A comparison of respiratory and peripheral muscle strength, functional exercise capacity, activities of daily living and physical fitness in patients with cystic fibrosis and healthy subjects

Research in Developmental Disabilities

Volumn 45-46, Issue , 2015, Pages 147-156

  Arikan, Hulya ^a   Yatar, Ilker ^b   Calik Kutukcu, Ebru ^a   Aribas, Zeynep ^c   Saglam, Melda ^a   Vardar Yagli, Naciye ^a   Savci, Sema ^d   Inal Ince, Deniz ^a   Ozcelik, Ugur ^a   Kiper, Nural ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

^b EASTERN MEDITERRANEAN UNIVERSITY   (Turkey)

^c GAZI UNIVERSITY   (Turkey)

^d DOKUZ EYLUL UNIVERSITY   (Turkey)

Author keywords

Cystic fibrosis; Daily living activities; Endurance; Exercise; Fitness; Muscle; Respiratory muscle; Strength

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BREATHING MUSCLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; COORDINATION; CYSTIC FIBROSIS; DAILY LIFE ACTIVITY; DISEASE SEVERITY; ENDURANCE; EXERCISE TEST; FEMALE; FITNESS; FORCED EXPIRATORY VOLUME; FUNCTIONAL ASSESSMENT; FUNCTIONAL STATUS; GLITTRE ADL TEST; HAND GRIP; HUMAN; JUMPING; MAJOR CLINICAL STUDY; MALE; MUNICH FITNESS TEST; MUSCLE EXERCISE; MUSCLE STRENGTH; PERIPHERAL MUSCLE STRENGTH; PHYSICAL CAPACITY; PHYSICAL PERFORMANCE; QUADRICEPS FEMORIS MUSCLE; RESPIRATORY MUSCLE STRENGTH; SCHOOL CHILD; SCORING SYSTEM; SHOULDER ABDUCTOR MUSCLE; SKELETAL MUSCLE; STANDING; VELOCITY; CASE CONTROL STUDY; COMPARATIVE STUDY; EXERCISE TOLERANCE; HAND STRENGTH; NORMAL HUMAN; PATHOPHYSIOLOGY; PHYSIOLOGY; YOUNG ADULT;

ACTIVITIES OF DAILY LIVING; ADOLESCENT; ADULT; CASE-CONTROL STUDIES; CHILD; CYSTIC FIBROSIS; EXERCISE TEST; EXERCISE TOLERANCE; FEMALE; FORCED EXPIRATORY VOLUME; HAND STRENGTH; HEALTHY VOLUNTEERS; HUMANS; MALE; MUSCLE STRENGTH; MUSCLE, SKELETAL; PHYSICAL FITNESS; QUADRICEPS MUSCLE; RESPIRATORY MUSCLES; YOUNG ADULT;

EID: 84939434821     PISSN: 08914222     EISSN: 18733379     Source Type: Journal    
DOI: 10.1016/j.ridd.2015.07.020     Document Type: Article

References (60)

