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Aggressive Use of Ribavirin and Prolonged Course of Peginterferon to Improve the Rate of Viral Response in Liver Transplant Patients with Recurrent Hepatitis C Viral Infection

机译:利巴韦林的积极使用和聚乙二醇干扰素的延长疗程可提高复发性丙型肝炎病毒感染的肝移植患者的病毒应答率

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Objectives: There are different approaches for treating recurrent hepatitis C viral infection after a liver transplant. However, sustained virologic response is achieved in < 40% of infected allografts. We examined sustained virologic response improvement using a prolonged course of peginterferon and aggressive use of ribavirin. Patients and Methods: From October 1998 to May 2008, 24 patients (13 male, 11 female; mean age at transplant, 49.4 ± 7.7 years) received a prolonged course of peginterferon and ribavirin (range, 48-180 weeks). The mean interval from liver transplant to hepatitis C antiviral therapy was 26.6 ± 27.8 months. Patients began weight-based standard dosages of peginterferon and ribavirin. In case of hemolysis, patients were treated with Epogen, with and without blood transfusions. Results: Fourteen patients (58.3%) had an end of treatment response, and 8 patients (33.3%) maintained sustained virologic response after the first course of therapy. Of 10 patients who did not respond to the first course, 6 received an extended course of antiviral therapy after a mean of 15 ± 4.6 weeks from completion of first course. Five of these 6 patients achieved end of treatment response and maintained a sustained virologic response, resulting in an overall end of treatment response in 17 patients and a sustained virologic response in 13 patients. Twenty-two patients experienced hemolysis and were treated with Epogen. Fifteen patients received blood transfusions. Ribavirin dosage was reduced in 12 patients, and peginterferon dosage was reduced in 2 patients. Conclusions: Aggressive use of ribavirin and prolonged course of peginterferon provided sustained virologic response in 54.1% of liver transplant recipients with recurrent hepatitis C virus-infection. More prospective studies are warranted to evaluate the benefit of this approach fully.
机译:目的:有多种方法可以治疗肝移植后复发的丙型肝炎病毒感染。但是,<40%的感染同种异体移植获得了持续的病毒学应答。我们研究了使用聚乙二醇干扰素的延长疗程和积极使用利巴韦林的持续病毒学应答改善。患者与方法:从1998年10月至2008年5月,有24例患者(男性13例,女性11例;平均移植年龄:49.4±7.7岁)接受了延长的聚乙二醇干扰素和利巴韦林疗程(范围48-180周)。从肝移植到丙型肝炎抗病毒治疗的平均间隔为26.6±27.8个月。患者开始使用基于重量的标准剂量的聚乙二醇干扰素和利巴韦林。如果发生溶血,则用Epogen进行治疗,有或没有输血。结果:14例患者(58.3%)的治疗反应终止,而8例患者(33.3%)在第一疗程后仍保持持续的病毒学应答。在对第一个疗程无反应的10例患者中,有6例在完成第一个疗程后平均15±4.6周后接受了延长的抗病毒治疗。这6例患者中有5例达到了治疗结束反应并维持了持续的病毒学应答,导致17例患者总体结束了治疗反应,而13例患者出现了持续的病毒学应答。 22名患者发生溶血并接受Epogen治疗。 15名患者接受了输血。利巴韦林剂量减少12例,聚乙二醇干扰素剂量减少2例。结论:利巴韦林的积极使用和聚乙二醇干扰素的延长疗程在54.1%的丙型肝炎病毒反复感染的肝移植受者中提供了持续的病毒学应答。必须进行更多的前瞻性研究,才能全面评估这种方法的益处。

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