Nutrition in adults with cystic fibrosis

Clinical Nutrition

Volumn 17, Issue 5, 1998, Pages 211-215

  Bell, S C ^b   Bowerman, A R ^a   Davies, C A ^a   Campbell, I A ^a   Shale, D J ^c   Elborn, J S ^a  

^a LLANDOUGH HOSPITAL   (United Kingdom)

^b THE PRINCE CHARLES HOSPITAL   (Australia)

^c BELFAST CITY HOSPITAL   (United Kingdom)

Author keywords

Cystic fibrosis; Enteral feeding; Malnutrition

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BODY HEIGHT; BODY MASS; BODY WEIGHT; CONTROLLED STUDY; CYSTIC FIBROSIS; DISEASE SEVERITY; ENTERIC FEEDING; FEMALE; FORCED EXPIRATORY VOLUME; GRAM NEGATIVE INFECTION; HUMAN; LUNG FUNCTION; LUNG TRANSPLANTATION; MAJOR CLINICAL STUDY; MALE; MALNUTRITION; NUTRITION; NUTRITIONAL STATUS; PSEUDOMONAS; SURVIVAL; VITAL CAPACITY;

EID: 0031782288     PISSN: 02615614     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0261-5614(98)80061-7     Document Type: Article

References (15)

1. Corey M, McLaughlin F J, Williams M, Levison H. A comparison of survival, growth and pulmonary function in patients with cystic fibrosis in Boston and Toronto. J Clin Epidemiol 1988; 41: 583-591
2. Ramsey B, Farrell P M, Pencharz P B and the Consensus Committee. Nutritional assessment and management in cystic fibrosis. A consensus report. Am J Clin Nutr 1992; 55: 108-116
3. Levy E, Gurbindo G, Lacaille F, Paradis K, Thibault L, Seidman E. Circulating tumour necrosis factor-alpha levels and lipid abnormalities in patients with cystic fibrosis. Pediatr Res 1993; 34: 162-166
4. Boland M P, Stoski D S, MacDonald N E, Soucy P, Patrick J. Chronic jejunostomy feeding with a non-elemental formula in undernourished patients with cystic fibrosis. Lancet 1986; i: 232-234
5. Steinkamp G, Van der Hardt H. Improvement of nutritional status and lung function after long-term nocturnal gastrostomy feedings in cystic fibrosis. J Pediatr 1994; 124: 244-249
6. Shepherd R W, Holt T L, Thomas B J, Ward L C Isles A, Francis P J. Nutritional rehabilitation in cystic fibrosis: controlled studies of the effects on nutritional growth retardation, body protein turnover and course of pulmonarydisease. J Pediatr 1984; 109: 788-794
7. Mansell A I, Anderson J C, Muttart C R et al. Short term pulmonary effects of total parental nutrition in children with cystic fibrosis. J Pediatr 1984; 104: 700-705
8. Sproul A, Huang N. Growth patterns in children with cystic fibrosis. J Pediatr 1964; 65: 664-667
9. Gaskin K. The impact of nutrition in cystic fibrosis: a review. J Pediatr Gastroent Nutr 1988; 7 (suppl 1): S12-S17
10. Fitzsimmons S C. The changing epidemiology of cystic fibrosis. J Pediatr 1993; 122: 1-9
11. Nir M, Lanng H, Johnasen K, Koch C. Long term survival and nutritional data in Danish Centre treated cystic fibrosis patients. Thorax 1996; 51: 1023-1027
12. Penketh A R L, Wise A, Mearns M B, Hodson M E, Batten J C. Cystic fibrosis in adolescents and adults. Thorax 1987; 42: 526-532
13. Gaskin K, Gurwitz D, Durie P, Corey M, Levison H, Forstner G. Improved respiratory prognosis in patients with cystic fibrosis with normal fat absorption. J Pediatr 1982; 100: 857-862
14. Kerem E, Corey M, Kerem B S et al. The relation between genotype and phenotype in cystic fibrosis - analysis of the most common mutation (AF508). N Eng J Med 1990; 323: 1517-1522
15. Pencharz P B, Durie P R. Nutritional management of cystic fibrosis. Ann Rev Nutr 1993; 13: 111-136