Relationship between nutritional status and maximum inspiratory and expiratory pressures in cystic fibrosis

Respiratory Care

Volumn 53, Issue 4, 2009, Pages 442-449

  Ziegler, Bruna ^a,b   Lukrafka, Janice L ^a   De Oliveira Abraão, Claudine L ^c   Rovedder, Paula M ^d   De Tarso Roth Dalcin, Paulo ^c,d  

^a Instituto Metodista IPA   (Brazil)

^b Hospital de Clínicas de   (Brazil)

^c HOSPITAL DE CLÍNICAS DE PORTO ALEGRE   (Brazil)

^d FEDERAL UNIVERSITY OF RIO GRANDE DO SUL   (Brazil)

Author keywords

Cystic fibrosis; Nutrition; Pulmonary function; Respiratory

Indexed keywords

ADULT; AGE DISTRIBUTION; ARM CIRCUMFERENCE; ARTICLE; BODY MASS; BRAZIL; BREATHING MUSCLE; CLINICAL ARTICLE; CONTROLLED STUDY; CYSTIC FIBROSIS; EXPIRATORY RESERVE VOLUME; FEMALE; FORCED EXPIRATORY VOLUME; HUMAN; INSPIRATORY RESERVE VOLUME; LUNG PRESSURE; MALE; MAXIMUM EXPIRATORY PRESSURE; MAXIMUM INSPIRATORY PRESSURE; MUSCLE STRENGTH; NUTRITIONAL DEFICIENCY; NUTRITIONAL STATUS; PROSPECTIVE STUDY; RESPIRATORY FUNCTION; SEX RATIO; SKINFOLD THICKNESS; SPIROMETRY; STATISTICAL SIGNIFICANCE; TRICEPS BRACHII MUSCLE; ADOLESCENT; CROSS-SECTIONAL STUDY; EXHALATION; PATHOPHYSIOLOGY; PHYSIOLOGY; VITAL CAPACITY;

ADOLESCENT; ADULT; BRAZIL; CROSS-SECTIONAL STUDIES; CYSTIC FIBROSIS; EXHALATION; FEMALE; FORCED EXPIRATORY VOLUME; HUMANS; MALE; NUTRITIONAL STATUS; VITAL CAPACITY;

EID: 48049086832     PISSN: 00201324     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (38)

