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Changes in physiological, functional and structural markers of cystic fibrosis lung disease with treatment of a pulmonary exacerbation

โœ Scribed by Horsley, A. R.; Davies, J. C.; Gray, R. D.; Macleod, K. A.; Donovan, J.; Aziz, Z. A.; Bell, N. J.; Rainer, M.; Mt-Isa, S.; Voase, N.; Dewar, M. H.; Saunders, C.; Gibson, J. S.; Parra-Leiton, J.; Larsen, M. D.; Jeswiet, S.; Soussi, S.; Bakar, Y.; Meister, M. G.; Tyler, P.; Doherty, A.; Hansell, D. M.; Ashby, D.; Hyde, S. C.; Gill, D. R.; Greening, A. P.; Porteous, D. J.; Innes, J. A.; Boyd, A. C.; Griesenbach, U.; Cunningham, S.; Alton, E. W.


Book ID
119944017
Publisher
BMJ Publishing Group
Year
2013
Tongue
English
Weight
629 KB
Volume
68
Category
Article
ISSN
0040-6376

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Chest physiotherapy (CPT) is recommended for the clearance of bronchial secretions in the management of patients with cystic fibrosis (CF). The Flutterยฎ valve (Scandipharm, Birmingham, AL) has been introduced as an alternative method to CPT for airway mucus clearance. The objective of this study was