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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2017
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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. |
format | Online Article Text |
id | pubmed-5405789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
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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