利福平联合用药对地高辛药代动力学的影响:一种真实世界的数据方法。

IF 1.1 Q4 PHARMACOLOGY & PHARMACY Translational and Clinical Pharmacology Pub Date : 2023-09-01 Epub Date: 2023-09-08 DOI:10.12793/tcp.2023.31.e13
JungJin Oh, Byungwook Kim, SeungHwan Lee
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引用次数: 0

摘要

地高辛是一种强心苷,通常用于治疗心力衰竭和心房颤动。由于地高辛是P-糖蛋白(P-gp)的底物,其血液浓度可能会被P-糖蛋白诱导物(如利福平)降低。为了评估这种药物相互作用的现实意义,在2012年至2017年间,对首尔国立大学医院的临床数据仓库进行了回顾性分析。确定了11名同时接受地高辛和利福平治疗且符合纳入/排除标准的患者。比较地高辛单药治疗与利福平联合治疗的疗效。结果表明,在同时使用利福平的情况下,口服地高辛的全身暴露量减少了40%。临床医生应该意识到地高辛和利福平之间的潜在药物相互作用,因为接受利福平或其他P-gp诱导药物的患者可能需要调整地高辛剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Effects of rifampin coadministration on the pharmacokinetics of digoxin: a real-world data approach.

Digoxin, a cardiac glycoside, is commonly prescribed to treat heart failure and atrial fibrillation. Because digoxin acts as a substrate of P-glycoprotein (P-gp), its blood concentration may be reduced by P-gp inducers such as rifampin. To assess the real-world implications of this drug-drug interaction, a retrospective analysis was carried out on the Clinical Data Warehouse at Seoul National University Hospital between 2012 and 2017. Eleven patients who received both digoxin and rifampin with satisfying the inclusion/exclusion criteria were identified. The Ctrough values of digoxin monotherapy were compared to those of the combination therapy with rifampin. Results demonstrated that the systemic exposure of orally administered digoxin decreased by 40% with the concurrent use of rifampin. Clinicians should be aware of potential drug interactions between digoxin and rifampin, as adjustments to digoxin dosage might be necessary for patients receiving rifampin or other P-gp inducer drugs.

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来源期刊
Translational and Clinical Pharmacology
Translational and Clinical Pharmacology Medicine-Pharmacology (medical)
CiteScore
1.60
自引率
11.10%
发文量
17
期刊介绍: Translational and Clinical Pharmacology (Transl Clin Pharmacol, TCP) is the official journal of the Korean Society for Clinical Pharmacology and Therapeutics (KSCPT). TCP is an interdisciplinary journal devoted to the dissemination of knowledge relating to all aspects of translational and clinical pharmacology. The categories for publication include pharmacokinetics (PK) and drug disposition, drug metabolism, pharmacodynamics (PD), clinical trials and design issues, pharmacogenomics and pharmacogenetics, pharmacometrics, pharmacoepidemiology, pharmacovigilence, and human pharmacology. Studies involving animal models, pharmacological characterization, and clinical trials are appropriate for consideration.
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