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MIC-based dose adjustment: facts and fables
Author(s) -
Johan W. Mouton,
Anouk E. Muller,
Rafael Cantón,
Christian G. Giske,
Gunnar Kahlmeter,
John Turnidge
Publication year - 2017
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkx427
Subject(s) - pharmacodynamics , pharmacokinetics , medicine , antimicrobial , antibiotics , drug , minimum inhibitory concentration , therapeutic drug monitoring , intensive care medicine , pharmacology , antimicrobial drug , clinical practice , biology , microbiology and biotechnology , family medicine
Over recent decades, several publications have described optimization procedures for antibiotic therapy in the individual patient based on antimicrobial MIC values. Most methods include therapeutic drug monitoring and use a single MIC determination plus the relevant pharmacokinetics/pharmacodynamics to adjust the dose to optimize antimicrobial drug exposure and antibacterial effects. However, the use of an MIC obtained by a single MIC determination is inappropriate. First, routine clinical laboratories cannot determine MICs with sufficient accuracy to guide dosage owing to the inherent assay variation in the MIC test. Second, the variation in any MIC determination, whatever method is used, must be accounted for. If dose adjustments are made based on therapeutic drug monitoring and include MIC determinations, MIC variation must be considered to prevent potential underdosing of patients. We present the problems and some approaches that could be used in clinical practice.

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