Airway clearance therapy in cystic fibrosis patients

Acta Biomedica de l'Ateneo Parmense

Volumn 80, Issue 2, 2009, Pages 102-106

  Pisi, Giovanna ^a   Chetta, Alfredo ^a  

^a UNIVERSITY HOSPITAL OF PARMA   (Italy)

Author keywords

Airway clearance; Chest physiotherapy; Cystic fibrosis

Indexed keywords

BREATHING EXERCISE; CAUCASIAN; CYSTIC FIBROSIS; HUMAN; LUNG CLEARANCE; LUNG CYSTIC FIBROSIS; LUNG GAS EXCHANGE; REVIEW; CHEST WALL OSCILLATION; METABOLISM; METHODOLOGY; MUCUS; PHYSIOTHERAPY; POSITIVE END EXPIRATORY PRESSURE; POSTURAL DRAINAGE; SECRETION; TREATMENT OUTCOME;

BREATHING EXERCISES; CHEST WALL OSCILLATION; CYSTIC FIBROSIS; DRAINAGE, POSTURAL; HUMANS; MUCUS; PHYSICAL THERAPY MODALITIES; POSITIVE-PRESSURE RESPIRATION; TREATMENT OUTCOME;

EID: 73349092769     PISSN: 03924203     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (37)

