Pediatric Glittre ADL-test in cystic fibrosis: Physiological parameters and respiratory mechanics

References

• Almajed A, Lands LC 2012 The evolution of exercise capacity and its limiting factors in cystic fibrosis. Paediatric Respiratory Reviews 13: 195–199.
   PubMed Web of Science ®Google Scholar
• Arikan H, Yatar I, Calik-Kutucku E, Aribas Z, Saglam M, Vardar-Yagli N, Savci S, Inal-Ince D, Ozcelik U, Kiper N 2015 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 45: 147–156.
   PubMed Web of Science ®Google Scholar
• Armitage P, Berry G 1994 The planning of statistical investigation. Statistical Methods in Medical Research 2: 179–185.
   Google Scholar
• Beydon N, Davis SD, Lombardi E, Allen JL, Arets HG, Aurora P, Bisgaard H, Davis GM, Ducharme FM, Eigen H, et al. 2007 An official American thoracic Society/European respiratory society statement: Pulmonary function testing in preschool children. American Journal of Respiratory and Critical Care Medicine 175: 1304–1345.
   PubMed Web of Science ®Google Scholar
• Buchs C, Coutier L, Vrielynck S, Jubin V, Mainguy C, Reix P 2015 An impulse oscillometry system is less efficient than spirometry in tracking lung function improvements after intravenous antibiotic therapy in pediatric patients with cystic fibrosis. Pediatric Pulmonology 50: 1073–1081.
   PubMed Web of Science ®Google Scholar
• Burtin C, Hebestreit H 2015 Rehabilitation in patients with chronic respiratory disease other than chronic obstructive pulmonary disease: Exercise and physical activity interventions in cystic fibrosis and non-cystic fibrosis bronchiectasis. Respiration 89: 181–189.
   PubMed Web of Science ®Google Scholar
• Cavallazzi TG, Cavallazzi RS, Cavalcante TD, Bettencourt AR, Diccini S 2005 Avaliação do uso da Escala Modificada de Borg na crise asmática [Evaluation of the use of the modified scale of Borg in the asthmatic crisis]. Acta Paulista de Enfermagem 18: 39–45.
   Google Scholar
• Cohen MA, Ribeiro MA, Ribeiro AF, Ribeiro JD, Morcillo AM 2011 Avaliação da qualidade de vida de pacientes com fibrose cística por meio do Cystic Fibrosis Questionnaire [Quality of life assessment in patients with cystic fibrosis by means of the cystic fibrosis questionnaire]. Jornal Brasileiro de Pneumologia 37: 184–192.
   PubMed Web of Science ®Google Scholar
• Corrêa KS, Karloh M, Martins LQ, Santos KD, Mayer AF 2011 Can the Glittre ADL test differentiate the functional capacity of COPD patients from that of healthy subjects? Brazilian Journal of Physical Therapy 15: 467–473.
   Web of Science ®Google Scholar
• Cunha MT, Rozov T, de Oliveira RC, Jardim JR 2006 Six‐minute walk test in children and adolescents with cystic fibrosis. Pediatric Pulmonology 41: 618–622.
   PubMed Web of Science ®Google Scholar
• Davi SF, Arcuri JF, Labadessa IG, Pessoa BV, Costa JN, Sentanin AC, Lorenzo VA 2014 Reprodutibilidade do teste de caminhada e do degrau de 6 minutos em adultos jovens saudáveis [Reproducibility of the six-minute walk and step tests in healthy young adults]. Revista Brasileira da Medicina do Esporte 20: 214–218.
   Google Scholar
• de Assumpção MS, Gonçalves RM, Martins R, Bobbio TG, Schivinski CI 2016 Reference equations for impulse oscilometry system parameters in healthy Brazilian children and adolescents. Respiratory Care 61: 1090–1099.
   PubMed Web of Science ®Google Scholar
• Dodd JD, Barry SC, Barry RB, Cawood TJ, McKenna MJ, Gallagher CG 2008 Bone mineral density in cystic fibrosis: Benefit of exercise capacity. Journal of Clinical Densitometry 11: 537–542.
