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Iohexol plasma clearance in children: validation of multiple formulas and two-point sampling times

BACKGROUND: In children, estimated glomerular filtration rate (eGFR) methods are hampered by inaccuracy, hence there is an obvious need for safe, simplified, and accurate measured GFR (mGFR) methods. The aim of this study was to evaluate different formulas and determine the optimal sampling points f...

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Autores principales: Tøndel, Camilla, Bolann, Bjørn, Salvador, Cathrin Lytomt, Brackman, Damien, Bjerre, Anna, Svarstad, Einar, Brun, Atle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203838/
https://www.ncbi.nlm.nih.gov/pubmed/27369694
http://dx.doi.org/10.1007/s00467-016-3436-z
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author Tøndel, Camilla
Bolann, Bjørn
Salvador, Cathrin Lytomt
Brackman, Damien
Bjerre, Anna
Svarstad, Einar
Brun, Atle
author_facet Tøndel, Camilla
Bolann, Bjørn
Salvador, Cathrin Lytomt
Brackman, Damien
Bjerre, Anna
Svarstad, Einar
Brun, Atle
author_sort Tøndel, Camilla
collection PubMed
description BACKGROUND: In children, estimated glomerular filtration rate (eGFR) methods are hampered by inaccuracy, hence there is an obvious need for safe, simplified, and accurate measured GFR (mGFR) methods. The aim of this study was to evaluate different formulas and determine the optimal sampling points for calculating mGFR based on iohexol clearance measurements on blood samples drawn at two time points (GFR2p). METHODS: The GFR of 96 children with different stages of chronic kidney disease (CKD) (median age 9.2 years, range 3 months to 17.5 years) was determined using the iohexol plasma clearance, with blood sampling at seven time points within 5 h (GFR7p) as the reference method. Median GFR7p was 65.9 (range 6.3–153) mL/min/1.73 m(2). The performance of seven different formulas with early and late normalization to body surface area (BSA) was validated against the reference. RESULTS: The highest percentage (95.8 %) of GFR2p within 10 % of the reference was calculated using the formula of Jødal and Brøchner–Mortensen (JBM) from 2009, with sampling at 2 and 5 h. Normalization to BSA before correction of the distribution phase improved the performance of the original Brøchner–Mortensen method from 1972; P10 of 92.7 % compared to P10 of 82.3 % with late normalization, and a similar result was obtained with other formulas. CONCLUSIONS: GFR2p performed well across a wide spectrum of GFR levels with the JBM formula. Several other formulas tested performed well provided that early BSA normalization was performed. Blood sampling at 2 and 5 h is recommended for an optimal GFR2p assessment.
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spelling pubmed-52038382017-01-13 Iohexol plasma clearance in children: validation of multiple formulas and two-point sampling times Tøndel, Camilla Bolann, Bjørn Salvador, Cathrin Lytomt Brackman, Damien Bjerre, Anna Svarstad, Einar Brun, Atle Pediatr Nephrol Original Article BACKGROUND: In children, estimated glomerular filtration rate (eGFR) methods are hampered by inaccuracy, hence there is an obvious need for safe, simplified, and accurate measured GFR (mGFR) methods. The aim of this study was to evaluate different formulas and determine the optimal sampling points for calculating mGFR based on iohexol clearance measurements on blood samples drawn at two time points (GFR2p). METHODS: The GFR of 96 children with different stages of chronic kidney disease (CKD) (median age 9.2 years, range 3 months to 17.5 years) was determined using the iohexol plasma clearance, with blood sampling at seven time points within 5 h (GFR7p) as the reference method. Median GFR7p was 65.9 (range 6.3–153) mL/min/1.73 m(2). The performance of seven different formulas with early and late normalization to body surface area (BSA) was validated against the reference. RESULTS: The highest percentage (95.8 %) of GFR2p within 10 % of the reference was calculated using the formula of Jødal and Brøchner–Mortensen (JBM) from 2009, with sampling at 2 and 5 h. Normalization to BSA before correction of the distribution phase improved the performance of the original Brøchner–Mortensen method from 1972; P10 of 92.7 % compared to P10 of 82.3 % with late normalization, and a similar result was obtained with other formulas. CONCLUSIONS: GFR2p performed well across a wide spectrum of GFR levels with the JBM formula. Several other formulas tested performed well provided that early BSA normalization was performed. Blood sampling at 2 and 5 h is recommended for an optimal GFR2p assessment. Springer Berlin Heidelberg 2016-07-01 2017 /pmc/articles/PMC5203838/ /pubmed/27369694 http://dx.doi.org/10.1007/s00467-016-3436-z Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Original Article
Tøndel, Camilla
Bolann, Bjørn
Salvador, Cathrin Lytomt
Brackman, Damien
Bjerre, Anna
Svarstad, Einar
Brun, Atle
Iohexol plasma clearance in children: validation of multiple formulas and two-point sampling times
title Iohexol plasma clearance in children: validation of multiple formulas and two-point sampling times
title_full Iohexol plasma clearance in children: validation of multiple formulas and two-point sampling times
title_fullStr Iohexol plasma clearance in children: validation of multiple formulas and two-point sampling times
title_full_unstemmed Iohexol plasma clearance in children: validation of multiple formulas and two-point sampling times
title_short Iohexol plasma clearance in children: validation of multiple formulas and two-point sampling times
title_sort iohexol plasma clearance in children: validation of multiple formulas and two-point sampling times
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203838/
https://www.ncbi.nlm.nih.gov/pubmed/27369694
http://dx.doi.org/10.1007/s00467-016-3436-z
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