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抗生素对细菌耐药性发展的药代动力学影响,特别是针对阿奇霉素

[Pharmacokinetic effects of antibiotics on the development of bacterial resistance particularly in reference to azithromycin].

作者信息

Wenisch C

机构信息

Klinischen Abteilung für Infektionen und Tropenmedizin, Medizinischen Universitätsklinik, Graz.

出版信息

Wien Med Wochenschr. 2000;150(3):37-41.

Abstract

Antibiotics reduce the mortality from infectious diseases but not the prevalence of these diseases. Use, and often abuse, of antimicrobial agents encourages the evolution of bacteria toward resistance, often resulting in therapeutic failure. There are two factors which influence potential utility of a drug in a specific clinical situation. The first is the measure of potency of the antibiotic for the pathogen in question (minimal inhibitory concentration [MIC], minimal bactericidal concentration [MBC]). The second is whichever relationship between the concentration-time profile and potency of the antibiotic linked most robustly to clinical outcome (time above MIC or MBC [T > MIC or T > MBC]; Peak/MIC or MBC; area under the curve [AUC]/MIC or AUC/MBC). Herein the effects of pharmacokinetics of antimicrobials on the evolution of antimicrobial resistance with particular reference to azithromycin are considered.

摘要

抗生素可降低传染病的死亡率,但无法降低这些疾病的患病率。抗菌药物的使用,且常常是滥用,促使细菌朝着耐药性方向进化,常常导致治疗失败。有两个因素会影响药物在特定临床情况下的潜在效用。第一个因素是抗生素针对所讨论病原体的效力衡量指标(最低抑菌浓度[MIC]、最低杀菌浓度[MBC])。第二个因素是抗生素的浓度-时间曲线与效力之间,与临床结果关联最为紧密的那种关系(高于MIC或MBC的时间[T > MIC或T > MBC];峰浓度/MIC或MBC;曲线下面积[AUC]/MIC或AUC/MBC)。本文将探讨抗菌药物的药代动力学对耐药性演变的影响,尤其以阿奇霉素为例。

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