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Acute inhalation of hypertonic saline does not improve mucociliary clearance in all children with cystic fibrosis

BACKGROUND: Little is known of how mucociliary clearance (MCC) in children with cystic fibrosis (CF) and normal pulmonary function compares with healthy adults, or how an acute inhalation of 7% hypertonic saline (HS) aerosol affects MCC in these same children. METHODS: We compared MCC in 12 children...

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Autores principales: Laube, Beth L, Sharpless, Gail, Carson, Kathryn A, Kelly, Amber, Mogayzel, Peter J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180295/
https://www.ncbi.nlm.nih.gov/pubmed/21896198
http://dx.doi.org/10.1186/1471-2466-11-45
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author Laube, Beth L
Sharpless, Gail
Carson, Kathryn A
Kelly, Amber
Mogayzel, Peter J
author_facet Laube, Beth L
Sharpless, Gail
Carson, Kathryn A
Kelly, Amber
Mogayzel, Peter J
author_sort Laube, Beth L
collection PubMed
description BACKGROUND: Little is known of how mucociliary clearance (MCC) in children with cystic fibrosis (CF) and normal pulmonary function compares with healthy adults, or how an acute inhalation of 7% hypertonic saline (HS) aerosol affects MCC in these same children. METHODS: We compared MCC in 12 children with CF and normal pulmonary function after an acute inhalation of 0.12% saline (placebo), or HS, admixed with the radioisotope (99 m)technetium sulfur colloid in a double-blind, randomized, cross-over study. Mucociliary clearance on the placebo day in the children was also compared to MCC in 10 healthy, non-CF adults. Mucociliary clearance was quantified over a 90 min period, using gamma scintigraphy, and is reported as MCC at 60 min (MCC60) and 90 min (MCC90). RESULTS: Median [interquartile range] MCC60 and MCC90 in the children on the placebo visit were 15.4 [12.4-24.5]% and 19.3 [17.3-27.8%]%, respectively, which were similar to the adults with 17.8 [6.4-28.7]% and 29.6 [16.1-43.5]%, respectively. There was no significant improvement in MCC60 (2.2 [-6.2-11.8]%) or MCC90 (2.3 [-1.2-10.5]%) with HS, compared to placebo. In addition, 5/12 and 4/12 of the children showed a decrease in MCC60 and MCC90, respectively, after inhalation of HS. A post hoc subgroup analysis of the change in MCC90 after HS showed a significantly greater improvement in MCC in children with lower placebo MCC90 compared to those with higher placebo MCC90 (p = 0.045). CONCLUSIONS: These data suggest that percent MCC varies significantly between children with CF lung disease and normal pulmonary functions, with some children demonstrating MCC values within the normal range and others showing MCC values that are below normal values. In addition, although MCC did not improve in all children after inhalation of HS, improvement did occur in children with relatively low MCC values after placebo. This finding suggests that acute inhalation of hypertonic saline may benefit a subset of children with low MCC values. TRIAL REGISTRATION: ClinicalTrials.gov: NCT01293084
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spelling pubmed-31802952011-09-27 Acute inhalation of hypertonic saline does not improve mucociliary clearance in all children with cystic fibrosis Laube, Beth L Sharpless, Gail Carson, Kathryn A Kelly, Amber Mogayzel, Peter J BMC Pulm Med Research Article BACKGROUND: Little is known of how mucociliary clearance (MCC) in children with cystic fibrosis (CF) and normal pulmonary function compares with healthy adults, or how an acute inhalation of 7% hypertonic saline (HS) aerosol affects MCC in these same children. METHODS: We compared MCC in 12 children with CF and normal pulmonary function after an acute inhalation of 0.12% saline (placebo), or HS, admixed with the radioisotope (99 m)technetium sulfur colloid in a double-blind, randomized, cross-over study. Mucociliary clearance on the placebo day in the children was also compared to MCC in 10 healthy, non-CF adults. Mucociliary clearance was quantified over a 90 min period, using gamma scintigraphy, and is reported as MCC at 60 min (MCC60) and 90 min (MCC90). RESULTS: Median [interquartile range] MCC60 and MCC90 in the children on the placebo visit were 15.4 [12.4-24.5]% and 19.3 [17.3-27.8%]%, respectively, which were similar to the adults with 17.8 [6.4-28.7]% and 29.6 [16.1-43.5]%, respectively. There was no significant improvement in MCC60 (2.2 [-6.2-11.8]%) or MCC90 (2.3 [-1.2-10.5]%) with HS, compared to placebo. In addition, 5/12 and 4/12 of the children showed a decrease in MCC60 and MCC90, respectively, after inhalation of HS. A post hoc subgroup analysis of the change in MCC90 after HS showed a significantly greater improvement in MCC in children with lower placebo MCC90 compared to those with higher placebo MCC90 (p = 0.045). CONCLUSIONS: These data suggest that percent MCC varies significantly between children with CF lung disease and normal pulmonary functions, with some children demonstrating MCC values within the normal range and others showing MCC values that are below normal values. In addition, although MCC did not improve in all children after inhalation of HS, improvement did occur in children with relatively low MCC values after placebo. This finding suggests that acute inhalation of hypertonic saline may benefit a subset of children with low MCC values. TRIAL REGISTRATION: ClinicalTrials.gov: NCT01293084 BioMed Central 2011-09-06 /pmc/articles/PMC3180295/ /pubmed/21896198 http://dx.doi.org/10.1186/1471-2466-11-45 Text en Copyright ©2011 Laube et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Laube, Beth L
Sharpless, Gail
Carson, Kathryn A
Kelly, Amber
Mogayzel, Peter J
Acute inhalation of hypertonic saline does not improve mucociliary clearance in all children with cystic fibrosis
title Acute inhalation of hypertonic saline does not improve mucociliary clearance in all children with cystic fibrosis
title_full Acute inhalation of hypertonic saline does not improve mucociliary clearance in all children with cystic fibrosis
title_fullStr Acute inhalation of hypertonic saline does not improve mucociliary clearance in all children with cystic fibrosis
title_full_unstemmed Acute inhalation of hypertonic saline does not improve mucociliary clearance in all children with cystic fibrosis
title_short Acute inhalation of hypertonic saline does not improve mucociliary clearance in all children with cystic fibrosis
title_sort acute inhalation of hypertonic saline does not improve mucociliary clearance in all children with cystic fibrosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180295/
https://www.ncbi.nlm.nih.gov/pubmed/21896198
http://dx.doi.org/10.1186/1471-2466-11-45
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