首页> 外文期刊>Journal of viral hepatitis. >Concentration-guided ribavirin dosing with darbepoetin support and peg-IFN alfa-2a for treatment of hepatitis C recurrence after liver transplantation
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Concentration-guided ribavirin dosing with darbepoetin support and peg-IFN alfa-2a for treatment of hepatitis C recurrence after liver transplantation

机译:浓度导向的利巴韦林配以达比泊汀支持和peg-IFN alfa-2a给药治疗肝移植后丙型肝炎复发

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Relapse of hepatitis C virus infection after liver transplantation is universal. Standard-of-care (SOC) treatment for relapse offers less satisfactory treatment response than in nontransplanted patients. Tolerance for treatment is suboptimal and withdrawals owing to adverse events induced by treatment frequent. To improve tolerance for SOC, and ribavirin (RBV) in particular, concentration-guided RBV dosing calculated by a formula taking renal function and weight into consideration was utilized. A serum RBV concentration of 10 μm was set as the goal. All patients were given maintenance darbepoetin therapy from 2 weeks prior to initiation of treatment. In total, 21 patients with a mean age of 52 (range 25-64) years were included. The mean RBV concentration at week 4 was 10.2 and 7.36 μm in genotype 1/4 and non-1/4 patients, respectively, and 11.7 and 9.42 at week 12. The mean haemoglobin drop was 25 g/L vs 21 g/L in the genotype 1/4 and non-1/4 group, respectively, a nonsignificant difference. With this treatment approach, 80-90% of patients could be kept adherent to treatment. Sustained viral response was achieved 8/16 (50%) with low-grade fibrosis (fibrosis stage ≤ 2) vs in none of five patients with advanced fibrosis (Fibrosis stage 3 and 4), P < 0.05. We conclude that a treatment algorithm utilizing concentration-guided RBV dosing during darbepoetin maintenance therapy substantially improves tolerance and allows high adherence to a SOC treatment schedule, and that therapy needs to be initiated before advanced fibrosis is developed.
机译:肝移植后丙型肝炎病毒感染的复发是普遍的。与非移植患者相比,用于复发的护理标准(SOC)治疗提供的治疗反应较差。治疗的耐受性欠佳,由于治疗引起的不良反应而戒断的情况经常发生。为了提高对SOC的耐受性,尤其是利巴韦林(RBV)的耐受性,采用了通过考虑肾脏功能和体重的公式计算出的浓度指导的RBV剂量。目标血清RBV浓度为10μm。从开始治疗前2周开始,所有患者均接受维持达比泊汀维持治疗。总共包括21例平均年龄为52岁(25-64岁)的患者。基因型1/4和非1/4患者在第4周的平均RBV浓度分别为10.2和7.36μm,在第12周时分别为11.7和9.42。平均血红蛋白滴为25 g / L,而在21周时为21 g / L。基因型1/4和非1/4组分别无显着性差异。通过这种治疗方法,80-90%的患者可以坚持治疗。低度纤维化(纤维化分期≤2)的持续病毒应答达到8/16(50%),而晚期纤维化(纤维化分期3和4)的五名患者中没有一个,P <0.05。我们得出的结论是,在达比泊汀维持治疗期间利用浓度指导的RBV剂量的治疗算法可显着提高耐受性,并允许对SOC治疗方案的高度依从性,并且需要在发展晚期纤维化之前开始治疗。

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