1. Adams G.M. Exercise physiology laboratory manual 1990, Wm. C. Brown Publishers, Dubuque, IA, USA. 1st ed.
2. Almajed A., Lands L.C. The evolution of exercise capacity and its limiting factors in cystic fibrosis. Paediatric Respiratory Reviews 2012, 13:195-199.
3. American Thoracic Society/European Respiratory Society ATS/ERS statement on respiratory muscle strength. American Journal of Respiratory Critical Care Medicine 2002, 166:518-624.
4. Arora N.S., Rochester D.F. Respiratory muscle strength and maximal voluntary ventilation in undernourished patients. American Review of Respiratory Disease 1982, 126:5-8.
5. ATS Committee on Proficiency Standards for Clinical Pulmonary Function Laboratories ATS statement: Guidelines for the six-minute walk test. American Journal of Respiratory Critical Care Medicine 2002, 166:111-117.
6. Aznar S., Gallardo C., Fiuza-Luces C., Santana-Sosa E., López-Mojares L.M., Santalla A., et al. Levels of moderate - vigorous physical activity are low in Spanish children with cystic fibrosis: A comparison with healthy controls. Journal of Cystic Fibrosis 2014, 13:335-340.
7. Bar-Or O., Rowland T. Pediatric exercise medicine. From physiologic principles to health care application 2004, Human Kinetics, Champaign, IL. 1st ed.
8. Barry S.C., Gallagher C.G. Corticosteroids and skeletal muscle function in cystic fibrosis. Journal of Applied Physiology 2003, 1985(95):1379-1384.
9. Beenakker E.A., van der Hoeven J.H., Fock J.M., Maurits N.M. Reference values of maximum isometric muscle force obtained in 270 children aged 4-16 years by hand-held dynamometry. Neuromuscular Disorders 2001, 11:441-446.
10. Boas S.R. Exercise recommendations for individuals with cystic fibrosis. Sports Medicine 1997, 24:17-37.
11. Bouchard C., Shepard R.J. Physical activity, fitness, and health international proceedings and consensus statement 1994, Human Kinetics, Champaign, IL. 1st ed.
12. Cabrera M.E., Lough M.D., Doershuk C.F., DeRivera G.A. Anaerobic performance assessed by the Wingate Test in patients with cystic fibrosis. Pediatric Exercise Science 1993, 5:78-87.
13. Chetta A., Pisi G., Zanini A., Foresi A., Grzincich G.L., Aiello M., et al. Six-minute walking test in cystic fibrosis adults with mild to moderate lung disease: Comparison to healthy subjects. Respiratory Medicine 2001, 95:986-991.
14. Cunha M.T., Rozov T., de Oliveira R.C., Jardim J.R. Six-minute walk test in children and adolescents with cystic fibrosis. Pediatric Pulmonology 2006, 41:618-622.
15. Coates A.L., Boyce P., Muller D., Mearns M., Godfrey S. The role of nutritional status, airway obstruction, hypoxia and abnormalities in serum lipid composition in limiting exercise tolerance in children with cystic fibrosis. Bulletin Europeen de Physiopathologie Respiratoire 1979, 15:341-342.
16. Corrêa K.S., Karloh M., Martins L.Q., dos Santos K., Mayer A.F. Can the Glittre ADL test differentiate the functional capacity of COPD patients from that of healthy subjects?. Revista Brasileira de Fisioterapia 2011, 15:467-473.
17. Dassios T. Determinants of respiratory pump function in patients with cystic fibrosis. Paediatric Respiratory Reviews 2014, pii:S1526-0542(14)00002-5. 10.1016/j.prrv.2014.01.001.
18. Dassios T., Katelari A., Doudounakis S., Mantagos S., Dimitriou G. Respiratory muscle function in patients with cystic fibrosis. Pediatric Pulmonology 2013, 48:865-873.
19. Davies J.C., Ebdon A.M., Orchard C. Recent advances in the management of cystic fibrosis. Archives of Disease in Childhood 2014, 0:1-4.
20. Dechman G., Scherer S.A. Outcome measures in cardiopulmonary physical therapy: Focus on the Glittre ADL-test for people with chronic obstructive pulmonary disease. Cardiopulmonary Physical Therapy Journal 2008, 19:115-118.
