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How to decrease bronchopulmonary dysplasia in your neonatal intensive care unit today and “tomorrow”

Bronchopulmonary dysplasia, or BPD, is the most common chronic lung disease in infants. Genetic predisposition and developmental vulnerability secondary to antenatal and postnatal infections, compounded with exposure to hyperoxia and invasive mechanical ventilation to an immature lung, result in per...

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Detalles Bibliográficos
Autores principales: Nelin, Leif D., Bhandari, Vineet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405789/
https://www.ncbi.nlm.nih.gov/pubmed/28503300
http://dx.doi.org/10.12688/f1000research.10832.1
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author Nelin, Leif D.
Bhandari, Vineet
author_facet Nelin, Leif D.
Bhandari, Vineet
author_sort Nelin, Leif D.
collection PubMed
description Bronchopulmonary dysplasia, or BPD, is the most common chronic lung disease in infants. Genetic predisposition and developmental vulnerability secondary to antenatal and postnatal infections, compounded with exposure to hyperoxia and invasive mechanical ventilation to an immature lung, result in persistent inflammation, culminating in the characteristic pulmonary phenotype of BPD of impaired alveolarization and dysregulated vascularization. In this article, we highlight specific areas in current management, and speculate on therapeutic strategies that are on the horizon, that we believe will make an impact in decreasing the incidence of BPD in your neonatal intensive care units.
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spelling pubmed-54057892017-05-12 How to decrease bronchopulmonary dysplasia in your neonatal intensive care unit today and “tomorrow” Nelin, Leif D. Bhandari, Vineet F1000Res Review Bronchopulmonary dysplasia, or BPD, is the most common chronic lung disease in infants. Genetic predisposition and developmental vulnerability secondary to antenatal and postnatal infections, compounded with exposure to hyperoxia and invasive mechanical ventilation to an immature lung, result in persistent inflammation, culminating in the characteristic pulmonary phenotype of BPD of impaired alveolarization and dysregulated vascularization. In this article, we highlight specific areas in current management, and speculate on therapeutic strategies that are on the horizon, that we believe will make an impact in decreasing the incidence of BPD in your neonatal intensive care units. F1000Research 2017-04-21 /pmc/articles/PMC5405789/ /pubmed/28503300 http://dx.doi.org/10.12688/f1000research.10832.1 Text en Copyright: © 2017 Nelin LD and Bhandari V http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Nelin, Leif D.
Bhandari, Vineet
How to decrease bronchopulmonary dysplasia in your neonatal intensive care unit today and “tomorrow”
title How to decrease bronchopulmonary dysplasia in your neonatal intensive care unit today and “tomorrow”
title_full How to decrease bronchopulmonary dysplasia in your neonatal intensive care unit today and “tomorrow”
title_fullStr How to decrease bronchopulmonary dysplasia in your neonatal intensive care unit today and “tomorrow”
title_full_unstemmed How to decrease bronchopulmonary dysplasia in your neonatal intensive care unit today and “tomorrow”
title_short How to decrease bronchopulmonary dysplasia in your neonatal intensive care unit today and “tomorrow”
title_sort how to decrease bronchopulmonary dysplasia in your neonatal intensive care unit today and “tomorrow”
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405789/
https://www.ncbi.nlm.nih.gov/pubmed/28503300
http://dx.doi.org/10.12688/f1000research.10832.1
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