International Physiotherapy Group for Cystic Fibrosis
|
|
|
|
|
| |
INTERNATIONAL PHYSIOTHERAPY PRACTICE IN INFANTS WITH CYSTIC FIBROSIS SURVEY RESULTS 1998 – 2000 . References.

1. Zach MS. Pathogenesis of lung disease in cystic fibrosis.
J R Soc Med 1991; 84:10-17. 2. Ramsey BW. Management of pulmonary disease in
patients with cystic fibrosis. N Engl J Med 1996; 335:179-188. 3. FitzSimmons
SC. The changing epidemiology of cystic fibrosis. J Pediatr 1993; 122: 1-9. 4.
Gibson RL, Burns JL, Ramsey BW. State of the art pathophysiology and management of pulmonary
infections in cystic fibrosis. Am J Respir Crit Care Med
2003;168(8):918-951. 5. Phelan PD, Olinsky A, Robertson CF. Cystic fibrosis.
In: Respiratory illness in children.4th edn. Oxford: Blackwell, 1994; 10:
207-251. 6. Sturgess J, Imrie J. Quantitative evaluation of the development of
tracheal submucosal glands in infants with cystic fibrosis and control infants. Am J Pathol 1982;
106: 303-311. 7. Armstrong DS, Grimwood K, Carzino R, Carlin JB, Olinsky A,
Phelan PD. Lower respiratory infection and inflammation in infants with newly diagnosed cystic
fibrosis. BMJ 1995; 310: 1571-1572. 8. Khan TZ, Wagener JS, Bost T, Martinez J,
Accurso FJ, Riches DW. Early pulmonary inflammation in infants with cystic fibrosis. Am J Respir
Crit Care Med 1995; 151: 1075-1082. 9. Tiddens HA. Detecting early structural
lung damage in cystic fibrosis. Pediatr Pulmonol 2002; 34(3):228-231. 10. Goss
CH. Airway clearance in cystic fibrosis. Respir Care 2003; 48: 20-21. 11.
Lannefors L, Button BM, McIlwaine M. Physiotherapy in infants and young children with CF: current
practice and future developments. J Royal Soc Med 2004; 44; 97: 8-25. 12.
Sutton P, Gemmell HG, Innes N, Davidson J, Smith FW, Legge JS, Friend JAR. Use of nebulised saline
and nebulised terbutaline as an adjunct to chest physiotherapy. Thorax 1988; 43:
57-60. 13. Ranganathan SC, Bush A, Dezateux C et al. Relative ability of full
and partial forced expiratory maneuvers to identify diminished airway function in infants with
cystic fibrosis. Am J Respir Crit Care Med 2002; 166: 1350-1357. 14. Hardy KA,
Wolfson MR, Schidlow DV, Shaffer TH. Mechanics and energetics of breathing in newly diagnosed
infants with cystic fibrosis: effect of combined bronchodilator and chest physical therapy. Pediatr
Pulmonol 1989; 6(2): 103-108. 15. Tepper RJ. Assessment of the respiratory
status of infants and toddlers with cystic fibrosis. J Pediatr 1998; 132:
380-381. 16. Connett GJ, Yeatman SL. Delayed diagnosis in cystic fibrosis
patients homozygous for the Delta F508 mutation results in increased treatment to maintain health in
childhood. Ped Pulm 2002; 24: 407A. 17. Button BM, Heine RG, Catto-Smith AG,
Phelan PD, Olinsky A. Postural drainage and gastro-oesophageal reflux in infants with cystic
fibrosis. Arch Dis Child 1997; 76:148-150. 18. Phelan PD, Olinsky A, Robertson
CF. Lung growth and development. In: Respiratory illness in children. 4th ed. Oxford: Blackwell,
1994; 1:1-7. 19. Orenstein SR, Whitington PF. Positioning for prevention of
infant gastroesophageal reflux. J Pediatr 1983; 103: 534-537. 20. Button BM,
Heine RG, Catto-Smith AG, Phelan PD, Olinsky A. Chest physiotherapy, gastro-oesophageal reflux, and
arousal in infants with cystic fibrosis. Arch Dis Child 2004; 89:435-439. 21.
Phillips GE, Pike SE, Rosenthal M, Bush A. Holding the baby: head downwards positioning for
physiotherapy does not cause gastro-esophageal reflux. Eur Respir J 1998; 12:
954-957. 22. Button BM, Heine RG, Catto-Smith AG, Olinsky A, Phelan PD,
Ditchfield MR, Story Chest physiotherapy in infants with cystic fibrosis: to tip or not? A five-year
study. Pediatr Pulmonol 2003; 35: 208-213. 23. Orenstein D. Editorial: Heads
UP! Clear those Airways. Pediatr Pulmonol 2003; 35:160-161. 24. Dab I,
Alexander F. The mechanism of autogenic drainage studied with flow-volume curves. Monogr Paediatr
1979; 10: 50-53. 25. Van Ginderdeuren F, Malfroot A, Verdonk J, Vanlaethem S,
Vandenpals Y. Influence of assisted autogenic drainage (AAD) and AAD combined with bouncing on
gastro-oesophageal reflux (GOR) in infants under the age of 5 months. J Cystic Fibrosis 2002; 2(l1):
A251. 26. Demont B, Escourrou P, Vincon C, Cambas CH, Grisan A, Odievre M.
Effects of respiratory physical therapy and nasopharyngeal suction on gastroesophageal reflux in
infants less than a year of age, with or without abnormal reflux. Arch Fr Pediatr 1991; 48(9):
621-625. 27. Andreasson B, Jonsson B, Kornfalt R, Nordmark E, Sandstrom S.
Long-term effects of physical exercise on working capacity and pulmonary function in cystic
fibrosis. Acta Pediatr Scand 1987; 76: 70-5. 28. Falk M, Kelstrup M, Andersen
JB, Kinoshita T, Falk P, Støvring S, Gøthgen I. Improving the ketchup bottle method with positive
expiratory pressure, PEP. A controlled study in patients with cystic fibrosis. Eur J Respr Dis 1984;
65: 423-432. 29. Frederiksen B, Thorsteinsson SL, Koch C, Høiby N. Improved
prognosis for patients with cystic fibrosis. A result of aggressive center-based treatment (article
in Danish). Ugeskr Laeger 1997; 159: 5790-5794. 30. Constantini D, Brivio A et
al. PEP-Mask versus Postural Drainage in CF infants a long-term comparative trial. Pediatr Pulmonol
2001; Suppl. 22: 308, A400. 31. Davidson AGF, Nadel H, Wong LTK. Delayed
gastric emptying in cystic fibrosis. Pediatr Pulmonol 1995 Suppl. A301. |
|
|
|
|
|
|
| |
|
|