Skip to main content
NCBI home page
Journal of the Royal Society of Medicine logoLink to Journal of the Royal Society of Medicine
. 1991;84(Suppl 18):28–35.

Nutritional strategies in cystic fibrosis: current issues.

A MacDonald 1, C Holden 1, G Harris 1
PMCID: PMC1293033  PMID: 1903449

Full text

PDF
28

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BILLE B. S., VAHLQUIST B. Idiopathic hypoproteinaemia versus hypoproteinaemia due to pancreatic dysfunction. Acta Paediatr. 1955 Sep;44(5):435–443. doi: 10.1111/j.1651-2227.1955.tb04266.x. [DOI] [PubMed] [Google Scholar]
  2. Bertrand J. M., Morin C. L., Lasalle R., Patrick J., Coates A. L. Short-term clinical, nutritional, and functional effects of continuous elemental enteral alimentation in children with cystic fibrosis. J Pediatr. 1984 Jan;104(1):41–46. doi: 10.1016/s0022-3476(84)80586-7. [DOI] [PubMed] [Google Scholar]
  3. Bertrand J. M., Morin C. L., Lasalle R., Patrick J., Coates A. L. Short-term clinical, nutritional, and functional effects of continuous elemental enteral alimentation in children with cystic fibrosis. J Pediatr. 1984 Jan;104(1):41–46. doi: 10.1016/s0022-3476(84)80586-7. [DOI] [PubMed] [Google Scholar]
  4. Beverley D. W., Kelleher J., MacDonald A., Littlewood J. M., Robinson T., Walters M. P. Comparison of four pancreatic extracts in cystic fibrosis. Arch Dis Child. 1987 Jun;62(6):564–568. doi: 10.1136/adc.62.6.564. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Boland M. P., Patrick J., Stoski D. S., Soucy P. Permanent enteral feeding in cystic fibrosis: advantages of a replaceable jejunostomy tube. J Pediatr Surg. 1987 Sep;22(9):843–847. doi: 10.1016/s0022-3468(87)80651-6. [DOI] [PubMed] [Google Scholar]
  6. 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 Feb 1;1(8475):232–234. doi: 10.1016/s0140-6736(86)90772-5. [DOI] [PubMed] [Google Scholar]
  7. Buchdahl R. M., Fulleylove C., Marchant J. L., Warner J. O., Brueton M. J. Energy and nutrient intakes in cystic fibrosis. Arch Dis Child. 1989 Mar;64(3):373–378. doi: 10.1136/adc.64.3.373. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Canciani M., Mastella G. Absorption of a new semielemental diet in infants with cystic fibrosis. J Pediatr Gastroenterol Nutr. 1985 Oct;4(5):735–740. doi: 10.1097/00005176-198510000-00009. [DOI] [PubMed] [Google Scholar]
  9. 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(6):583–591. doi: 10.1016/0895-4356(88)90063-7. [DOI] [PubMed] [Google Scholar]
  10. Daniels L. A., Davidson G. P. Current issues in the nutritional management of children with cystic fibrosis. Aust Paediatr J. 1989 Oct;25(5):261–266. doi: 10.1111/j.1440-1754.1989.tb01473.x. [DOI] [PubMed] [Google Scholar]
  11. Daniels L., Davidson G. P., Martin A. J., Pouras T. Supplemental nasogastric feeding in cystic fibrosis patients during treatment for acute exacerbation of chest disease. Aust Paediatr J. 1989 Jun;25(3):164–167. doi: 10.1111/j.1440-1754.1989.tb01443.x. [DOI] [PubMed] [Google Scholar]
  12. Dodge J. A. The nutritional state and nutrition. Acta Paediatr Scand Suppl. 1985;317:31–37. doi: 10.1111/j.1651-2227.1985.tb14932.x. [DOI] [PubMed] [Google Scholar]
  13. Durie P. R., Newth C. J., Forstner G. G., Gall D. G. Malabsorption of medium-chain triglycerides in infants with cystic fibrosis: correction with pancreatic enzyme supplement. J Pediatr. 1980 May;96(5):862–864. doi: 10.1016/s0022-3476(80)80559-2. [DOI] [PubMed] [Google Scholar]
  14. Eid N. S., Shoemaker L. R., Samiec T. D. Vitamin A in cystic fibrosis: case report and review of the literature. J Pediatr Gastroenterol Nutr. 1990 Feb;10(2):265–269. [PubMed] [Google Scholar]
