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Individual and population pharmacokinetic compartment analysis: a graphic procedure for quantification of predictive performance
OBJECTIVES: Pharmacokinetic studies are important for optimizing of drug dosing, but requires proper validation of the used pharmacokinetic procedures. However, simple and reliable statistical methods suitable for evaluation of the predictive performance of pharmacokinetic analysis are essentially l...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Maney Publishing
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937653/ https://www.ncbi.nlm.nih.gov/pubmed/27536447 http://dx.doi.org/10.3109/21556660.2013.838569 |
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author | Eksborg, Staffan |
author_facet | Eksborg, Staffan |
author_sort | Eksborg, Staffan |
collection | PubMed |
description | OBJECTIVES: Pharmacokinetic studies are important for optimizing of drug dosing, but requires proper validation of the used pharmacokinetic procedures. However, simple and reliable statistical methods suitable for evaluation of the predictive performance of pharmacokinetic analysis are essentially lacking. The aim of the present study was to construct and evaluate a graphic procedure for quantification of predictive performance of individual and population pharmacokinetic compartment analysis. METHODS: Original data from previously published pharmacokinetic compartment analyses after intravenous, oral, and epidural administration, and digitized data, obtained from published scatter plots of observed vs predicted drug concentrations from population pharmacokinetic studies using the NPEM algorithm and NONMEM computer program and Bayesian forecasting procedures, were used for estimating the predictive performance according to the proposed graphical method and by the method of Sheiner and Beal. RESULTS: The graphical plot proposed in the present paper proved to be a useful tool for evaluation of predictive performance of both individual and population compartment pharmacokinetic analysis. CONCLUSION: The proposed method is simple to use and gives valuable information concerning time- and concentration-dependent inaccuracies that might occur in individual and population pharmacokinetic compartment analysis. Predictive performance can be quantified by the fraction of concentration ratios within arbitrarily specified ranges, e.g. within the range 0.8–1.2. |
format | Online Article Text |
id | pubmed-4937653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Maney Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-49376532016-08-17 Individual and population pharmacokinetic compartment analysis: a graphic procedure for quantification of predictive performance Eksborg, Staffan J Drug Assess Original Articles OBJECTIVES: Pharmacokinetic studies are important for optimizing of drug dosing, but requires proper validation of the used pharmacokinetic procedures. However, simple and reliable statistical methods suitable for evaluation of the predictive performance of pharmacokinetic analysis are essentially lacking. The aim of the present study was to construct and evaluate a graphic procedure for quantification of predictive performance of individual and population pharmacokinetic compartment analysis. METHODS: Original data from previously published pharmacokinetic compartment analyses after intravenous, oral, and epidural administration, and digitized data, obtained from published scatter plots of observed vs predicted drug concentrations from population pharmacokinetic studies using the NPEM algorithm and NONMEM computer program and Bayesian forecasting procedures, were used for estimating the predictive performance according to the proposed graphical method and by the method of Sheiner and Beal. RESULTS: The graphical plot proposed in the present paper proved to be a useful tool for evaluation of predictive performance of both individual and population compartment pharmacokinetic analysis. CONCLUSION: The proposed method is simple to use and gives valuable information concerning time- and concentration-dependent inaccuracies that might occur in individual and population pharmacokinetic compartment analysis. Predictive performance can be quantified by the fraction of concentration ratios within arbitrarily specified ranges, e.g. within the range 0.8–1.2. Maney Publishing 2013-09-03 /pmc/articles/PMC4937653/ /pubmed/27536447 http://dx.doi.org/10.3109/21556660.2013.838569 Text en © 2013 The Author(s). Published by Taylor & Francis. 2013 http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Original Articles Eksborg, Staffan Individual and population pharmacokinetic compartment analysis: a graphic procedure for quantification of predictive performance |
title | Individual and population pharmacokinetic compartment analysis: a graphic procedure for quantification of predictive performance |
title_full | Individual and population pharmacokinetic compartment analysis: a graphic procedure for quantification of predictive performance |
title_fullStr | Individual and population pharmacokinetic compartment analysis: a graphic procedure for quantification of predictive performance |
title_full_unstemmed | Individual and population pharmacokinetic compartment analysis: a graphic procedure for quantification of predictive performance |
title_short | Individual and population pharmacokinetic compartment analysis: a graphic procedure for quantification of predictive performance |
title_sort | individual and population pharmacokinetic compartment analysis: a graphic procedure for quantification of predictive performance |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937653/ https://www.ncbi.nlm.nih.gov/pubmed/27536447 http://dx.doi.org/10.3109/21556660.2013.838569 |
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