1. Dodge JA, Lewis PA. Cystic fibrosis is no longer an important cause of childhood death in the UK. Arch Dis Child 2005; 90: 547.
2. Elborn JS, Shale DJ, Britton JR. Cystic fibrosis: current survival and population estimates to the year 2000. Thorax 1991; 46: 881-5.
3. Cystic Fibrosis Foundation Patient Registry: 2003 Annual Data Report to the Center Directors. Bethesda, Md: Cystic Fibrosis Foundation; 2004.
4. Matsui H, Grubb B R, Tarran R, et al. Evidence for pericil-iary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airway disease. Cell 1998; 95: 1005-1015.
5. Matsui H, Wagner VE, Hill DB, et al. A physical linkage between cystic fibrosis airway surface dehydration and Pseudomonas aeruginosa biofilm. Proc Natl Acad Sci 2006; 103: I8131-I8136.
6. Rowe SM, Miller S, Sarscher EJ. Mechanisms of disease: cystic fibrosis. NEJM 2005; 352: 1992-2001.
7. Chilvers MA, O'Callaghan C. Local mucociliary defence mechanisms, Paediatr Respir Rev, 2000; 1: 27-34
8. Van der Schans CP, Postma DS, Koeter GH, et al. Physiotherapy and bronchial mucus transport. Eur Respir J 1999; 13: 1477-86.
9. Selsby D, Jones JG. Some physiological and clinical aspects of chest physiotherapy. Br J Anaesth 1990; 64: 621-31.
10. Matthews LW, Doershuk CF, Wise M, et al. A therapeutic regimen for patients with cystic fibrosis. J Pediatr 1964; 65: 558-75.
11. Reisman JJ, Rivington-Law B, Corey M, et al. Role of conventional physiotherapy in cystic fibrosis. J Pediatr, 1988; 113: 632-36.
12. Thomas J, Cook DJ, Brooks D. Chest physiotherapy management of patients with cystic fibrosis. Am J Respir Crit Care Med 1995; 151: 846-50.
13. Giles DR, Wagener JS, Accurso FJ, et al. Short term effects of postural drainage with clapping versus autogenic drainage on oxygen saturation and sputum recovery in patients with cystic fibrosis. Chest 1995; 108: 952-4.
14. Button BM, Heine RG, Catto-Smith AG, et al. Postural drainage and gastro-oesophageal reflux in infants with cystic fibrosis. Arch Dis Child 1997; 76: 148-50.
15. Campbell AH, O'Connell JM, Wilson M. The effect of chest physiotherapy upon the FEV1 in chronic bronchitis. Med J Aust 1975; 1: 33-5.
16. Naylor JM, Chow CM, McLean AS. Cardiovascular responses to short term head-down positioning in healthy young and older adults. Physiother Res Int 2005; 10: 32-47.
17. Lapin C. Conventional postural drainage and percussion: is this still the gold standard? Pediatr Pulmonol 1994; (Suppl. 10): 87-8.
18. Czajkowski DR, Koocher GP. Predicting medical compliance among adolescents with cystic fibrosis. Health Psych 1986; 5: 297-305.
19. Pryor JC, Webber BA, Hodson ME, et al. Evaluation of the forced expiration technique as an adjunct to postural drainage in treatment of cystic fibrosis. Br Med J 1979; 2: 417-18.
20. Chevaillier J. Autogenic drainage. In: Lawson D (ed.), Cys-ticFibrosis Horizons, Chichester: John Wiley, 1984; 235.
21. Main E, Prasad A, van der Schans C. Conventional chest physiotherapy compared to other airway clearance techniques for cystic fibrosis. Cochrane Database Syst Rev 2005; (1): CD002011.
22. Davidson AGF, Wong LTK, Pirie GE, et al. Long-term comparative trial of conventional percussion and drainage physiotherapy to autogenic drainage in cystic fibrosis. Pedi-atr Pulmonol 1992; (Suppl. 6): 298 (Abstract 235).
23. Webber BA, Hodson ME. Effect of chest physiotherapy on oxygen saturation in patients with cystic fibrosis. Thorax 1990; 45: 77.
24. Giles DR, Wagener JS, Accurso FJ, et al. Short term effects of postural drainage with clapping versus autogenic drainage on oxygen saturation and sputum recovery in patients with cystic fibrosis. Chest 1995; 108: 952-4.
25. Mahlmeister M, Fink J, Hoffman J, et al. Positive-expiratory pressure mask therapy: theoretical and practical considerations and a review of the literature. Respire Care 1991; 36: 1218-29.
26. Marks JH. Airway clearance devices in cystic fibrosis. Pae-diatr Resp Rev 2007; 8: 17-23.
27. Elkins MR, Jones A, van der Schans C. Positive expiratory pressure physiotherapy for airway clearance in people with cystic fibrosis. Cochrane Database Syst Rev 2006; (2): CD003147.
28. Hansen LG, Warwick WJ, Hansen KL. Mucus transport mechanisms in relation to the effect of high frequency chest compression (HFCC) on mucus clearance. Pediatr Pul-monol 1994; 17: 113-8.
29. Tomkiewicz RP, Biviji AA, King M. Effects of oscillating air on the reological properties and clearability for mucus gel stimulant. Biorheology 1994; 124: 689-93.
30. Grzincich GL, Longo F, Faverzani S, et al. Short-term effects of high-frequency chest compression (HFCC) and positive expiratory pressure (PEP) in adults with cystic fi-brosis. Eur Respir J 2008; 32: 502s.
31. Braggion C, Cappelletti LM, Cornacchia M, et al. Short-term effects of three chest physiotherapy regimens in patients hospitalized for pulmonary exacerbations of cystic fi-brosis: a crossover randomized study. Pediatr Pulmonol 1995; 19: 16-22.
32. Arens R, Gozal D, Omlin KJ, et al. Comparison of high frequency chest compression and conventional chest physiotherapy in hospitalized patients with cystic fibrosis. Am J Respir Crit Care Med 1994; 150: 1154-7.
33. Kluft J, Beker L, Castagnino M, et al. A comparison of bronchial drainage treatments in cystic fibrosis. Pediatr Pul-monol 1996; 22: 271-4.
34. Phillips GE, Pike SE, Jaffe A, et al. Comparison of active cycle of breathing and high-frequency oscillation jacket in children with cystic fibrosis. Pediatr Pulmonol 2004; 37: 71-5.
35. Warwick WJ, Hansen LG. The long-term effect of high frequency chest compression therapy on pulmonary complications of cystic fibrosis. Pediatr Pulmonol 1991; 11: 265-71.
36. Tecklin JS, Clayton RG, Scanlin TF. High frequency chest wall oscillation vs. traditional chest physical therapy in CF-A large, one-year, controlled study. Pediatr Pulmonol 2000; 20: 304-5.
37. Greece CA. Effectiveness of high frequency chest compression: a 3-year retrospective study. Pediatr Pulmonol 2000; 20: 302-3.