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The role of positive expiratory pressure (PEP) in physiotherapy of patients with cystic fibrosis. Comparison with oscillating positive expiratory pressure (OPEP) Cover

The role of positive expiratory pressure (PEP) in physiotherapy of patients with cystic fibrosis. Comparison with oscillating positive expiratory pressure (OPEP)

Open Access
|Jul 2018

References

  1. Walkowiak J, Pogorzelski A, Sands D, Skorupa W, Milanowski A, Orlik T, et al. Zasady rozpoznawania i leczenia mukowiscydozy. Standardy Medyczne/pediatria 2009;3(6).
  2. Pryor JA, Webber BA. Physiotherapy for cystic fibrosis – which technique? Physiotherapy 1992;78(2):105-8.
  3. Pryor JA, Webber BA, Hodson ME. Effect of chest physiotherapy on oxygen saturation in patients with cystic fibrosis. Thorax 1990;45(1):77.
  4. Reisman JJ, Rivington-Law B, Corey M, Marcotte J, Wannamaker E, Harcourt D, et al. Role of conventional physiotherapy in cystic fibrosis. J Pediatr 1988; 113:632-6.
  5. Orlik T. Współczesne techniki fizjoterapii klatki piersiowej stosowane w leczeniu chorych na mukowiscydozę. Med Wieku Roz 1997; 1(3):397-406.
  6. Orlik T. Ocena efektywności wybranych metod fizjoterapii klatki piersiowej stosowanej w leczeniu chorych na mukowiscydozę. Med Wieku Roz 2000;4(3):233-46.
  7. Orenstein SR, Whitngton PF. Positioning for prevention of infant gastroesophageal reflux. J Pediatr 1983;103:534-7.
  8. Vandenplast Y, Diericx A, Blecker U, Lanciers S, Deneyer M. Esophagel pH monitoring data during chest physiotherapy. J Ped Gastroenterol Nutr 1991;13:23-6.
  9. Button BM, Heine R, Catto-Smith A, Phelan P, Olinsky A. Postural drainage techniques and gastro-oesophageal reflux in infants with cystic fibrosis. Eur Resp J 1999; 14:1456.
  10. Orlik T. Ocena metod autodrenażu w wybranej grupie chorych na mukowiscydozę z uwzględnieniem czynnika środowiskowego. Med Wieku Roz 2000; 4(3):247-59.
  11. Falk M, Kelstrup M, Andersen JB, Kinoshita T, Falk P, Stovring S, et al. Improving the ketchup bottle method with positive expiratory pressure, PEP, in cystic fibrosis. Eur J Respir Dis 1984;65(6):423-32.
  12. Hofmeyr JL, Webber BA, Hodson M E. Ewaluation of positive expiratory pressure as an adjunct to chest physiotherapy in the treatment of cystic fibrosis. Thorax 1986;41(12):951-4.
  13. Andersen JB, Qvist J, Kann T. Recruiting collapsed lung through collateral channels with positive and expiratory pressure. Scan J Res Dis 1979;60:260-6.
  14. McIlwaine M. Physiotherapy and airway clearance techniques and devices. Pediatr Respir Rev 2006;7(suppl):220-2.
  15. Morrison L, Agnew J. Oscillating devices for airway clearance in people with cystic fibrosis. Cochrane Database Syst 2014 doi: 10 1002/14651858 CD006842 pub3
  16. Lannefors L, Wollmer P. Mucus clearance with three chest physiotherapy regimes in cystic fibrosis: a comparison between postural drainage, PEP and physical exercise. Eur Respir J 1992;5(6):748-53.
  17. Mortensen J, Falk M, Groth S, Jensen C. The effects of postural drainage and positive expiratory pressure physiotherapy on tracheobronchial clearance in cystic fibrosis. Chest 1991;100(5):1350-57.
  18. Darbee JC, Kanga JF, Ohtake PJ. Physiologic evidence for high frequency chest wall oscillation and positive airway clearance technique in patients with cystic fibrosis. Phys Ther 2004;84(6):524-37.
  19. McIlwaine PM, Wong LT, Peacok D, Davidson AG. Long-term comparative trial of conventional postural drainage and percussion versus positive expiratory pressure physiotherapy in the treatment of cystic fibrosis. J Pediatr 1997;131(4):570-4.
