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Acute viral bronchiolitis as a cause of pediatric acute respiratory distress syndrome

The Pediatric Acute Lung Injury Consensus Conference (PALICC) published pediatric-specific guidelines for the definition, management, and research in pediatric acute respiratory distress syndrome (PARDS). Acute viral bronchiolitis (AVB) remains one of the leading causes of admission to PICU. Respira...

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Autores principales: Ghazaly, Marwa M. H., Abu Faddan, Nagla H., Raafat, Duaa M., Mohammed, Nagwa A., Nadel, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648537/
https://www.ncbi.nlm.nih.gov/pubmed/33161501
http://dx.doi.org/10.1007/s00431-020-03852-9
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author Ghazaly, Marwa M. H.
Abu Faddan, Nagla H.
Raafat, Duaa M.
Mohammed, Nagwa A.
Nadel, Simon
author_facet Ghazaly, Marwa M. H.
Abu Faddan, Nagla H.
Raafat, Duaa M.
Mohammed, Nagwa A.
Nadel, Simon
author_sort Ghazaly, Marwa M. H.
collection PubMed
description The Pediatric Acute Lung Injury Consensus Conference (PALICC) published pediatric-specific guidelines for the definition, management, and research in pediatric acute respiratory distress syndrome (PARDS). Acute viral bronchiolitis (AVB) remains one of the leading causes of admission to PICU. Respiratory syncytial virus (RSV) is the most common cause of AVB. We aimed to evaluate the incidence of PARDS in AVB and identify the risk of RSV as a trigger pathogen for PARDS. This study is a retrospective single-center observational cohort study including children < 2 years of age admitted to the pediatric intensive care unit at St Mary’s Hospital, London, and presented with AVB in 3 years (2016–2018). Clinical and demographic data was collected; PALICC criteria were applied to define PARDS. Data was expressed as median (IQR range); non-parametric tests were used. In this study, 144 infants with acute viral bronchiolitis were admitted to PICU in the study period. Thirty-nine infants fulfilled criteria of PARDS with RSV as the most common virus identified. Bacterial infection was identified as a risk factor for development of PARDS in infants with AVB. Conclusion: AVB is an important cause of PARDS in infants. RSV is associated with a higher risk of PARDS in AVB. Bacterial co-infection is a significant risk factor for development of PARDS in AVB. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00431-020-03852-9.
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spelling pubmed-76485372020-11-09 Acute viral bronchiolitis as a cause of pediatric acute respiratory distress syndrome Ghazaly, Marwa M. H. Abu Faddan, Nagla H. Raafat, Duaa M. Mohammed, Nagwa A. Nadel, Simon Eur J Pediatr Original Article The Pediatric Acute Lung Injury Consensus Conference (PALICC) published pediatric-specific guidelines for the definition, management, and research in pediatric acute respiratory distress syndrome (PARDS). Acute viral bronchiolitis (AVB) remains one of the leading causes of admission to PICU. Respiratory syncytial virus (RSV) is the most common cause of AVB. We aimed to evaluate the incidence of PARDS in AVB and identify the risk of RSV as a trigger pathogen for PARDS. This study is a retrospective single-center observational cohort study including children < 2 years of age admitted to the pediatric intensive care unit at St Mary’s Hospital, London, and presented with AVB in 3 years (2016–2018). Clinical and demographic data was collected; PALICC criteria were applied to define PARDS. Data was expressed as median (IQR range); non-parametric tests were used. In this study, 144 infants with acute viral bronchiolitis were admitted to PICU in the study period. Thirty-nine infants fulfilled criteria of PARDS with RSV as the most common virus identified. Bacterial infection was identified as a risk factor for development of PARDS in infants with AVB. Conclusion: AVB is an important cause of PARDS in infants. RSV is associated with a higher risk of PARDS in AVB. Bacterial co-infection is a significant risk factor for development of PARDS in AVB. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00431-020-03852-9. Springer Berlin Heidelberg 2020-11-07 2021 /pmc/articles/PMC7648537/ /pubmed/33161501 http://dx.doi.org/10.1007/s00431-020-03852-9 Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Ghazaly, Marwa M. H.
Abu Faddan, Nagla H.
Raafat, Duaa M.
Mohammed, Nagwa A.
Nadel, Simon
Acute viral bronchiolitis as a cause of pediatric acute respiratory distress syndrome
title Acute viral bronchiolitis as a cause of pediatric acute respiratory distress syndrome
title_full Acute viral bronchiolitis as a cause of pediatric acute respiratory distress syndrome
title_fullStr Acute viral bronchiolitis as a cause of pediatric acute respiratory distress syndrome
title_full_unstemmed Acute viral bronchiolitis as a cause of pediatric acute respiratory distress syndrome
title_short Acute viral bronchiolitis as a cause of pediatric acute respiratory distress syndrome
title_sort acute viral bronchiolitis as a cause of pediatric acute respiratory distress syndrome
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648537/
https://www.ncbi.nlm.nih.gov/pubmed/33161501
http://dx.doi.org/10.1007/s00431-020-03852-9
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