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Variation in Target Attainment of Beta-Lactam Antibiotic Dosing Between International Pediatric Formularies.

Gastine, S; Hsia, Y; Clements, M; Barker, CIS; Bielicki, J; Hartmann, C; Sharland, M; Standing, JF (2021) Variation in Target Attainment of Beta-Lactam Antibiotic Dosing Between International Pediatric Formularies. Clin Pharmacol Ther, 109 (4). pp. 958-970. ISSN 1532-6535 https://doi.org/10.1002/cpt.2180
SGUL Authors: Sharland, Michael Roy Bielicki, Julia Anna

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Abstract

As antimicrobial susceptibility of common bacterial pathogens decreases, ensuring optimal dosing may preserve the use of older antibiotics in order to limit the spread of resistance to newer agents. Beta-lactams represent the most widely prescribed antibiotic class, yet most were licensed prior to legislation changes mandating their study in children. As a result, significant heterogeneity persists in the pediatric doses used globally, along with quality of evidence used to inform dosing. This review summarizes dosing recommendations from the major pediatric reference sources and tries to answer the questions: Does beta-lactam dose heterogeneity matter? Does it impact pharmacodynamic target attainment? For three important severe clinical infections-pneumonia, sepsis, and meningitis-pharmacokinetic models were identified for common for beta-lactam antibiotics. Real-world demographics were derived from three multicenter point prevalence surveys. Simulation results were compared with minimum inhibitory concentration distributions to inform appropriateness of recommended doses in targeted and empiric treatment. While cephalosporin dosing regimens are largely adequate for target attainment, they also pose the most risk of neurotoxicity. Our review highlights aminopenicillin, piperacillin, and meropenem doses as potentially requiring review/optimization in order to preserve the use of these agents in future.

Item Type: Article
Additional Information: © 2021 The Authors. Clinical Pharmacology & Therapeutics published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Keywords: Pharmacology & Pharmacy, 1115 Pharmacology and Pharmaceutical Sciences
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Clin Pharmacol Ther
ISSN: 1532-6535
Language: eng
Dates:
DateEvent
26 March 2021Published
28 February 2021Published Online
15 January 2021Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
UNSPECIFIEDGlobal Antibiotic Research and Development Partnership (GARDP)UNSPECIFIED
UNSPECIFIEDNational Institute for Health Research (NIHR)UNSPECIFIED
UNSPECIFIEDNational Institute for Health Research Biomedical Research Centre at Great Ormond Street Hospital for Children NHS Foundation TrustUNSPECIFIED
UNSPECIFIEDUniversity College LondonUNSPECIFIED
UNSPECIFIEDNIHR Biomedical Research Centre based at Guy's and St Thomas' NHS Foundation TrustUNSPECIFIED
UNSPECIFIEDKing's College LondonUNSPECIFIED
MR/M008665/1UK Medical Research CouncilUNSPECIFIED
MC_UU_12023/22UK Medical Research CouncilUNSPECIFIED
PubMed ID: 33521971
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/112924
Publisher's version: https://doi.org/10.1002/cpt.2180

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