Physical activity participation by adults with cystic fibrosis: An observational study

Respirology

Volumn 21, Issue 3, 2016, Pages 511-518

  Cox, Narelle S ^a   Alison, Jennifer A ^b   Button, Brenda M ^c,d   Wilson, John W ^c,d   Morton, Judith M ^e,f   Holland, Anne E ^a,c  

^a LA TROBE UNIVERSITY   (Australia)

^b ALFRED HOSPITAL   (Australia)

^c MONASH UNIVERSITY   (Australia)

^d SOUTHERN HEALTH   (Australia)

^e UNIVERSITY OF SYDNEY   (Australia)

^f ROYAL PRINCE ALFRED HOSPITAL   (Australia)

Author keywords

cystic fibrosis; exercise; habitual activity; hospitalization; physical activity

Indexed keywords

ADULT; ARTICLE; CYSTIC FIBROSIS; DISEASE EXACERBATION; EXERCISE; EXERCISE TEST; FEMALE; FORCED EXPIRATORY VOLUME; HOSPITAL ADMISSION; HOSPITAL DISCHARGE; HOSPITALIZATION; HUMAN; LENGTH OF STAY; LUNG FUNCTION; MAJOR CLINICAL STUDY; MALE; MODERATE VIGOROUS PHYSICAL ACTIVITY; MODIFIED SHUTTLE TEST; OBSERVATIONAL STUDY; OUTCOME ASSESSMENT; PHYSICAL ACTIVITY; PRIORITY JOURNAL; PROSPECTIVE STUDY; QUALITY OF LIFE; SEX DIFFERENCE; CLINICAL TRIAL; LUNG; MOTOR ACTIVITY; MULTICENTER STUDY; PATHOPHYSIOLOGY; PHYSIOLOGY;

ADULT; CYSTIC FIBROSIS; EXERCISE; EXERCISE TEST; FEMALE; HUMANS; LUNG; MALE; MOTOR ACTIVITY; QUALITY OF LIFE;

EID: 84952837696     PISSN: 13237799     EISSN: 14401843     Source Type: Journal    
DOI: 10.1111/resp.12719     Document Type: Article

References (46)

