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Validation of a population pharmacokinetic model for adjunctive lamotrigine therapy in children
Author(s) -
Chen Chao
Publication year - 2000
Publication title -
british journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.216
H-Index - 146
eISSN - 1365-2125
pISSN - 0306-5251
DOI - 10.1046/j.1365-2125.2000.00237.x
Subject(s) - lamotrigine , covariate , nonmem , pharmacokinetics , population , medicine , physiologically based pharmacokinetic modelling , population pharmacokinetics , statistics , epilepsy , pharmacology , mathematics , psychiatry , environmental health
AimsThis analysis was performed to validate a previously developed population pharmacokinetic model for lamotrigine in order to establish a basis for dosage recommendations for children.Methods(a) The importance of the covariates in the final model was confirmed using the model validation dataset. Population and individual (Bayesian estimate) pharmacokinetic parameters were estimated using both the initial model, which included none of the covariates, and the final model. Accuracy and precision of parameter estimation and of concentration prediction were compared between the two models. (b) The performance in predicting the validation concentrations by the final model parameters obtained previously from the model development dataset was assessed. (c) The parameters of the final model were refined using a dataset combining both the development and validation data.ResultsPrediction performance of the final pharmacostatistical model was superior to that of the initial model. The results of the validation confirmed that concomitant antiepileptic drugs that increased or reduced lamotrigine clearance in adults had similar effects in children. The validation also verified the linear relationship between weight and clearance. The previously seen small sex effect on clearance was found statistically insignificant.ConclusionsThe current analysis confirmed the previous findings. To achieve the same concentrations, children receiving enzyme‐inducing antiepileptic drugs without valproate require higher doses than those receiving valproate; and heavier children require higher doses.