喹硫平与HIV蛋白酶抑制剂合用时的剂量建议。

IF 2.9 4区 医学
Journal of Clinical Pharmacology Pub Date : 2019-04-01 Epub Date: 2018-11-19 DOI:10.1002/jcph.1345
Mario R Sampson, Kelly Y Cao, Paula L Gish, Kyong Hyon, Poonam Mishra, William Tauber, Ping Zhao, Esther H Zhou, Islam R Younis
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引用次数: 10

摘要

尽管目前喹硫平的标签建议与强细胞色素P450 (CYP)3A抑制剂合用时,其剂量应降低6倍,但有报道称,一名接受喹硫平与洛匹那韦和利托那韦联合使用的患者出现昏迷,这促使对喹硫平与人类免疫缺陷病毒(HIV)蛋白酶抑制剂合用时喹硫平剂量的标签建议进行重新评估。文献和数据库(FDA不良事件报告系统和United States Symphony Health Solutions' Integrated Dataverse database)检索使我们能够识别涉及喹硫平和HIV蛋白酶抑制剂联合使用的昏迷病例和相关不良事件,并估计同时使用的频率。文献回顾和基于生理的药代动力学模型使我们能够估计CYP3A抑制可能导致与HIV蛋白酶抑制剂-喹硫平共给药相关的不良事件。我们在3个报告中发现了喹硫平和HIV蛋白酶抑制剂联合使用后的过度镇静,没有明显的混杂因素。在处方索赔数据中,0.4%的喹硫平患者同时使用利托那韦处方。在90%的治疗事件中,利托那韦开始时喹硫平剂量没有减少。现有数据表明,所有HIV蛋白酶抑制剂联合利托那韦可能是强CYP3A抑制剂。我们预测利托那韦会增加喹硫平的暴露,与强CYP3A抑制剂酮康唑相当。目前喹硫平与强CYP3A抑制剂(即喹硫平剂量低6倍)联合使用的推荐剂量是适当的,当喹硫平与HIV蛋白酶抑制剂联合使用时,应遵循推荐剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dosing Recommendations for Quetiapine When Coadministered With HIV Protease Inhibitors.

Although current quetiapine labeling recommends that its dosage should be lowered 6-fold when coadministered with strong cytochrome P450 (CYP)3A inhibitors, a reported case of coma in a patient receiving quetiapine with lopinavir and ritonavir prompted the reevaluation of labeling recommendations for the dosing of quetiapine when coadministered with human immunodeficiency virus (HIV) protease inhibitors. Literature and database (FDA Adverse Event Reporting System and United States Symphony Health Solutions' Integrated Dataverse Database) searches allowed us to identify cases of coma and related adverse events involving the coadministration of quetiapine and HIV protease inhibitors and to estimate the frequency of concomitant use. Literature review and physiologically based pharmacokinetic modeling allowed us to estimate the potential for CYP3A inhibition to contribute to adverse events related to HIV protease inhibitor-quetiapine coadministration. We identified excess sedation following coadministration of quetiapine and an HIV protease inhibitor in 3 reports without obvious confounders. In prescription claims data, 0.4% of quetiapine patients were dispensed a concurrent ritonavir prescription. The quetiapine dose was not reduced on ritonavir initiation in 90% of therapy episodes. Available data indicate to us that all HIV protease inhibitors combined with ritonavir are likely to be strong CYP3A inhibitors. We predicted that ritonavir would increase quetiapine exposure comparable to the strong CYP3A inhibitor ketoconazole. The current dosing recommendations for use of quetiapine with strong CYP3A inhibitors (ie, 6-fold lower quetiapine dose) are appropriate and should be followed when quetiapine is coadministered with HIV protease inhibitors.

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来源期刊
Journal of Clinical Pharmacology
Journal of Clinical Pharmacology PHARMACOLOGY & PHARMACY-
自引率
3.40%
发文量
0
期刊介绍: The Journal of Clinical Pharmacology (JCP) is a Human Pharmacology journal designed to provide physicians, pharmacists, research scientists, regulatory scientists, drug developers and academic colleagues a forum to present research in all aspects of Clinical Pharmacology. This includes original research in pharmacokinetics, pharmacogenetics/pharmacogenomics, pharmacometrics, physiologic based pharmacokinetic modeling, drug interactions, therapeutic drug monitoring, regulatory sciences (including unique methods of data analysis), special population studies, drug development, pharmacovigilance, womens’ health, pediatric pharmacology, and pharmacodynamics. Additionally, JCP publishes review articles, commentaries and educational manuscripts. The Journal also serves as an instrument to disseminate Public Policy statements from the American College of Clinical Pharmacology.
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