期刊
EXPERT REVIEW OF ANTI-INFECTIVE THERAPY
卷 17, 期 8, 页码 571-582出版社
TAYLOR & FRANCIS LTD
DOI: 10.1080/14787210.2019.1647781
关键词
Antimicrobials; beta-lactamases; multi-drug resistance; pharmacodynamics; pharmacokinetics
Introduction: beta-lactamase production in Gram-negative bacteria is a leading cause of antimicrobial resistance. beta-lactamase inhibitors are therapeutic agents used in combination with a partner antimicrobial to overcome the production of these enzymes and restore antimicrobial activity. To address the ongoing threat of multi-drug resistant bacteria, a recent wave of beta-lactamase inhibitor development has occurred. Emphasis on the pharmacokinetics and pharmacodynamics of these agents is needed to optimize their clinical impact. Areas covered: This review will describe methods currently used to define the pharmacokinetics/pharmacodynamics of beta-lactamase inhibitors. Minimal focus will be on the structure and mechanism of beta-lactamase inhibitors. Emphasis will be placed on the use of specific thresholds to normalize beta-lactamase inhibitor exposure. In vitro and in vivo pharmacokinetic/pharmacodynamic data specific to FDA approved and pipeline beta-lactamase inhibitors will be explored. Expert opinion: Describing the exposure-response relationship of beta-lactamase inhibitors is an ongoing challenge due to the dynamic relationship of the beta-lactamase inhibitor with the active partner compound. Pharmacokinetic/pharmacodynamic indices and target exposures lack generalizability, as they are often specific to the infecting organism and/or beta-lactamase, rather than beta-lactamase inhibitor class. Selected dosage regimens of new agents should be validated via the use of population target attainment analyses.
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