Vancomycin pharmacokinetics in preterm neonates and the prediction of adult clearance
- 21 July 2006
- journal article
- Published by Wiley in British Journal of Clinical Pharmacology
- Vol. 63 (1), 75-84
- https://doi.org/10.1111/j.1365-2125.2006.02725.x
Abstract
*Effects of size, renal function, age (postnatal age, gestational age and postmenstrual age) as predictors of vancomycin clearance in premature neonates are established, but the relative contribution of each component remains poorly quantified, largely because these variables are closely correlated. *We have quantified the covariates contributing to vancomycin clearance population parameter variability in order to establish the major covariates required for dosing predictions. Size, standardized using allometric models, was the primary covariate used in our analysis. *Size explained 49.8%, postmenstrual age 18.2% and renal function 14.1% of clearance variability. *Descriptors of the relationship between age and clearance in premature neonates vary. *The use of a variable slope sigmoidal model to describe the relationship between clearance and postmenstrual age predicted an adult clearance of 3.79 l h(-1) 70 kg(-1) (95% confidence interval 2.76, 4.98) from premature neonatal data. To identify and quantify factors describing the variability of vancomycin clearance in premature neonates. Population pharmacokinetics were estimated (NONMEM) in 214 neonates [postmenstrual age (PMA) 30.4 weeks, range 24-34 weeks; postnatal age 11.9 days, range 1-27 days; weight 1.30 kg, range 0.42-2.6 kg] using therapeutic drug monitoring data. Covariate analysis included weight, PMA, serum creatinine, use of inotropes or ibuprofen, positive blood culture and respiratory support. A one-compartment linear disposition model with zero order input and first-order elimination was used to describe the data (604 observations). The population estimate for volume of distribution (V) was 39 l 70 kg(-1) (coefficient of variation 19.4%). Clearance (CL) increased from 0.897 l h(-1) 70 kg(-1) at 24 weeks PMA to 2.02 l h(-1) 70 kg(-1) by 34 weeks PMA. The between-subject variability for CL was 18.6% and the between-occasion variability was 12.2%. The use of ibuprofen reduced clearance, but this effect was attributable to reduced renal function. Overall, 82% of the variability of CL was predictable. Size explained 49.8%, PMA 18.2% and renal function 14.1%. The use of a variable slope sigmoidal model to describe the relationship between clearance and PMA predicted an adult clearance of 3.79 l h(-1) 70 kg(-1) (95% confidence interval 2.76, 4.98). Size, renal function and PMA are the major contributors to clearance variability in premature neonates. The small (18%) unexplained variability in clearance suggests target concentration intervention is unnecessary if size, age and renal function are used to predict the dose. Extrapolation to an adult clearance from neonatal data is possible using allometric size models and a function describing clearance maturation.Keywords
This publication has 36 references indexed in Scilit:
- Prediction of Cytochrome P450-Mediated Hepatic Drug Clearance in Neonates, Infants and ChildrenClinical Pharmacokinetics, 2006
- Limited predictability of amikacin clearance in extreme premature neonates at birthBritish Journal of Clinical Pharmacology, 2005
- COMMENTARY ON BROWN ET AL.'S “TOWARD A METABOLIC THEORY OF ECOLOGY”Ecology, 2004
- VancomycinClinical Pharmacokinetics, 2004
- Serum creatinine concentration, urinary creatinine excretion and creatinine clearance during the first 9 weeks in preterm infants with a birth weight below 1500 gEuropean Journal of Pediatrics, 1996
- A Size Standard for PharmacokineticsClinical Pharmacokinetics, 1996
- Pharmacokinetic parameters of vancomycin for therapeutic regimens in neutropenic adult patientsInternational Journal of Bio-Medical Computing, 1994
- Comparison of Vancomycin Pharmacokinetics in Hospitalized Elderly and Young Patients Using a Bayesian ForecasterThe Journal of Clinical Pharmacology, 1993
- Developmental patterns of renal functional maturation compared in the human neonateThe Journal of Pediatrics, 1978
- Prediction of Creatinine Clearance from Serum CreatinineNephron, 1976