Drug-induced CYP induction as therapy for tacrolimus intoxication.

John M Hoppe, Alexander Holderied, Ulf Schönermarck, Volker Vielhauer, Hans-Joachim Anders, Michael Fischereder
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引用次数: 1

Abstract

Management of calcineurin inhibitor (CNI) therapy in kidney transplant recipients may be complicated due to polypharmacy. As CNI undergo extensive metabolism by cytochrome-P450 enzymes (CYP), drug-mediated CYP inhibition poses a risk for elevated CNI blood concentrations. Here, we report on 2 kidney transplant recipients treated with tacrolimus who presented with signs of tacrolimus intoxication at admission. Patient A was started on antiviral medication ombitasvir, paritaprevir, ritonavir, and dasabuvir for hepatitis C virus treatment 3 days prior to hospitalization. Patient B was treated with clarithromycin for pneumonia. Both therapies cause drug-mediated CYP inhibition, and both patients displayed highly elevated tacrolimus serum concentrations and acute kidney injury (Table 1). After application of the CYP-inducing agents rifampicin and phenytoin, respectively, tacrolimus levels were rapidly reduced, and renal function recovered. Treating severe CNI intoxication is an infrequent yet emergent condition. These results add to the knowledge of therapeutic drug-induced CYP induction as rescue therapy.

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药物诱导CYP治疗他克莫司中毒。
肾移植受者钙调磷酸酶抑制剂(CNI)治疗的管理可能由于多种药物而复杂。由于CNI经过细胞色素- p450酶(CYP)的广泛代谢,药物介导的CYP抑制可能导致CNI血药浓度升高。在这里,我们报告了2例接受他克莫司治疗的肾移植受者,他们在入院时出现他克莫司中毒的迹象。患者A在住院前3天开始使用抗病毒药物ombitasvir、paritaprevir、利托那韦和达沙布韦治疗丙型肝炎病毒。患者B接受克拉霉素治疗肺炎。两种治疗方法均引起药物介导的CYP抑制,两例患者均表现出他克莫司血清浓度高和急性肾损伤(表1)。分别应用促CYP药物利福平和苯妥英后,他克莫司水平迅速降低,肾功能恢复。治疗严重的CNI中毒是一种罕见但紧急的情况。这些结果增加了治疗性药物诱导CYP作为抢救治疗的认识。
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