Journal of Antimicrobial Chemotherapy, Vol 39, 677-686, Copyright © 1997 by The British Society for Antimicrobial Chemotherapy
CD Freeman, DP Nicolau, PP Belliveau and CH Nightingale
The use of higher-dose, extended interval (i.e., once-daily) aminoglycoside
regimens to optimize bacterial killing is justified by a pharmacodynamic
principle of aminoglycosides, namely concentration- dependent killing, and
by the partial attribution of the toxicity of aminoglycosides to prolonged
serum concentrations. Numerous in-vitro and animal studies have supported
using once-daily aminoglycoside dosing. Clinical studies show at least
equal effectiveness and no greater toxicity when compared with traditional
regimens. A dose of 5-7 mg/kg of gentamicin, tobramycin, or netilmicin,
with at least a 24 h dosing interval should be employed and a similar
regimen can be applied to amikacin dosing. As yet, there are some patient
populations that have not been adequately studied to determine whether or
not once-daily aminoglycoside dosing would be a better choice than
traditional dosing regimens.
REVIEW, TUTORIAL
Once-daily dosing of aminoglycosides: review and recommendations for clinical practice
Department of Medicine, University of Missouri-Kansas City School of Medicine, 64108, USA. cfreeman@cctr.umkc.edu
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