Literature DB >> 20610985

Population pharmacokinetics and pharmacodynamics in anesthesia, intensive care and pain medicine.

Eleonora H Heeremans1, Johannes H Proost, Douglas J Eleveld, Anthony R Absalom, Michel M R F Struys.   

Abstract

PURPOSE OF REVIEW: Population modeling is a relatively new pharmacological discipline, the development of which has largely been stimulated by the need for accurate models for the pharmacokinetics and dynamics of anesthetic agents. RECENT
FINDINGS: Population-based modeling is now considered superior to older, more traditional modeling methods. Nonlinear mixed-effect modeling - a commonly used population-based modeling approach - estimates intraindividual and interindividual variability, limits the influence of outlying samples and individuals through the use of Bayesian statistical analysis, and provides a potential means of optimizing drug delivery regimens, especially when used to define pharmacokinetic-dynamic models for target-controlled infusion systems. In addition to being used for pharmacokinetic modeling, in which the influence of factors such as age, weight and illness can be studied, it is a powerful tool for the study of the influence of multiple factors on drug pharmacodynamics.
SUMMARY: Nonlinear mixed-effect population-based modeling has become the gold standard method of pharmacokinetic and pharmacodynamic analysis during new drug development and during subsequent pharmacological studies. Population-based modeling techniques have been applied to numerous aspects of drug delivery in anesthesia, intensive care and pain medicine.

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Year:  2010        PMID: 20610985     DOI: 10.1097/ACO.0b013e32833a1d2f

Source DB:  PubMed          Journal:  Curr Opin Anaesthesiol        ISSN: 0952-7907            Impact factor:   2.706


  3 in total

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Authors:  Pornswan Ngamprasertwong; Alexander A Vinks; Anne Boat
Journal:  Int Anesthesiol Clin       Date:  2012

2.  The elimination half-life of crystalloid fluid is shorter in female than in male volunteers: a retrospective population kinetic analysis.

Authors:  Robert G Hahn
Journal:  Biol Sex Differ       Date:  2016-10-07       Impact factor: 5.027

3.  Effects of vasoactive drugs on crystalloid fluid kinetics in septic sheep.

Authors:  Yuhong Li; Zheng Xiaozhu; Ru Guomei; Ding Qiannan; Robert G Hahn
Journal:  PLoS One       Date:  2017-02-23       Impact factor: 3.240

  3 in total

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