Literature DB >> 17324223

Age-related differences in the pharmacokinetics of stavudine in 272 children from birth to 16 years: a population analysis.

V Jullien1, A Raïs, S Urien, J Dimet, C Delaugerre, M Bouillon-Pichault, E Rey, G Pons, S Blanche, J M Tréluyer.   

Abstract

AIMS: To develop a population pharmacokinetic model for stavudine in children and to investigate the consistency of the currently recommended dose based on adult target concentrations.
METHODS: The pharmacokinetics of stavudine were investigated using a population approach. Individual estimates of CL/F were used to calculate the stavudine dose required to achieve the area under the concentration-time curve reported in adults given recommended doses.
RESULTS: Stavudine pharmacokinetics were well described by a one-compartment model with zero-order absorption. Typical population estimates (% interindividual variability) of the apparent distribution volume (V/F) and plasma clearance (CL/F) were 40.9 l (32%) and 16.5 l h(-1) (38%), respectively. Stavudine V/F and CL/F were similarly related to age. Mean calculated doses (0.61 mg kg(-1) for children less than 2 weeks, 1.23 mg kg(-1) for children more than 2 weeks with bodyweight less than 30 kg, and 31.5 mg for children with a bodyweight between 30 and 60 kg) were in agreement with the current paediatric doses (0.5 mg kg(-1), 1 mg kg(-1), and 30 mg, respectively).
CONCLUSIONS: Our findings support the current recommended paediatric dosage regimens for stavudine, as they result in the same exposure to the drug as in adults.

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Year:  2007        PMID: 17324223      PMCID: PMC2000613          DOI: 10.1111/j.1365-2125.2007.02854.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


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