Activity levels and the relationship to lung function and nutritional status in children with cystic fibrosis

American Journal of Physical Medicine and Rehabilitation

Volumn 76, Issue 4, 1997, Pages 311-315

  Boucher, G P ^a   Lands, L C ^a   Hay, J A ^a   Hornby, L ^a  

^a MONTREAL CHILDREN S HOSPITAL   (Canada)

Author keywords

Activity; Cystic Fibrosis; Exercise; Nutrition

Indexed keywords

NUTRITION; PULMONARY DISEASES;

CYSTIC FIBROSIS; FORCED EXPIRATORY VOLUME (FEV); HABITUAL ACTIVITY ESTIMATION SCALE;

PEDIATRICS;

ADOLESCENT; ARTICLE; BODY MASS; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; CYSTIC FIBROSIS; FEMALE; FORCED EXPIRATORY VOLUME; HUMAN; LUNG FUNCTION; MALE; NUTRITIONAL STATUS; PHYSICAL ACTIVITY; QUALITY OF LIFE;

ADOLESCENT; CHILD; CYSTIC FIBROSIS; EXERCISE; FEMALE; FORCED EXPIRATORY VOLUME; HUMANS; MALE; NUTRITIONAL STATUS; PHYSICAL FITNESS; RESPIRATION;

EID: 0031194825     PISSN: 08949115     EISSN: None     Source Type: Journal    
DOI: 10.1097/00002060-199707000-00010     Document Type: Article

References (21)

1. Cooper DM. Rethinking exercise testing in children. a challenge. Am J Respir Crit Care Med 1995;152:1154-1157.
2. Lands LC, Heigenhauser GJ, Jones NL. Analysis of factors limiting maximal exercise performance in cystic fibrosis. Clin Sei 1992;83:391-397.
3. Babb TG, Viggiano R, Hurley B, Staats B, Rodarte Effect of mild-to-moderate airflow limitation on exercise capacity. J Appl Physiol 1991;70:223-230.
4. Coates AL, 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. Ada Paediatr Scand 1980;69:353-358.
5. Lands LC, Desmond KJ, Demizio D, Pavilanis A, Coates AL. The effects of nutritional status and hyperinflation on respiratory muscle strength in children and young adults. Am Rev Respir Dis 1990;141:1506-1509.
6. Wang X, Dockery DW, Wypij D, Fay ME, Ferris BG Pulmonary function between 6 and 18 years of age. Pediatr Pulmonol 1993;15:75-88.
7. Hay J, Atkinson SA, Haiton J. An Examination of the Reliability of the Habitual Activity Estimation Scale (HAES). Proceeding of the Pediatrie Work Physiology Symposium XVIII, 1995, p 49.
8. Bland JM, Altman DG. Statistical methods for assessing agreement between two methods of clinical measurement. Lancet 1986;1:307-310.
9. Moelgaard C. Bone mineralization during growth. the influence of growth, puberty and calcium intake. University of Copenhagen (Denmark), PhD thesis, 1996.
10. Hay J. Adequacy in and predilectation for physical activity in children. Clin J Sports Med 1992;2:191-201.
11. Atkinson SA, Halton J, Hay J, Gordon C, Webber C. Normative values for lumbar spine bone mass in children in relation to age, gender, dietary intake and physical activity. J Bone Miner Kes 1991;6:S241.
12. Russell DM, Walker PM, Leiter LA, et al.. Metabolic and structural changes in skeletal muscle during hypocaloric dieting. Am J Clin Nittr 1984;39:503-513.
13. Pencharz P, Hill R, Archibald E, Levy L, Newth C. Energy needs and nutritional rehabilitation in undernourished adolescents and young adult patients with cystic fibrosis. J Pediatr Gastroenterol Nittr 1984;3(suppl 1):S147-S153.
14. Marcotte JE, Canny GJ, Grisdale R, et al.. Effects of nutritional status on exercise performance in advanced cystic fibrosis. Chest 1986;90:375-379.
15. Spicher V, Roulet M, Schutz Y. Assessment of total energy expenditure in free-living patients with cystic fibrosis. / Pediatr 1991;118:865-872.
16. Fried MD, Durie PR, Tsui LC, Corey M, Levison H, Pencharz PB. The cystic fibrosis gene and resting energy expenditure. / Pediatr 1991;119:913-916.
17. Grunow JE, Azcue MP, Derail G, Pencharz PB. Energy expenditure in cystic fibrosis during activities of daily living. / Pediatr 1993;122:243-246.
18. Hay J. The stability of children's self-perceptions regarding activity. a 5-year follow-up (abstract). Pediatr Exercise Sei 1995; 7:A217.
19. Gurwitz D, Corey M, Francis P, Crozier D, Levison H. Perspectives in cystic fibrosis. Pedintr Clin Nortli Am 1979;26:603-615.
20. Gaskin K, Gurwitz D, Durie P, Corey M, Levison H, Forstner G. Improved respiratory prognosis in patients wvith cystic fibrosis with normal fat absorption. / Pediatr 1982;100:857-862.
21. Kraemer R, Rudeberg A, Hadorn B, Rossi E. Relative underweight in cystic fibrosis and its prognostic value. Ada Paediatr Scand 1978;67:33-37.