Publication Cover
Physiotherapy Theory and Practice
An International Journal of Physical Therapy
Volume 38, 2022 - Issue 13
475
Views
1
CrossRef citations to date
0
Altmetric
Descriptive Report

Relationship between peripheral muscle strength, exercise capacity and body composition in children and adolescents with cystic fibrosis

, MSc, PTORCID Icon, , MSc, PTORCID Icon, , MSc, PTORCID Icon, , PhDORCID Icon & , PhD, PTORCID Icon
Pages 3010-3017 | Received 28 Aug 2020, Accepted 18 Jul 2021, Published online: 01 Sep 2021

References

  • Almajed A, Lands LC 2012 The evolution of exercise capacity and its limiting factors in cystic fibrosis. Paediatric Respiratory Reviews 13: 195–199 10.1016/j.prrv.2012.01.001
  • Arikan H, Yatar I, Calik-Kutukcu 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 45-46: 147–156 10.1016/j.ridd.2015.07.020
  • Athanazio RA, da Silva Filho LV, Vergara AA, Ribeiro AF, Riedi CA, Procianoy EF, Adde FV, Reis FJ, Ribeiro JD, Torres LA, et al. 2017 Brazilian guidelines for the diagnosis and treatment of cystic fibrosis. Jornal Brasileiro De Pneumologia 43: 219–245.
  • Beenakker EA, Van der Hoeven JH, Fock JM, Maurits NM 2001 Reference values of maximum isometric muscle force obtained in 270 children aged 4-16 years by hand-held dynamometry. Neuromuscular Disorders 11: 441–446 10.1016/S0960-8966(01)00193-6
  • Bongers BC, Werkman MS, Arets HG, Takken T, Hulzebos HJ 2014 A possible alternative exercise test for youths with cystic fibrosis: The steep ramp test. Medicine and Science in Sports and Exercise 47: 485–492 10.1249/MSS.0000000000000440
  • Bradley J, Howard J, Wallace E, Elborn S 1999 Validity of a modified shuttle test in adult cystic fibrosis. Thorax 54: 437–439 10.1136/thx.54.5.437
  • Button BM, Wilson C, Dentice R, Cox NS, Middleton A, Tannenbaum E, Bishop J, Cobb R, Burton K, Wood M, et al. 2016 Physiotherapy for cystic fibrosis in Australia and New Zealand: A clinical practice guideline. Respirology 21: 656–667. 10.1111/resp.12764
  • Calik-Kutukcu E, Arikan H, Saglam M, Vardar-Yagli N, Oksuz C, Inal-Ince D, Savci S, Duger T, Coplu L 2017 Arm strength training improves activities of daily living and occupational performance in patients with COPD. Clinical Respiratory Journal 11: 820–832 10.1111/crj.12422
  • Campos NE, Vendrusculo FM, Gheller MF, de Almeida IS, Becker NA, Heinzmann-Filho JP, Ruiz MP, Donadio MV 2020 Association of peripheral muscle strength with exercise capacity and use of antibiotics in patients with cystic fibrosis. Journal of Cystic Fibrosis 19: S139 10.1016/S1569-1993(20)30625-1
  • Dancey C, Reidy J 2018 Estatística sem matemática para psicologia (7th ed). 624. Brasil: Penso.
  • De Meer K, Jeneson JA, Gulmans VA, Van Der Laag J, Berger R 1995 Efficiency of oxidative work performance of skeletal muscle in patients with cystic fibrosis. Thorax 50: 980–983 10.1136/thx.50.9.980
  • Doerschuk CF, Matthews LR, 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 10.1016/S0022-3476(64)80152-9
  • Fagher K, Fritzson A, Drake AM 2016 Test-retest reliability of isokinetic knee strength measurements in children aged 8 to 10 years. Sports Health 8: 255–259 10.1177/1941738116632506
  • Fess E 1992 American society of hand therapists. Clinical assessment recommendations. 2 ed. Chicago: The Society.
  • Graham BL, Steenbruggen I, Barjaktarevic IZ, Cooper BG, Hall GL, Hallstrand TS, Kaminsky DA, McCarthy K, McCormack MC, Miller MR, et al. 2019 Standardization of spirometry 2019 update. An Official American Thoracic Society and European Respiratory Society Technical Statement. American Journal of Respiratory and Critical Care Medicine 200: e70–e88.
  • Gruet M, Troosters T, Verges S 2017 Peripheral muscle abnormalities in cystic fibrosis: Etiology, clinical implications and response to therapeutic interventions. Journal of Cystic Fibrosis 16: 538–552 10.1016/j.jcf.2017.02.007
  • Hulley S, Cummings S, Browner W, Grady D, Newman T 2015 Delineando A pesquisa clínica 4th 400. Brasil: Artmed.
  • 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 10.1249/MSS.0000000000000344
  • 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 10.1016/S0149-2918(99)80035-6
  • Kaymaz D, İÇ C, Ergün P, Demir N, Taşdemir F, Demir P 2018 Relation between upper-limb muscle strength with exercise capacity, quality of life and dyspnea in patients with severe chronic obstructive pulmonary disease. Clinical Respiratory Journal 12: 1257–1263 10.1111/crj.12659
