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艾尔巴韦/格拉瑞韦在接受血液透析的肝移植术后患者中的应用。

Elbasvir/Grazoprevir Use in Postliver Transplantation Patients on Hemodialysis.

作者信息

Martin Michelle T, Koppe Sean

机构信息

1 Pharmacy Practice, University of Illinois at Chicago College of Pharmacy, University of Illinois Hospital and Health Sciences System, Chicago, IL. 2 University of Illinois Hospital and Health Sciences System, University of Illinois at Chicago College of Medicine, Chicago, IL.

出版信息

Transplantation. 2017 Sep;101(9):2088-2091. doi: 10.1097/TP.0000000000001758.

Abstract

BACKGROUND

Current national hepatitis C virus (HCV) guidelines do not recommend the use of elbasvir (EBR)/grazoprevir (GZR) in postliver transplantation (LT) patients due to drug-drug interactions with immunosuppression agents. However, recommendations do not address the treatment of HCV in renally impaired post-LT patients. Treatment regimens that are recommended for post-LT patients are not safe in patients with severe renal impairment and patients on dialysis. EBR/GZR is approved for use in patients with renal impairment and patients on dialysis, but not in the post-LT setting.

METHODS

Authors reviewed the electronic medical records of 3 treatment-naive HCV genotype 1a male post-LT patients on hemodialysis who were treated with EBR/GZR with or without ribavirin for 12 or 16 weeks.

RESULTS

No patients had serious adverse drug events during treatment and no patients stopped treatment early or died. Providers monitored immunosuppression levels; both patients who were taking tacrolimus required immunosuppression dose adjustments during HCV treatment. No patients experienced organ rejection. All patients achieved sustained virologic response.

CONCLUSIONS

Current HCV guidelines do not address the treatment options for post-LT patients with severe renal impairment or who are on dialysis, nor do published accounts of use of EBR/GZR in this patient population exist. Clinicians may benefit from exposure to real-world cases of HCV treatment in this historically difficult-to-cure patient population. Providers must address drug-drug interactions with EBR/GZR and monitor for changes in immunosuppression levels to ensure safety with its use in post-LT patients.

摘要

背景

由于与免疫抑制剂存在药物相互作用,目前的国家丙型肝炎病毒(HCV)指南不建议在肝移植(LT)后患者中使用艾尔巴韦(EBR)/格拉瑞韦(GZR)。然而,这些建议并未涉及LT后肾功能受损患者的HCV治疗。推荐用于LT后患者的治疗方案在严重肾功能受损患者和透析患者中并不安全。EBR/GZR已获批用于肾功能受损患者和透析患者,但未获批用于LT后患者。

方法

作者回顾了3例LT后接受血液透析、初治的HCV基因1a型男性患者的电子病历,这些患者接受了EBR/GZR治疗,联合或不联合利巴韦林,治疗12周或16周。

结果

治疗期间无患者发生严重不良药物事件,无患者提前停药或死亡。医护人员监测免疫抑制水平;2例服用他克莫司的患者在HCV治疗期间需要调整免疫抑制剂量。无患者发生器官排斥反应。所有患者均实现持续病毒学应答。

结论

目前的HCV指南未涉及LT后严重肾功能受损或正在接受透析患者的治疗选择,也没有关于EBR/GZR在该患者群体中使用情况的公开报道。临床医生可能会从这一历史上难以治愈的患者群体中HCV治疗的真实病例中受益。医护人员必须处理EBR/GZR的药物相互作用,并监测免疫抑制水平的变化,以确保在LT后患者中使用的安全性。

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