Exercise-induced changes of oxygen saturation in patients with cystic fibrosis;Belastungsabhangige Veranderungen der Sauerstoffsattigung bei Patienten mit Mukoviszidose

Monatsschrift fur Kinderheilkunde

Volumn 144, Issue 9, 1996, Pages 910-917

  Stern, M ^a   Strauss H ^a  

^a UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

Author keywords

cystic fibrosis; exercise testing; oxygen saturation; pulse oxymetry; spiroergometry

Indexed keywords

ARTICLE; BLOOD PRESSURE MEASUREMENT; BREATHING RATE; CLINICAL ARTICLE; CONTROLLED STUDY; CYSTIC FIBROSIS; DISEASE SEVERITY; EXERCISE; GRAM NEGATIVE INFECTION; HEART RATE; HUMAN; LUNG FUNCTION TEST; OXYGEN SATURATION; PROGNOSIS; PSEUDOMONAS AERUGINOSA; PULSE OXIMETRY; WORK CAPACITY;

EID: 0029812869     PISSN: 00269298     EISSN: None     Source Type: Journal    
DOI: 10.1007/s001120050059     Document Type: Article

References (50)

1. Bachl N (1986) Submaximale Belastungsverfahren. In: Prokop L (Hrsg) Kinder-Sportmedizin. Fischer, Stuttgart New York, S 114-118
2. Beier FR, Renzetti AD, Mitchell M, Watanabe S (1966) Pulmonary pathophysiology in cystic fibrosis. Am Rev Respir Dis 94: 430-440
3. Betancourt M, Slade G, Dinwiddie R (1991) Oxygen saturation in cystic fibrosis. Arch Dis Child 66: 1075-1076
4. Breuer H-WM, Groeben H, Worth H (1990) Comparative analysis of arterial oxygen saturations during exercise by pulse oximetry, photometric measurements and calculation procedures. Int J Sports Med 11: 22-25
5. Bruce RA, Blackman JR, Jones JW, Strait G (1963) Exercise testing in adult normal subjects and cardiac patients. Pediatrics 32: 742
6. Cerny FJ (1989) Relative effects of bronchial drainage and exercise for inhospital care of patients with cystic fibrosis. Phys Ther 69: 633-639
7. Cerny FJ, Orenstein D (1993) Cystic fibrosis. In: Skinner JS (ed) Exercise testing and exercise prescription for special cases, 2nd edn. Lea & Febiger, Philadelphia, pp 241-250
8. Cerny FJ, Pullano TP, Cropp GJA (1982) Cardiorespiratory adaptations to exercise in cystic fibrosis. Am Rev Respir Dis 126: 217-220
9. Chrispin AR, Norman AP (1974) The systematic evaluation of the chest radiograph in cystic fibrosis. Pediatr Radiol 2: 101-106
10. Coates AG, Canny G, Zinman R, Grisdale R, Desmond K, Roumeliotis D, Levison H (1988) The effects of chronic airflow limitation, increased dead space, and the pattern of ventilation on gas exchange during maximal exercise in advanced cystic fibrosis. Am Rev Respir Dis 138: 1524-1531
11. Coates AL, Boyce P, Muller D, Mearns M, Godfrey S (1980) The role of nutritional status, airway obstruction, hypoxia and abnormalities in serum lipid composition in limiting exercise tolerance in children with cystic fibrosis. Acta Paediatr 69: 353-359
12. Cooper PJ, Robertson CF, Hudson IL, Phelan PD (1990) Variability of pulmonary function tests in cystic fibrosis. Pediatr Pulmonol 8: 16-22
13. Cropp GJ, Pullano TP, Cerny FJ, Nathanson IT (1982) Exercise tolerance and cardiorespiratory adjustments at peak work capacity in cystic fibrosis. Am Rev Respir Dis 126: 211-216
14. Cumming GR, Everatt D, Hastmann L (1978) Bruce treadmill test in children: normal values in a clinic population. Am J Cardiol 41: 69-75
15. Döring G, Høiby N (1983) Longitudinal study of immune response to 'Pseudomonas aeruginosa' antigens in cystic fibrosis. Infect Immun 42: 197-201
16. Eichinger T, Zimmermann T (1991) Laufbandbelastung bei Kindern und Jugendlichen mit Mucoviscidose (CF). Pneumologie 45: 906-909
17. Escourrou PJL, Delaperche MF, Visseaux A (1990) Reliability of pulse oximetry during exercise in pulmonary patients. Chest 97: 635-638
18. Gaisl G, Wiesspeiner G (1987) A noninvasive method of determining the anaerobic treshold in children. Int J Sports Med 8: 41-44
19. Godfrey S, Mearns M (1971) Pulmonary function and response to exercise in cystic fibrosis. Arch Dis Child 46: 144-151
20. Gruber W, Leister E, Linse P (1994) Körperliche Aktivität und Sport in der Behandlung von Patienten mit Mukoviszidose. Arbeitskreis Physiotherapie Mukoviszidose e.V. (Hrsg) Physiothérapie bei Mukoviszidose, Bonn, S 113-117
21. Harms HK, Bertele RM, Weidl B, Fendel H (1983) Die Wertigkeit des Chrispin-Norman-Score in der Beurteilung der pulmonalen Situation von Patienten mit Cystischer Fibröse. Klin Pädiatr 195: 24-28