  • Knudson RJ, Slatin RC, Lebowitz M, Burrows B 1976 The maximal expiratory flow volume curve. Normal standards, variability, and effects of age. American Review of Respiratory Disease 113: 587–600.
  • Lamhonwah AM, Bear CE, Huan LJ, Chiaw PK, Ackerley CA, Tein I 2010 Cystic fibrosis trans-membrane conductance regulator in human muscle dysfunction causes abnormal metabolic recovery in exercise. Annals of Neurology 67: 802–808
  • Lanza FD, Zagatto ED, Silva JC, Selman JP, Imperatori TB, Zanatta DJ, Carvalho LN, Reimberg MM, Dal Corso S 2015 Reference equation for the incremental shuttle walk test in children and adolescents. Journal of Pediatrics 167: 1057–1061 10.1016/j.jpeds.2015.07.068
  • Lima CA, de Andrade AD, Campos SL, Brandão DC, Mourato IP, Britto MC 2018 Six-minute walk test as a determinant of the functional capacity of children and adolescents with cystic fibrosis: A systematic review. Respiratory Medicine 137: 83–88 10.1016/j.rmed.2018.02.016
  • Machado FA, Denadai BS 2011 Validity of maximum heart rate prediction equations for children and adolescents. Arquivos Brasileiros De Cardiologia 97: 136–140 10.1590/S0066-782X2011005000078
  • Maltais F, Decramer M, Casaburi R, Barreiro E, Burelle Y, Debigaré R, Dekhuijzen R, Franssen F, Gayan-Ramirez G, Gea J, et al. 2014 ATS/ERS Ad Hoc committee on limb muscle dysfunction in COPD 2014 An official American Thoracic Society/European respiratory society statement: Update on limb muscle dysfunction in chronic obstructive pulmonary disease. American Journal of Respiratory and Critical Care Medicine 189: e15–e62. 10.1164/rccm.201402-0373ST
  • Ministério da Saúde 2012 Brasil: Programa Telessaúde Brasil. https://aps.bvs.br/apps/calculadoras/.
  • Ozipek M, Arikan H, Calik-Kutukcu E, Kerem-Gunel M, Saglam M, Inal-Ince D, Vardar-Yagli N, Livanelioglu A, Bozdemir-Ozel C, Cakmak A, et al. 2020 Deviations of body functions and structure, activity limitations, and participation restrictions of the International Classification of functioning, disability, and health model in children with cystic fibrosis and non–cystic fibrosis bronchiectasis. Pediatric Pulmonology 55: 1207–1216. 10.1002/ppul.24708
  • Papalexopoulou N, Dassios TG, Lunt A, Bartlett F, Perrin F, Bossley CJ, Wyatt HA, Greenough A 2018 Nutritional status and pulmonary outcome in children and young people with cystic fibrosis. Respiratory Medicine 142: 60–65 10.1016/j.rmed.2018.07.016
  • 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
  • Quanjer PH, Stanojevic S, Cole TJ, Baur X, Hall GL, Culver BH, Enright P, Hankinson J, Ip M, Zheng J 2012 Multi-ethnic reference values for spirometry for the 3-95-yr age range: The global lung function 2012 equations. European Respiratory Journal 40: 1324–1343 10.1183/09031936.00080312
  • Ramírez-Vélez R, Peña-Ibagon JC, Martínez-Torres J, Tordecilla-Sanders A, Correa-Bautista JE, Lobelo F, García-Hermoso A 2017 Handgrip strength cutoff for cardiometabolic risk index among Colombian children and adolescents: The FUPRECOL Study. Scientific Reports 7: 42622 10.1038/srep42622
  • Ramsey BW, Boat TF 1994 Outcome measures for clinical trials in cystic fibrosis: Summary of a cystic fibrosis foundation consensus conference. Journal of Pediatrics 124: 177–192 10.1016/S0022-3476(94)70301-9
  • Troosters T, Langer D, Vrijsen B, Segers J, Wouters K, Janssens W, Gosselink R, Decramer M, Dupont L 2009 Skeletal muscle weakness, exercise tolerance and physical activity in adults with cystic fibrosis. European Respiratory Journal 33: 99–106 10.1183/09031936.00091607
  • Urquhart DS, Vendrusculo FM 2017 Clinical interpretation of cardiopulmonary exercise testing in cystic fibrosis and implications for exercise counselling. Paediatric Respiratory Reviews 24: 72–78 10.1016/j.prrv.2015.09.009
  • Vaidya T, Beaumont M, de Bisschop C, Bazerque L, Le Blanc C, Vincent A, Ouksel H, Chambellan A 2018 Determining the minimally important difference in quadriceps strength in individuals with COPD using a fixed dynamometer. International Journal of COPD 13: 2685–2693 10.2147/COPD.S161342
  • Vendrusculo FM, Aquino ES, Campos NE, Almeida IS, Heinzmann-Filho JP, Queiroz KC, Leite LR, Donadio MV 2020 Determinants of exercise capacity assessed with the modified shuttle test in individuals with cystic fibrosis. Respiratory Care 65: 643–649 10.4187/respcare.07326
  • Vendrusculo FM, Heinzmann-Filho JP, Da Silva JS, Perez Ruiz M, Donadio MV 2019 Peak oxygen uptake and mortality in cystic fibrosis: Systematic review and meta-analysis. Respiratory Care 64: 91–98 10.4187/respcare.06185

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.