用抗病毒药物治疗其他病毒性疾病的HIV患者的药物相互作用。

Adaora Okoli, Onyema Ogbuagu
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引用次数: 0

摘要

背景:HIV感染者(PWH)从有效的抗逆转录病毒(ARV)治疗中获益良多。然而,PWH感染与艾滋病毒传播方式相同的其他病毒感染(如丙型肝炎和MPox)或机会性感染(如巨细胞病毒)的风险增加。这些合并感染显著增加了PWH的发病率和死亡率,需要有效的治疗来优化患者的预后。然而,由于药物-药物相互作用(ddi)与抗逆转录病毒药物之间的相互作用,它们的管理变得复杂。涵盖领域:讨论了用于治疗常见和临床相关病毒合并感染的经批准的抗逆转录病毒药物和选定的抗病毒药物之间的代谢途径和ddi。文献综述包括检索1981年6月30日至2024年6月1日期间已发表的论文、会议摘要(IAS、CROI、IDWeek、EACS、Glasgow)以及PubMed、谷歌和谷歌Scholar中已批准的药物处方信息和监管提交的未发表数据。专家意见:管理药物相互作用对于维持抗逆转录病毒药物和其他联合给药的抗病毒治疗的有效性和安全性至关重要。现在有更长效的药物可用于治疗艾滋病毒,这延长了药物相互作用可能发生的时间。新兴的新型纳米颗粒载体靶向丙型肝炎和艾滋病毒治疗可能减轻(如果不能消除)它们的药物-药物相互作用倾向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug interactions in people with HIV treated with antivirals for other viral illnesses.

Introduction: Background: People with HIV (PWH) have benefited tremendously from effective antiretroviral(ARV) treatments. However, PWH are at increased risk for other viral infections transmitted in the same way as HIV (such as hepatitis C and MPox) or that are opportunistic (e.g. cytomegalovirus). These coinfections contribute significantly to morbidity and mortality among PWH and require effective treatments to optimize patient outcomes. However, their management is complicated by drug-drug interactions (DDIs) with ARVs.

Areas covered: Metabolism pathways and DDIs between approved ARVs and selected antiviral agents used for the treatment of common and clinically relevant viral coinfections are discussed. Literature review included search of published papers, conference abstracts (IAS, CROI, IDWeek, EACS, Glasgow) as well as unpublished data from approved drug prescribing information and regulatory submissions sourced from PubMed, Google, and Google Scholar available between June 30 1981 through June 1, 2024.

Expert opinion: Management of drug interactions is essential for maintaining efficacy and safety of ARV and other co-administered antiviral therapies. Longer acting agents are now available for treatment of HIV and this lengthens the period during which drug interactions may occur. Emerging novel nanoparticle-carrier targeted hepatitis C and HIV treatments may mitigate, if not eliminate, their propensity for drug-drug interactions.

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