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Inhaled corticosteroids in ventilated preterm neonates: a non-randomized dose-ranging study

BACKGROUND: Inhaled corticosteroids (ICS) offer targeted treatment for bronchopulmonary dysplasia (BPD) with minimal systemic effects compared to systemic steroids. However, dosing of ICS in the management of infants at high-risk of developing BPD is not well established. The objective of this study...

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Autores principales: Raghuram, Kamini, Dunn, Michael, Jangaard, Krista, Reilly, Maureen, Asztalos, Elizabeth, Kelly, Edmond, Vincer, Michael, Shah, Vibhuti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5938808/
https://www.ncbi.nlm.nih.gov/pubmed/29734948
http://dx.doi.org/10.1186/s12887-018-1134-7
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author Raghuram, Kamini
Dunn, Michael
Jangaard, Krista
Reilly, Maureen
Asztalos, Elizabeth
Kelly, Edmond
Vincer, Michael
Shah, Vibhuti
author_facet Raghuram, Kamini
Dunn, Michael
Jangaard, Krista
Reilly, Maureen
Asztalos, Elizabeth
Kelly, Edmond
Vincer, Michael
Shah, Vibhuti
author_sort Raghuram, Kamini
collection PubMed
description BACKGROUND: Inhaled corticosteroids (ICS) offer targeted treatment for bronchopulmonary dysplasia (BPD) with minimal systemic effects compared to systemic steroids. However, dosing of ICS in the management of infants at high-risk of developing BPD is not well established. The objective of this study was to determine an effective dose of ICS for the treatment of ventilator-dependent infants to facilitate extubation or reduce fractional inspired oxygen concentration. METHODS: Forty-one infants born at < 32 weeks gestational age (GA) or < 1250 g who were ventilator-dependent at 10–28 days postnatal age were included. A non-randomized dose-ranging trial was performed using aerosolized inhaled beclomethasone with hydrofluoralkane propellant (HFA-BDP). Four dosing groups (200, 400, 600 and 800 μg twice daily for 1 week) with 11, 11, 10 and 9 infants in each group, respectively, were studied. The primary outcome was therapeutic efficacy (successful extubation or reduction in FiO(2) of > 75% from baseline) in ≥60% of infants in the group. Oxygen requirements, complications and long-term neurodevelopmental outcomes were also assessed. RESULTS: The median age at enrollment was 22 (10–28) postnatal days. The primary outcome, therapeutic efficacy as defined above, was not achieved in any group. However, there was a significant reduction in post-treatment FiO(2) at a dose of 800 μg bid. No obvious trends were seen in long-term neurodevelopmental outcomes. CONCLUSIONS: Therapeutic efficacy was not achieved with all studied doses of ICS. A significant reduction in oxygen requirements was noted in ventilator-dependent preterm infants at 10–28 days of age when given 800 μg of HFA-BDP bid. Larger randomized trials of ICS are required to determine efficacy for the management of infants at high-risk for development of BPD. TRIAL REGISTRATION: This clinical trial was registered retrospectively on clinicaltrials.gov. The registration number is NCT03503994.
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spelling pubmed-59388082018-05-11 Inhaled corticosteroids in ventilated preterm neonates: a non-randomized dose-ranging study Raghuram, Kamini Dunn, Michael Jangaard, Krista Reilly, Maureen Asztalos, Elizabeth Kelly, Edmond Vincer, Michael Shah, Vibhuti BMC Pediatr Research Article BACKGROUND: Inhaled corticosteroids (ICS) offer targeted treatment for bronchopulmonary dysplasia (BPD) with minimal systemic effects compared to systemic steroids. However, dosing of ICS in the management of infants at high-risk of developing BPD is not well established. The objective of this study was to determine an effective dose of ICS for the treatment of ventilator-dependent infants to facilitate extubation or reduce fractional inspired oxygen concentration. METHODS: Forty-one infants born at < 32 weeks gestational age (GA) or < 1250 g who were ventilator-dependent at 10–28 days postnatal age were included. A non-randomized dose-ranging trial was performed using aerosolized inhaled beclomethasone with hydrofluoralkane propellant (HFA-BDP). Four dosing groups (200, 400, 600 and 800 μg twice daily for 1 week) with 11, 11, 10 and 9 infants in each group, respectively, were studied. The primary outcome was therapeutic efficacy (successful extubation or reduction in FiO(2) of > 75% from baseline) in ≥60% of infants in the group. Oxygen requirements, complications and long-term neurodevelopmental outcomes were also assessed. RESULTS: The median age at enrollment was 22 (10–28) postnatal days. The primary outcome, therapeutic efficacy as defined above, was not achieved in any group. However, there was a significant reduction in post-treatment FiO(2) at a dose of 800 μg bid. No obvious trends were seen in long-term neurodevelopmental outcomes. CONCLUSIONS: Therapeutic efficacy was not achieved with all studied doses of ICS. A significant reduction in oxygen requirements was noted in ventilator-dependent preterm infants at 10–28 days of age when given 800 μg of HFA-BDP bid. Larger randomized trials of ICS are required to determine efficacy for the management of infants at high-risk for development of BPD. TRIAL REGISTRATION: This clinical trial was registered retrospectively on clinicaltrials.gov. The registration number is NCT03503994. BioMed Central 2018-05-07 /pmc/articles/PMC5938808/ /pubmed/29734948 http://dx.doi.org/10.1186/s12887-018-1134-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Raghuram, Kamini
Dunn, Michael
Jangaard, Krista
Reilly, Maureen
Asztalos, Elizabeth
Kelly, Edmond
Vincer, Michael
Shah, Vibhuti
Inhaled corticosteroids in ventilated preterm neonates: a non-randomized dose-ranging study
title Inhaled corticosteroids in ventilated preterm neonates: a non-randomized dose-ranging study
title_full Inhaled corticosteroids in ventilated preterm neonates: a non-randomized dose-ranging study
title_fullStr Inhaled corticosteroids in ventilated preterm neonates: a non-randomized dose-ranging study
title_full_unstemmed Inhaled corticosteroids in ventilated preterm neonates: a non-randomized dose-ranging study
title_short Inhaled corticosteroids in ventilated preterm neonates: a non-randomized dose-ranging study
title_sort inhaled corticosteroids in ventilated preterm neonates: a non-randomized dose-ranging study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5938808/
https://www.ncbi.nlm.nih.gov/pubmed/29734948
http://dx.doi.org/10.1186/s12887-018-1134-7
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