Population pharmacokinetics of paracetamol across the human age-range from (pre)term neonates, infants, children to adults
Journal of Clinical Pharmacology , Volume 54 - Issue 6 p. 619- 629
In order to characterize the variation in pharmacokinetics of paracetamol across the human age span, we performed a population pharmacokinetic analysis from preterm neonates to adults with specific focus on clearance. Concentration-time data obtained in 220 neonates (post-natal age 1-76 days, gestational age 27-42 weeks), infants (0.11-1.33 yrs), children (2-7 yrs) and adults (19-34 yrs) were analyzed using NONMEM 7.2. In the covariate analysis, linear functions, power functions, and a power function with a bodyweight-dependent exponent were tested. Between preterm neonates and adults, linear bodyweight functions were identified for Q2, Q3, V1, V2, and V3, while for CL a power function with a bodyweight-dependent exponent k was identified (CLi=CLp×(BW/70)k). The exponent k was found to decrease in a sigmoidal manner with bodyweight from 1.2 to 0.75, with half the decrease in exponent reached at 12.2kg. No other covariates such as age were identified. A pharmacokinetic model for paracetamol characterizing changes in pharmacokinetic parameters across the pediatric age-range was developed. Clearance was found to change in a nonlinear manner with bodyweight. Based on the final model, dosing guidelines are proposed from preterm neonates to adolescents resulting in similar exposure across all age ranges.
|allometry, clearance, paracetamol, pediatric, pharmacokinetics|
|Journal of Clinical Pharmacology|
|Organisation||Department of Pediatric Surgery|
Wang, C, Allegaert, K.M, Tibboel, D, Danhof, M, van der Marel, C.D, Mathot, R.A, & Knibbe, C.A.J. (2014). Population pharmacokinetics of paracetamol across the human age-range from (pre)term neonates, infants, children to adults. Journal of Clinical Pharmacology, 54(6), 619–629. doi:10.1002/jcph.259