1. Steinkamp G, Wiedemann B. Relationship between nutritional status and lung function in cystic fibrosis: cross sectional and longitudinal analyses from the German CF quality assurance (CFQA) project. Thorax 2002;57(7):596-601.
2. Gulmans VA, de Meer K, Brackel HJ, Helders PJ. Maximal work capacity in relation to nutritional status in children with cystic fibrosis. Eur Respir J 1997;10(9):2014-2017.
3. Zemel BSP, Jawad A. Longitudinal relationship among growth, nutritional status, and pulmonary function in children with cystic fi-brosis: analysis of the cystic fibrosis foundation national CF patients registry. J Pediatr 1985;107(2):225-230.
4. Ionescu AA, Chatham K, Davies CA, Nixon LS, Enright S, Shale DJ. Inspiratory muscle function and body composition in cystic fibrosis. Am J Respir Crit Care Med 1998;158(4):1271-1276.
5. Lands LC, Heigenhauser GJ, Jones NL. Respiratory and peripheral muscle function in cystic fibrosis. Am Rev Respir Dis 1993;147(4): 865-869.
6. Mier A, Redington A, Brophy C, Hodson M, Green M. Respiratory muscle function in cystic fibrosis. Thorax 1990;45(10):750-752.
7. Pradal U, Polese G, Braggion C, Poggi R, Zanolla L, Mastella G, et al. Determinants of maximal transdiaphragmatic pressure in adults with cystic fibrosis. Am J Respir Crit Care Med 1994;150(1):167- 173.
8. Szeinberg A, England S, Mindorff C, Fraser IM, Levison H. Maximal inspiratory and expiratory pressures are reduced in hyperin- flated, malnourished, young adult male patients with cystic fibrosis. Am Rev Respir Dis 1985;132(4):766-769.
9. Alison JA, Regnis JA, Donnelly PM, Adams RD, Sutton JR, Bye PT. Evaluation of supported upper limb exercise capacity in patients with cystic fibrosis. Am J Respir Crit Care Med 1997;156(5):1541-1548.
10. Bradley S, Solin P, Wilson J, Johns D, Walters EH, Naughton MT. Hypoxemia and hypercapnia during exercise and sleep in patients with cystic fibrosis. Chest 1999;116(3):647-654.
11. Hanning RM, Blimkie CJ, Bar-Or O, Lands LC, Moss LA, Wilson WM. Relationships among nutritional status and skeletal and respiratory muscle function in cystic fibrosis: does early dietary supplementation make a difference? Am J Clin Nutr 1993;57(4):580-587.
12. Lands L, Desmond KJ, Demizio D, Pavilanis A, Coates AL. The effects of nutritional status and hyperinflation on respiratory muscle strength in children and young adults. Am Rev Respir Dis 1990; 141(6):1506-1509.
13. Mansell AL, Andersen JC, Muttart CR, Ores CN, Loeff DS, Levy JS, et al. Short-term pulmonary effects of total parenteral nutrition in children with cystic fibrosis. J Pediatr 1984;104(5):700-705.
14. Asher MI, Pardy RL, Coates AL, Thomas E, Macklem PT. The effects of inspiratory muscle training in patients with cystic fibrosis. Am Rev Respir Dis 1982;126(5):855-859.
15. Marks J, Pasterkamp H, Tal A, Leahy F. Relationship between respiratory muscle strength, nutritional status, and lung volume in cystic fibrosis and asthma. Am Rev Respir Dis 1986;133(3):414-417.
16. O'Neill S, Leahy F, Pasterkamp H, Tal A. The effects of chronic hyperinflation, nutritional status, and posture on respiratory muscle strength in cystic fibrosis. Am Rev Respir Dis 1983;128(6):1051-1054.
17. Pinet C, Cassart M, Scillia P, Lamotte M, Knoop C, Casimir G, et al. Function and bulk of respiratory and limb muscles in patients with cystic fibrosis. Am J Respir Crit Care Med 2003;168(8):989-994.
18. American Thoracic Society, European Respiratory Society. Statement on respiratory muscle testing. Am J Respir Crit Care Med 2002;166(4):518-624.
19. Sharma R, Florea VG, Bolger AP, Doehner W, Florea ND, Coats AJ, et al. Wasting as an independent predictor of mortality in patients with cystic fibrosis. Thorax 2001;56(10):746-750.
20. Rosenstein BJ, Cutting GR. The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel. J Pe-diatr 1998;132(4):589-595.
21. Volianitis S, McConnell AK, Jones DA. Assessment of maximum inspiratory pressure. Respiration 2001;68:22-27.
22. Neder JA, Andreoni S, Lerario MC, Nery LE. Reference values for lung function tests. II. Maximal respiratory pressures and voluntary ventilation. Braz J Med Biol Res 1999;32(6):719-727.
23. Shwachman H, Kulczycki LL. Long-term study of one hundred five patients with cystic fibrosis; studies made over a five-to-fourteen- year period. AMA J Dis Child 1958;96(1):6-15.
24. Brasfield D, Hicks G, Soong S, Tiller RE. The chest roentgenogram in cystic fibrosis: a new scoring system. Pediatrics 1979;63(1):24-29.
25. American Thoracic Society. Standardization of spirometry, 1994 update. Am J Respir Crit Care Med 1995;152(3):1107-1136.
26. Knudson RJ, Slatin RC, Lebowitz MD, Burrows B. The maximal expiratory flow-volume curve. Normal standards, variability, and effects of age. Am Rev Respir Dis 1976;113(5):587-600.
27. Borowitz D, Baker RD, Stallings V. Consensus report on nutrition for pediatric patients with cystic fibrosis. J Pediatr Gastroenterol Nutr 2002;35(3):246-259.
28. World Health Organization Expert Committee. Physical status: the use and interpretation of anthropometry. Technical Reports Series: 854;1995:Geneva.
29. Frisancho AR. New norms of upper limb fat and muscle areas for assessment of nutritional status. Am J Clin Nutr 1981;34(11):2540-2545.
30. Hulley SB, Cummings SR, Browner WS, Grady D, Hearst N, Newman TB. Designing clinical research: an epidemiological approach. Lippincott Williams & Wilkins, 2001, Philadelphia.
31. Wilson SH, Cooke NT, Edwards RH, Spiro SG. Predicted normal values for maximal respiratory pressures in caucasian adults and children. Thorax 1984;39(7):535-538.
32. Enright S, Unnithan VB, Davies D. Reproducibility ofmeasurements of inspiratory work capacity in cystic fibrosis patients. Respir Physiol Neurobiol 2006;150(1):35-43.
33. Romer LM, McConnell AK. Inter-test reliability for non-invasive measures of respiratory muscle function in healthy humans. Eur J Appl Physiol 2004;91(2-3):167-176.
34. Enright S, Chatham K, Ionescu AA, Unnithan VB, Shale DJ. In- spiratory muscle training improves lung function and exercise capacity in adults with cystic fibrosis. Chest 2004;126(2):405-411.
35. Bell SC, Saunders MJ, Elborn JS, Shale DJ. Resting energy expenditure and oxygen cost of breathing in patients with cystic fibrosis. Thorax 1996;51(2):126-131.
36. O'Rawe A, McIntosh I, Dodge JA, Brock DJ, Redmond AO, Ward R, et al. Increased energy expenditure in cystic fibrosis is associated with specific mutations. Clin Sci (Lond) 1992;82(1): 71-76.
37. Ionescu AA, Evans WD, Pettit RJ, Nixon LS, Stone MD, Shale DJ. Hidden depletion of fat-free mass and bone mineral density in adults with cystic fibrosis. Chest 2003;124(6):2220-2228.
38. Fernandes AK, Mallmann F, John AB, Faccin CS, Dalcin PTR, Menna Barreto SS. Relationship between functional and X-ray alterations in patients with cystic fibrosis. J Pneumologia 2003;29: 196-201.