Skip to main content
Top

2008 | OriginalPaper | Hoofdstuk

9 Inspanning bij patiënten met cystic fibrose (CF)

Auteur : Dr. H.J. Hulzebos

Gepubliceerd in: Inspanningsfysiologie bij kinderen

Uitgeverij: Bohn Stafleu van Loghum

share
DELEN

Deel dit onderdeel of sectie (kopieer de link)

  • Optie A:
    Klik op de rechtermuisknop op de link en selecteer de optie “linkadres kopiëren”
  • Optie B:
    Deel de link per e-mail

Samenvatting

Cystic fibrose (CF) is een autosomaal recessief erfelijke ziekte met een progressief beloop en beperkte levensverwachting. De geschatte incidentie in Nederland is 1:4750; de mediane leeftijd van overleving voor patiënten met CF is door verbeterde behandeling gestegen tot rond de 40 jaar (Slieker et al., 2005).
Literatuur
go back to reference Alison JA, Regnis JA, Donnelly PM, Adams RD, Sullivan CE, Bye PT. End-expiratory lung volume during arm and leg exercise in normal subjects and patients with cystic fibrosis. Am J Respir Crit Care Med. 1998 Nov;158(5 Pt 1):1450-8.PubMedCrossRef Alison JA, Regnis JA, Donnelly PM, Adams RD, Sullivan CE, Bye PT. End-expiratory lung volume during arm and leg exercise in normal subjects and patients with cystic fibrosis. Am J Respir Crit Care Med. 1998 Nov;158(5 Pt 1):1450-8.PubMedCrossRef
go back to reference American College of Sports Medicine Position Stand. The recommended quantity and quality of exercise for developing and maintaining cardiorespiratory and muscular fitness, and flexibility in healthy adults. Review. Med Sci Sports Exerc. 1998 Jun;30(6):975-91.CrossRef American College of Sports Medicine Position Stand. The recommended quantity and quality of exercise for developing and maintaining cardiorespiratory and muscular fitness, and flexibility in healthy adults. Review. Med Sci Sports Exerc. 1998 Jun;30(6):975-91.CrossRef
go back to reference 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. 1997 Jul-Aug;76(4):311-5.PubMedCrossRef 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. 1997 Jul-Aug;76(4):311-5.PubMedCrossRef
go back to reference Bradley J, Moran F. Physical training for Cystic Fibrosis (Cochrane Review). The Cochrane Library 2003;(4):1-19. Bradley J, Moran F. Physical training for Cystic Fibrosis (Cochrane Review). The Cochrane Library 2003;(4):1-19.
go back to reference Britto MT, Garrett JM, Konrad TR, Majure JM, Leigh MW. Comparison of physical activity in adolescents with Cystic Fibrosis versus age-matched controls. Pediatr Pulmonol. 2000; 30:86-91.PubMedCrossRef Britto MT, Garrett JM, Konrad TR, Majure JM, Leigh MW. Comparison of physical activity in adolescents with Cystic Fibrosis versus age-matched controls. Pediatr Pulmonol. 2000; 30:86-91.PubMedCrossRef
go back to reference Butcher SJ, Jones RL. The impact of exercise training intensity on change in physiological function in patients with chronic obstructive pulmonary disease. Review. Sports Med. 2006;36(4):307-25.PubMedCrossRef Butcher SJ, Jones RL. The impact of exercise training intensity on change in physiological function in patients with chronic obstructive pulmonary disease. Review. Sports Med. 2006;36(4):307-25.PubMedCrossRef
go back to reference Faigenbaum AD, Westcott WL, Loud RL, Long C. The effects of different resistance training protocols on muscular strength and endurance development in children. Pediatrics. 1999; 104:e5.PubMedCrossRef Faigenbaum AD, Westcott WL, Loud RL, Long C. The effects of different resistance training protocols on muscular strength and endurance development in children. Pediatrics. 1999; 104:e5.PubMedCrossRef
