Literature DB >> 9623407

Maintenance of growth in cystic fibrosis despite reduction in pancreatic enzyme supplementation.

J Lowdon1, M C Goodchild, H C Ryley, I J Doull.   

Abstract

Twenty one children with cystic fibrosis were advised to decrease their pancreatic enzyme supplement (PES) dose to less than 10,000 units lipase/kg/day. Mean PES dosage was significantly decreased in 15 patients from 18,380 to 8647 units lipase/kg/day. There were no significant changes in energy or fat intake, but there were significant increases in weight SD score, height SD score, and weight/height ratio.

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Year:  1998        PMID: 9623407      PMCID: PMC1717525          DOI: 10.1136/adc.78.4.377

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


  2 in total

1.  High-dose pancreatic-enzyme supplements and fibrosing colonopathy in children with cystic fibrosis.

Authors:  S C FitzSimmons; G A Burkhart; D Borowitz; R J Grand; T Hammerstrom; P R Durie; J D Lloyd-Still; A B Lowenfels
Journal:  N Engl J Med       Date:  1997-05-01       Impact factor: 91.245

2.  Fibrosing colonopathy in cystic fibrosis: results of a case-control study.

Authors:  R L Smyth; D Ashby; U O'Hea; E Burrows; P Lewis; D van Velzen; J A Dodge
Journal:  Lancet       Date:  1995-11-11       Impact factor: 79.321

  2 in total
  3 in total

Review 1.  Control of malabsorption in cystic fibrosis.

Authors:  J M Littlewood; S P Wolfe
Journal:  Paediatr Drugs       Date:  2000 May-Jun       Impact factor: 3.022

2.  Lipid, nitrogen, water and energy content of a single stool sample in healthy children and children with cystic fibrosis.

Authors:  Anita Maria Van den Neucker; Pierre-Philippe Forget; Bernard van Kreel
Journal:  Eur J Pediatr       Date:  2003-08-27       Impact factor: 3.183

Review 3.  Update on intestinal strictures.

Authors:  J M Littlewood
Journal:  J R Soc Med       Date:  1999       Impact factor: 18.000

  3 in total

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