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ABSTRACT: Purpose
Clearance via renal replacement therapy (RRT) can significantly alter the pharmacokinetic profile of drugs. The aim of this study was (i) to improve the use of clinical trial data and (ii) to provide a model that allows quantification of all aspects of drug elimination via RRT including adsorption to dialysis membranes and/or degradation of the drug in the dialysate.Methods
An integrated dialysis pharmacometric (IDP) model was developed to simultaneously incorporate all available RRT information. The sensitivity, accuracy and precision of the IDP model was compared to conventional approaches in clinical trial simulations and applied to clinical datasets of teicoplanin and doripenem.Results
The IDP model was more accurate, precise and sensitive than conventio
SUBMITTER: Broeker A
PROVIDER: S-EPMC7225193 | biostudies-literature | 2020 May
REPOSITORIES: biostudies-literature