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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2018
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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. |
format | Online Article Text |
id | pubmed-5938808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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