Division of Clinical Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Clin Pharmacol Ther. 2010 Nov;88(5):712-9. doi: 10.1038/clpt.2010.130. Epub 2010 Jul 28.
Combination antiretroviral therapy (cART) has improved survival rates in HIV-infected patients; however, patients now experience comorbidities that require pharmacological intervention, thereby increasing the risk of drug-drug interactions (DDIs). HIV protease inhibitors (PIs), non-nucleoside reverse transcriptase inhibitors (NNRTIs), and the CCR5 antagonist maraviroc are primarily metabolized via the cytochrome P450 (CYP) system and are prone to pharmacokinetic interactions.(1,2) This article addresses some key challenges that prescribers face when using available drug interaction-data resources in making day-to-day clinical decisions.
联合抗逆转录病毒疗法(cART)提高了感染 HIV 患者的存活率;然而,现在患者出现了需要药物干预的合并症,从而增加了药物-药物相互作用(DDI)的风险。HIV 蛋白酶抑制剂(PI)、非核苷类逆转录酶抑制剂(NNRTI)和 CCR5 拮抗剂马拉维若主要通过细胞色素 P450(CYP)系统代谢,容易发生药代动力学相互作用。(1,2)本文讨论了临床医生在日常临床决策中使用现有的药物相互作用数据资源时面临的一些关键挑战。