21. de Meer K., Gulmans V.A., van Der Laag J. Peripheral muscle weakness and exercise capacity in children with cystic fibrosis. American Journal of Respiratory Critical Care Medicine 1999, 159:748-754.
22. Dogru D., Pekcan S., Yalcin E., Ozcelik U., Kiper N., Gurcan N., et al. The role of serum Pseudomonas aeruginosa antibodies in the diagnosis and follow-up of cystic fibrosis. Turkish Journal of Pediatrics 2013, 55:50-57.
23. Domenech-Clar R., Lopez-Andreu J.A., Compte-Torrero L., De Diego Damiá A., Macián-Gisbert V., Perpiñá-Tordera M., et al. Maximal static respiratory pressures in children and adolescents. Pediatric Pulmonology 2003, 35:126-132.
24. DuBois D.C., Almon R.R. Disuse atrophy of skeletal muscle is associated with an increase in number of glucocorticoid receptors. Endocrinology 1980, 107:1649-1651.
25. Elkin S.L., Williams L., Moore M., Hodson M.E., Rutherford O.M. Relationship of skeletal muscle mass, muscle strength and bone mineral density in adults with cystic fibrosis. Clinical Science (London) 2000, 99:309-314.
26. Enright S., Catham K., Alina A., Viswanath B. The influence of body composition on respiratory muscle, lung function and diaphragm thickness in adults with cystic fibrosis. Journal of Cystic Fibrosis 2007, 6:384-390.
27. Gardner R.M., Hankinson J.L. Standardization of spirometry - 1987 ATS update (American Thoracic Society). Journal of Occupational and Environmental Medicine 1988, 30:272-273.
28. Green S.B., Salkind N.J. Using SPSS for Windows and Macintosh: Analyzing and understanding data 2013, Pearson, USA. 7th ed.
29. Gruber W., Orenstein D.M., Braumann K.M., Hüls G. Health-related fitness and trainability in children with cystic fibrosis. Pediatric Pulmonology 2008, 43:953-964.
30. Hayran M., Hayran M. Sağlik Araştirmalari I˙çin Temel I˙statistik 2011, Omega yayinlari, Ankara. 1st ed.
31. Hebestreit H. Exercise in cystic fibrosis. ERS Monograph 2014, 64:203-218.
32. Hulzebos E.H., Bomhof-Roordink H., van de Weert-van Leeuwen P.B., Twisk J.W., Arets H.G., van der Ent C.K., et al. Prediction of mortality in adolescents with cystic fibrosis. Medicine & Science in Sports & Exercise 2014, 46:2047-2052.
33. Hussey J., Gormley J., Leen G., Greally P. Peripheral muscle strength in young males with cystic fibrosis. Journal of Cystic Fibrosis 2002, 1:116-121.
34. Jamieson N., Fitzgerald D., Singh-Grewal D., Hanson C.S., Craig J.C., Tong A. Children's experiences of cystic fibrosis: A systematic review of qualitative studies. Pediatrics 2014, 133:e1683-e1697.
35. Janaudis-Ferreira T., Beauchamp M.K., Robles P.G., Goldstein R.S., Brooks D. Measurement of activities of daily living in patients with COPD: A systematic review. Chest 2014, 145:253-271.
36. Johnson M.R., Ferkol T.W., Shepherd R.W. Energy cost of activity and exercise in children and adolescents with cystic fibrosis. Journal of Cystic Fibrosis 2006, 5:53-58.
37. Kerem E., Conway S., Elborn S., Heijerman H., Consensus Committee Standards of care for patients with cystic fibrosis: A European consensus. Journal of Cystic Fibrosis 2005, 4:7-26.
38. Lands L., Desmond K.J., Demizio D., Pavilanis A., Coates A.L. The effects of nutritional status and hyperinflation on respiratory muscle strength in children and young adults. American Review of Respiratory Disease 1990, 141:1506-1509.
39. Li A.M., Yin J., Au J.T., So H.K., Tsang T., Wong E., et al. Standard reference for the six-minute-walk test in healthy children aged 7 to 16 years. American Journal of Respiratory Critical Care Medicine 2007, 176:174-181.
40. Li A.M., Yin J., Yu C.C., Tsang T., So H.K., Wong E., et al. The six-minute walk test in healthy children: Reliability and validity. European Respiratory Journal 2005, 25:1057-1060.
