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Dose optimisation of antibiotics in children: application of pharmacokinetics/pharmacodynamics in paediatrics

Journal

INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS
Volume 43, Issue 3, Pages 223-230

Publisher

ELSEVIER
DOI: 10.1016/j.ijantimicag.2013.11.006

Keywords

Dose optimisation; Pharmacokinetics; Pharmacodynamics; PK/PD; Antibiotics

Funding

  1. Eunice Kennedy Shriver National Institute of Child Health and Human Development under a fellowship training grant [NIH 5 T32 HD069054]
  2. Joint Commission and Pfizer Independent Grants for Learning Change [8116513]

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The judicious use of antibiotics to combat infections in children relies upon appropriate selection of an agent, dose and duration to maximise efficacy and to minimise toxicity. Critical to dose optimisation is an understanding of the pharmacokinetics and pharmacodynamics of available drugs. Optimal dosing strategies may take advantage of pharmacokinetic/pharmacodynamic (PK/PD) principles so that antibiotic dosing can be individualised to assure effective bacterial killing in patients who have altered pharmacokinetics or who have infections with less susceptible or resistant organisms. This review will outline the fundamentals of antimicrobial pharmacokinetics/pharmacodynamics through discussion of antibacterial agents most often used in children. We aim to highlight the importance of dose optimisation in paediatrics and describe non-conventional dosing strategies that can take advantage of PK/PD principles at the bedside. (C) 2013 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.

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