   PubMed Web of Science ®Google Scholar
• Doeurshuk CF, Matthews LW, Tucker AS, Nudelman H, Eddy G, Wise M, Spector S 1964 A 5 year clinical evaluation of a therapeutic program for patients with Cystic fibrosis. Journal of Pediatrics 65: 677–693.
   PubMed Web of Science ®Google Scholar
• Farrell PM, White TB, Ren CL, Hempstead SE, Accurso F, Derichs N, Howenstine M, McColley SA, Rocha M, Rosenfeld M, et al. 2017 Diagnosis of cystic fibrosis: Consensus guidelines from the cystic fibrosis foundation. Journal of Pediatrics 181: S4–S15.
   PubMed Web of Science ®Google Scholar
• Holland AE, Spruit MA, Troosters T, Puhan MA, Pepin V, Saey D, McCormack MC, Carlin BW, Sciurba FC, Pitta F, et al. 2014 An official European Respiratory Society/American thoracic society technical standard: Field walking tests in chronic respiratory disease. European Respiratory Journal 44: 1428–1446.
   PubMed Web of Science ®Google Scholar
• Hommerding PX, Donadio MV, Paim TF, Marostica PJ 2010 The Borg escale is accurate in children and adolescents older than 9 years with cystic fibrosis. Respiratory Care 55: 729–733.
   PubMed Web of Science ®Google Scholar
• Hulzebos EH, Bomhof-Roordink H, van de Weert-van Leeuwen PB, Twisk JW, Arets HG, van der Ent CK, Takken T 2014 Prediction of mortality in adolescents with cystic fibrosis. Medicine and Science in Sports and Exercise 46: 2047–2052.
   PubMed Web of Science ®Google Scholar
• Hussey J, Gormley J, Leen G, Greally P 2002 Peripheral muscle strength in young males with cystic fibrosis. Journal of Cystic Fibrosis 1: 116–121.
   PubMedGoogle Scholar
• Kanga J, Kuhn R, Craigmyle L, Haverstock D, Church D 1999 Cystic fibrosis clinical score: A new scoring system to evaluate acute pulmonary exacerbation. Clinical Therapeutics 21: 1343–1356.
   PubMed Web of Science ®Google Scholar
• Klijn PH, van der Net J, Kimpen JL, Helders PJ, van der Ent CK 2003 Longitudinal determinants of peak aerobic performance in children with cystic fibrosis. Chest 124: 2215–2219.
   PubMed Web of Science ®Google Scholar
• Knudson RJ, Slatin RC, Lebowitz MD, Burrows B 1976 The maximal expiratory flow-volume curves: Normal standards, variability, and effects of age. American Review of Respiratory Disease 113: 587–600.
   PubMed Web of Science ®Google Scholar
• Lamhonwah AM, Bear CE, Huan LJ, Kim Chiaw P, Ackerley CA, Tein I 2010 Cystic fibrosis transmembrane conductance regulator in human muscle: Dysfunction causes abnormal metabolic recovery in exercise. Annals of Neurology 67: 802–808.
   PubMed Web of Science ®Google Scholar
• Machado F, Denadai BS 2011 Validade das equações preditivas da frequência cardíaca máxima para crianças e adolescentes [Validity of maximum heart rate prediction equations for children and adolescents]. Arquivo Brasileiro De Cardiologia 97: 136–140.
   PubMed Web of Science ®Google Scholar
• Martins R, Assumpcao MS, Bobbio TG, Mayer AF, Schivinski CI 2018 The validity and reliability of the ADL-Glittre Test for children. Physiotherapy Theory and Practice. doi:10.1080/09593985.2018.1457747. Epub ahead of print.
   PubMed Web of Science ®Google Scholar
• Miller MR, Crapo R, Hankinson J, Brusasco V, Burgos F, Casaburi R, Coates A, Enright P, van der Grinten CPM, Gustafsson P, et al. 2005 General considerations for lung function testing. European Respiratory Journal 26: 153–161.
   PubMed Web of Science ®Google Scholar
• Moço VR, Lopes AJ, dos Santos Vigário P, de Almeida VP, de Menezes SL, Guimarães FS 2015 Pulmonary function, functional capacity and quality of life in adults with cystic fibrosis. Revista Portuguesa De Pneumologia 21: 198–202.