1. Simmonds NJ,. Ageing in cystic fibrosis and long-term survival. Paediatr. Respir. Rev. 2013; 14 (Suppl. 1): 6-9.
2. Selvadurai HC, Blimkie CJ, Cooper PJ, Mellis CM, Van Asperen PP,. Gender differences in habitual activity in children with cystic fibrosis. Arch. Dis. Child. 2004; 89: 928-933.
3. Schneiderman JE, Wilkes DL, Atenafu EG, Nguyen T, Wells GD, Alarie N, Tullis E, Lands LC, Coates AL, Corey M, et al. Longitudinal relationship between physical activity and lung health in patients with cystic fibrosis. Eur. Respir. J. 2014; 43: 817-823.
4. Collaco JM, Blackman SM, Raraigh KS, Morrow CB, Cutting GR, Paranjape SM,. Self-reported exercise and longitudinal outcomes in cystic fibrosis: a retrospective cohort study. BMC Pulm. Med. 2014; 14: 159.
5. WHO. Global Recommendations for Physical Activity and Health. WHO Press, Geneva, 2010.
6. Haskell W, Lee I-M, Pate RR, Powel K, Blair S, Franklin B, Macera C, Heath GW, Thompson P, Bauman A,. Physical activity and public health: updated recommendation for adults from the American College of Sports Medicine and the American Heart Association. Med. Sci. Sports Exerc. 2007; 39: 1423-1434.
7. Thompson PD, Buchner D, Pina IL, Balady GJ, Williams MA, Marcus BH, Berra K, Blair SN, Costa F, Franklin B, et al. This statement was reviewed B, has received the endorsement of the American College of Sports M. Exercise and physical activity in the prevention and treatment of atherosclerotic cardiovascular disease: a statement from the council on clinical cardiology (subcommittee on exercise, rehabilitation, and prevention) and the council on nutrition, physical activity, and metabolism (subcommittee on physical activity). Arterioscler. Thromb. Vasc. Biol. 2003; 23: e42-49.
8. Bradley J, Moran F,. Physical training for cystic fibrosis. Cochrane Database Syst. Rev. 2008; (2008): CD002768.
9. Schneiderman-Walker J, Pollock SL, Corey M, Wilkes DD, Canny GJ, Pedder L, Reisman JJ,. A randomized controlled trial of a 3-year home exercise program in cystic fibrosis. J. Pediatr. 2000; 136: 304-310.
10. Hebestreit H, Kieser S, Junge S, Ballmann M, Hebestreit A, Schindler C, Schenk T, Posselt HG, Kriemler S,. Long-term effects of a partially supervised conditioning programme in cystic fibrosis. Eur. Respir. J. 2010; 35: 578-583.
11. Selvadurai HC, Blimkie CJ, Meyers N, Mellis CM, Cooper PJ, Van Asperen PP,. Randomized controlled study of in-hospital exercise training programs in children with cystic fibrosis. Pediatr. Pulmonol. 2002; 33: 194-200.
12. Nixon P, Orenstein D, Kelsey S, Doershuk C,. The prognostic value of exercise testing in patients with cystic fibrosis. N. Engl. J. Med. 1992; 327: 1785-1788.
13. Pianosi P, Le Blanc J, Almudevar A,. Peak oxygen uptake in children with cystic fibrosis. Thorax 2005; 60: 50-54.
14. Murphy MH, Nevill AM, Neville C, Biddle S, Hardman AE,. Accumulating brisk walking for fitness, cardiovascular risk, and psychological health. Med. Sci. Sports Exerc. 2002; 34: 1468-1474.
15. Rosenfeld M, Emerson J, Williams-Warren J, Pepe M, Smith A, Montgomery B, Ramsey B,. Defining a pulmonary exacerbation in cystic fibrosis. J. Pediatr. 2001; 139: 359-365.
16. Bourka A, Tiede H, Liebich L, Dumitrascu R, Hecker C, Reichenberger F, Mayer K, Seeger W, Schultz R,. Quality of life in clinically stable adult cystic fibrosis out-patients: associations with daytime sleepiness and sleep quality. Respir. Med. 2012; 106: 1244-1249.
17. Cox NS, Alison JA, Button BM, Wilson JW, Morton JM, Dowman LM, Holland AE,. Validation of a multi-sensor armband during free-living activity in adults with cystic fibrosis. J. Cyst. Fibros. 2014; 13: 347-350.
18. Trost S, McIver K, Pate RR,. Conducting accelerometer-based activity assessments in field-based research. Med. Sci. Sports Exerc. 2005; 37: S531-543.
19. Hebestreit H, Kieser S, Rudiger S, Schenk T, Junge S, Hebestreit A, Ballmann M, Posselt H-G, Kriemler S,. Physical activity is independently related to aerobic capacity in cystic fibrosis. Eur. Respir. J. 2006; 28: 734-739.
20. Us Department of Health and Human Services. Physical Activity and Health: A Report of the Surgeon General, 1996.
21. Troosters T, Langer D, Vrijsen B, Segers J, Wouters K, Janssens W, Gosselink R, Decramer M, Dupont L,. Skeletal muscle weakness, exercise tolerance and physical activity in adults with cystic fibrosis. Eur. Respir. J. 2009; 33: 99-106.
22. Ward N, White D, Rowe H, Stiller K, Sullivan T,. Physical activity levels of patients with cystic fibrosis hospitalised with an acute respiratory exacerbation. Respir. Med. 2013; 107: 1014-1020.
