| Literature DB >> 25750489 |
Seongho Kim1, Adam E Gaweda2, Dongfeng Wu3, Lang Li4, Shesh N Rai3, Michael E Brier5.
Abstract
Warfarin is a frequently used oral anticoagulant for long-term prevention and treatment of thromboembolic events. Due to its narrow therapeutic range and large inter-individual dose-response variability, it is highly desirable to personalize warfarin dosing. However, the complexity of the conventional kinetic-pharmacodynamic (K-PD) models hampers the development of the personalized dose management. To avert this challenge, we propose simplified PD models for warfarin dose-response relationship, which is motivated by ideas from control theory. The simplified models were further applied to longitudinal data of 37 patients undergoing anticoagulation treatment using the standard two-stage approach and then compared with the conventional K-PD models. Data analysis shows that all models have a similar predictive ability, but the simplified models are most parsimonious.Entities:
Keywords: dose-response model; kinetic-pharmacodynamics; mixed-effects model; standard two-stage approach
Year: 2015 PMID: 25750489 PMCID: PMC4349334 DOI: 10.4015/S1016237215500015
Source DB: PubMed Journal: Biomed Eng (Singapore) ISSN: 1016-2372