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Pharmacological Interactions Between Rifampicin and Antiretroviral Drugs: Challenges and Research Priorities for Resource-Limited Settings

机译:利福平和抗逆转录病毒药物之间的药理相互作用:资源受限环境的挑战和研究重点

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Coadministration of antituberculosis and antiretroviral therapy is often inevitable in high-burden countries where tuberculosis (TB) is the most common opportunistic infection associated with HIV/AIDS. Concurrent use of rifampicin and many antiretroviral drugs is complicated by pharmacokinetic drug-drug interactions. Rifampicin is a very potent enzyme inducer, which can result in subtherapeutic antiretroviral drug concentrations. In addition, TB drugs and antiretroviral drugs have additive (pharmacodynamic) interactions as reflected in overlapping adverse effect profiles. This review provides an overview of the pharmacological interactions between rifampicin-based TB treatment and antiretroviral drugs in adults living in resource-limited settings. Major progress has been made to evaluate the interactions between TB drugs and antiretroviral therapy; however, burning questions remain concerning nevirapine and efavirenz effectiveness during rifampicin-based TB treatment, treatment options for TB-HIV-coinfected patients with nonnucleoside reverse transcriptase inhibitor resistance or intolerance, and exact treatment or dosing schedules for vulnerable patients including children and pregnant women. The current research priorities can be addressed by maximizing the use of already existing data, creating new data by conducting clinical trials and prospective observational studies and to engage a lobby to make currently unavailable drugs available to those most in need.
机译:在结核病是与艾滋病毒/艾滋病相关的最常见机会性感染的高负担国家,抗结核药物和抗逆转录病毒疗法的并用往往是不可避免的。同时使用利福平和许多抗逆转录病毒药物会使药代动力学药物-药物相互作用变得复杂。利福平是一种非常有效的酶诱导剂,可导致亚治疗性抗逆转录病毒药物浓度升高。此外,结核病药物和抗逆转录病毒药物具有加性(药效学)相互作用,如重叠的不良反应图所反映。这篇综述概述了生活在资源有限的成年人中,基于利福平的结核病治疗与抗逆转录病毒药物之间的药理相互作用。在评估结核病药物与抗逆转录病毒疗法之间的相互作用方面取得了重大进展;然而,在利福平为基础的结核病治疗期间,奈韦拉平和依非韦伦的有效性,结核病-艾滋病毒感染的非核苷类逆转录酶抑制剂耐药或不耐受患者的治疗选择以及弱势患者(包括儿童和孕妇)的确切治疗或用药时间表仍然令人担忧。当前的研究重点可以通过以下方式来解决:最大限度地利用现有数据,通过进行临床试验和前瞻性观察研究创建新数据,并邀请游说者为最需要的人提供当前无法获得的药物。

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