一感染患者,对非血友病患者的反应率相似。相反,在接受高活性抗逆转录病毒治疗的HIV合并感染的血友病患者中,它与严重的毒性和非常差的持续病毒学应答率有关。在该人群中开始治疗之前,需要仔细评估和几点考虑。

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