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为未来保护抗生素:从药代动力学和药效学角度看,新旧药物的新用途。

Conserving antibiotics for the future: new ways to use old and new drugs from a pharmacokinetic and pharmacodynamic perspective.

机构信息

Department of Medical Microbiology, Radboud University Nijmegen Medical Center, The Netherlands.

出版信息

Drug Resist Updat. 2011 Apr;14(2):107-17. doi: 10.1016/j.drup.2011.02.005. Epub 2011 Mar 26.

Abstract

There is a growing need to optimize the use of old and new antibiotics to treat serious as well as less serious infections. The topic of how to use pharmacokinetic and pharmacodynamic (PK/PD) knowledge to conserve antibiotics for the future was elaborated on in a workshop of the conference (The conference "The Global Need for Effective Antibiotics - moving towards concerted action", ReAct, Uppsala, Sweden, 2010). The optimization of dosing regimens is accomplished by choosing the dose and schedule that results in the antimicrobial exposure that will achieve the microbiological and clinical outcome desired while simultaneously suppressing emergence of resistance. PK/PD of antimicrobial agents describe how the therapeutic drug effect is dependent on the potency of a drug against a microorganism and the exposure (the concentration of antimicrobial available for effect over time). The description and modeling of these relationships quantitatively then allow for a rational approach to dose optimization and several strategies to that purpose are described. These strategies include not only the dosing regimen itself but also the duration of therapy, preventing collateral damage through inappropriate use and the application of PK/PD in drug development. Furthermore, PK/PD relationships of older antibiotics need to be urgently established. The need for global harmonization of breakpoints is also suggested and would add efficacy to antibiotic therapy. For each of the strategies, a number of priority actions are provided.

摘要

现在越来越需要优化利用新旧抗生素来治疗严重和不太严重的感染。在会议的一个研讨会上详细阐述了如何利用药代动力学和药效学(PK/PD)知识来为未来保存抗生素的主题(会议主题为“全球对有效抗生素的需求-迈向协同行动”,ReAct,瑞典乌普萨拉,2010 年)。通过选择能够达到所需微生物和临床结果的抗菌药物暴露量来优化给药方案,同时抑制耐药性的产生。抗菌药物的 PK/PD 描述了治疗药物效果如何取决于药物对微生物的效力和暴露量(随时间变化的抗菌药物的有效浓度)。对这些关系进行定量描述和建模,然后可以为剂量优化提供合理的方法,并描述了几种达到这一目的的策略。这些策略不仅包括给药方案本身,还包括治疗持续时间,通过不当使用来防止产生副作用,以及在药物开发中应用 PK/PD。此外,还迫切需要建立旧抗生素的 PK/PD 关系。还建议对临界点进行全球协调统一,以增强抗生素治疗的效果。对于每种策略,都提供了一些优先行动。

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