Accuracy of single intravenous access iohexol GFR in children is hampered by marker contamination

Abstract Measurement of glomerular filtration rate (GFR) in children by iohexol injection and blood sampling from the contralateral arm is widely used. A single intravenous access for iohexol injection and subsequent blood sampling has the obvious advantages of being less painful and easier to perfo...

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Autores principales: Thea Tislevoll Eide, Karl Ove Hufthammer, Atle Brun, Damien Brackman, Einar Svarstad, Camilla Tøndel
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/493e1ab0acb948d2bb7e7a3ee96f6c26
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spelling oai:doaj.org-article:493e1ab0acb948d2bb7e7a3ee96f6c262021-12-05T12:13:08ZAccuracy of single intravenous access iohexol GFR in children is hampered by marker contamination10.1038/s41598-021-02759-12045-2322https://doaj.org/article/493e1ab0acb948d2bb7e7a3ee96f6c262021-12-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-02759-1https://doaj.org/toc/2045-2322Abstract Measurement of glomerular filtration rate (GFR) in children by iohexol injection and blood sampling from the contralateral arm is widely used. A single intravenous access for iohexol injection and subsequent blood sampling has the obvious advantages of being less painful and easier to perform. The purpose of our study was to determine if blood samples drawn from the injection access are feasible and accurate for iohexol GFR (iGFR) measurements. Thirty-one children, median age 10.5 (range 6–17) years, with chronic kidney disease were given a bolus of iohexol followed by extended saline flushing and subsequent venous blood samples collected from the injection access as well as from a cannula in the contralateral arm, the latter serving as the reference method. Paired venous blood samples were collected at four time points (2, 3, 3.5 and 4 h) after the iohexol bolus. Blood sample discarding preceded and saline flushing followed each blood sampling to avoid marker contamination. iGFR based on samples drawn from the injection access at 2 and 3 h showed significantly lower iGFR than measurement from the contralateral arm (p < 0.01). Singlepoint iGFR did not differ significantly after 3–4 repeated procedures of blood discarding and saline flusing (3.5 and 4 h). Despite thorough saline flushing there is still a relatively high risk of falsely low iGFR due to marker contamination in blood samples from the injection site. Hence, blood sampling from a second intravenous access is recommended for routine iohexol GFR measurements in children. Clinical trial registration: ClinicalTrials.gov, Identifier NCT01092260, https://clinicaltrials.gov/ct2/show/NCT01092260?term=tondel&rank=2 .Thea Tislevoll EideKarl Ove HufthammerAtle BrunDamien BrackmanEinar SvarstadCamilla TøndelNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-7 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Thea Tislevoll Eide
Karl Ove Hufthammer
Atle Brun
Damien Brackman
Einar Svarstad
Camilla Tøndel
Accuracy of single intravenous access iohexol GFR in children is hampered by marker contamination
description Abstract Measurement of glomerular filtration rate (GFR) in children by iohexol injection and blood sampling from the contralateral arm is widely used. A single intravenous access for iohexol injection and subsequent blood sampling has the obvious advantages of being less painful and easier to perform. The purpose of our study was to determine if blood samples drawn from the injection access are feasible and accurate for iohexol GFR (iGFR) measurements. Thirty-one children, median age 10.5 (range 6–17) years, with chronic kidney disease were given a bolus of iohexol followed by extended saline flushing and subsequent venous blood samples collected from the injection access as well as from a cannula in the contralateral arm, the latter serving as the reference method. Paired venous blood samples were collected at four time points (2, 3, 3.5 and 4 h) after the iohexol bolus. Blood sample discarding preceded and saline flushing followed each blood sampling to avoid marker contamination. iGFR based on samples drawn from the injection access at 2 and 3 h showed significantly lower iGFR than measurement from the contralateral arm (p < 0.01). Singlepoint iGFR did not differ significantly after 3–4 repeated procedures of blood discarding and saline flusing (3.5 and 4 h). Despite thorough saline flushing there is still a relatively high risk of falsely low iGFR due to marker contamination in blood samples from the injection site. Hence, blood sampling from a second intravenous access is recommended for routine iohexol GFR measurements in children. Clinical trial registration: ClinicalTrials.gov, Identifier NCT01092260, https://clinicaltrials.gov/ct2/show/NCT01092260?term=tondel&rank=2 .
format article
author Thea Tislevoll Eide
Karl Ove Hufthammer
Atle Brun
Damien Brackman
Einar Svarstad
Camilla Tøndel
author_facet Thea Tislevoll Eide
Karl Ove Hufthammer
Atle Brun
Damien Brackman
Einar Svarstad
Camilla Tøndel
author_sort Thea Tislevoll Eide
title Accuracy of single intravenous access iohexol GFR in children is hampered by marker contamination
title_short Accuracy of single intravenous access iohexol GFR in children is hampered by marker contamination
title_full Accuracy of single intravenous access iohexol GFR in children is hampered by marker contamination
title_fullStr Accuracy of single intravenous access iohexol GFR in children is hampered by marker contamination
title_full_unstemmed Accuracy of single intravenous access iohexol GFR in children is hampered by marker contamination
title_sort accuracy of single intravenous access iohexol gfr in children is hampered by marker contamination
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/493e1ab0acb948d2bb7e7a3ee96f6c26
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AT atlebrun accuracyofsingleintravenousaccessiohexolgfrinchildrenishamperedbymarkercontamination
AT damienbrackman accuracyofsingleintravenousaccessiohexolgfrinchildrenishamperedbymarkercontamination
AT einarsvarstad accuracyofsingleintravenousaccessiohexolgfrinchildrenishamperedbymarkercontamination
AT camillatøndel accuracyofsingleintravenousaccessiohexolgfrinchildrenishamperedbymarkercontamination
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