go back to reference Gulmans VAM, Meer K de, Brackel HJL, Faber JAJ, Berger R, Helders PJM. Outpatient exercise training in children with Cystic Fibrosis: physiological effects, perceived competence, and acceptability. Pediatr Pulmonol. 1999; 28:39-46.PubMedCrossRef Gulmans VAM, Meer K de, Brackel HJL, Faber JAJ, Berger R, Helders PJM. Outpatient exercise training in children with Cystic Fibrosis: physiological effects, perceived competence, and acceptability. Pediatr Pulmonol. 1999; 28:39-46.PubMedCrossRef
go back to reference Hart N, Polkey MI, Clément A, Boulé M, Moxham J, Lofaso F, Fauroux B. Changes in pulmonary mechanics with increasing disease severity in children and young adults with cystic fibrosis. Am J Respir Crit Care Med. 2002 Jul 1;166(1):61-6.PubMedCrossRef Hart N, Polkey MI, Clément A, Boulé M, Moxham J, Lofaso F, Fauroux B. Changes in pulmonary mechanics with increasing disease severity in children and young adults with cystic fibrosis. Am J Respir Crit Care Med. 2002 Jul 1;166(1):61-6.PubMedCrossRef
go back to reference Hayot M, Guillaumont S, Ramonatxo M, Voisin M, Préfaut C. Determinants of the tension-time index of inspiratory muscles in children with cystic fibrosis. Pediatr Pulmonol. 1997 May;23(5):336-43.PubMedCrossRef Hayot M, Guillaumont S, Ramonatxo M, Voisin M, Préfaut C. Determinants of the tension-time index of inspiratory muscles in children with cystic fibrosis. Pediatr Pulmonol. 1997 May;23(5):336-43.PubMedCrossRef
go back to reference Hebestreit H, Kieser S, Rüdiger S, Schenk T, Junge S, Hebestreit A, Ballmann M, Posselt HG, Kriemler S. Physical activity is independently related to aerobic capacity in cystic fibrosis. Eur Respir J. 2006 Oct;28(4):734-9. Epub 2006 Jun 28.PubMedCrossRef Hebestreit H, Kieser S, Rüdiger S, Schenk T, Junge S, Hebestreit A, Ballmann M, Posselt HG, Kriemler S. Physical activity is independently related to aerobic capacity in cystic fibrosis. Eur Respir J. 2006 Oct;28(4):734-9. Epub 2006 Jun 28.PubMedCrossRef
go back to reference Hussey J, Gormley J, Leen G, Greally P. Peripheral muscle strength in young males with cystic fibrosis. J Cyst Fibros. 2002 Sep;1(3):116-21.PubMedCrossRef Hussey J, Gormley J, Leen G, Greally P. Peripheral muscle strength in young males with cystic fibrosis. J Cyst Fibros. 2002 Sep;1(3):116-21.PubMedCrossRef
go back to reference Kaplan TA, Zebranek JD, McKey RM. Use of exercise in the management of cystic fibrosis. Pediatr Pulmonol. 1991; 10:205-7.PubMedCrossRef Kaplan TA, Zebranek JD, McKey RM. Use of exercise in the management of cystic fibrosis. Pediatr Pulmonol. 1991; 10:205-7.PubMedCrossRef
go back to reference Keochkerian D, Chlif M, Delanaud S, Gauthier R, Maingourd Y, Ahmaidi S. Timing and driving components of the breathing strategy in children with cystic fibrosis during exercise. Pediatr Pulmonol. 2005 Nov;40(5):449-56.PubMedCrossRef Keochkerian D, Chlif M, Delanaud S, Gauthier R, Maingourd Y, Ahmaidi S. Timing and driving components of the breathing strategy in children with cystic fibrosis during exercise. Pediatr Pulmonol. 2005 Nov;40(5):449-56.PubMedCrossRef
go back to reference Klijn PH, Oudshoorn A, Ent CK van de, Net J van der, Kimpen JL, Helders PJM. Effects of anaerobic training in children with Cystic Fibrosis: a randomized controlled study. Chest. 2004;125(4):1299-1305.PubMedCrossRef Klijn PH, Oudshoorn A, Ent CK van de, Net J van der, Kimpen JL, Helders PJM. Effects of anaerobic training in children with Cystic Fibrosis: a randomized controlled study. Chest. 2004;125(4):1299-1305.PubMedCrossRef
