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Optimising an Infusion Protocol Containing Cefepime to Limit Particulate Load to Newborns in a Neonatal Intensive Care Unit

Background: In neonatal intensive care units (NICUs), the simultaneous administration of drugs requires complex infusion methods. Such practices can increase the risk of drug incompatibilities resulting in the formation of a particulate load with possible clinical consequences. Methods: This paper e...

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Autores principales: Martin Mena, Anthony, Masse, Morgane, Négrier, Laura, Nguyen, Thu Huong, Ladam, Bruno, Storme, Laurent, Barthélémy, Christine, Odou, Pascal, Genay, Stéphanie, Décaudin, Bertrand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001063/
https://www.ncbi.nlm.nih.gov/pubmed/33800228
http://dx.doi.org/10.3390/pharmaceutics13030351
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author Martin Mena, Anthony
Masse, Morgane
Négrier, Laura
Nguyen, Thu Huong
Ladam, Bruno
Storme, Laurent
Barthélémy, Christine
Odou, Pascal
Genay, Stéphanie
Décaudin, Bertrand
author_facet Martin Mena, Anthony
Masse, Morgane
Négrier, Laura
Nguyen, Thu Huong
Ladam, Bruno
Storme, Laurent
Barthélémy, Christine
Odou, Pascal
Genay, Stéphanie
Décaudin, Bertrand
author_sort Martin Mena, Anthony
collection PubMed
description Background: In neonatal intensive care units (NICUs), the simultaneous administration of drugs requires complex infusion methods. Such practices can increase the risk of drug incompatibilities resulting in the formation of a particulate load with possible clinical consequences. Methods: This paper evaluates strategies to reduce the particulate load of a protocol commonly used in NICUs with a potential medical incompatibility (vancomycin/cefepime combination). The protocol was reproduced in the laboratory and the infusion line directly connected to a dynamic particle counter to evaluate the particulate matter administered during infusion. A spectrophotometry UV assay of cefepime evaluated the impact of filters on the concentration of cefepime administered. Results: A significant difference was observed between the two infusion line configurations used in the NICU, with higher particulate load for cefepime infused via the emergency route. There was no change in particulate load in the absence of vancomycin. A filter on the emergency route significantly reduced this load without decreasing the cefepime concentration infused. Preparation of cefepime seemed to be a critical issue in the protocol as the solution initially contained a high level of particles. Conclusion: This study demonstrated the impact of a reconstitution method, drug dilution and choice of infusion line configuration on particulate load.
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spelling pubmed-80010632021-03-28 Optimising an Infusion Protocol Containing Cefepime to Limit Particulate Load to Newborns in a Neonatal Intensive Care Unit Martin Mena, Anthony Masse, Morgane Négrier, Laura Nguyen, Thu Huong Ladam, Bruno Storme, Laurent Barthélémy, Christine Odou, Pascal Genay, Stéphanie Décaudin, Bertrand Pharmaceutics Article Background: In neonatal intensive care units (NICUs), the simultaneous administration of drugs requires complex infusion methods. Such practices can increase the risk of drug incompatibilities resulting in the formation of a particulate load with possible clinical consequences. Methods: This paper evaluates strategies to reduce the particulate load of a protocol commonly used in NICUs with a potential medical incompatibility (vancomycin/cefepime combination). The protocol was reproduced in the laboratory and the infusion line directly connected to a dynamic particle counter to evaluate the particulate matter administered during infusion. A spectrophotometry UV assay of cefepime evaluated the impact of filters on the concentration of cefepime administered. Results: A significant difference was observed between the two infusion line configurations used in the NICU, with higher particulate load for cefepime infused via the emergency route. There was no change in particulate load in the absence of vancomycin. A filter on the emergency route significantly reduced this load without decreasing the cefepime concentration infused. Preparation of cefepime seemed to be a critical issue in the protocol as the solution initially contained a high level of particles. Conclusion: This study demonstrated the impact of a reconstitution method, drug dilution and choice of infusion line configuration on particulate load. MDPI 2021-03-08 /pmc/articles/PMC8001063/ /pubmed/33800228 http://dx.doi.org/10.3390/pharmaceutics13030351 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Martin Mena, Anthony
Masse, Morgane
Négrier, Laura
Nguyen, Thu Huong
Ladam, Bruno
Storme, Laurent
Barthélémy, Christine
Odou, Pascal
Genay, Stéphanie
Décaudin, Bertrand
Optimising an Infusion Protocol Containing Cefepime to Limit Particulate Load to Newborns in a Neonatal Intensive Care Unit
title Optimising an Infusion Protocol Containing Cefepime to Limit Particulate Load to Newborns in a Neonatal Intensive Care Unit
title_full Optimising an Infusion Protocol Containing Cefepime to Limit Particulate Load to Newborns in a Neonatal Intensive Care Unit
title_fullStr Optimising an Infusion Protocol Containing Cefepime to Limit Particulate Load to Newborns in a Neonatal Intensive Care Unit
title_full_unstemmed Optimising an Infusion Protocol Containing Cefepime to Limit Particulate Load to Newborns in a Neonatal Intensive Care Unit
title_short Optimising an Infusion Protocol Containing Cefepime to Limit Particulate Load to Newborns in a Neonatal Intensive Care Unit
title_sort optimising an infusion protocol containing cefepime to limit particulate load to newborns in a neonatal intensive care unit
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001063/
https://www.ncbi.nlm.nih.gov/pubmed/33800228
http://dx.doi.org/10.3390/pharmaceutics13030351
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