Toronto General Hospital, 585 University Avenue, 13N-1314, Toronto, ON, M5G 2N2, Canada,
Curr Infect Dis Rep. 2012 Feb;14(1):67-82. doi: 10.1007/s11908-011-0229-1.
Advances in antiretroviral therapy have turned HIV into a chronic, manageable disease. Patients often require treatment for co-morbid conditions as well as HIV, and consequently, pharmacokinetic interactions between antiretrovirals (ARVs) and other drug classes are an increasing concern. Protease inhibitors and non-nucleoside reverse transcriptase inhibitors are involved in the CYP450 or other transporter systems, and may be associated with higher risk of clinically significant drug interactions. One reverse transcriptase inhibitor, abacavir, has demonstrated weak inhibition of CYP3A4, 2D6 and 2C9 in vitro, but is not associated with any clinically significant interactions involving the CYP450 system. The integrase inhibitor raltegravir is not involved in the CYP450 system, and may be a suitable option to use when trying to minimize interactions with other drug classes. This review summarizes recently published data on clinically significant drug interactions between ARVs and other drug classes including antineoplastics, immunosuppressant transplant drugs, directly acting antivirals for hepatitis C, antifungals, antimalarials, corticosteroids, psychotropics, hormonal contraceptives, anticoagulants, drugs for pulmonary hypertension, and herbal products. In situations of suspected or potential interactions, close monitoring is warranted, and dose adjustments or substitutions may be required.
抗逆转录病毒疗法的进步使 HIV 成为一种慢性、可管理的疾病。患者通常需要治疗合并症以及 HIV,因此抗逆转录病毒药物(ARV)与其他药物类别的药代动力学相互作用成为一个日益关注的问题。蛋白酶抑制剂和非核苷类逆转录酶抑制剂涉及 CYP450 或其他转运体系统,可能与更高的临床显著药物相互作用风险相关。一种逆转录酶抑制剂阿巴卡韦在体外显示出对 CYP3A4、2D6 和 2C9 的弱抑制作用,但与涉及 CYP450 系统的任何临床显著相互作用无关。整合酶抑制剂拉替拉韦不涉及 CYP450 系统,当试图最小化与其他药物类别的相互作用时,可能是一个合适的选择。这篇综述总结了最近发表的关于 ARV 与其他药物类别的临床显著药物相互作用的数据,包括抗肿瘤药物、免疫抑制移植药物、直接作用抗 HCV 药物、抗真菌药物、抗疟药物、皮质类固醇、精神药物、激素避孕药、抗凝药物、肺动脉高压药物和草药产品。在怀疑或潜在相互作用的情况下,需要密切监测,并可能需要调整剂量或替代药物。