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Expert Review of Respiratory Medicine Volume 7, 2013 - Issue 6
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Measurement of physical activity in patients with cystic fibrosis: a systematic review

Erik HulzebosChild Development & Exercise Center, Wilhelmina Children’s Hospital, Room KB.02.056, University Medical Center Utrecht, P.O. Box 85090, 3508 AB Utrecht, The Netherlands;Cystic Fibrosis Center and Department of Pediatric Respiratory Medicine, Wilhelmina Children’s Hospital, University Medical Center Utrecht, The NetherlandsCorrespondence[email protected]
,
Tessa DademaFaculty of Human Movement Sciences, VU University Amsterdam, Amsterdam, The Netherlands
&
Tim TakkenChild Development & Exercise Center, Wilhelmina Children’s Hospital, Room KB.02.056, University Medical Center Utrecht, P.O. Box 85090, 3508 AB Utrecht, The Netherlands;Partner of Shared Utrecht Pediatric Exercise Research (SUPER) Lab, Utrecht, The Netherlands
Pages 647-653 | Published online: 09 Jan 2014

References

  • Davis PB, Drumm M, Konstan MW. Cystic fibrosis – state of the art. Am. J. Respir. Crit. Care Med. 154, 1229–1256 (1996).
  • Hodson ME, Norman AP, Batten JC. Cystic Fibrosis. Balliere Tindall, London (1983).
  • Blomquist M, Freyschuss U, Wiman LG, Strandvik B. Physical activity and self-treatment in cystic fibrosis. Arch. Dis. Child. 61, 362–367 (1986).
  • Lands LC, Heigenhauser GJ, Jones NL. Analysis of factors limiting maximal exercise performance in cystic fibrosis. Clin. Sci. 83(4), 391–397 (1992).
  • Boucher GP, Lands LC, Hay JA, Hornby L. Activity levels and the relationship to lung function and nutritional status in children with cystic fibrosis. Am. J. Phys. Med. Rehabil. 76(4), 311–315 (1997).
  • Webb AK, Dodd ME, Moorcroft J. Exercise and cystic fibrosis. J. R. Soc. Med. 88(S25), 30–36 (1995).
  • Tepper RS, Hiatt P, Eigen H, Scott P, Grosfeld J, Cohen M. Infants with cystic fibrosis: pulmonary function at diagnosis. Pediatr. Pulmonol. 5(1), 15–18 (1988).
  • Corey M. Modelling survival in cystic fibrosis. Thorax 56(10), 743 (2001).
  • Schluchter MD, Konstan MW, David PB. Jointly modelling the relationship between survival and pulmonary function in cystic fibrosis patients. Statist. Med. 21, 1271–1287 (2002).
  • Wilkes DL, Scheiderman JE, Nguyen T et al. Exercise and physical activity in children with cystic fibrosis. Pediatr. Respir. Rev. 10, 105–109 (2009).
  • Nixon PA, Orenstein DM, Kelsey SF, Doershuk CF. The prognostic value of exercise testing in patients with cystic fibrosis. N. Engl. J. Med. 327(25), 1785–1788 (1992).
  • Orenstein D, Nixon P, Ross E, Kaplan R. The quality of well-being in cystic fibrosis. Chest 95, 344–347 (1989).
  • Hebestreit H, Kieser S, Rüdiger S et al. Physical activity is independently related to aerobic capacity in cystic fibrosis. Eur. Respir. J. 28(4), 734–739 (2006).
  • Schneiderman-walker J, Wilkes DL, Strug L et al. Sex differences in habitual physical activity and lung function decline in children with CF. J. Pediatr. 147, 321–326 (2005).
  • Nixon PA, Orenstein DM, Kelsey SF. Habitual physical activity in children and adolescents with cystic fibrosis. Med. Sci. Sports Exerc. 33(1), 30–35 (2001).
  • Swisher AK, Erickson M. Perceptions of physical activity in a group of adolescents with cystic fibrosis. Cardiopulm. Phys. Ther. J. 19(4), 107–113 (2008).
  • Ruf K, Fehn S, Bachmann M et al. Validation of activity questionnaires in patients with cystic fibrosis by accelerometry and cycle ergometry. BMC Med. Res. Methodol. 3, 12–43 (2012).
  • Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred reporting items for systematic reviews and meta-analyses: The PRISMA Statement. Ann. Intern. Med. 151(4), 264–269 (2009).
  • Wells GD, Wilkes DL, Schneiderman-Walker J et al. reliability and validity of the habitual activity estimation scale (HAES) in patients with cystic fibrosis. Pediatr. Pulmonol. 43, 345–353 (2008).
  • Kent L, O’Neill B, Murray J, Reid A, Elborn JS, Bradley J. Habitual physical activity in children with cystic fibrosis: reliability and relationship with quality of life and lung function. J. Cyst. Fibros. 10(1), S64 (2011).
  • Adams A, MacKenzie R, Lenton J, Brickley G, Seddon R. Physical activity and fitness in children with Cystic Fibrosis. J. Cyst. Fibros. 5(1), S80 (2006).
  • Button BM, Rasekaba T, Wilson JW, Holland AE. Validation of the international physical activity questionnaire (IPAQ) in adults with cystic fibrosis. J. Cyst.. Fibros. 10(1), S65 (2006).
  • Dwyer TJ, Alison JA, McKeough ZJ, Elkins MR, Bye PTP. Evaluation of the SenseWear activity monitor during exercise in cystic fibrosis and in health. Respir. Med. 103, 1511–1517 (2009).
  • Quon BS, Patrick DL, Edwards TC et al. Feasibility of using pedometers to measure daily step counts in cystic fibrosis and an assessment of its responsiveness to changes in health state. J. Cyst. Fibros. 11, 216–222 (2012).
  • Hay JA, Cairney J. Development of the habitual activity estimation scale for clinical research: a systematic approach. Pediatr. Exerc. Sci. 18, 193–202 (2006).
  • Hopkins WG. Quantification of training in competitive sports: methods and applications. Sports Med. 12(3), 161–183 (1991).
  • Van Remoortel H, Raste Y, Louvaris Z et al. Validity of six activity monitors in chronic obstructive pulmonary disease: a comparison with indirect calorimetry. PLoS ONE 7(6), e39198 (2012).
  • Turner LJ, Houchen L, Williams J, Singh SJ. Reliability of pedometers to measure step counts in patients with chronic respiratory disease. J. Cardiopulm. Rehabil. Prev. 32(5), 284–291 (2012).

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