Journal
JOURNAL OF CLINICAL PHARMACOLOGY
Volume 46, Issue 4, Pages 433-442Publisher
WILEY
DOI: 10.1177/0091270006286433
Keywords
opioid; pediatric; pharmocokinetics
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Young children are often undertreated for pain. One barrier to effective pain treatment is understanding the pharmacokinetic behavior of analgesics in this age group. Oxycodone is a commonly prescribed opioid for severe pain, yet little is known about its pharmacokinetics in young children. This article used population pharmacokinetic modeling to synthesize pharmacokinetic data from several studies into a model. A single Population model that described the observed pharmacokinetics was developed. The combined data were best described with a 2-compartment linear model with different first-order absorption rates depending on route of administration. Weight was found to significantly influence both clearance (CL) and volume of distribution (Vd). The following model adequately describes the population pharmacokinetic profile of oxycodone where absolute bioavailability (F) is estimated for each administration route: CL/F = 55 x (body weight/70)(0.87); V/F= 86 x (body weight/70)(1.16). The interindividual coefficients of variation in CL and 114 were 20.2 and 19.7%.. respectively This finding confirms that the allometric scaling using the above model explained most of the variability in exposure observed among children. This model confirms using a vveight-based dose for oxycodone without adjustment for age between 6 months and 7 years and is valuable for evaluating dosing schedules and dosing routes.
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