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格卡瑞韦-哌柏瑞韦与炔雌醇诱发的非肝硬化患者肝损伤

Glecaprevir-Pibrentasvir and Ethinyl Estradiol-Induced Liver Injury in a Patient Without Cirrhosis.

作者信息

Wiese Jennifer, Derian Nayiri A, Ghimire Shristee, Bambhroliya Zarna, Joshi Tejas

机构信息

Internal Medicine, Marshall University Joan C. Edwards School of Medicine, Huntington, USA.

Internal Medicine, University of Science & Technology Chattogram, Chattogram, BGD.

出版信息

Cureus. 2024 Jun 8;16(6):e61980. doi: 10.7759/cureus.61980. eCollection 2024 Jun.

Abstract

Most drug liver injury cases are the result of an unexpected interaction with medications. We present a 33-year-old woman, four months postpartum, on ethinyl estradiol/norgestrel, who presented in the ED with nausea, vomiting, abdominal pain, and severe pruritus six weeks after starting glecaprevir-pibrentasvir (GP) treatment. The patient was suspected to have a drug-induced liver injury (DILI), and GP was discontinued. Other potential causes of liver injury were ruled out via labs, imaging, and liver biopsy. The patient's liver function significantly improved after discontinuing GP. Few cases of DILI secondary to GP have been reported. However, to the best of our knowledge, DILI from the interaction of ethinyl estradiol and GP does not exist in published literature. In our case, DILI was likely due to the effect of GP and ethinyl estradiol on the liver's cytochrome 450 (CYP 450) system. The aim of this report is to raise awareness and improve pharmacovigilance, especially in patients receiving medications that are metabolized by the liver's CYP 450 system. Early detection of DILI secondary to drug-interaction and discontinuation of the culprit medication is the mainstay of treatment. However, there is a lack of evidence-based management strategies for premature discontinuation of GP in the setting of DILI while treating chronic hepatitis C virus (HCV) infection. Further investigations are warranted.

摘要

大多数药物性肝损伤病例是药物意外相互作用的结果。我们报告一名33岁产后4个月的女性,正在服用炔雌醇/炔诺孕酮,在开始glecaprevir-pibrentasvir(GP)治疗六周后因恶心、呕吐、腹痛和严重瘙痒就诊于急诊科。患者被怀疑患有药物性肝损伤(DILI),停用了GP。通过实验室检查、影像学检查和肝活检排除了其他潜在的肝损伤原因。停用GP后患者肝功能显著改善。继发于GP的DILI病例报道较少。然而,据我们所知,已发表的文献中不存在炔雌醇与GP相互作用导致的DILI。在我们的病例中,DILI可能是由于GP和炔雌醇对肝脏细胞色素P450(CYP 450)系统的影响。本报告的目的是提高认识并加强药物警戒,尤其是在接受经肝脏CYP 450系统代谢药物的患者中。早期发现药物相互作用继发的DILI并停用致病药物是治疗的关键。然而,在治疗慢性丙型肝炎病毒(HCV)感染时,在DILI情况下过早停用GP缺乏循证管理策略。有必要进行进一步研究。

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