23. Tejero Garcia S, Giraldez Sanchez M, Cejudo P, Quintana Gallego E, Dapena J, Carcia Jimenez R, Can Luis P, Gomez De Terreros I,. Bone health, daily physical activity, and exercise tolerance in patients with cystic fibrosis. Chest 2011; 140: 475-481. [Epub 2011 Feb 3].
24. Miller MR, Hankinson J, Brusasco V, Burgos F, Casaburi R, Coates A, Crapo R, Enright P, Van Der Grinten C, Gustafsson P,. Standardisation of spirometry. Eur. Respir. J. 2005; 26: 319-338.
25. Bradley J, Howard J, Wallace E, Elborn S,. Validity of a modified shuttle test in adult cystic fibrosis. Thorax 1999; 54: 437-439.
26. Bradley J, Howard J, Wallace E, Elborn S,. Reliability, repeatability, and sensitivity of the modified shuttle test in adult cystic fibrosis. Chest 2000; 117: 1666-1671.
27. Rogers D, Smith P, John N, Oliver W, Doull I,. Validity of a modified shuttle walk test as a measure of exercise tolerance in paediatric CF patients [Abstract]. J. Cyst. Fibros. 2002; 1: 22.
28. Quittner AL, Buu A, Messer MA, Modi AC, Watrous M,. Development and validation of The Cystic Fibrosis Questionnaire in the United States: a health-related quality-of-life measure for cystic fibrosis. Chest 2005; 128: 2347-2354.
29. Liou TG, Elkin EP, Pasta DJ, Jacobs JR, Konstan MW, Morgan WJ, Wagener JS,. Year-to-year changes in lung function in individuals with cystic fibrosis. J. Cyst. Fibros. 2010; 9: 250-256.
30. Pallant J,. SPSS Survival Manual, 4th edn. Allen & Unwin, Crows Nest, NSW, 2011.
31. Rasekaba TM, Button BM, Wilson JW, Holland AE,. Reduced physical activity associated with work and transport in adults with cystic fibrosis. J. Cyst. Fibros. 2013; 12: 229-233.
32. Matthews CE, Moore SC, George SM, Sampson J, Bowles HR,. Improving self-reports of active and sedentary behaviors in large epidemiologic studies. Exerc. Sport Sci. Rev. 2012; 40: 118-126.
33. Reilly J, Vpenpraze V, Hislop J, Davies G, Grant S, Paton J,. Objective measurement of physical activity and sedentary behaviour: review with new data. Arch. Dis. Child. 2008; 93: 614-619.
34. Ruf K, Fehn S, Moeller A, Roth K, Kriemler S, Hebestreit H,. Validation of activity questionnaires in patients with cystic fibrosis by accelerometry and cycle ergometry. BMC Med. Res. Methodol. 2012; 12: 1-9.
35. Savi D, Quattrucci S, Internullo M, De Biase RV, Calverley PMA, Palange P,. Measuring habitual physical activity in adults with cystic fibrosis. Respir. Med. 2013; 107: 1888-1894.
36. Boreham C, Kennedy R, Murphy M, Tully M, Wallace W, Young I,. Training effects of short bouts of stair climbing on cardiorespiratory fitness, blood lipids, and homocysteine in sedentary young women. Br. J. Sports Med. 2005; 39: 590-593.
37. Donaire-Gonzalez D, Gimeno-Santos E, Balcells E, Rodríguez DA, Farrero E, Batlle JD, Benet M, Ferrer A, Barberà JA, Gea J, et al. Physical activity in COPD patients: patterns and bouts. Eur. Respir. J. 2013; 42: 993-1002.
38. Dentro K, Beals K, Crouter S, Eisenmann J, McKenzie T, Pate RR, Saelens BE, Sisson S, Spruijt-Metz D, Sothern M, et al. Results from the United States' 2014 report card on physical activity for children and youth. J. Phys. Act. Health 2014; 11: S105-112.
39. Bray SR, Born HA,. Transition to university and vigorous physical activity: implications for health and psychological well-being. J. Am. Coll. Health 2004; 52: 181-188.
40. Dodge JA, Lewis PA, Stanton M, Wilsher J,. Cystic fibrosis mortality and survival in the UK: 1947-2003. Eur. Respir. J. 2007; 29: 522-526.
41. Schneiderman-Walker J, Wilkes DL, Strug L, Lands LC, Pollock SL, Selvadurai HC, Hay J, Coates AL, Corey M,. Sex differences in habitual physical activity and lung function decline in children with cystic fibrosis. J. Pediatr. 2005; 147: 321-326.
42. Spruit MA, Gosselink R, Troosters T, Kasran A, Gayan-Ramirez G, Bogaerts P, Bouillon R, Decramer M,. Muscle force during an acute exacerbation in hospitalised patients with COPD and its relationship with CXCL8 and IGF-I. Thorax 2003; 58: 752-756.
43. Pitta F, Troosters T, Probst VS, Spruit MA, Decramer M, Gosselink R,. Physical activity and hospitalization for exacerbation of COPD. Chest 2006; 129: 536-544.
44. Swisher AK, Erickson M,. Perceptions of physical activity in a group of adolescents with cystic fibrosis. Cardiopulm. Phys. Ther. J. 2008; 19: 107-113.
45. Sawicki GS, Sellers DE, Robinson WM,. High treatment burden in adults with cystic fibrosis: challenges to disease self-management. J. Cyst. Fibros. 2009; 8: 91-96.
46. Pivarnik JM, Reeves MJ, Rafferty AP,. Seasonal variation in adult leisure-time physical activity. Med. Sci. Sports Exerc. 2003; 35: 1004-1008.