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Antimicrobial Agents and Chemotherapy, May 2002, p. 1381-1387, Vol. 46, No. 5
0066-4804/02/$04.00+0     DOI: 10.1128/AAC.46.5.1381-1387.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Nonparametric Population Pharmacokinetic Analysis of Amikacin in Neonates, Infants, and Children

J. M. Tréluyer,1* Y. Merlé,2 S. Tonnelier,1 E. Rey,1 and G. Pons1

Pharmacologie Périnatale et Pédiatrique, Universite Rene-Descartes, Hopital Saint Vincent de Paul,1 INSERM U436, CHU Pitié-Salpetriere, Paris, France2

Received 8 March 2001/ Returned for modification 27 October 2001/ Accepted 31 January 2002

The therapeutic and toxic effects of amikacin are known to depend on its concentration in plasma, but the pharmacokinetics of this drug in neonates, infants, and children and the influences of clinical and biological variables have been only partially assessed. Therapeutic drug monitoring data collected from 155 patients (49 neonates, 77 infants, and 29 children) receiving amikacin were analyzed by a nonparametric population-based approach, the nonparametric maximum-likelihood method. We assessed the effects of gestational and postnatal age, weight, Apgar score, and plasma creatinine and urea concentrations on pharmacokinetic parameters. There is no specific formulation of amikacin for neonates and infants. We therefore used an error model to account for errors due to dilution during preparation of the infusion. The covariates that reduced the variance of clearance from plasma and the volume of distribution by more than 10% were postnatal age (43 and 28%, respectively) and body weight (30.4 and 17.4%, respectively). The expected reduction of clearance was about 10% for the plasma creatinine concentration. The other covariates studied (Apgar scores, plasma urea concentration, gestational age, sex) were found to have little effect. Simulations showed that a smaller percentage of patients had a maximum concentration in plasma/MIC ratio greater than 8 with a regimen of 7.5 mg/kg of body weight twice daily than with a regimen of 15 mg/kg once a day for MICs of 1 to 8 mg/liter.


* Corresponding author. Mailing address: Pharmacologie Périnatale et Pédiatrique, Groupe Hospitalier Cochin-Saint Vincent de Paul (AP-HP), 82 avenue Denfert Rochereau, 75674 Paris Cedex 14, France. Phone: 33-1-40488212. Fax: 33-1-40488328. E-mail: jm.treluyer{at}svp.ap-hop-paris.fr.


Antimicrobial Agents and Chemotherapy, May 2002, p. 1381-1387, Vol. 46, No. 5
0066-4804/02/$04.00+0     DOI: 10.1128/AAC.46.5.1381-1387.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.







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