   PubMedGoogle Scholar
• Peirano KR 2010 Oscilometría de impulso (IOS) em niños [Impulse oscillometry system (IOS) in children]. Neumologia Pediatrica 5: 89–95.
   PubMedGoogle Scholar
• Polgar G, Weng TR 1979 The functional development of the respiratory system from the period of gestation to adulthood. American Review of Respiratory Disease 120: 625–695.
   PubMed Web of Science ®Google Scholar
• Quanjer PH, Stanojevic S, Cole TJ, Baur X, Hall GL, Culver B, Enright PL, Hankinson JL, Ip MS, Zheng J; ERS Global Lung Function Initiative et al. 2012 Multi-ethnic reference values for spirometry for the 3–95year age range: The global lung function 2012 equations. European Respiratory Journal 40: 1324–1343.
   PubMed Web of Science ®Google Scholar
• Radtke T, Hebestreit H, Gallati S, Schneiderman JE, Braun J, Stevens D, Hulzebos EH, Takken T, Boas SR, Urquhart DS, et al. 2017 CFTR-exercise study group 2018 CFTR genotype and maximal exercise capacity in cystic fibrosis: A cross-sectional study. Annals of the American Thoracic Society 15: 209–216.
   PubMed Web of Science ®Google Scholar
• Raj D, Sharma GK, Lodha R, Kabra SK 2014 Correlation between impulse oscillometry and spirometry parameters in Indian patients with cystic fibrosis. Chronic Respiratory Disease 11: 139–149.
   PubMed Web of Science ®Google Scholar
• Ramsey BW 1996 Management of pulmonary disease in patients with cystic fibrosis. New England Journal of Medicine 335: 179–188.
   PubMed Web of Science ®Google Scholar
• Saglam M, Vardar-Yagli N, Savci S, Inal-Ince D, Aribas Z, Bosnak-Guclu M, Arikan H, Calik-Kutukcu E, Gunes-Yalcin E 2016 Six minute walk test versus incremental shuttle walk test in cystic fibrosis. Pediatrics International 58: 887–893.
   PubMed Web of Science ®Google Scholar
• Scalco JC 2015 Respostas ventilatórias, cardiovasculares e metabólicas induzidas por testes de exercício em escolares saudáveis [Ventilatory, cardiovascular and metabolic responses in exercise-induced tests in healthy school children]. Dissertação de Mestrado. Universidade do Estado de Santa Catarina.
   Google Scholar
• Silva FB, Carneiro AK, Storni JG, Carvalho NA, Damaceno N, Muramatu LH, Barroso R 2010 Comparação das variáveis fisiológicas e análise de preferência entre testes de tolerância em portadores de fibrose cística [Comparison of physiological variables and analysis of preference between tests of tolerance in patients with cystic fibrosis]. Medicina de Reabilitação 29: 45–51.
   Google Scholar
• Skumlien S, Hagelund T, Bjørtuft Ø, Ryg MS 2006 A field test of functional status as performance of activities of daily living in COPD patients. Respiratory Medicine 100: 316–323.
   PubMed Web of Science ®Google Scholar
• van de Weert-van Leeuwen PB, Slieker MG, Hulzebos HJ, Kruitwagen CL, van der Ent CK, Arets HG 2012 Chronic infection and inflammation affect exercise capacity in cystic fibrosis. European Respiratory Journal 39: 893–898.
   PubMed Web of Science ®Google Scholar
• Wieboldt J, Atallah L, Kelly JL, Shrikrishna D, Gyi KM, Lo B, Yang GZ, Bilton D, Polkey MI, Hopkinson NS 2012 Effect of acute exacerbations on skeletal muscle strength and physical activity in cystic fibrosis. Journal of Cystic Fibrosis 11: 209–215.
   PubMed Web of Science ®Google Scholar
• Ziegler B, Rovedder PM, Lukrafka JL, Abraão CL, Dalcin PD 2007 Estado nutricional em pacientes atendidos por um programa de adultos em fibrose cística [Nutritional status in patients seen at an adult program for cystic fibrosis patients]. Revista HCPA 27: 13–19.
   Google Scholar