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Serious interaction between mibefradil and tacrolimus.

机译:米贝拉地尔和他克莫司之间存在严重的相互作用。

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摘要

BACKGROUND/AIMS: Tacrolimus is metabolized by cytochrome P450 3A4 and 2D6 and has a narrow therapeutic range. We report a serious kinetic interaction between tacrolimus and mibefradil, a potent cytochrome P450 inhibitor. CASE REPORT: A 62-year-old women who had undergone liver transplantation was treated with tacrolimus for immunosuppression. For control of blood pressure, the patient was treated with nifedipine. She developed ankle edema, and nifedipine was replaced by mibefradil. Four days later, she presented with mental confusion, renal failure, and hyperglycemia, compatible with tacrolimus toxicity. In agreement with this assumption, the tacrolimus blood concentration was 100 ng/ml. Mibefradil and tacrolimus were both stopped, and the patient recovered within 1 week. Eight days after stopping mibefradil, tacrolimus was restarted at the same dosage and the subsequent plasma concentrations remained in the therapeutic range. CONCLUSIONS: Mibefradil increases the tacrolimus blood concentration by inhibiting its metabolism and should, therefore, not be used in patients treated with tacrolimus.
机译:背景/目的:他克莫司被细胞色素P450 3A4和2D6代谢,治疗范围狭窄。我们报告了他克莫司和米贝拉地尔(一种有效的细胞色素P450抑制剂)之间存在严重的动力学相互作用。病例报告:接受肝移植的62岁妇女接受了他克莫司的免疫抑制治疗。为了控制血压,患者接受硝苯地平治疗。她发展为脚踝浮肿,硝苯地平被硝苯地平代替。四天后,她表现出精神错乱,肾衰竭和高血糖症,与他克莫司毒性相适应。与该假设一致,他克莫司的血药浓度为100 ng / ml。 Mibefradil和他克莫司都停止使用,患者在1周内康复。停止米贝拉地尔八天后,以相同剂量重新开始他克莫司,随后的血浆浓度保持在治疗范围内。结论:米贝拉地尔通过抑制他克莫司的代谢来增加他克莫司的血药浓度,因此,不宜用于他克莫司治疗的患者。

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