Acapella vs. PEP mask therapy: A randomised trial in children with cystic fibrosis during respiratory exacerbation

References

• App EM, Kieselmann R, Reinhardt D, Lindemann H, Dasgupta B, King M, Brand P 1998 Sputum rheology changes in cystic fibrosis lung disease following two different types of physiotherapy. Flutter vs autogenic drainage. Chest 114:171–177
   PubMed Web of Science ®Google Scholar
• Bradley J, Howard J, Wallace E, Elborn S 1999 Validity of a modified shuttle test in adult cystic fibrosis. Thorax 54:437–439
   PubMed Web of Science ®Google Scholar
• Bradley J, Howard J, Wallace E, Elborn S 2000 Reliability, repeatability and sensitivity of the modified shuttle test in adult cystic fibrosis. Chest 117:1666–1671
   PubMed Web of Science ®Google Scholar
• Braggion C, Cappelletti L, Cornacchia M, Zanolla L, Mastella G 1995 Short-term effects of three chest physiotherapy regimens in patients hospitalized for pulmonary exacerbations of cystic fibrosis: A cross-over randomized study. Pediatric Pulmonology 19:16–22
   PubMed Web of Science ®Google Scholar
• Cox NS, Follett J, McKay K 2006 Modified shuttle test performance in hospitalized children and adolescents with cystic fibrosis. Journal of Cystic Fibrosis 5:165–170
   PubMed Web of Science ®Google Scholar
• Desmond KJ, Schwenk WF, Thomas E, Beaudry PH, Coates AL 1983 Immediate and long-term effects of chest physiotherapy in patients with cystic fibrosis. Journal of Pediatrics 103:538–542
   PubMed Web of Science ®Google Scholar
• Elkins MR, Jones A, van der Schans C 2006 Positive expiratory pressure physiotherapy for airway clearance in people with cystic fibrosis. Cochrane Database of Systematic Reviews Issue 2. Art. No.: CD003147. DOI: 10.1002/14651858.CD003147.pub3
   PubMed Web of Science ®Google Scholar
• Falk M, Kelstrup M, Andersen J, Kinoshita T, Stovring S, Gothgen I 1984 Improving the ketchup bottle method with positive expiratory pressure, PEP, in cystic fibrosis. European Journal of Respiratory Disease 65:423–432
   PubMedGoogle Scholar
• Groth G, Stafanger G, Dirksen H, Andersen JB, Falk M, Kelstrup M 1985 Positive expiratory pressure (PEP mask) physiotherapy improves ventilation and reduces volume of trapped gas in cystic fibrosis. European Physiopathological Respiratory Bulletin 21:339–343
   PubMedGoogle Scholar
• Lannefors L, Wollmer P 1992 Mucus clearance with three chest physiotherapy regimes in cystic fibrosis: A comparison between postural drainage, PEP and physical exercise. European Respiratory Journal 5:748–753
   PubMed Web of Science ®Google Scholar
• Main E, Prasad A, van der Schans C 2005 Conventional chest physiotherapy compared to other airway clearance techniques for cystic fibrosis. Cochrane Database of Systematic Reviews, Issue 1. Art. No.: CD002011. DOI: 10.1002/14651858.CD002011.pub2
   PubMed Web of Science ®Google Scholar
• McIlwaine PM, Wong LT, Peacock D, Davidson AG 1997 Long-term comparative trial of conventional postural drainage and percussion versus positive expiratory pressure physiotherapy in the treatment of cystic fibrosis. Journal of Pediatrics 131:570–574
   PubMed Web of Science ®Google Scholar
• Mortenson J, Falk M, Groth S, Jensen C 1991 The effects of postural drainage and positive expiratory pressure physiotherapy on tracheobronchial clearance in cystic fibrosis. Chest 100:1350–1357
   PubMed Web of Science ®Google Scholar
• Oberwaldner B, Evans JC, Zach MS 1986 Forced expirations against a variable resistance: A new chest physiotherapy method in cystic fibrosis. Pediatric Pulmonology 2:358–367
   PubMed Web of Science ®Google Scholar
• Oermann C, Swank P, Sockrider M 2000 Validation of an instrument measuring patient satisfaction with chest physiotherapy techniques in cystic fibrosis. Chest 118:92–97
   PubMed Web of Science ®Google Scholar
• Pike SE, Prasad SA, Balfour-Lynn IM 2001 Effect of intravenous antibiotics on exercise tolerance (3 min step test) in cystic fibrosis. Pediatric Pulmonology 32:38–43
   PubMed Web of Science ®Google Scholar
• Polgar G, Promadhat V 1971 Pulmonary function testing in children: Techniques and standards. Philadelphia, W.B., Saunders Co
   Google Scholar
• Reisman JJ, Rivington-Law B, Corey M, Marcotte J, Wannamaker E, Harcourt D 1988 Role of conventional physiotherapy in cystic fibrosis. Journal of Pediatrics 113:632–636
   PubMed Web of Science ®Google Scholar
• Rossman CM, Waldes R, Sampson D, Newhouse MT 1982 Effect of chest physiotherapy on the removal of mucus in patients with cystic fibrosis. American Review of Respiratory Disease 126:131–135
   PubMed Web of Science ®Google Scholar
• Shwachman H, Kulczycki L 1958 Long term study of 105 patients with cystic fibrosis. American Journal of Diseases in Childhood 96:6–15
   PubMedGoogle Scholar
• Steen HJ, Redmond AO, O'Neill D, Beattie F 1991 Evaluation of the PEP mask in cystic fibrosis. Acta Paediatrica Scandinavia 80:51–56
   PubMed Web of Science ®Google Scholar
• Tonneson P, Stovring S 1984 Positive expiratory pressure (PEP) as lung physiotherapy in cystic fibrosis: A pilot study. European Journal of Respiratory Disease 65:419–422
   PubMedGoogle Scholar
• Tyrrell JC, Hiller EJ, Martin J 1986 Face mask physiotherapy in cystic fibrosis. Archives of Disease in Childhood 61:598–611
   PubMed Web of Science ®Google Scholar
• van der Schans C, Prasad A, Main E 2000 Chest physiotherapy compared to no chest physiotherapy for cystic fibrosis. Cochrane Database of Systematic Reviews, Issue 2. Art. No.: CD001401. DOI: 10.1002/14651858.CD001401
   PubMedGoogle Scholar
• Van Asperen PP, Jackson L, Hennessy P, Brown J 1987 Comparison of a positive expiratory pressure (PEP) mask with postural drainage in patients with cystic fibrosis. Australian Journal of Paediatrics 23:283–284
   PubMedGoogle Scholar
• Wood LG, Fitzgerald DA, Gibson PG, Cooper DM, Garg ML 2002 Increased plasma fatty acid concentrations after respiratory exacerbations are associated with elevated oxidative stress in cystic fibrosis patients. American Journal of Clinical Nutrition 75:668–675
   PubMed Web of Science ®Google Scholar