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Less invasive surfactant administration and complications of preterm birth

In a large cohort study of the German Neonatal Network (GNN) we aimed to evaluate whether less invasive surfactant administration (LISA) strategy is associated with complications of preterm birth. Within the observational period n = 7533 very-low-birth-weight infants (VLBWI) with gestational age 22...

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Autores principales: Härtel, Christoph, Paul, Pia, Hanke, Kathrin, Humberg, Alexander, Kribs, Angela, Mehler, Katrin, Vochem, Matthias, Wieg, Christian, Roll, Claudia, Herting, Egbert, Göpel, Wolfgang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974027/
https://www.ncbi.nlm.nih.gov/pubmed/29844331
http://dx.doi.org/10.1038/s41598-018-26437-x
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author Härtel, Christoph
Paul, Pia
Hanke, Kathrin
Humberg, Alexander
Kribs, Angela
Mehler, Katrin
Vochem, Matthias
Wieg, Christian
Roll, Claudia
Herting, Egbert
Göpel, Wolfgang
author_facet Härtel, Christoph
Paul, Pia
Hanke, Kathrin
Humberg, Alexander
Kribs, Angela
Mehler, Katrin
Vochem, Matthias
Wieg, Christian
Roll, Claudia
Herting, Egbert
Göpel, Wolfgang
author_sort Härtel, Christoph
collection PubMed
description In a large cohort study of the German Neonatal Network (GNN) we aimed to evaluate whether less invasive surfactant administration (LISA) strategy is associated with complications of preterm birth. Within the observational period n = 7533 very-low-birth-weight infants (VLBWI) with gestational age 22 0/7 to 28 6/7 weeks were enrolled in GNN; n = 1214 VLBWI never received surfactant, n = 2624 VLBWI were treated according to LISA procedure, n = 3695 VLBWI had surfactant via endotracheal tube (ETT). LISA was associated with a reduced risk for adverse outcome measures including mortality [odds ratio (OR) 0.66 (95% CI: 0.51–0.84), p < 0.001] bronchopulmonary dysplasia [BPD; OR 0.55 (95% CI: 0.49–0.62), p < 0.001], intracerebral hemorrhage (ICH) grade II-IV [OR 0.55 (95% CI: 0.48–0.64), p < 0.001] and retinopathy of prematurity [ROP; OR 0.62 (95% CI: 0.45–0.85), p < 0.001]. Notably, LISA was associated with an increased risk for focal intestinal perforation [FIP; OR 1.49 (95% CI: 1.14–1.95), p = 0.002]. The differences in FIP rates were primarily observed in VLBWI born <26 weeks (LISA: 10.0 vs. ETT: 7.4%, p = 0.029). Our observational data confirm that LISA is associated with improved outcome. In infants <26 weeks we noted an increased risk for FIP. Future randomized controlled trials including LISA need to integrate safety analyses for this particular subgroup.
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spelling pubmed-59740272018-05-31 Less invasive surfactant administration and complications of preterm birth Härtel, Christoph Paul, Pia Hanke, Kathrin Humberg, Alexander Kribs, Angela Mehler, Katrin Vochem, Matthias Wieg, Christian Roll, Claudia Herting, Egbert Göpel, Wolfgang Sci Rep Article In a large cohort study of the German Neonatal Network (GNN) we aimed to evaluate whether less invasive surfactant administration (LISA) strategy is associated with complications of preterm birth. Within the observational period n = 7533 very-low-birth-weight infants (VLBWI) with gestational age 22 0/7 to 28 6/7 weeks were enrolled in GNN; n = 1214 VLBWI never received surfactant, n = 2624 VLBWI were treated according to LISA procedure, n = 3695 VLBWI had surfactant via endotracheal tube (ETT). LISA was associated with a reduced risk for adverse outcome measures including mortality [odds ratio (OR) 0.66 (95% CI: 0.51–0.84), p < 0.001] bronchopulmonary dysplasia [BPD; OR 0.55 (95% CI: 0.49–0.62), p < 0.001], intracerebral hemorrhage (ICH) grade II-IV [OR 0.55 (95% CI: 0.48–0.64), p < 0.001] and retinopathy of prematurity [ROP; OR 0.62 (95% CI: 0.45–0.85), p < 0.001]. Notably, LISA was associated with an increased risk for focal intestinal perforation [FIP; OR 1.49 (95% CI: 1.14–1.95), p = 0.002]. The differences in FIP rates were primarily observed in VLBWI born <26 weeks (LISA: 10.0 vs. ETT: 7.4%, p = 0.029). Our observational data confirm that LISA is associated with improved outcome. In infants <26 weeks we noted an increased risk for FIP. Future randomized controlled trials including LISA need to integrate safety analyses for this particular subgroup. Nature Publishing Group UK 2018-05-29 /pmc/articles/PMC5974027/ /pubmed/29844331 http://dx.doi.org/10.1038/s41598-018-26437-x Text en © The Author(s) 2018 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
Härtel, Christoph
Paul, Pia
Hanke, Kathrin
Humberg, Alexander
Kribs, Angela
Mehler, Katrin
Vochem, Matthias
Wieg, Christian
Roll, Claudia
Herting, Egbert
Göpel, Wolfgang
Less invasive surfactant administration and complications of preterm birth
title Less invasive surfactant administration and complications of preterm birth
title_full Less invasive surfactant administration and complications of preterm birth
title_fullStr Less invasive surfactant administration and complications of preterm birth
title_full_unstemmed Less invasive surfactant administration and complications of preterm birth
title_short Less invasive surfactant administration and complications of preterm birth
title_sort less invasive surfactant administration and complications of preterm birth
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974027/
https://www.ncbi.nlm.nih.gov/pubmed/29844331
http://dx.doi.org/10.1038/s41598-018-26437-x
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