  15. FLEISHER D. S., DIGEORGE A. M., BARNESS L. A., CORNFELD D. HYPOPROTEINEMIA AND EDEMA IN INFANTS WITH CYSTIC FIBROSIS OF THE PANCREAS. J Pediatr. 1964 Mar;64:341–348. doi: 10.1016/s0022-3476(64)80186-4. [DOI] [PubMed] [Google Scholar]
  16. Farrell P. M., Mischler E. H., Sondel S. A., Palta M. Predigested formula for infants with cystic fibrosis. J Am Diet Assoc. 1987 Oct;87(10):1353–1356. [PubMed] [Google Scholar]
  17. Gauderer M. W., Ponsky J. L., Izant R. J., Jr Gastrostomy without laparotomy: a percutaneous endoscopic technique. J Pediatr Surg. 1980 Dec;15(6):872–875. doi: 10.1016/s0022-3468(80)80296-x. [DOI] [PubMed] [Google Scholar]
  18. Geertsma M. A., Hyams J. S., Pelletier J. M., Reiter S. Feeding resistance after parenteral hyperalimentation. Am J Dis Child. 1985 Mar;139(3):255–256. doi: 10.1001/archpedi.1985.02140050049020. [DOI] [PubMed] [Google Scholar]
  19. Gerson W. T., Swan P., Walker W. A. Nutrition support in cystic fibrosis. Nutr Rev. 1987 Dec;45(12):353–360. doi: 10.1111/j.1753-4887.1987.tb02703.x. [DOI] [PubMed] [Google Scholar]
  20. Goodchild M. C. Nutritional management of cystic fibrosis. Digestion. 1987;37 (Suppl 1):61–67. doi: 10.1159/000199543. [DOI] [PubMed] [Google Scholar]
  21. Holden C. E., Puntis J. W., Charlton C. P., Booth I. W. Nasogastric feeding at home: acceptability and safety. Arch Dis Child. 1991 Jan;66(1):148–151. doi: 10.1136/adc.66.1.148. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Kane R. E., Black P. Glucose intolerance with low-, medium-, and high-carbohydrate formulas during nighttime enteral feedings in cystic fibrosis patients. J Pediatr Gastroenterol Nutr. 1989 Apr;8(3):321–326. doi: 10.1097/00005176-198904000-00010. [DOI] [PubMed] [Google Scholar]
  23. Knowles M. R., Fernald G. W. Diabetes and cystic fibrosis: new questions emerging from increased longevity. J Pediatr. 1988 Mar;112(3):415–416. doi: 10.1016/s0022-3476(88)80322-6. [DOI] [PubMed] [Google Scholar]
  24. Laughlin J. J., Brady M. S., Eigen H. Changing feeding trends as a cause of electrolyte depletion in infants with cystic fibrosis. Pediatrics. 1981 Aug;68(2):203–207. [PubMed] [Google Scholar]
  25. Levy L. D., Durie P. R., Pencharz P. B., Corey M. L. Effects of long-term nutritional rehabilitation on body composition and clinical status in malnourished children and adolescents with cystic fibrosis. J Pediatr. 1985 Aug;107(2):225–230. doi: 10.1016/s0022-3476(85)80130-x. [DOI] [PubMed] [Google Scholar]
  26. Littlewood J. M., MacDonald A. Rationale of modern dietary recommendations in cystic fibrosis. J R Soc Med. 1987;80 (Suppl 15):16–24. [PMC free article] [PubMed] [Google Scholar]
  27. MacDonald A., Kelleher J., Littlewood J. M. A normal fat diet for cystic fibrosis: is a dietitian still needed? Scand J Gastroenterol Suppl. 1988;143:157–159. doi: 10.3109/00365528809090238. [DOI] [PubMed] [Google Scholar]
  28. 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 May;43(5):732–737. doi: 10.1093/ajcn/43.5.732. [DOI] [PubMed] [Google Scholar]
  29. Pelekanos J. T., Holt T. L., Ward L. C., Cleghorn G. J., Shepherd R. W. Protein turnover in malnourished patients with cystic fibrosis: effects of elemental and nonelemental nutritional supplements. J Pediatr Gastroenterol Nutr. 1990 Apr;10(3):339–343. doi: 10.1097/00005176-199004000-00013. [DOI] [PubMed] [Google Scholar]
  30. Pencharz P. B., Berall G., Corey M., Durie P., Vaisman N. Energy intake in cystic fibrosis. Nutr Rev. 1989 Jan;47(1):31–32. doi: 10.1111/j.1753-4887.1989.tb02750.x. [DOI] [PubMed] [Google Scholar]
