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Lung Volume, Breathing Pattern and Ventilation Inhomogeneity in Preterm and Term Infants
BACKGROUND: Morphological changes in preterm infants with bronchopulmonary dysplasia (BPD) have functional consequences on lung volume, ventilation inhomogeneity and respiratory mechanics. Although some studies have shown lower lung volumes and increased ventilation inhomogeneity in BPD infants, con...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2645689/ https://www.ncbi.nlm.nih.gov/pubmed/19247491 http://dx.doi.org/10.1371/journal.pone.0004635 |
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author | Latzin, Philipp Roth, Stefan Thamrin, Cindy Hutten, Gerard J. Pramana, Isabelle Kuehni, Claudia E. Casaulta, Carmen Nelle, Matthias Riedel, Thomas Frey, Urs |
author_facet | Latzin, Philipp Roth, Stefan Thamrin, Cindy Hutten, Gerard J. Pramana, Isabelle Kuehni, Claudia E. Casaulta, Carmen Nelle, Matthias Riedel, Thomas Frey, Urs |
author_sort | Latzin, Philipp |
collection | PubMed |
description | BACKGROUND: Morphological changes in preterm infants with bronchopulmonary dysplasia (BPD) have functional consequences on lung volume, ventilation inhomogeneity and respiratory mechanics. Although some studies have shown lower lung volumes and increased ventilation inhomogeneity in BPD infants, conflicting results exist possibly due to differences in sedation and measurement techniques. METHODOLOGY/PRINCIPAL FINDINGS: We studied 127 infants with BPD, 58 preterm infants without BPD and 239 healthy term-born infants, at a matched post-conceptional age of 44 weeks during quiet natural sleep according to ATS/ERS standards. Lung function parameters measured were functional residual capacity (FRC) and ventilation inhomogeneity by multiple breath washout as well as tidal breathing parameters. Preterm infants with BPD had only marginally lower FRC (21.4 mL/kg) than preterm infants without BPD (23.4 mL/kg) and term-born infants (22.6 mL/kg), though there was no trend with disease severity. They also showed higher respiratory rates and lower ratios of time to peak expiratory flow and expiratory time (t (PTEF)/t (E)) than healthy preterm and term controls. These changes were related to disease severity. No differences were found for ventilation inhomogeneity. CONCLUSIONS: Our results suggest that preterm infants with BPD have a high capacity to maintain functional lung volume during natural sleep. The alterations in breathing pattern with disease severity may reflect presence of adaptive mechanisms to cope with the disease process. |
format | Text |
id | pubmed-2645689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-26456892009-02-27 Lung Volume, Breathing Pattern and Ventilation Inhomogeneity in Preterm and Term Infants Latzin, Philipp Roth, Stefan Thamrin, Cindy Hutten, Gerard J. Pramana, Isabelle Kuehni, Claudia E. Casaulta, Carmen Nelle, Matthias Riedel, Thomas Frey, Urs PLoS One Research Article BACKGROUND: Morphological changes in preterm infants with bronchopulmonary dysplasia (BPD) have functional consequences on lung volume, ventilation inhomogeneity and respiratory mechanics. Although some studies have shown lower lung volumes and increased ventilation inhomogeneity in BPD infants, conflicting results exist possibly due to differences in sedation and measurement techniques. METHODOLOGY/PRINCIPAL FINDINGS: We studied 127 infants with BPD, 58 preterm infants without BPD and 239 healthy term-born infants, at a matched post-conceptional age of 44 weeks during quiet natural sleep according to ATS/ERS standards. Lung function parameters measured were functional residual capacity (FRC) and ventilation inhomogeneity by multiple breath washout as well as tidal breathing parameters. Preterm infants with BPD had only marginally lower FRC (21.4 mL/kg) than preterm infants without BPD (23.4 mL/kg) and term-born infants (22.6 mL/kg), though there was no trend with disease severity. They also showed higher respiratory rates and lower ratios of time to peak expiratory flow and expiratory time (t (PTEF)/t (E)) than healthy preterm and term controls. These changes were related to disease severity. No differences were found for ventilation inhomogeneity. CONCLUSIONS: Our results suggest that preterm infants with BPD have a high capacity to maintain functional lung volume during natural sleep. The alterations in breathing pattern with disease severity may reflect presence of adaptive mechanisms to cope with the disease process. Public Library of Science 2009-02-27 /pmc/articles/PMC2645689/ /pubmed/19247491 http://dx.doi.org/10.1371/journal.pone.0004635 Text en Latzin et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Latzin, Philipp Roth, Stefan Thamrin, Cindy Hutten, Gerard J. Pramana, Isabelle Kuehni, Claudia E. Casaulta, Carmen Nelle, Matthias Riedel, Thomas Frey, Urs Lung Volume, Breathing Pattern and Ventilation Inhomogeneity in Preterm and Term Infants |
title | Lung Volume, Breathing Pattern and Ventilation Inhomogeneity in Preterm and Term Infants |
title_full | Lung Volume, Breathing Pattern and Ventilation Inhomogeneity in Preterm and Term Infants |
title_fullStr | Lung Volume, Breathing Pattern and Ventilation Inhomogeneity in Preterm and Term Infants |
title_full_unstemmed | Lung Volume, Breathing Pattern and Ventilation Inhomogeneity in Preterm and Term Infants |
title_short | Lung Volume, Breathing Pattern and Ventilation Inhomogeneity in Preterm and Term Infants |
title_sort | lung volume, breathing pattern and ventilation inhomogeneity in preterm and term infants |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2645689/ https://www.ncbi.nlm.nih.gov/pubmed/19247491 http://dx.doi.org/10.1371/journal.pone.0004635 |
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