Association among posture, lung function and functional capacity in cystic fibrosis;Associação entre postura, função pulmonar e capacidade funcional na fibrose quística

Revista Portuguesa de Pneumologia

Volumn 19, Issue 1, 2013, Pages 1-6

  Penafortes, J T S ^a   Guimaraes F S ^a   Moco V J R ^a   Almeida, V P ^a   Dias, R F ^a   Lopes, A J ^a,b  

^a Universidade Augusto Motta   (Brazil)

^b STATE UNIVERSITY OF RIO DE JANEIRO   (Brazil)

Author keywords

Cystic fibrosis; Postural balance; Respiratory function tests

Indexed keywords

CARBON MONOXIDE;

AIRWAY RESISTANCE; ARTICLE; BODY PLETHYSMOGRAPHY; BODY POSTURE; CLINICAL ARTICLE; CROSS-SECTIONAL STUDY; FEMALE; FORCED EXPIRATORY VOLUME; FUNCTIONAL STATUS; HUMAN; LUNG FIBROSIS; LUNG FUNCTION; MALE; QUALITY OF LIFE; QUESTIONNAIRE; SPIROMETRY; TOTAL LUNG CAPACITY;

ADULT; CROSS-SECTIONAL STUDIES; CYSTIC FIBROSIS; FEMALE; HUMANS; LUNG; MALE; POSTURE; RESPIRATORY FUNCTION TESTS; YOUNG ADULT;

EID: 84876728401     PISSN: 08732159     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.rppneu.2012.07.001     Document Type: Article

References (30)

