Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9005903 | Clinical Therapeutics | 2005 | 9 Pages |
Abstract
Based on the findings of this study, sparse TDM data can be used for PPK modeling of CBZ clearance in children with epilepsy, and these models can be used to predict Cl at steady state in pediatric patients. However, to estimate additional pharmacokinetic model parameters (eg, the absorption rate constant and Vd), it would be necessary to combine sparse TDM data with additional well-timed samples. This would allow development of more informative PPK models that could be used as part of Bayesian dose-individualization strategies.
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Authors
MSc Carlsson, PhD Hoem, MD Glauser, PhD Vinks,