go back to reference Klijn PH, Terheggen-Lagro SW, Ent CK van de, Net J van der, Kimpen JL, Helders PJM. Anaerobic exercise in pediatric cystic fibrosis. Pediatr Pulmonol. 2003; 36(3):223-9.PubMedCrossRef Klijn PH, Terheggen-Lagro SW, Ent CK van de, Net J van der, Kimpen JL, Helders PJM. Anaerobic exercise in pediatric cystic fibrosis. Pediatr Pulmonol. 2003; 36(3):223-9.PubMedCrossRef
go back to reference Kwaliteitsinstituut voor de gezondheidszorg CBO. Conceptrichtlijn Diagnostiek en Behandeling Cystic Fibrosis 2007. Utrecht: Kwaliteitsinstituut voor de gezondheidszorg CBO. pp. 1-249. Kwaliteitsinstituut voor de gezondheidszorg CBO. Conceptrichtlijn Diagnostiek en Behandeling Cystic Fibrosis 2007. Utrecht: Kwaliteitsinstituut voor de gezondheidszorg CBO. pp. 1-249.
go back to reference Lands LC, Heigenhauser GJ, Jones NL. Analysis of factors limiting maximal exercise performance in cystic fibrosis. Clin Sci (Lond). 1992 Oct;83(4):391-7.PubMed Lands LC, Heigenhauser GJ, Jones NL. Analysis of factors limiting maximal exercise performance in cystic fibrosis. Clin Sci (Lond). 1992 Oct;83(4):391-7.PubMed
go back to reference Laursen PB, Jenkins DG. The scientific basis for high-intensity interval training: optimising training programmes and maximising performance in highly trained endurance athletes. Review. Sports Med. 2002;32(1):53-73.PubMedCrossRef Laursen PB, Jenkins DG. The scientific basis for high-intensity interval training: optimising training programmes and maximising performance in highly trained endurance athletes. Review. Sports Med. 2002;32(1):53-73.PubMedCrossRef
go back to reference Marcotte JE, Canny GJ, Grisdale R, Desmond K, Corey M, Zinman R, et al. Effects of nutritional status on exercise performance in advanced cystic fibrosis. Chest. 1986;90(3):375-9.PubMedCrossRef Marcotte JE, Canny GJ, Grisdale R, Desmond K, Corey M, Zinman R, et al. Effects of nutritional status on exercise performance in advanced cystic fibrosis. Chest. 1986;90(3):375-9.PubMedCrossRef
go back to reference McKone EF, Barry SC, FitzGerald MX, Gallagher CG. The role of supplemental oxygen during submaximal exercise in patients with. Eur Respir J. 2002;20:134-42.PubMedCrossRef McKone EF, Barry SC, FitzGerald MX, Gallagher CG. The role of supplemental oxygen during submaximal exercise in patients with. Eur Respir J. 2002;20:134-42.PubMedCrossRef
go back to reference Meer K de, Gulmans VAM, Laag J van der. Peripheral muscle weakness and exercise capacity in children with cystic fibrosis. Am J Respir Crit Care Med. 1999; 159:748-54.PubMedCrossRef Meer K de, Gulmans VAM, Laag J van der. Peripheral muscle weakness and exercise capacity in children with cystic fibrosis. Am J Respir Crit Care Med. 1999; 159:748-54.PubMedCrossRef
go back to reference Meyer K, Samek L, Schwaibold M, Westbrook S, Hajric R, Beneke R, Lehmann M, Roskamm H. Interval training in patients with severe chronic heart failure: analysis and recommendations for exercise procedures. Med Sci Sports Exerc. 1997 Mar;29(3):306-12.PubMedCrossRef Meyer K, Samek L, Schwaibold M, Westbrook S, Hajric R, Beneke R, Lehmann M, Roskamm H. Interval training in patients with severe chronic heart failure: analysis and recommendations for exercise procedures. Med Sci Sports Exerc. 1997 Mar;29(3):306-12.PubMedCrossRef
