Literature DB >> 3926979

Effects of long-term nutritional rehabilitation on body composition and clinical status in malnourished children and adolescents with cystic fibrosis.

L D Levy, P R Durie, P B Pencharz, M L Corey.   

Abstract

Fourteen patients aged 4.9 to 21.5 years with cystic fibrosis and moderate to severe lung disease, malnutrition, or growth failure were given nocturnal supplemental feeding by gastrostomy tube. Mean follow-up was for 1.1 years (range 0.8 to 2.78 years). Patients were studied to observe the effect of nutritional support on body composition, growth, pulmonary function, and quality of life. A contemporary group of patients with CF was retrospectively pair matched to the study group. The supplemental feeding resulted in positive changes in body composition and in growth velocity. Weight, as a percentage of standard in the control group, declined by 3% over 1 year, whereas it increased by 2% in the treatment group (P less than 0.05). Pulmonary function, assessed as a percent of predicted FVC and FEV1, did not change significantly in the treatment group over 1.1 years, whereas FVC declined by 12% (P less than 0.01) and FEV1 declined by 13% (P less than 0.01) in the control group. There was a marked increase in patient ability to participate in activities of daily living, even in those patients in whom pulmonary function deteriorated during the study.

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Year:  1985        PMID: 3926979     DOI: 10.1016/s0022-3476(85)80130-x

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


  25 in total

Review 1.  Cystic fibrosis. 6. Gastrointestinal and nutritional aspects.

Authors:  H Kopelman
Journal:  Thorax       Date:  1991-04       Impact factor: 9.139

Review 2.  Pathogenesis and management of lung disease in cystic fibrosis.

Authors:  M S Zach
Journal:  J R Soc Med       Date:  1991       Impact factor: 5.344

Review 3.  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

4.  Cows' milk sensitive enteropathy in cystic fibrosis.

Authors:  S M Hill; A D Phillips; M Mearns; J A Walker-Smith
Journal:  Arch Dis Child       Date:  1989-09       Impact factor: 3.791

Review 5.  Nutritional strategies in cystic fibrosis: current issues.

Authors:  A MacDonald; C Holden; G Harris
Journal:  J R Soc Med       Date:  1991       Impact factor: 5.344

6.  Percutaneous endoscopic gastrostomy feeding in patients with cystic fibrosis.

Authors:  S G Williams; F Ashworth; A McAlweenie; S Poole; M E Hodson; D Westaby
Journal:  Gut       Date:  1999-01       Impact factor: 23.059

7.  A prognostic model for the prediction of survival in cystic fibrosis.

Authors:  K M Hayllar; S G Williams; A E Wise; S Pouria; M Lombard; M E Hodson; D Westaby
Journal:  Thorax       Date:  1997-04       Impact factor: 9.139

8.  Nutrition and survival in cystic fibrosis.

Authors:  J S Elborn; S C Bell
Journal:  Thorax       Date:  1996-10       Impact factor: 9.139

Review 9.  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

10.  Increasing calorie consumption in children with cystic fibrosis: replication with 2-year follow-up.

Authors:  L J Stark; L G Knapp; A M Bowen; S W Powers; E Jelalian; S Evans; M A Passero; M M Mulvihill; M Hovell
Journal:  J Appl Behav Anal       Date:  1993
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