Literature DB >> 381615

Cystic fibrosis and malnutrition.

H P Chase, M A Long, M H Lavin.   

Abstract

Cystic fibrosis as a specific disease entity has been known to be associated with malnutrition for almost half a century. The importance of the malnutrition in the disease process remains unknown, as does much information about specific nutritional deficiencies in CF. Supplements for children with CF should include extra energy as fat or carbohydrate, a form of linoleic acid that can be absorbed, hydrolyzed protein, fat-soluble vitamins with vitamins A and E in a water emulsion, vitamin B12, probably B vitamins and vitamin C, and trace minerals. Routine measurements of nutritional status, particularly in children with growth failure, should be made at regular intervals and should include a three-day diet record and a simultaneous 72-hour stool fat determination. If fat malabsorption is not controlled by pancreatic enzymes, the use of antacids or cimetidine should be considered. The true role of nutrition in patients with CF will not be known until the appropriate studies are completed.

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Year:  1979        PMID: 381615     DOI: 10.1016/s0022-3476(79)80504-1

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  34 in total

Review 1.  Energy balance and growth in cystic fibrosis.

Authors:  S A Wootton; J L Murphy; S A Bond; J E Ellis; A A Jackson
Journal:  J R Soc Med       Date:  1991       Impact factor: 5.344

Review 2.  A rational approach to the nutritional care of patients with cystic fibrosis.

Authors:  P R Durie; P B Pencharz
Journal:  J R Soc Med       Date:  1989       Impact factor: 5.344

3.  Peripheral nerve dysfunction in adult patients with cystic fibrosis.

Authors:  J I O'Riordan; J Hayes; M X Fitzgerald; J Redmond
Journal:  Ir J Med Sci       Date:  1995 Jul-Sep       Impact factor: 1.568

4.  Bone mineral content in cystic fibrosis patients: correlation with fat-free mass.

Authors:  F Salamoni; M Roulet; F Gudinchet; M Pilet; D Thiébaud; P Burckhardt
Journal:  Arch Dis Child       Date:  1996-04       Impact factor: 3.791

Review 5.  Rationale of modern dietary recommendations in cystic fibrosis.

Authors:  J M Littlewood; A MacDonald
Journal:  J R Soc Med       Date:  1987       Impact factor: 5.344

6.  Cystic fibrosis of the lungs.

Authors:  J S Jagadish
Journal:  Indian J Pediatr       Date:  1989 Mar-Apr       Impact factor: 1.967

7.  Energy and nutrient intakes in cystic fibrosis.

Authors:  R M Buchdahl; C Fulleylove; J L Marchant; J O Warner; M J Brueton
Journal:  Arch Dis Child       Date:  1989-03       Impact factor: 3.791

8.  Absorption of safflower oil and structured lipid preparations in patients with cystic fibrosis.

Authors:  V S Hubbard; M C McKenna
Journal:  Lipids       Date:  1987-06       Impact factor: 1.880

9.  Effect of intrajejunal acidity on aqueous phase bile acid and lipid concentrations in pancreatic steatorrhoea due to cystic fibrosis.

Authors:  P L Zentler-Munro; W J Fitzpatrick; J C Batten; T C Northfield
Journal:  Gut       Date:  1984-05       Impact factor: 23.059

Review 10.  Chronic illness and disordered eating: a discussion of the literature.

Authors:  Virginia M Quick; Carol Byrd-Bredbenner; Dianne Neumark-Sztainer
Journal:  Adv Nutr       Date:  2013-05-01       Impact factor: 8.701

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