go back to reference Moorcroft AJ, Dodd ME, Morris J, Webb AK. Symptoms, lactate and exercise limitation at peak cycle ergometry in adults with cystic fibrosis. Eur Respir J. 2005 Jun;25(6):1050-6.PubMedCrossRef Moorcroft AJ, Dodd ME, Morris J, Webb AK. Symptoms, lactate and exercise limitation at peak cycle ergometry in adults with cystic fibrosis. Eur Respir J. 2005 Jun;25(6):1050-6.PubMedCrossRef
go back to reference Nici L, Donner C, Wouters E, Zuwallack R, Ambrosino N, Bourbeau J, Carone M, Celli B, Engelen M, Fahy B, Garvey C, Goldstein R, Gosselink R, Lareau S, MacIntyre N, Maltais F, Morgan M, O’Donnell D, Prefault C, Reardon J, Rochester C, Schols A, Singh S, Troosters T; ats/ers Pulmonary Rehabilitation Writing Committee. American Thoracic Society/European Respiratory Society statement on pulmonary rehabilitation. Am J Respir Crit Care Med. 2006 Jun 15;173(12):1390-413.PubMedCrossRef Nici L, Donner C, Wouters E, Zuwallack R, Ambrosino N, Bourbeau J, Carone M, Celli B, Engelen M, Fahy B, Garvey C, Goldstein R, Gosselink R, Lareau S, MacIntyre N, Maltais F, Morgan M, O’Donnell D, Prefault C, Reardon J, Rochester C, Schols A, Singh S, Troosters T; ats/ers Pulmonary Rehabilitation Writing Committee. American Thoracic Society/European Respiratory Society statement on pulmonary rehabilitation. Am J Respir Crit Care Med. 2006 Jun 15;173(12):1390-413.PubMedCrossRef
go back to reference Nixon PA, Orenstein DM, Kelsey SF, Doershuk CF. The prognostic value of exercise testing in patients with cystic fibrosis. N Engl J Med. 1992; 327:1785-8.PubMedCrossRef Nixon PA, Orenstein DM, Kelsey SF, Doershuk CF. The prognostic value of exercise testing in patients with cystic fibrosis. N Engl J Med. 1992; 327:1785-8.PubMedCrossRef
go back to reference Nixon PA, Orenstein DM, Kelsey SF. Habitual physical activity in children and adolescents with cystic fibrosis. Med Sci Sports Exerc. 2001; 33(1):30-5.PubMedCrossRef Nixon PA, Orenstein DM, Kelsey SF. Habitual physical activity in children and adolescents with cystic fibrosis. Med Sci Sports Exerc. 2001; 33(1):30-5.PubMedCrossRef
go back to reference O’Donnell DE. Ventilatory limitations in chronic obstructive pulmonary disease. Review. Med Sci Sports Exerc. 2001 Jul;33(7 Suppl):S647-55.CrossRef O’Donnell DE. Ventilatory limitations in chronic obstructive pulmonary disease. Review. Med Sci Sports Exerc. 2001 Jul;33(7 Suppl):S647-55.CrossRef
go back to reference Pianosi P, Pelech A. Stroke volume during exercise in cystic fibrosis. Am J Respir Crit Care Med. 1996 Mar;153(3):1105-9.PubMedCrossRef Pianosi P, Pelech A. Stroke volume during exercise in cystic fibrosis. Am J Respir Crit Care Med. 1996 Mar;153(3):1105-9.PubMedCrossRef
go back to reference Pinet C, Cassart M, Scillia P, Lamotte M, Knoop C, Casimir G, Mélot C, Estenne M. Function and bulk of respiratory and limb muscles in patients with cystic fibrosis. Am J Respir Crit Care Med. 2003 Oct 15;168(8):989-94. Epub 2003 Jun 26.PubMedCrossRef Pinet C, Cassart M, Scillia P, Lamotte M, Knoop C, Casimir G, Mélot C, Estenne M. Function and bulk of respiratory and limb muscles in patients with cystic fibrosis. Am J Respir Crit Care Med. 2003 Oct 15;168(8):989-94. Epub 2003 Jun 26.PubMedCrossRef
go back to reference Prasad A, Cerny FJ. Factors that influence adherence to exercise and their effectiveness: application to cystic fibrosis. Pediatr Pulmonol. 2003. Prasad A, Cerny FJ. Factors that influence adherence to exercise and their effectiveness: application to cystic fibrosis. Pediatr Pulmonol. 2003.
