Literature DB >> 8660059

Nutritional management of cystic fibrosis.

A MacDonald1.   

Abstract

Nutritional support is an integral part of the management of cystic fibrosis patients. It is arguably best provided by a qualified dietitian and nutritional care sister working in conjunction with the rest of the cystic fibrosis team. The patient's nutritional needs should be assessed, regularly reviewed, and nutritional treatment tailored to meet the changing clinical and psychosocial needs of the patient. Nutritional intervention is not without complications, and in particular attention to normal feeding behaviour and vigilance when instituting supplementary nutrition may prevent many feeding difficulties.

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Year:  1996        PMID: 8660059      PMCID: PMC1511597          DOI: 10.1136/adc.74.1.81

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  58 in total

1.  Fat-soluble-vitamin status during the first year of life in infants with cystic fibrosis identified by screening of newborns.

Authors:  R J Sokol; M C Reardon; F J Accurso; C Stall; M Narkewicz; S H Abman; K B Hammond
Journal:  Am J Clin Nutr       Date:  1989-11       Impact factor: 7.045

2.  Night blindness and conjunctival xerosis caused by vitamin A deficiency in patients with cystic fibrosis.

Authors:  R J Rayner; J C Tyrrell; E J Hiller; C Marenah; M A Neugebauer; S A Vernon; G Brimlow
Journal:  Arch Dis Child       Date:  1989-08       Impact factor: 3.791

3.  Energy expenditure of patients with cystic fibrosis.

Authors:  N Vaisman; P B Pencharz; M Corey; G J Canny; E Hahn
Journal:  J Pediatr       Date:  1987-10       Impact factor: 4.406

4.  Increased resting energy expenditure in cystic fibrosis.

Authors:  R M Buchdahl; M Cox; C Fulleylove; J L Marchant; A M Tomkins; M J Brueton; J O Warner
Journal:  J Appl Physiol (1985)       Date:  1988-05

5.  A comparison of enteric coated microspheres with enteric coated tablet pancreatic enzyme preparations in cystic fibrosis. A controlled study.

Authors:  H Vyas; D J Matthew; P J Milla
Journal:  Eur J Pediatr       Date:  1990-01       Impact factor: 3.183

6.  Enteric coated microspheres of pancreatin in the treatment of cystic fibrosis: comparison with a standard enteric coated preparation.

Authors:  R J Stead; I Skypala; M E Hodson; J C Batten
Journal:  Thorax       Date:  1987-07       Impact factor: 9.139

7.  A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto.

Authors:  M Corey; F J McLaughlin; M Williams; H Levison
Journal:  J Clin Epidemiol       Date:  1988       Impact factor: 6.437

8.  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

9.  Comparison of four pancreatic extracts in cystic fibrosis.

Authors:  D W Beverley; J Kelleher; A MacDonald; J M Littlewood; T Robinson; M P Walters
Journal:  Arch Dis Child       Date:  1987-06       Impact factor: 3.791

10.  Bone mineral density and body composition in adult patients with cystic fibrosis.

Authors:  A B Grey; R W Ames; R D Matthews; I R Reid
Journal:  Thorax       Date:  1993-06       Impact factor: 9.139

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  12 in total

1.  Perceived body image and eating behavior in young adults with cystic fibrosis and their healthy peers.

Authors:  J Abbott; S Conway; C Etherington; J Fitzjohn; L Gee; A Morton; H Musson; A K Webb
Journal:  J Behav Med       Date:  2000-12

Review 2.  The role of vitamins in cystic fibrosis.

Authors:  S B Carr; J McBratney
Journal:  J R Soc Med       Date:  2000       Impact factor: 5.344

3.  Relation between dietary intake and nutritional status in cystic fibrosis.

Authors:  H Anthony; J Bines; P Phelan; S Paxton
Journal:  Arch Dis Child       Date:  1998-05       Impact factor: 3.791

4.  Adequacy of clinical formulae for estimation of energy requirements in children with cystic fibrosis.

Authors:  J J Reilly; T J Evans; J Wilkinson; J Y Paton
Journal:  Arch Dis Child       Date:  1999-08       Impact factor: 3.791

5.  Dietary fibre and the occurrence of gut symptoms in cystic fibrosis.

Authors:  J Gavin; J Ellis; A L Dewar; C J Rolles; G J Connett
Journal:  Arch Dis Child       Date:  1997-01       Impact factor: 3.791

6.  The nature and prevalence of eating disorders and eating disturbance in adolescents with cystic fibrosis.

Authors:  J E Shearer; M Bryon
Journal:  J R Soc Med       Date:  2004       Impact factor: 5.344

Review 7.  Quality of life in children and adolescents with cystic fibrosis: implications for optimizing treatments and clinical trial design.

Authors:  Janice Abbott; Louise Gee
Journal:  Paediatr Drugs       Date:  2003       Impact factor: 3.022

Review 8.  Dental treatment for people with cystic fibrosis.

Authors:  N Harrington; P J Barry; S M Barry
Journal:  Eur Arch Paediatr Dent       Date:  2016-05-04

9.  Oral protein energy supplements for children with cystic fibrosis: CALICO multicentre randomised controlled trial.

Authors:  Vanessa J Poustie; Jayne E Russell; Ruth M Watling; Deborah Ashby; Rosalind L Smyth
Journal:  BMJ       Date:  2006-02-08

10.  Long term clinical outcome of home and hospital intravenous antibiotic treatment in adults with cystic fibrosis.

Authors:  J Thornton; R Elliott; M P Tully; M Dodd; A K Webb
Journal:  Thorax       Date:  2004-03       Impact factor: 9.139

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