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Published on: August 30, 2018
Approaches for dosage individualisation in critically ill patients
M del Mar Fernández de Gatta1, Ana Martin-Suarez, Jose M Lanao
1University of Salamanca, Institute of Biomedical Research of Salamanca (IBSAL), Department of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy , Avda. Licenciado Méndez Núñez, 37007 Salamanca , Spain +0034 923 294 536 ; +0034 923 294 515 ; gatta@usal.es.
Dosage individualisation strategies are crucial for critically ill patients due to pharmacokinetic variability. Therapeutic drug monitoring (TDM) and pharmacogenomics can optimize drug exposure and improve treatment outcomes.
Area of Science:
- Pharmacology
- Critical Care Medicine
- Pharmacokinetics
Background:
- Critically ill patients exhibit significant pharmacokinetic variability due to complex pathophysiological and clinical factors.
- Standard drug dosages may lead to unpredictable drug exposure, impacting treatment efficacy and safety.
- Dosage individualisation is essential in critical care settings to optimize therapeutic outcomes.
Purpose of the Study:
- To review and discuss various approaches for drug dosage individualisation in critically ill patients.
- To highlight the role of therapeutic drug monitoring (TDM) and pharmacogenomics in optimizing drug therapy.
- To explore the application of population pharmacokinetic models and Bayesian forecasting for improved drug dosing.
Main Methods:
- Review of established and innovative methods for dosage individualisation.
- Focus on therapeutic drug monitoring (TDM) and pharmacogenomics.
- Summary of population pharmacokinetic models and Bayesian forecasting techniques.
- Consideration of Monte Carlo simulations for dosage strategy selection.
Main Results:
- Pharmacokinetic/pharmacodynamic (PK/PD) modelling and individualised dosing strategies improve pharmacologic treatment in critically ill patients.
- Integration of pharmacogenomics into critical care practice requires substantial effort.
- Therapeutic drug monitoring (TDM) remains valuable due to the lack of target biomarkers for dosage adjustment.
Conclusions:
- Mathematical and statistical methods for dosage individualisation enhance pharmacologic treatment in critical care.
- Further research and integration efforts are needed for pharmacogenomics in critical care.
- Therapeutic drug monitoring (TDM) is a key strategy for controlling treatment outcome variability in critically ill patients.
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