1. Boyle M.P. Adult cystic fibrosis. JAMA 2007, 298:1787-1793.
2. Simmonds N.J., MacNeill S., Culliman P., Hodson M.E. Cystic fibrosis and survival to 40 years: a case control study. Eur Respir J 2010, 36:1277-1283.
3. Yankaskas J.R., Marshall B.C., Sufian B., Simon R.H., Rodman D. Cystic fibrosis adult care: consensus conference report. Chest 2004, 125(Supp 1):1S-39S.
4. Andrade E.F., Fonseca D.F.O., Abreu e Silva F.A., Menna-Barreto S.S. Avaliação evolutiva da espirometria na fibrose cística. J Pneumol 2001, 27:130-136.
5. Ramsey B.W. Management of pulmonary disease in patients with cystic fibrosis. N Engl J Med 1996, 335:179-188.
6. Penha P.J., João S.M.A., Casarotto R.A., Amino C.J., Penteado D.C.P. Postural assessment of girls between 7 and 10 years of age. Clinics 2005, 60:9-16.
7. Souza J.A., Pasinato F., Basso D., Corrêa E.C.R., Silva A.M.T. Biofotogrametria: confiabilidade das medidas do protocolo do software para avaliação postural (SAPO). Rev Bras Cineantropom Desempenho Hum 2011, 13:299-305.
8. Boulay C., Tardieu C., Hecquet J., Benaim C., Mouilleseaux B., Marty C., et al. Sagittal alignment of spine and pelvis regulated by pelvic incidence: standard values and prediction of lordosis. Eur Spine J 2006, 15:415-422.
9. Tattersall R., Walshaw M.J. Posture and cystic fibrosis. J R Soc Med 2003, 96(Suppl. 43):18-22.
10. Butcher S.J., Meshke J.M., Sheppard M.S. Reductions in functional balance, coordination, and mobility measures among patients with stable chronic obstructive pulmonary disease. J Cardiopulm Rehabil 2004, 24:274-280.
11. Denton J.R., Tietjen R., Gaerlan P.F. Thoracic kyphosis in cystic fibrosis. Clin Orthop Relat Res 1981, 155:71-74.
12. Modi A.C., Quittner A.L. Validation of a disease-specific measure of health-related quality of life for children with cystic fibrosis. J Pediatr Psychol 2003, 28:535-545.
13. Cohen M.A., Ribeiro M.A.G.O., Ribeiro A.F., Ribeiro J.D., Morcillo A.M. Avaliação da qualidade de vida de pacientes com fibrose cística por meio do Cystic Fibrosis Questionnaire. J Bras Pneumol 2011, 37:184-192.
14. Ferreira E.A.G., Duarte M., Maldonado E.P., Burke T.N., Marques A.P. Postural assessment software (PAS/SAPO): validation and reliability. Clinics 2010, 65:675-681.
15. Miller M.R., Hankinson J., Brusasco V. ATS/ERS Task Force. Standardization of spirometry. Eur Respir J 2005, 26:319-338.
16. Pereira C.A.C., Rodrigues S.C., Sato T. Novos valores de referência para espirometria forçada em brasileiros adultos de raça branca. J Bras Pneumol 2007, 33:397-406.
17. Neder J.A., Andreoni S., Peres C., Nery L.E. Reference values for lung function tests I. Static volumes. Braz J Med Biol Res 1999, 32:703-717.
18. Neder J.A., Andreoni S., Peres C, Nery L.E. Reference values for lung function tests III. Carbon monoxide diffusing capacity (transfer factor). Braz J Med Biol Res 1999, 32:729-737.
19. Gibbons W.J., Fruchter N., Sloan S., Levy R.D. Reference values for a multiple repetition 6-minute walk test in healthy adults older than 20 years. J Cardiopulm Rehabil 2011, 21:87-93.
20. American Thoracic Society ATS statement: guidelines for the six-minute walk test. Am J Respir Crit Care Med 2000, 166:111-117.
21. Pachioni C.A.S., Ferrante J.A., Panissa T.S.D., Ferreira D.M.A.F., Ramos D., Moreira G.L., et al. Avaliação postural em pacientes com doença pulmonar obstrutiva crônica. Fisioter Pesq 2011, 18:341-345.
22. Figueiredo R.V., Amaral A.C., Shimano A.C. Fotogrametria na identificação de assimetrias posturais em cadetes e pilotos da academia da força aérea brasileira. Rev Bras Fisioter 2012, 16:54-60.
23. Dunk N.M., Chung Y.Y., Compton D.S., Callaghan J.P. The reliability of quantifying upright standing postures as a baseline diagnostic clinical tool. J Manipulative Physiol Ther 2004, 27:91-96.
24. Lima A.N., Lopes A.J., Jansen U., Capone D., Jansen J.M. Fibrose cística em adultos: aspectos clínicos, funcionais e tomográficos. Pulmão RJ 2004, 13:90-96.
25. Cunha M.T., Rozov T., Oliveira R.C., Jardim J.R. Six-minute walk test in children and adolescents with cystic fibrosis. Pediatr Pulmonol 2006, 41:618-622.
26. Stevens D., Williams C.A. Exercise testing and training with the young cystic fibrosis patient. J Sports Science Med 2007, 6:286-291.
27. Ziegler B., Rovedder M.E., Oliveira C.L., Schuh S.J., Silva F.A., Dalcin P.T.R. Preditores da dessaturação do oxigênio no teste da caminhada de seis minutos em pacientes com fibrose cística. J Bras Pneumol 2009, 35:957-965.
28. Henry B., Aussage P., Grosskopf C., Goehrs J.M. Development of the Cystic Fibrosis Questionnaire (CFQ) for assessing quality of life in pediatric and adult patients. Qual Life Res 2003, 12:63-76.
29. Elbasan B., Tunali N., Duzgun I., Ozcelik U. Effects of chest physiotherapy and aerobic exercise training on physical fitness in young children with cystic fibrosis. Ital J Pediatr 2012, 10:2.
30. Dunnink M.A., Doeleman W.R., Trappenburg J.C.A., de Vries W.R. Respiratory muscle strength in stable adolescent and adult patients with cystic fibrosis. J Cyst Fibros 2009, 8:31-36.