41. Mall M.A., Boucher R.C. Pathophysiology of cystic fibrosis lung disease. ERS Monograph 2014, 64:1-13.
42. Marks J., Pasterkamp H., Tal A., Leahy F. Relationship between respiratory muscle strength, nutritional status, and lung volume in cystic fibrosis and asthma. American Review of Respiratory Disease 1986, 133:414-417.
43. Nixon P.A., Orenstein D.M., Kelsey S.F. Habitual physical activity in children and adolescents with cystic fibrosis. Medicine & Science in Sports & Exercise 2001, 33:30-35.
44. O'Neill S., Leahy F., Pasterkamp H., Tal A. The effects of chronic hyperinflation, nutritional status, and posture on respiratory muscle strength in cystic fibrosis. American Review of Respiratory Disease 1983, 128:1051-1054.
45. Orenstein D.M., Rosenstein B., Stern R. Cystic fibrosis medical care 2000, Lippincott Williams & Wilkins, Philadelphia, PA. 1st ed.
46. Pastre J., Prevotat A., Tardif C., Langlois C., Duhamel A., Wallaert B. Determinants of exercise capacity in cystic fibrosis patients with mild-to-moderate lung disease. BMC Pulmonary Medicine 2014, 14:74.
47. Pinet C., Assart M., Scillia P., Lamotte M., Knoop C., Casimir G., et al. Function and bulk of respiratory and limb muscles in patients with cystic fibrosis. American Journal of Respiratory and Critical Care Medicine 2003, 168:989-994.
48. Radtke T., Stevens D., Benden C., Williams C.A. Clinical exercise testing in children and adolescents with cystic fibrosis. Pediatric Physical Therapy 2009, 21:275-281.
49. Rupper G.L. Manual of pulmonary function testing 2008, Mosby, St. Louis, MO. 9th ed.
50. Rusch H., Bradfisch J., Irrgang W. Auswahltest sportforderunterricht. Haltung bewegung 1994, 14:4-17.
51. Schneiderman Walker J., Wilkes D., Strug L., Lands L.C., Pollock S.L., Selvadurai H.C., et al. Sex differences in habitual physical activity and lung function decline in children with cystic fibrosis. Journal of Pediatrics 2005, 147:321-326.
52. Selvadurai H.C., Blimkie C.J., Meyers N., Melis C.M., Cooper P.J., Van Asperen P.P. Randomised controlled study of in-hospital exercise training programs in children with cystic fibrosis. Pediatric Pulmonology 2002, 33:194-200.
53. Skumlien S., Hagelund T., Bjortuft O., Ryg M.S. A field test of functional status as performance of activities of daily living in COPD patients. Respiratory Medicine 2006, 100:316-323.
54. Stocks J., Sly P.D., Morris M.G., Frey U. Standards for infant respiratory function testing: What (ever) next?. European Respiratory Journal 2000, 16:581-584.
55. Stuberg W.A., Metkalf W.K. Reliability of quantitative muscle testing in healthy children and in children with Duchenne muscular dystrophy using a hand-held dynamometer. Physical Therapy 1988, 68:977-982.
56. Szeinberg A., England S., Mindorf C., Fraser I.M., Levison H. Maximal inspiratory and expiratory pressures are reduced in hyperinflated, malnourished, young adult male patients with cystic fibrosis. American Review of Respiratory Disease 1985, 132:766-769.
57. Troosters T., Langer D., Vrijsen B., Segers J., Wouters K., Janssens W., et al. Skeletal muscle weakness, exercise tolerance and physical activity in adults with cystic fibrosis. European Respiratory Journal 2009, 33:99-106.
58. van der Ploeg R.J., Fidler V., Oosterhuis H.J. Hand-held myometry: Reference values. Journal of Neurology, Neurosurgery & Psychiatry 1991, 54:244-247.
59. Wilkes D.L., Schneiderman J.E., Nguyen T., Heale L., Mola F., Ratjen F., et al. Exercise and physical activity in children with cystic fibrosis. Paediatric Respiratory Reviews 2009, 10:105-109.
60. World Health Organization Physical status: The use and interpretation of anthropometry, report of the WHO Expert Committee 1995, (WHO Technical Report Series, No: 854), World Health Organization, Geneva.