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Effect of airway clearance therapies on mucociliary clearance in adults with cystic fibrosis: A randomized controlled trial
BACKGROUND: Cystic fibrosis (CF) is an inherited disorder causing impaired mucociliary clearance within the respiratory tract, and is associated with bronchiectasis, chronic respiratory infections, and early death. Airway clearance therapies have long been a cornerstone of management of individuals...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122229/ https://www.ncbi.nlm.nih.gov/pubmed/35594286 http://dx.doi.org/10.1371/journal.pone.0268622 |
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author | Trimble, Aaron Zeman, Kirby Wu, Jihong Ceppe, Agathe Bennett, William Donaldson, Scott |
author_facet | Trimble, Aaron Zeman, Kirby Wu, Jihong Ceppe, Agathe Bennett, William Donaldson, Scott |
author_sort | Trimble, Aaron |
collection | PubMed |
description | BACKGROUND: Cystic fibrosis (CF) is an inherited disorder causing impaired mucociliary clearance within the respiratory tract, and is associated with bronchiectasis, chronic respiratory infections, and early death. Airway clearance therapies have long been a cornerstone of management of individuals with CF, although evidence supporting their use is lacking. We designed a randomized controlled trial to quantitatively compare the effects of different forms of airway clearance on mucociliary clearance. METHODS: Three different physiotherapy methods to augment cough-clearance were studied in addition to cough-clearance alone: high-frequency chest-wall oscillating vest, oscillatory positive expiratory pressure, and whole-body vibration. We used gamma scintigraphy after inhalation of radiolabeled particles to quantify mucus clearance before, during, and after physiotherapy. As secondary endpoints, we measured concentrations of small molecules in exhaled breath that may impact mucus clearance. RESULTS: Ten subjects were enrolled and completed study procedures. No differences were identified between any method of airway clearance, including cough clearance alone. We did identify changes in certain small molecule concentrations in exhaled breath following airway clearance. CONCLUSIONS: Due to the limitations of this study, we do not believe the negative results suggest a change in clinical practice with regard to airway clearance. Findings pertaining to small molecules in exhaled breath may serve as future opportunities for study. |
format | Online Article Text |
id | pubmed-9122229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-91222292022-05-21 Effect of airway clearance therapies on mucociliary clearance in adults with cystic fibrosis: A randomized controlled trial Trimble, Aaron Zeman, Kirby Wu, Jihong Ceppe, Agathe Bennett, William Donaldson, Scott PLoS One Research Article BACKGROUND: Cystic fibrosis (CF) is an inherited disorder causing impaired mucociliary clearance within the respiratory tract, and is associated with bronchiectasis, chronic respiratory infections, and early death. Airway clearance therapies have long been a cornerstone of management of individuals with CF, although evidence supporting their use is lacking. We designed a randomized controlled trial to quantitatively compare the effects of different forms of airway clearance on mucociliary clearance. METHODS: Three different physiotherapy methods to augment cough-clearance were studied in addition to cough-clearance alone: high-frequency chest-wall oscillating vest, oscillatory positive expiratory pressure, and whole-body vibration. We used gamma scintigraphy after inhalation of radiolabeled particles to quantify mucus clearance before, during, and after physiotherapy. As secondary endpoints, we measured concentrations of small molecules in exhaled breath that may impact mucus clearance. RESULTS: Ten subjects were enrolled and completed study procedures. No differences were identified between any method of airway clearance, including cough clearance alone. We did identify changes in certain small molecule concentrations in exhaled breath following airway clearance. CONCLUSIONS: Due to the limitations of this study, we do not believe the negative results suggest a change in clinical practice with regard to airway clearance. Findings pertaining to small molecules in exhaled breath may serve as future opportunities for study. Public Library of Science 2022-05-20 /pmc/articles/PMC9122229/ /pubmed/35594286 http://dx.doi.org/10.1371/journal.pone.0268622 Text en © 2022 Trimble et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Trimble, Aaron Zeman, Kirby Wu, Jihong Ceppe, Agathe Bennett, William Donaldson, Scott Effect of airway clearance therapies on mucociliary clearance in adults with cystic fibrosis: A randomized controlled trial |
title | Effect of airway clearance therapies on mucociliary clearance in adults with cystic fibrosis: A randomized controlled trial |
title_full | Effect of airway clearance therapies on mucociliary clearance in adults with cystic fibrosis: A randomized controlled trial |
title_fullStr | Effect of airway clearance therapies on mucociliary clearance in adults with cystic fibrosis: A randomized controlled trial |
title_full_unstemmed | Effect of airway clearance therapies on mucociliary clearance in adults with cystic fibrosis: A randomized controlled trial |
title_short | Effect of airway clearance therapies on mucociliary clearance in adults with cystic fibrosis: A randomized controlled trial |
title_sort | effect of airway clearance therapies on mucociliary clearance in adults with cystic fibrosis: a randomized controlled trial |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122229/ https://www.ncbi.nlm.nih.gov/pubmed/35594286 http://dx.doi.org/10.1371/journal.pone.0268622 |
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