The Short-Term Effect of Breathing Tasks Via an Incentive Spirometer on Lung Function Compared With Autogenic Drainage in Subjects With Cystic Fibrosis

References

1. 1.↵
   1. van der Schans C,
   2. Prasad A,
   3. Main E

   . Chest physiotherapy compared to no chest physiotherapy for cystic fibrosis. Cochrane Database Syst Rev 2000;(2):CD001401.
2. 2.
   1. Konstan MW,
   2. Berger M

   . Current understanding of the inflammatory process in cystic fibrosis: onset and etiology. Pediatr Pulmonol 1997;24(2):137–142; discussion 159-161.

   OpenUrlCrossRefPubMedWeb of Science
3. 3.↵
   1. Hess DR

   . The evidence for secretion clearance techniques. Respir Care 2001;46(11):1276–1293.

   OpenUrlPubMed
4. 4.
   1. McCool FD,
   2. Rosen MJ

   . Nonpharmacologic airway clearance therapies: ACCP evidence-based clinical practice guidelines. Chest 2006;129(1 Suppl):250S–259S.

   OpenUrlCrossRefPubMedWeb of Science
5. 5.↵
   1. Elkins MR,
   2. Jones A,
   3. van der Schans C

   . Positive expiratory pressure physiotherapy for airway clearance in people with cystic fibrosis. Cochrane Database Syst Rev 2006;19(2):CD003147.

   OpenUrl
6. 6.↵
   1. Main E,
   2. Prasad A,
   3. van der Schans CP

   . Conventional chest physiotherapy compared to other airway clearance techniques for cystic fibrosis. Cochrane Database Syst Rev 2005;1:CD002011.

   OpenUrlPubMed
7. 7.↵
   1. Morrison L,
   2. Agnew J

   . Oscillating devices for airway clearance in people with cystic fibrosis. Cochrane Database Syst Rev 2009;1:CD006842.

   OpenUrlPubMed
8. 8.↵
   1. Lawson D

   1. Chevallier J

   . Autogenic drainage. In: Lawson D, editor. Cystic fibrosis: horizons. New York: John Wiley & Sons; 1984:235.
9. 9.↵
   1. McIlwaine PM,
   2. Wong LT,
   3. Peacock D,
   4. 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):570–574.

   OpenUrlCrossRefPubMedWeb of Science
10. 10.↵
    1. Marks JH

    . Airway clearance devices in cystic fibrosis. Paediatr Respir Rev 2007;8(1):17–23.

    OpenUrlCrossRefPubMed
11. 11.
    1. Hristara-Papadopoulou A,
    2. Tsanakas J,
    3. Diomou G,
    4. Papadopoulou O

    . Current devices of respiratory physiotherapy. Hippokratia 2008;12(4):211–220.

    OpenUrlPubMedWeb of Science
12. 12.
    1. Hardy KA,
    2. Anderson BD

    . Noninvasive clearance of airway secretions. Respir Care Clin N Am 1996;2(2):323–345.

    OpenUrlPubMed
13. 13.
    1. Falk M,
    2. Kelstrup M,
    3. Andersen JB,
    4. Kinoshita T,
    5. Falk P,
    6. Støvring S,
    7. Gøthgen I

    . Improving the ketchup bottle method with positive expiratory pressure, PEP, in cystic fibrosis. Eur J Respir Dis 1984;65(6):423–432.

    OpenUrlPubMedWeb of Science
14. 14.↵
    1. Volsko TA,
    2. DiFiore J,
    3. Chatburn RL

    . Performance comparison of two oscillating positive expiratory pressure devices: Acapella versus Flutter. Respir Care 2003;48(2):124–130.

    OpenUrlAbstract/FREE Full Text
15. 15.↵
    1. Oberwaldner B,
    2. Evans JC,
    3. Zach MS

    . Forced expirations against a variable resistance: a new chest physiotherapy method in cystic fibrosis. Pediatr Pulmonol 1986;2(6):358–367.

    OpenUrlCrossRefPubMedWeb of Science
16. 16.↵
    1. Stock MC,
    2. Downs JB,
    3. Gauer PK,
    4. Alster JM,
    5. Imrey PB

    . Prevention of postoperative pulmonary complications with CPAP, incentive spirometry, and conservative therapy. Chest 1985;87(2):151–157.

    OpenUrlCrossRefPubMedWeb of Science
17. 17.↵
    1. Basoglu OK,
    2. Atasever A,
    3. Bacakoglu F

    . The efficacy of incentive spirometry in patients with COPD. Respirology 2005;10(3):349–353.

    OpenUrlCrossRefPubMed
18. 18.↵
    1. Pellegrino R,
    2. Viegi G,
    3. Brusasco V,
    4. Crapo RO,
    5. Burgos F,
    6. Casaburi R,
    7. et al

    . Interpretative strategies for lung function tests. Eur Respir J 2005;26(5):948–968.

    OpenUrlFREE Full Text
19. 19.
    1. Rodriguez Hortal MC,
    2. Hjelte L

    . Time point to perform lung function tests evaluating the effects of an airway clearance therapy session in cystic fibrosis. Respir Care 2014;59(10):1537–1541.

    OpenUrlAbstract/FREE Full Text
20. 20.↵
    1. Placidi G,
    2. Cornacchia M,
    3. Polese G,
    4. Zanolla L,
    5. Assael BM,
    6. Braggion C

    . Chest physiotherapy with positive airway pressure: a pilot study of short-term effects on sputum clearance in patients with cystic fibrosis and severe airway obstruction. Respir Care 2006;51(10):1145–1153.

    OpenUrlAbstract/FREE Full Text
21. 21.↵
    1. Homnick DN

    . Making airway clearance successful. Paediatr Respir Rev 2007;8(1):40–45.

    OpenUrlCrossRefPubMedWeb of Science
22. 22.↵
    1. Chatham K,
    2. Ionescu AA,
    3. Nixon LS,
    4. Shale DJ

    . A short-term comparison of two methods of sputum expectoration in cystic fibrosis. Eur Respir J 2004;23(3):435–439.

    OpenUrlAbstract/FREE Full Text
23. 23.↵
    1. Andersen JB,
    2. Qvist J,
    3. Kann T

    . Recruiting collapsed lung through collateral channels with positive end-expiratory pressure. Scand J Respir Dis 1979;60(5):260–266.

    OpenUrlPubMedWeb of Science
24. 24.↵
    1. Darbee JC,
    2. Ohtake PJ,
    3. Grant BJ,
    4. Cerny FJ

    . Physiologic evidence for the efficacy of positive expiratory pressure as an airway clearance technique in patients with cystic fibrosis. Phys Ther 2004;84(6):524–537.

    OpenUrlAbstract/FREE Full Text
25. 25.
    1. Lapin C

    . Airway physiology, autogenic drainage, and active cycle. Respir Care 2002;47(7):778–785.

    OpenUrlPubMed
26. 26.↵
    1. Delaunois L

    . Anatomy and physiology of collateral respiratory pathways. Eur Respir J 1989;2(9):893–904.

    OpenUrlAbstract/FREE Full Text
27. 27.↵
    1. Bennett WD,
    2. Zeman KL

    . Effect of enhanced supramaximal flows on cough clearance. J Appl Physiol 1994;77(4):1577–1583.

    OpenUrlAbstract/FREE Full Text