2009
DOI: 10.1097/aco.0b013e32832c3c6c
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Pharmacokinetic–pharmacodynamic modeling in anesthesia, intensive care and pain medicine

Abstract: Progress was made by improving population pharmacokinetic/pharmacodynamic models, developing new indexes to measure drug effect and using them in an adaptive delivery system to the individual patient.

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Cited by 16 publications
(9 citation statements)
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“…The model becomes linear when =1.In this paper (Cr=remifentanil concentration, Cp =propofol concentration) is obtained by respecting Loewe additivity [7].…”
Section: Interaction Modelmentioning
confidence: 99%
See 1 more Smart Citation
“…The model becomes linear when =1.In this paper (Cr=remifentanil concentration, Cp =propofol concentration) is obtained by respecting Loewe additivity [7].…”
Section: Interaction Modelmentioning
confidence: 99%
“…Diverse models have been proposed for modeling the drug effect, such as experimental models, compartmental models and physiological models [6].Out of all the modeling options available, the standard modeling paradigm that has been commonly used to describe the relationship between anesthetic input and patient output is that of compartmental models. Compartmental models are formulated based on the minimum number of compartments that effectively fit the observed data [7]. Physiologically based models are more near to the actual representation of drug kinetics.…”
Section: Introductionmentioning
confidence: 99%
“…[2] Prediction of therapeutically effective plasma levels is also valuable in designing rational dosage regimes in clinical psychopharmacology. [34] Models have also been devised for optimizing the dose of capecitabine for breast cancer chemotherapy,[5] prediction of therapeutically effective plasma levels of antipsychotics,[6] and prediction of the onset and duration of the pharmacological effect of diazepam. [7] …”
Section: Introductionmentioning
confidence: 99%
“…EDICAL Medical experience with critically ill Medical experience with critically ill patients has revealed that standard dosing guidelines often result in an inappropriate under-or over-sedation which is leading to increased mortality due to huge inter-patient pharmacological variability [1], [2], [3].Open-loop control (manual control) by clinical personnel can be tedious, imprecise, timeconsuming, and sometimes of poor quality. Hence, the need for active control (closed-loop control) in medical systems is significant, with the potential for improving the quality of medical care as well as curtailing the increasing cost of health care.…”
Section: Introductionmentioning
confidence: 99%