Efficacy of the Flutter device for airway mucus clearance in patients with cystic fibrosis

1994 ◽  
Vol 124 (5) ◽  
pp. 689-693 ◽  
Author(s):  
Michael W. Konstan ◽  
Robert C. Stern ◽  
Carl F. Doershuk
2018 ◽  
Vol 52 (6) ◽  
pp. 1801297 ◽  
Author(s):  
David B. Hill ◽  
Robert F. Long ◽  
William J. Kissner ◽  
Eyad Atieh ◽  
Ian C. Garbarine ◽  
...  

Cystic fibrosis (CF) is a recessive genetic disease that is characterised by airway mucus plugging and reduced mucus clearance. There are currently alternative hypotheses that attempt to describe the abnormally viscous and elastic mucus that is a hallmark of CF airways disease, including: 1) loss of CF transmembrane regulator (CFTR)-dependent airway surface volume (water) secretion, producing mucus hyperconcentration-dependent increased viscosity, and 2) impaired bicarbonate secretion by CFTR, producing acidification of airway surfaces and increased mucus viscosity.A series of experiments was conducted to determine the contributions of mucus concentration versus pH to the rheological properties of airway mucus across length scales from the nanoscopic to macroscopic.For length scales greater than the nanoscopic, i.e. those relevant to mucociliary clearance, the effect of mucus concentration dominated over the effect of airway acidification.Mucus hydration and chemical reduction of disulfide bonds that connect mucin monomers are more promising therapeutic approaches than alkalisation.


1995 ◽  
Vol 39 (2) ◽  
pp. 133
Author(s):  
MICHAEL W. KONSTAN ◽  
ROBERT C. STERN ◽  
CARL F. DOERSHUK

1996 ◽  
Vol 128 (1) ◽  
pp. 165-166
Author(s):  
Michael W. Konstan ◽  
Robert C. Stern ◽  
Carl F. Doershuk, MD

1996 ◽  
Vol 128 (1) ◽  
pp. 165 ◽  
Author(s):  
Vinit K. Mahesh ◽  
Julie A. McDougal ◽  
Lisa Haluszka

1995 ◽  
Vol 39 (2) ◽  
pp. 133
Author(s):  
MICHAEL W. KONSTAN ◽  
ROBERT C. STERN ◽  
CARL F. DOERSHUK

2019 ◽  
Vol 53 (4) ◽  
pp. 1801793 ◽  
Author(s):  
Tiffany J. Dwyer ◽  
Evangelia Daviskas ◽  
Rahizan Zainuldin ◽  
Jordan Verschuer ◽  
Stefan Eberl ◽  
...  

Exercise improves mucus clearance in people without lung disease and those with chronic bronchitis. No study has investigated exercise alone for mucus clearance in cystic fibrosis (CF). The aim of this study was to compare the effects of treadmill exercise to resting breathing and airway clearance with positive expiratory pressure (PEP) therapy on mucus clearance in adults with CF.This 3-day randomised, controlled, crossover trial included 14 adults with mild to severe CF lung disease (forced expiratory volume in 1 s % predicted 31–113%). Interventions were 20 min of resting breathing (control), treadmill exercise at 60% of the participant's peak oxygen consumption or PEP therapy (including huffing and coughing). Mucus clearance was measured using the radioaerosol technique and gamma camera imaging.Treadmill exercise improved whole lung mucus clearance compared to resting breathing (mean difference 3%, 95% CI 2–4); however, exercise alone was less effective than PEP therapy (mean difference −7%, 95% CI −6– −8). When comparing treadmill exercise to PEP therapy, there were no significant differences in mucus clearance from the intermediate and peripheral lung regions, but significantly less clearance from the central lung region (likely reflecting the huffing and coughing that was only in PEP therapy).It is recommended that huffing and coughing are included to maximise mucus clearance with exercise.


1999 ◽  
Vol 14 (3) ◽  
pp. 678 ◽  
Author(s):  
M. Robinson ◽  
E. Daviskas ◽  
S. Eberl ◽  
J. Baker ◽  
H-K Chan ◽  
...  

Radiology ◽  
2017 ◽  
Vol 285 (1) ◽  
pp. 261-269 ◽  
Author(s):  
Gaël Dournes ◽  
Patrick Berger ◽  
John Refait ◽  
Julie Macey ◽  
Stephanie Bui ◽  
...  

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