Ontology highlight
ABSTRACT: Aims
To build a population pharmacokinetic model that describes the apparent clearance of tacrolimus and the potential demographic, clinical and genetically controlled factors that could lead to inter-patient pharmacokinetic variability within children following liver transplantation.Methods
The present study retrospectively examined tacrolimus whole blood pre-dose concentrations (n = 628) of 43 children during their first year post-liver transplantation. Population pharmacokinetic analysis was performed using the non-linear mixed effects modelling program (nonmem) to determine the population mean parameter estimate of clearance and influential covariates.Results
The final model identified time post-transplantation and CYP3A5*1 allele as influential covariates on ta
SUBMITTER: Jalil MH
PROVIDER: S-EPMC3895354 | biostudies-literature | 2014 Jan
REPOSITORIES: biostudies-literature