Tseng A L, Foisy M M
Toronto Hospital, Ontario, Canada.
Ann Pharmacother. 1999 Apr;33(4):461-73. doi: 10.1345/aph.18240.
To provide an update on relevant antiretroviral interactions and psychotropic medications for healthcare practitioners managing complex HIV-related pharmacotherapy.
Information was retrieved via a MEDLINE search (January 1966-September 1998) using MeSH headings human immunodeficiency virus, drug interactions, psychiatry, psychotropics, psychiatric illness, and names of medications commonly prescribed for the management of HIV infection. Abstracts of international and national conferences (until February 1999), review articles, textbooks, and references of all articles also were searched.
Literature on pharmacokinetic interactions was considered for inclusion. Pertinent information was selected and summarized for discussion. In the absence of specific data, pharmacokinetic and pharmacodynamic properties were considered in order to predict the likelihood of potential drug interactions.
All protease inhibitors and nonnucleoside reverse transcriptase inhibitors are substrates of the cytochrome P450 system and possess enzyme-inhibiting and/or -inducing properties. Psychotropic medications also possess similar metabolic characteristics and may interact with antiretrovirals. Modifications in drug selection, dose, or dosing regimen may be needed to ensure adequate antiretroviral concentrations and thus minimize the risk of incomplete viral suppression and/or development of drug resistance. In the absence of specific data, consideration of metabolic characteristics may assist practitioners in predicting the likelihood of possible interactions.
The incidence and implications of antiretroviral drug interactions are reviewed. Practical management strategies are also discussed. Comprehensive tables on clinically significant interactions with antiretroviral combinations and with psychiatric medications are provided.
Given the increasing use of multiple-drug therapy, the potential for drug interactions is extremely high. Drug interactions may lead to undesirable outcomes including subtherapeutic drug concentrations and risk of antiretroviral resistance. Practitioners need to consider pharmacokinetic, pharmacologic, therapeutic, and adherence factors when managing interactions with complex antiretroviral therapy.
为处理复杂的HIV相关药物治疗的医护人员提供有关抗逆转录病毒药物相互作用和精神药物的最新信息。
通过MEDLINE检索(1966年1月至1998年9月)获取信息,使用医学主题词“人类免疫缺陷病毒”、“药物相互作用”、“精神病学”、“精神药物”、“精神疾病”以及常用于治疗HIV感染的药物名称。还检索了国际和国内会议摘要(截至1999年2月)、综述文章、教科书以及所有文章的参考文献。
考虑纳入有关药代动力学相互作用的文献。选择并总结相关信息以供讨论。在缺乏具体数据时,考虑药代动力学和药效学特性以预测潜在药物相互作用的可能性。
所有蛋白酶抑制剂和非核苷类逆转录酶抑制剂都是细胞色素P450系统的底物,并具有酶抑制和/或诱导特性。精神药物也具有类似的代谢特征,可能与抗逆转录病毒药物相互作用。可能需要调整药物选择、剂量或给药方案,以确保足够的抗逆转录病毒药物浓度,从而将病毒抑制不完全和/或耐药性发展的风险降至最低。在缺乏具体数据时,考虑代谢特征可能有助于医护人员预测可能相互作用的可能性。
综述了抗逆转录病毒药物相互作用的发生率及其影响。还讨论了实际管理策略。提供了关于抗逆转录病毒药物组合和精神药物临床显著相互作用的综合表格。
鉴于多药疗法的使用日益增加,药物相互作用的可能性极高。药物相互作用可能导致不良后果,包括药物浓度低于治疗水平以及产生抗逆转录病毒耐药性的风险。医护人员在处理复杂的抗逆转录病毒治疗相互作用时,需要考虑药代动力学、药理学、治疗和依从性因素。