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Estimation of glomerular filtration rate in paediatric cancer patients using (51)CR-EDTA population pharmacokinetics
Estimation of glomerular filtration rate (GFR) using the clearance of chromium 51 EDTA ((51)Cr-EDTA) (or other radiolabelled isotopes) is reliable, but invasive and not always practicable. Mathematical models have been devised for estimating GFR using readily obtainable patient characteristics. Unfo...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2004
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395308/ https://www.ncbi.nlm.nih.gov/pubmed/14710207 http://dx.doi.org/10.1038/sj.bjc.6601484 |
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author | Cole, M Price, L Parry, A Keir, M J Pearson, A D J Boddy, A V Veal, G J |
author_facet | Cole, M Price, L Parry, A Keir, M J Pearson, A D J Boddy, A V Veal, G J |
author_sort | Cole, M |
collection | PubMed |
description | Estimation of glomerular filtration rate (GFR) using the clearance of chromium 51 EDTA ((51)Cr-EDTA) (or other radiolabelled isotopes) is reliable, but invasive and not always practicable. Mathematical models have been devised for estimating GFR using readily obtainable patient characteristics. Unfortunately, these models were developed using various patient populations and may not provide the optimal prediction of GFR in children with cancer. The current study uses population pharmacokinetics to determine the relationship between (51)Cr-EDTA clearance, and patient covariates in 50 paediatric cancer patients. These models were validated using a separate group of 43 children and were compared with previously published models of renal function. Body size was the major determinant of (51)Cr-EDTA clearance and inclusion of weight or surface area reduced the residual variability between individuals (coefficient of variation) from 61 to 32%. Serum creatinine was the only other parameter that significantly improved the model. Mean percentage error values of –5.0 and –1.1% were observed for models including weight alone or weight and creatinine, respectively, with precision estimates of 21.7 and 20.0%. These simple additive models provide a more rationale approach than the use of complex formulae, involving additional parameters, to predict renal function. |
format | Text |
id | pubmed-2395308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23953082009-09-10 Estimation of glomerular filtration rate in paediatric cancer patients using (51)CR-EDTA population pharmacokinetics Cole, M Price, L Parry, A Keir, M J Pearson, A D J Boddy, A V Veal, G J Br J Cancer Clinical Estimation of glomerular filtration rate (GFR) using the clearance of chromium 51 EDTA ((51)Cr-EDTA) (or other radiolabelled isotopes) is reliable, but invasive and not always practicable. Mathematical models have been devised for estimating GFR using readily obtainable patient characteristics. Unfortunately, these models were developed using various patient populations and may not provide the optimal prediction of GFR in children with cancer. The current study uses population pharmacokinetics to determine the relationship between (51)Cr-EDTA clearance, and patient covariates in 50 paediatric cancer patients. These models were validated using a separate group of 43 children and were compared with previously published models of renal function. Body size was the major determinant of (51)Cr-EDTA clearance and inclusion of weight or surface area reduced the residual variability between individuals (coefficient of variation) from 61 to 32%. Serum creatinine was the only other parameter that significantly improved the model. Mean percentage error values of –5.0 and –1.1% were observed for models including weight alone or weight and creatinine, respectively, with precision estimates of 21.7 and 20.0%. These simple additive models provide a more rationale approach than the use of complex formulae, involving additional parameters, to predict renal function. Nature Publishing Group 2004-01-12 2004-01-06 /pmc/articles/PMC2395308/ /pubmed/14710207 http://dx.doi.org/10.1038/sj.bjc.6601484 Text en Copyright © 2004 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Cole, M Price, L Parry, A Keir, M J Pearson, A D J Boddy, A V Veal, G J Estimation of glomerular filtration rate in paediatric cancer patients using (51)CR-EDTA population pharmacokinetics |
title | Estimation of glomerular filtration rate in paediatric cancer patients using (51)CR-EDTA population pharmacokinetics |
title_full | Estimation of glomerular filtration rate in paediatric cancer patients using (51)CR-EDTA population pharmacokinetics |
title_fullStr | Estimation of glomerular filtration rate in paediatric cancer patients using (51)CR-EDTA population pharmacokinetics |
title_full_unstemmed | Estimation of glomerular filtration rate in paediatric cancer patients using (51)CR-EDTA population pharmacokinetics |
title_short | Estimation of glomerular filtration rate in paediatric cancer patients using (51)CR-EDTA population pharmacokinetics |
title_sort | estimation of glomerular filtration rate in paediatric cancer patients using (51)cr-edta population pharmacokinetics |
topic | Clinical |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395308/ https://www.ncbi.nlm.nih.gov/pubmed/14710207 http://dx.doi.org/10.1038/sj.bjc.6601484 |
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