Abstract
BackgroundCystic 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.MethodsThree 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.ResultsTen 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.ConclusionsDue 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.
Funder
Cystic Fibrosis Foundation
Publisher
Public Library of Science (PLoS)
Reference33 articles.
1. Cystic fibrosis;JS Elborn;The Lancet,2016
2. Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease;H Matsui;Cell,1998
3. Mucus clearance as a primary innate defense mechanism for mammalian airways;MR Knowles;The Journal of clinical investigation,2002
4. Effective mucus clearance is essential for respiratory health;SH Randell;American journal of respiratory cell and molecular biology,2006
5. Cystic fibrosis pulmonary guidelines: airway clearance therapies.;PA Flume;Respiratory care,2009
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