The use of an alternate side lying positioning strategy during inhalation therapy does not prolong nebulisation time in adults with Cystic Fibrosis: a randomised crossover trial
Author:
Funder
National Health and Medical Research Council
Cystic Fibrosis Foundation
Publisher
Springer Science and Business Media LLC
Subject
Pulmonary and Respiratory Medicine
Link
http://link.springer.com/content/pdf/10.1186/s12890-017-0568-2.pdf
Reference23 articles.
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2. Fuchs HJ, Borowitz DS, Christiansen DH, Morris EM, Nash ML, Ramsey BW, et al. Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme study group. New Engl J Med. 1994;331(10):637–42.
3. Elkins MR, Robinson M, Rose BR, Harbour C, Moriarty CP, Marks GB, et al. A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis. New Engl J Med. 2006;354(3):229–40.
4. Ballmann M, von der Hardt H. Hypertonic saline and recombinant human DNase: a randomised cross-over pilot study in patients with cystic fibrosis. J Cyst Fibros. 2002;1:35–7.
5. Amis T, Jones H, Hughes J. Effect of posture on inter-regional distribution of pulmonary perfusion and VA/Q ratios in man. Respir Physiol. 1984;56(2):169–82.
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