Factors Affecting Clinical Outcome in Gastrostomy-Fed Children with Cystic Fibrosis

Pediatric Pulmonology

Volumn 37, Issue 4, 2004, Pages 324-329

  Oliver, Mark R ^a   Heine, Ralf G ^a   Ng, Chi Hang ^a   Volders, Evelyn ^a   Olinsky, Anthony ^a  

^a ROYAL CHILDREN'S HOSPITAL   (Australia)

Author keywords

Cystic fibrosis; Gastrostomy; Nutrition; Pulmonary function; Survival

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUSTRALIA; BODY WEIGHT; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; CORRELATION ANALYSIS; CYSTIC FIBROSIS; FEMALE; FOLLOW UP; FORCED EXPIRATORY VOLUME; GASTROESOPHAGEAL REFLUX; GASTROSTOMY; HUMAN; LUNG DISEASE; LUNG FUNCTION TEST; MALE; MEASUREMENT; MEDICAL RECORD; NUTRITIONAL STATUS; OUTCOMES RESEARCH; PATIENT COMPLIANCE; PRIORITY JOURNAL; RISK FACTOR; SCORING SYSTEM; SEX DIFFERENCE; SPUTUM CULTURE; SURVIVAL RATE; TUBE FEEDING; WEIGHT GAIN;

ADOLESCENT; ADULT; BODY WEIGHT; CHILD; CHILD, PRESCHOOL; CYSTIC FIBROSIS; ENTERAL NUTRITION; FEMALE; FORCED EXPIRATORY VOLUME; GASTROESOPHAGEAL REFLUX; GASTROSTOMY; HUMANS; MALE; OUTCOME ASSESSMENT (HEALTH CARE); PREDICTIVE VALUE OF TESTS; RETROSPECTIVE STUDIES; SEX FACTORS;

EID: 1942441643     PISSN: 87556863     EISSN: None     Source Type: Journal    
DOI: 10.1002/ppul.10321     Document Type: Article

References (22)

1. Ramsey BW, Farrell PM, Pencharz P. Nutritional assessment and management in cystic fibrosis: a consensus report. The Consensus Committee. Am J Clin Nutr 1992;55:108-116.
2. Roulet M. Protein-energy malnutrition in cystic fibrosis patients. Acta Paediatr [Suppl] 1994;83:43-48.
3. Zemel BS, Kawchak DA, Cnaan A, Zhao H, Scanlin TF, Stallings VA. Prospective evaluation of resting energy expenditure, nutritional status, pulmonary function, and genotype in children with cystic fibrosis. Pediatr Res 1996;40:578-586.
4. Pencharz PB, Durie PR. Pathogenesis of malnutrition in cystic fibrosis, and its treatment. Clin Nutr 2000;19:387-394.
5. Anthony H, Paxton S, Catto-Smith A, Phelan P. Physiological and psychosocial contributors to malnutrition in children with cystic fibrosis: review. Clin Nutr 1999;18:327-335.
6. Williams SG, Ashworth F, McAlweenie A, Poole S, Hodson ME, Westaby D. Percutaneous endoscopic gastrostomy feeding in patients with cystic fibrosis. Gut 1999;44:87-90.
7. Rosenfeld M, Casey S, Pepe M, Ramsey BW. Nutritional effects of long-term gastrostomy feedings in children with cystic fibrosis. J Am Diet Assoc 1999:99:191-194.
8. Jelalian E, Stark LJ, Reynolds L, Seifer R. Nutrition intervention for weight gain in cystic fibrosis: a meta analysis. J Pediatr 1998; 132:486-492.
9. Steinkamp G, von 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.
10. Akobeng AK, Miller V, Thomas A. Percutaneous endoscopic gastrostomy feeding improves nutritional status and stabilizes pulmonary function in patients with cystic fibrosis. J Pediatr Gastroenterol Nutr 1999:29:485-486.
11. Walker SA, Gozal D. Pulmonary function correlates in the prediction of long-term weight gain in cystic fibrosis patients with gastrostomy tube feedings. J Pediatr Gastroenterol Nutr 1998;27: 53-56.
12. Scott RB, O'Loughlin EV, Gall DG. Gastroesophageal reflux in patients with cystic fibrosis. J Pediatr 1985;106:223-227.
13. Stringer DA, Sprigg A, Juodis E, Corey M, Daneman A, Levison HJ, Durie PR. The association of cystic fibrosis, gastroesophageal reflux, and reduced pulmonary function. Can Assoc Radiol J 1988;39:100-102.
14. Davidson PM, Catto-Smith AG, Beasley SW. Technique and complications of percutaneous endoscopic gastrostomy in children. Aust N Z J Surg 1995;65:194-196.
15. Dibley MJ, Goldsby JB, Staehling NW, Trowbridge FL. Development of normalized curves for the international growth reference: historical and technical considerations. Am J Clin Nutr 1987;46:736-748.
16. Crapo RO, Morris AH, Gardner RM. Reference spirometric values using techniques and equipment that meet ATS recommendations. Am Rev Respir Dis 1981;123:659-664.
17. Dalzell AM, Shepherd RW, Dean B, Cleghorn GJ, Holt TL, Francis PJ. Nutritional rehabilitation in cystic fibrosis: a 5 year follow-up study. J Pediatr Gastroenterol Nutr 1992;15:141-145.
18. Levy L, Durie P, Pencharz P, Corey M. Effects of long-term nutritional rehabilitation on body composition and clinical status in malnourished children and adolescents with cystic fibrosis. J Pediatr 1985;107:225-230.
19. Shepherd RW, Holt TL, Thomas BJ, Kay L, Isles A, Francis PJ, Ward LC. Nutritional rehabilitation in cystic fibrosis: controlled studies of effects on nutritional growth retardation, body protein turnover, and course of pulmonary disease. J Pediatr 1986;109: 788-794.
20. O'Loughlin E, Forbes D, Parsons H, Scott B, Cooper D, Gall G. Nutritional rehabilitation of malnourished patients with cystic fibrosis. Am J Clin Nutr 1986;43:732-737.
21. Boland MP, Stoski DS, MacDonald NE, Soucy P, Patrick J. Chronic jejunostomy feeding with a non-elemental formula in undernourished patients with cystic fibrosis. Lancet 1986;1:232-234.
22. Rosenfeld M, Davis R, FitzSimmons S, Pepe M, Ramsey B. Gender gap in cystic fibrosis mortality. Am J Epidemiol 1997; 145:794-803.