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In-line filtration in very preterm neonates: a randomized controlled trial

In-line filtration is increasingly used in critically-ill infants but its benefits, by preventing micro-particle infusion in very preterm neonates, remain to be demonstrated. We conducted a randomized controlled trial among very preterm infants allocated to receive either in-line filtration of all t...

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Autores principales: Virlouvet, Anne-Laure, Pansiot, Julien, Toumazi, Artemis, Colella, Marina, Capewell, Andreas, Guerriero, Emilie, Storme, Thomas, Rioualen, Stéphane, Bourmaud, Aurélie, Biran, Valérie, Baud, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081338/
https://www.ncbi.nlm.nih.gov/pubmed/32193413
http://dx.doi.org/10.1038/s41598-020-61815-4
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author Virlouvet, Anne-Laure
Pansiot, Julien
Toumazi, Artemis
Colella, Marina
Capewell, Andreas
Guerriero, Emilie
Storme, Thomas
Rioualen, Stéphane
Bourmaud, Aurélie
Biran, Valérie
Baud, Olivier
author_facet Virlouvet, Anne-Laure
Pansiot, Julien
Toumazi, Artemis
Colella, Marina
Capewell, Andreas
Guerriero, Emilie
Storme, Thomas
Rioualen, Stéphane
Bourmaud, Aurélie
Biran, Valérie
Baud, Olivier
author_sort Virlouvet, Anne-Laure
collection PubMed
description In-line filtration is increasingly used in critically-ill infants but its benefits, by preventing micro-particle infusion in very preterm neonates, remain to be demonstrated. We conducted a randomized controlled trial among very preterm infants allocated to receive either in-line filtration of all the intra-venous lines or standard care without filters. The primary outcome was differences greater than 20% in the median changes in pro-inflammatory cytokine serum concentrations measured at day 3 and day 8 (+/−1) using a Luminex multianalytic profiling technique. Major neonatal complications were analyzed as secondary predefined outcomes. We randomized 146 infants, assigned to filter (n = 73) or control (n = 73) group. Difference over 20% in pro-inflammatory cytokine concentration between day 3 and day 8 was not found statistically different between the two groups, both in intent-to-treat (with imputation) and per protocol (without imputation) analyses. The incidences of most of neonatal complications were found to be similar. Hence, this trial did not evidence a beneficial effect of in-line filtration in very preterm infants on the inflammatory response syndrome and neonatal morbidities. These data should be interpreted according to local standards in infusion preparation and central line management.
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spelling pubmed-70813382020-03-23 In-line filtration in very preterm neonates: a randomized controlled trial Virlouvet, Anne-Laure Pansiot, Julien Toumazi, Artemis Colella, Marina Capewell, Andreas Guerriero, Emilie Storme, Thomas Rioualen, Stéphane Bourmaud, Aurélie Biran, Valérie Baud, Olivier Sci Rep Article In-line filtration is increasingly used in critically-ill infants but its benefits, by preventing micro-particle infusion in very preterm neonates, remain to be demonstrated. We conducted a randomized controlled trial among very preterm infants allocated to receive either in-line filtration of all the intra-venous lines or standard care without filters. The primary outcome was differences greater than 20% in the median changes in pro-inflammatory cytokine serum concentrations measured at day 3 and day 8 (+/−1) using a Luminex multianalytic profiling technique. Major neonatal complications were analyzed as secondary predefined outcomes. We randomized 146 infants, assigned to filter (n = 73) or control (n = 73) group. Difference over 20% in pro-inflammatory cytokine concentration between day 3 and day 8 was not found statistically different between the two groups, both in intent-to-treat (with imputation) and per protocol (without imputation) analyses. The incidences of most of neonatal complications were found to be similar. Hence, this trial did not evidence a beneficial effect of in-line filtration in very preterm infants on the inflammatory response syndrome and neonatal morbidities. These data should be interpreted according to local standards in infusion preparation and central line management. Nature Publishing Group UK 2020-03-19 /pmc/articles/PMC7081338/ /pubmed/32193413 http://dx.doi.org/10.1038/s41598-020-61815-4 Text en © The Author(s) 2020 Open Access 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 http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Virlouvet, Anne-Laure
Pansiot, Julien
Toumazi, Artemis
Colella, Marina
Capewell, Andreas
Guerriero, Emilie
Storme, Thomas
Rioualen, Stéphane
Bourmaud, Aurélie
Biran, Valérie
Baud, Olivier
In-line filtration in very preterm neonates: a randomized controlled trial
title In-line filtration in very preterm neonates: a randomized controlled trial
title_full In-line filtration in very preterm neonates: a randomized controlled trial
title_fullStr In-line filtration in very preterm neonates: a randomized controlled trial
title_full_unstemmed In-line filtration in very preterm neonates: a randomized controlled trial
title_short In-line filtration in very preterm neonates: a randomized controlled trial
title_sort in-line filtration in very preterm neonates: a randomized controlled trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081338/
https://www.ncbi.nlm.nih.gov/pubmed/32193413
http://dx.doi.org/10.1038/s41598-020-61815-4
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