  20. Pryor JA, Webber BA, Hodson ME. The Flutter VRP1 as an adjunct to chest physiotherapy in cystic fibrosis. Respir Med 1994;88(9):677-81.
  21. App EM, Kieselmann R, Reinhardt D, Lindemann H, Dasgupta B, King M, et al. Sputum rheology changes in cystic fibrosis lung disease following two different types of physiotherapy: flutter vs autogenic drainage. Chest 1998;114(1):171-7.
  22. Konstan MW, Stern RC, Doershuk CF. Efficacy of the Flutter device for airway mucus clearance in patients with cystic fibrosis. J Pediatr 1994;124(5):689-93.
  23. Orlik T, Sands D. Długofalowa ocena skuteczności wybranych metod fizjoterapii klatki piersiowej stosowanych w leczeniu chorych na mukowiscydozę. Med Wieku Roz 2001;5(3): 245-57.
  24. Lagerkvist AL, Sten GM, Redfors SB, Lindblad AG, Hjalmarson O. Immediate changes in blood gas tensions during chest physiotherapy pressure in patients with cystic fibrosis. Respir Care 2006;51(10):1154-61.
  25. McIlwaine PM, Webber BA, Hodson ME. Long-term comparative trial of positive expiratory pressure versus oscillating positive expiratory pressure (flutter) physiotherapy in the treatment of cystic fibrosis. J Pediatr 2001;138(6):845-50.
  26. Van Winden CM, Visser A, Hop W, Sterk PJ, Becker S, de Jongste JC. Effects of flutter and PEP mask physiotherapy on symptoms and lung function in children with cystic fibrosis. Eur Respir J 1998;12(1):143-7.
  27. Borka P, Gyurkovits K, Bódis J. Comparative study of PEP mask and Flutter on expectoration in cystic fibrosis patients. Acta Physiol Hung 2012 Sep;99(3):324-31. doi: 10.1556/APhysiol.99.2012.3.9.
  28. Homnick DN, Anderson K, Marks JH. Comparison of the flutter device to standard chest physiotherapy in hospitalized patients with cystic fibrosis: a pilot study. Chest 1998;114:993-7.
  29. Newhouse PA, White F, Marks JH. The intrapulmonary percussive ventilator and flutter device compared to standard chest physiotherapy in patients with cystic fibrosis. Clin Pediatr 1998;37:427-32.
  30. Gondor M, Nixon PA, Mutich R, Rebovich P, Orenstein DM. Comparison of Flutter device and chest physical therapy in the treatment of cystic fibrosis pulmonary exacerbation. Pediatr Pulmo 1999;28:255-60.
  31. Oermann CM, Sockrider MM, Gilles D, Sontag MK, Accurso FJ, Castile RG. Comparison of high-frequency chest wall oscillation and oscillating positive expiratory pressure in the home management of cystic fibrosis: a pilot study. Pediatr Pulmo 2001;32:372-7.
  32. McIlwaine M, Button B, Dwan K. Positive expiratory pressure physiotherapy for airway clearance in people with cystic fibrosis. Cochrane Database Syst Rev 2015 Jun 17;(6):CD003147. doi: 10.1002/14651858.CD003147.pub4.
  33. Morrison L, Innes S, Oscillating devices for airway clearance in people with cystic fibrosis. Cochrane Database Syst Rev 2017 May 4;5; doi: 10 1002/14651858 CD006842 pub4.
  34. Orlik T, Milanowski A, Skorupa W, Kluba L, Korzeniewska A, Majka L i wsp. Długofalowy model postępowania fizjoterapeutycznego w mukowiscydozie. Standardy Medyczne 2003;10 (48):1306-1314.
  35. Hoo ZH, Daniels T, Wildman M, Teare MD, Bradley JM. Airway clearance techniques used by people with cystic fibrosis in the UK. Physiotherapy 2015;101(4):340-8. doi: 10.1016/j.physio.2015.01.008. Epub 2015 Mar 14.
Language: English
Page range: 39 - 45
Published on: Jul 4, 2018
In partnership with: Paradigm Publishing Services

© 2018 Teresa Orlik, Anna Wyka-Wojeńska, published by University of Physical Education in Warsaw
This work is licensed under the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License.