  31. Pencharz P. B., Berall G., Vaisman N., Corey M., Canny G. Energy expenditure in children with cystic fibrosis. Lancet. 1988 Aug 27;2(8609):513–514. doi: 10.1016/s0140-6736(88)90163-8. [DOI] [PubMed] [Google Scholar]
  32. Pencharz P., Hill R., Archibald E., Levy L., Newth C. Energy needs and nutritional rehabilitation in undernourished adolescents and young adult patients with cystic fibrosis. J Pediatr Gastroenterol Nutr. 1984;3 (Suppl 1):S147–S153. doi: 10.1097/00005176-198400031-00022. [DOI] [PubMed] [Google Scholar]
  33. Reardon M. C., Hammond K. B., Accurso F. J., Fisher C. D., McCabe E. R., Cotton E. K., Bowman C. M. Nutritional deficits exist before 2 months of age in some infants with cystic fibrosis identified by screening test. J Pediatr. 1984 Aug;105(2):271–274. doi: 10.1016/s0022-3476(84)80128-6. [DOI] [PubMed] [Google Scholar]
  34. Scott R. B., O'Loughlin E. V., Gall D. G. Gastroesophageal reflux in patients with cystic fibrosis. J Pediatr. 1985 Feb;106(2):223–227. doi: 10.1016/s0022-3476(85)80291-2. [DOI] [PubMed] [Google Scholar]
  35. Sheehan J. P., Ulchaker M. M., Doershuk C. F., Stern R. C., Amini S. B. Diet, cystic fibrosis, and diabetes: making friends with the perfect enemy. Lancet. 1990 Aug 25;336(8713):501–501. doi: 10.1016/0140-6736(90)92046-k. [DOI] [PubMed] [Google Scholar]
  36. Shepherd R. W., Holt T. L., Cleghorn G., Ward L. C., Isles A., Francis P. Short-term nutritional supplementation during management of pulmonary exacerbations in cystic fibrosis: a controlled study, including effects of protein turnover. Am J Clin Nutr. 1988 Aug;48(2):235–239. doi: 10.1093/ajcn/48.2.235. [DOI] [PubMed] [Google Scholar]
  37. Shepherd R. W., Holt T. L., Thomas B. J., Kay L., Isles A., Francis P. J., Ward L. C. Nutritional rehabilitation in cystic fibrosis: controlled studies of effects on nutritional growth retardation, body protein turnover, and course of pulmonary disease. J Pediatr. 1986 Nov;109(5):788–794. doi: 10.1016/s0022-3476(86)80695-3. [DOI] [PubMed] [Google Scholar]
  38. Shepherd R. W., Holt T. L., Vasques-Velasquez L., Coward W. A., Prentice A., Lucas A. Increased energy expenditure in young children with cystic fibrosis. Lancet. 1988 Jun 11;1(8598):1300–1303. doi: 10.1016/s0140-6736(88)92119-8. [DOI] [PubMed] [Google Scholar]
  39. Sokol R. J., Reardon M. C., Accurso F. J., Stall C., Narkewicz M., Abman S. H., Hammond K. B. Fat-soluble-vitamin status during the first year of life in infants with cystic fibrosis identified by screening of newborns. Am J Clin Nutr. 1989 Nov;50(5):1064–1071. doi: 10.1093/ajcn/50.5.1064. [DOI] [PubMed] [Google Scholar]
  40. Soutter V. L., Kristidis P., Gruca M. A., Gaskin K. J. Chronic undernutrition/growth retardation in cystic fibrosis. Clin Gastroenterol. 1986 Jan;15(1):137–155. [PubMed] [Google Scholar]
  41. Sullivan M. M., Denning C. R. Diabetic microangiopathy in patients with cystic fibrosis. Pediatrics. 1989 Oct;84(4):642–647. [PubMed] [Google Scholar]
  42. Taylor C. J., McIntyre S., Baxter P. S. Nutrition in cystic fibrosis. Arch Dis Child. 1990 Jun;65(6):646–647. doi: 10.1136/adc.65.6.646-a. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Wilson-Goodman V., Taylor M. L., Mueller D., Palmer J. Factors affecting the dietary habits of adolescents with cystic fibrosis. J Am Diet Assoc. 1990 Mar;90(3):429–431. [PubMed] [Google Scholar]

Articles from Journal of the Royal Society of Medicine are provided here courtesy of Royal Society of Medicine Press

RESOURCES