go back to reference Regnis JA, Donnelly PM, Robinson M, Alison JA, Bye PT. Ventilatory mechanics at rest and during exercise in patients with cystic fibrosis. Am J Respir Crit Care Med. 1996 Nov;154(5):1418-25.PubMedCrossRef Regnis JA, Donnelly PM, Robinson M, Alison JA, Bye PT. Ventilatory mechanics at rest and during exercise in patients with cystic fibrosis. Am J Respir Crit Care Med. 1996 Nov;154(5):1418-25.PubMedCrossRef
go back to reference Schneiderman-Walker J, Pollock SL, Corey M, Wilkes DD, Canny GJ, Pedder L et al. A randomized controlled trial of a 3-year home exercise program in cystic fibrosis. J Pediatr. 2000;136(3):279-80.CrossRef Schneiderman-Walker J, Pollock SL, Corey M, Wilkes DD, Canny GJ, Pedder L et al. A randomized controlled trial of a 3-year home exercise program in cystic fibrosis. J Pediatr. 2000;136(3):279-80.CrossRef
go back to reference 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. 2003; 33:194-200.CrossRef 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. 2003; 33:194-200.CrossRef
go back to reference Selvadurai HC, Cooper PJ, Meyers N, Blimkie CJ, Smith L, Mellis CM, et al. Validation of shuttle tests in children with cystic fibrosis. Pediatr Pulmonol. 2003;35(2):133-8.PubMedCrossRef Selvadurai HC, Cooper PJ, Meyers N, Blimkie CJ, Smith L, Mellis CM, et al. Validation of shuttle tests in children with cystic fibrosis. Pediatr Pulmonol. 2003;35(2):133-8.PubMedCrossRef
go back to reference Shah AR, Gozal D, Keens TG. Determinants of aerobic and anaerobic exercise performance in cystic fibrosis. Am J Respir Crit Care Med. 1998 Apr;157(4 Pt 1):1145-50.PubMedCrossRef Shah AR, Gozal D, Keens TG. Determinants of aerobic and anaerobic exercise performance in cystic fibrosis. Am J Respir Crit Care Med. 1998 Apr;157(4 Pt 1):1145-50.PubMedCrossRef
go back to reference Slieker MG, Uiterwaal CS, Sinaasappel M, Heijerman HG, Laag J van der, Ent CK van der. Birth prevalence and survival in cystic fibrosis: a national cohort study in the Netherlands. Chest. 2005 Oct;128(4):2309-15.PubMedCrossRef Slieker MG, Uiterwaal CS, Sinaasappel M, Heijerman HG, Laag J van der, Ent CK van der. Birth prevalence and survival in cystic fibrosis: a national cohort study in the Netherlands. Chest. 2005 Oct;128(4):2309-15.PubMedCrossRef
go back to reference Stein R, Selvadurai H, Coates A, Wilkes DL, Schneiderman-Walker J, Corey M. Determination of maximal voluntary ventilation in children with cystic fibrosis. Pediatr Pulmonol. 2003 Jun;35(6):467-71.PubMedCrossRef Stein R, Selvadurai H, Coates A, Wilkes DL, Schneiderman-Walker J, Corey M. Determination of maximal voluntary ventilation in children with cystic fibrosis. Pediatr Pulmonol. 2003 Jun;35(6):467-71.PubMedCrossRef
go back to reference Takken T. Inspanningstests. Maarssen: Elsevier Gezondheidszorg; 2007. Takken T. Inspanningstests. Maarssen: Elsevier Gezondheidszorg; 2007.
go back to reference Thin AG, Dodd JD, Gallagher CG, Fitzgerald MX, Mcloughlin P. Effect of respiratory rate on airway deadspace ventilation during exercise in cystic fibrosis. Respir Med. 2004 Nov;98(11):1063-70.PubMedCrossRef Thin AG, Dodd JD, Gallagher CG, Fitzgerald MX, Mcloughlin P. Effect of respiratory rate on airway deadspace ventilation during exercise in cystic fibrosis. Respir Med. 2004 Nov;98(11):1063-70.PubMedCrossRef
Metagegevens
Titel
9 Inspanning bij patiënten met cystic fibrose (CF)
Auteur
Dr. H.J. Hulzebos
Copyright
2008
Uitgeverij
Bohn Stafleu van Loghum
DOI
https://doi.org/10.1007/978-90-313-6560-9_9