22. Heijerman HG, Bakker W, Sterk PJ, Dijkman JH (1991) Oxygen-assisted exercise training in adult cystic fibrosis patients with pulmonary limitation to exercise. Int J Rehabil Res 14: 101-115
23. Henke KG, Orenstein DM (1984) Oxygen saturation during exercise in cystic fibrosis. Am Rev Respir Dis 129: 708-711
24. Hjeltnes N, Stanghelle JK, Skyberg D (1984) Pulmonary function and oxygen uptake during exercise in 16-year old boys with cystic fibrosis. Acta Paediatr 73: 548-553
25. Hodson ME, Geddes DM (1995) Cystic fibrosis. Chapman & Hall, London
26. James FW, Blomqvist CG, Freed MD, Miller WW, Moller JH, Nugent EW, Riopel DA, Strong WB, Wessel HU (1982) AHA special report: standards of exercise testing in the pediatric age group. Circulation 66: 1377-1395
27. Knox AJ, Morrison JFJ, Muers MF (1988) Reproducibility of walking test results in chronic obstructive airways disease. Thorax 43: 388-392
28. Kraemer R, Rüdeberg A, Kläy E, Rossi E (1979) Relationship between clinical conditions, radiographic findings and pulmonary functions in patients with cystic fibrosis. Helv Paediatr Acta 34: 417-428
29. Lands L, Heigenhauser GJ, Jones NL (1992) Analysis of factors limiting maximal exercise performance in cystic fibrosis. Clin Sci 83: 391-397
30. Lebecque P, Lapierre J-G, Lamarre A, Coates AL (1987) Diffusion capacity and oxygen desaturation effects on exercise in patients with cystic fibrosis. Chest 91: 693-697
31. Leupold W (1989) Lungenfunktion und körperliche Leistungsfähigkeit bei Patienten mit Mukoviszidose. Z Erkr Atmungsorgane 171: 190-198
32. Lindemann H (1993) Pneumologische Aspekte der Mukoviszidose. Monatsschr Kinderheilkd 141: 333-342
33. Marcotte JE, Grisdale RK, Levison H, Coates AL, Canny GL (1986) Multiple factors limit exercise capacity in cystic fibrosis. Pediatr Pulmonol 2: 274-281
34. Nickerson BG, Lernen RJ, Gerdes CB, Wegmann MJ, Robertson G (1980) Within-subject variability and per cent change for significance of spirometry in normal subjects and in patients with cystic fibrosis. Am Rev Respir Dis 122: 859-866
35. Nixon PA, Orenstein DM, Curtis SE, Rosse EA (1990) Oxygen supplementation during exercise in cystic fibrosis. Am Rev Respir Dis 142: 807-811
36. Nixon PA, Orenstein DM, Kelsey SF, Doershuk CF (1992) The prognostic value of exercise testing in patients with cystic fibrosis. N Engl J Med 327: 1785-1788
37. Orenstein MD (1988) Exercise tolerance and exercise conditioning in children with chronic lung disease. J Pediatr 112: 1043-1047
38. Orenstein MD, Curtis SE, Nixon PA, Hartigan ER (1993) Accuracy of three pulse oximeters during exercise and hypoxemia in patients with cystic fibrosis. Chest 104: 1187-1190
39. Pradal U, Braggion C, Mastella G (1990) Transcutaneous blood gas analysis during sleep and exercise in cystic fibrosis. Pediatr Pulmonol 8: 162-167
40. Schuemer R, Ströhlein G, Gogolok J (1990) Datenverarbeitung und statistische Auswertung mit SAS, B II. Komplexe statistische Analyseverfahren. Fischer, Stuttgart New York
41. Sly PD, Robertson CF (1990) A review of pulmonary function testing in children. J Asthma 27: 137-147
42. Stanghelle JK (1988) Physical exercise for patients with cystic fibrosis: a review. Int J Sports Med [Suppl] 9: 6-18
43. Taussig CM (1984) Cystic fibrosis, 2nd edn. Thieme, Stuttgart New York
44. Tepper RS, Hiatt P, Eigen H, Scott P, Grosfeld J, Cohen M (1988) Infants with cystic fibrosis: pulmonary function at diagnosis. Pediatr Pulmonol 5: 15-18
45. Versteegh FGA, Bogaad GM, Raatgever JW, Stam H, Neijens HJ, Kerrebijn KF (1990) Relationship between airway obstruction, desaturation during exercise and nocturnal hypoxaemia in cystic fibrosis patients. Eur Respir J 3: 68-73
46. Von der Hardt H, Nowak-Beneke R (1976) Lung volumes in healthy boys and girls, 6-15 years of age. Lung 154: 51-63
47. Von Forche G, Stadlober E, Zach M, Harnoncourt K (1984) Spirometrische Normalwerte für Kinder. Atemw Lungenkrankh 10: 501-506
48. Webb RK, Ralton AC, Runciman WB (1991) Potential errors in pulse oximetry. Anaesthesia 46: 207-212
49. Wiesemann HG (1985) Bedeutung der Lungenfunktionsuntersuchung in der klinischen Betreuung von Patienten mit Mucoviscidose. Monatsschr Kinderheilkd 133: 726-729
50. Winnie GB, Cowan RG (1991) Respiratory tract colonization with pseudomonas aeruginosa in cystic fibrosis: correlations between anti-pseudomonas aeruginosa antibody levels and pulmonary function. Pediatr Pulmonol 10: 92-100