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Impact of insulin adsorption in various containers during hyperkalaemia treatment
BACKGROUND: Insulin–glucose therapy in hyperkalaemia treatment has a narrow therapeutic index for a safe and efficient use. We assess the variability of the effective delivered insulin under conditions used in the setting of hyperkalaemia treatment. METHODS: A range of simulated insulin infusions wa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8483685/ https://www.ncbi.nlm.nih.gov/pubmed/34603702 http://dx.doi.org/10.1093/ckj/sfab033 |
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author | Robert, Thomas Vanelle, Patrice Brunet, Philippe Martin, Nathalie Burtey, Stéphane Curti, Christophe |
author_facet | Robert, Thomas Vanelle, Patrice Brunet, Philippe Martin, Nathalie Burtey, Stéphane Curti, Christophe |
author_sort | Robert, Thomas |
collection | PubMed |
description | BACKGROUND: Insulin–glucose therapy in hyperkalaemia treatment has a narrow therapeutic index for a safe and efficient use. We assess the variability of the effective delivered insulin under conditions used in the setting of hyperkalaemia treatment. METHODS: A range of simulated insulin infusions was studied using different containers (bag or syringes) according to the different hyperkalaemia treatment procedures of our institution. Insulin concentration was assayed using a chromatographic method on an automatic high-performance liquid chromatography. We calculated the effective delivered insulin and compared the time average of percentage delivered insulin (TAdi) between all the procedures. RESULTS: The TAdi was significantly decreased to 63.3% of the expected insulin delivery in the polyurethane (PE) bag compared with allover container. The procedure duration and the insulin concentration influenced the variability of the insulin delivery in the PE and glass bag. The polyvinyl chloride bag had the highest TAdi at 93.8%, without significant variation during the time. TAdi reaches ∼90% of the expected insulin with all the syringe procedure without variation according to the solute used to dilute insulin. CONCLUSIONS: Clinically significant variations in intravenous insulin delivery occur in the setting of hyperkalaemia treatment according to the container. The use of propylene syringe limits the insulin delivery variation. In the future, clinical studies on hyperkalaemia treatment by insulin–glucose therapy should detail the procedure precisely. |
format | Online Article Text |
id | pubmed-8483685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-84836852021-10-01 Impact of insulin adsorption in various containers during hyperkalaemia treatment Robert, Thomas Vanelle, Patrice Brunet, Philippe Martin, Nathalie Burtey, Stéphane Curti, Christophe Clin Kidney J Original Articles BACKGROUND: Insulin–glucose therapy in hyperkalaemia treatment has a narrow therapeutic index for a safe and efficient use. We assess the variability of the effective delivered insulin under conditions used in the setting of hyperkalaemia treatment. METHODS: A range of simulated insulin infusions was studied using different containers (bag or syringes) according to the different hyperkalaemia treatment procedures of our institution. Insulin concentration was assayed using a chromatographic method on an automatic high-performance liquid chromatography. We calculated the effective delivered insulin and compared the time average of percentage delivered insulin (TAdi) between all the procedures. RESULTS: The TAdi was significantly decreased to 63.3% of the expected insulin delivery in the polyurethane (PE) bag compared with allover container. The procedure duration and the insulin concentration influenced the variability of the insulin delivery in the PE and glass bag. The polyvinyl chloride bag had the highest TAdi at 93.8%, without significant variation during the time. TAdi reaches ∼90% of the expected insulin with all the syringe procedure without variation according to the solute used to dilute insulin. CONCLUSIONS: Clinically significant variations in intravenous insulin delivery occur in the setting of hyperkalaemia treatment according to the container. The use of propylene syringe limits the insulin delivery variation. In the future, clinical studies on hyperkalaemia treatment by insulin–glucose therapy should detail the procedure precisely. Oxford University Press 2021-02-03 /pmc/articles/PMC8483685/ /pubmed/34603702 http://dx.doi.org/10.1093/ckj/sfab033 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of ERA-EDTA. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Articles Robert, Thomas Vanelle, Patrice Brunet, Philippe Martin, Nathalie Burtey, Stéphane Curti, Christophe Impact of insulin adsorption in various containers during hyperkalaemia treatment |
title | Impact of insulin adsorption in various containers during hyperkalaemia treatment |
title_full | Impact of insulin adsorption in various containers during hyperkalaemia treatment |
title_fullStr | Impact of insulin adsorption in various containers during hyperkalaemia treatment |
title_full_unstemmed | Impact of insulin adsorption in various containers during hyperkalaemia treatment |
title_short | Impact of insulin adsorption in various containers during hyperkalaemia treatment |
title_sort | impact of insulin adsorption in various containers during hyperkalaemia treatment |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8483685/ https://www.ncbi.nlm.nih.gov/pubmed/34603702 http://dx.doi.org/10.1093/ckj/sfab033 |
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