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Ventilation inhomogeneities in children with congenital thoracic malformations

BACKGROUND: Congenital thoracic malformations (CTM) are rare lung lesions that are managed with surgical resection or active surveillance. The objective of this study was to comprehensively assess large and small airway function in children with CTM who underwent lobectomy in early life. We hypothes...

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Autores principales: Mandaliya, Payal H, Morten, Matthew, Kumar, Rajendra, James, Alan, Deshpande, Aniruddh, Murphy, Vanessa E, Gibson, Peter G, Whitehead, Bruce, Robinson, Paul, Mattes, Joerg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4417263/
https://www.ncbi.nlm.nih.gov/pubmed/25887144
http://dx.doi.org/10.1186/s12890-015-0023-1
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author Mandaliya, Payal H
Morten, Matthew
Kumar, Rajendra
James, Alan
Deshpande, Aniruddh
Murphy, Vanessa E
Gibson, Peter G
Whitehead, Bruce
Robinson, Paul
Mattes, Joerg
author_facet Mandaliya, Payal H
Morten, Matthew
Kumar, Rajendra
James, Alan
Deshpande, Aniruddh
Murphy, Vanessa E
Gibson, Peter G
Whitehead, Bruce
Robinson, Paul
Mattes, Joerg
author_sort Mandaliya, Payal H
collection PubMed
description BACKGROUND: Congenital thoracic malformations (CTM) are rare lung lesions that are managed with surgical resection or active surveillance. The objective of this study was to comprehensively assess large and small airway function in children with CTM who underwent lobectomy in early life. We hypothesise that sensitive measures of lung function will demonstrate residual impairments in CTM compared to healthy children. METHODS: Nitrogen lung clearance index (LCI), reactance and resistance (X5Hz and R5Hz), forced expiratory volume in 1 s and forced vital capacity (FEV1 and FVC) were prospectively measured in 10 children with CTM (mean age/SD: 7.6/1.3) who had undergone surgical resection in early life and in 17 healthy children (mean age/SD: 4.8/0.4). Total lung capacity (TLC) was also conducted in children older than 7 years of age with CTM (n = 8). RESULTS: Mean LCI was 8.0 (95% CI 7.5 to 8.5) in the CTM group and 7.3 (95% CI 7.0 to 7.6) in healthy children (p = 0.016). Mean X5Hz was −0.44kPa/l/s (95% CI −0.58 to −0.31) in the CTM group and −0.31kPa/l/s (95% CI −0.35 to −0.27) in healthy children (p = 0.02). Mean Z score for X5Hz was −2.11 (95% CI −3.59 to −0.63) in the CTM group and −0.11 (95% CI −0.55 to 0.33) in healthy children (p = 0.0008). Mean FEV1 was 1.21 L (95% CI 0.97 to 1.45) in the CTM group and 1.02 L (95% CI 0.90 to 1.15) in healthy children (p = 0.22). Mean % predicted FEV1 was 83% (95% CI 74 to 92) in the CTM group and 97% (95% CI 87 to 107) in healthy children (p < 0.05). Mean % predicted TLC in CTM children was 121.3% (95% CI 88.45 to 154.1). Mean LCI was inversely correlated with height z-scores in the CTM group (rs = −0.88, p = 0.002) but not in healthy children (rs = 0.22, p = 0.4). CONCLUSIONS: Children with CTM have impaired lung function as demonstrated by the significant differences in LCI, reactance and FEV1 but not FVC, resistance and TLC. These findings may be of clinical relevance as ventilation inhomogeneities are closely correlated with somatic growth in this study. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12890-015-0023-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-44172632015-05-03 Ventilation inhomogeneities in children with congenital thoracic malformations Mandaliya, Payal H Morten, Matthew Kumar, Rajendra James, Alan Deshpande, Aniruddh Murphy, Vanessa E Gibson, Peter G Whitehead, Bruce Robinson, Paul Mattes, Joerg BMC Pulm Med Research Article BACKGROUND: Congenital thoracic malformations (CTM) are rare lung lesions that are managed with surgical resection or active surveillance. The objective of this study was to comprehensively assess large and small airway function in children with CTM who underwent lobectomy in early life. We hypothesise that sensitive measures of lung function will demonstrate residual impairments in CTM compared to healthy children. METHODS: Nitrogen lung clearance index (LCI), reactance and resistance (X5Hz and R5Hz), forced expiratory volume in 1 s and forced vital capacity (FEV1 and FVC) were prospectively measured in 10 children with CTM (mean age/SD: 7.6/1.3) who had undergone surgical resection in early life and in 17 healthy children (mean age/SD: 4.8/0.4). Total lung capacity (TLC) was also conducted in children older than 7 years of age with CTM (n = 8). RESULTS: Mean LCI was 8.0 (95% CI 7.5 to 8.5) in the CTM group and 7.3 (95% CI 7.0 to 7.6) in healthy children (p = 0.016). Mean X5Hz was −0.44kPa/l/s (95% CI −0.58 to −0.31) in the CTM group and −0.31kPa/l/s (95% CI −0.35 to −0.27) in healthy children (p = 0.02). Mean Z score for X5Hz was −2.11 (95% CI −3.59 to −0.63) in the CTM group and −0.11 (95% CI −0.55 to 0.33) in healthy children (p = 0.0008). Mean FEV1 was 1.21 L (95% CI 0.97 to 1.45) in the CTM group and 1.02 L (95% CI 0.90 to 1.15) in healthy children (p = 0.22). Mean % predicted FEV1 was 83% (95% CI 74 to 92) in the CTM group and 97% (95% CI 87 to 107) in healthy children (p < 0.05). Mean % predicted TLC in CTM children was 121.3% (95% CI 88.45 to 154.1). Mean LCI was inversely correlated with height z-scores in the CTM group (rs = −0.88, p = 0.002) but not in healthy children (rs = 0.22, p = 0.4). CONCLUSIONS: Children with CTM have impaired lung function as demonstrated by the significant differences in LCI, reactance and FEV1 but not FVC, resistance and TLC. These findings may be of clinical relevance as ventilation inhomogeneities are closely correlated with somatic growth in this study. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12890-015-0023-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-03-25 /pmc/articles/PMC4417263/ /pubmed/25887144 http://dx.doi.org/10.1186/s12890-015-0023-1 Text en © Morten et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Mandaliya, Payal H
Morten, Matthew
Kumar, Rajendra
James, Alan
Deshpande, Aniruddh
Murphy, Vanessa E
Gibson, Peter G
Whitehead, Bruce
Robinson, Paul
Mattes, Joerg
Ventilation inhomogeneities in children with congenital thoracic malformations
title Ventilation inhomogeneities in children with congenital thoracic malformations
title_full Ventilation inhomogeneities in children with congenital thoracic malformations
title_fullStr Ventilation inhomogeneities in children with congenital thoracic malformations
title_full_unstemmed Ventilation inhomogeneities in children with congenital thoracic malformations
title_short Ventilation inhomogeneities in children with congenital thoracic malformations
title_sort ventilation inhomogeneities in children with congenital thoracic malformations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4417263/
https://www.ncbi.nlm.nih.gov/pubmed/25887144
http://dx.doi.org/10.1186/s12890-015-0023-1
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