成人患者利福平-双丙戊酸-药物相互作用:1例报告。

The Mental Health Clinician Pub Date : 2021-01-08 eCollection Date: 2021-01-01 DOI:10.9740/mhc.2021.01.019
Christine Doran, Michael Moro, Jennifer Green, Kristen N Gardner
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引用次数: 1

摘要

双丙戊酸(DVP)包装说明书指出,利福平可使口服丙戊酸清除率提高40%,并且在开始或停止利福平时可能需要调整丙戊酸衍生物的剂量。然而,鉴于有限的临床结果数据已发表,这种药物-药物相互作用的总体临床意义尚不清楚。本病例描述了一名患有双相情感障碍、边缘型人格障碍和创伤后应激障碍的52岁女性,她以前稳定的药物治疗方案包括DVP延迟释放500mg每天早上和1500mg每天晚上(基线稳定状态通过99.8 mcg/mL)。在利福平治疗潜伏性结核病的整个过程中,她需要增加DVP的给药频率,从每天2次增加到3次,DVP的剂量增加75%,以保持临床稳定性。在4个月的利福平疗程中,丙戊酸谷浓度范围为56.4至75.9微克/毫升。该报告支持dvp -利福平相互作用可能具有临床意义,并且比包装说明书所建议的程度更大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Rifampin-divalproex drug-drug interaction in an adult patient: A case report.

Rifampin-divalproex drug-drug interaction in an adult patient: A case report.

The divalproex (DVP) package insert states that rifampin may increase the oral clearance of valproate by 40% and that valproic acid derivative dose adjustments may be required when starting or stopping rifampin. However, the overall clinical significance of this drug-drug interaction remains unclear given that limited clinical outcome data has been published. This case describes a 52-year-old female with bipolar disorder, borderline personality disorder, and PTSD who was previously stable on a medication regimen consisting of DVP delayed-release 500 mg every morning and 1500 mg every evening (baseline steady-state trough 99.8 mcg/mL). Throughout rifampin therapy for latent tuberculosis treatment, she required an increase in both the frequency of DVP administration, from 2 to 3 times daily, and DVP dose by 75% to maintain clinical stability. Valproic acid trough concentrations ranged from 56.4 to 75.9 mcg/mL during the 4-month course of rifampin. This report supports that the DVP-rifampin interaction may be clinically significant and of a greater magnitude than suggested by the package insert.

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