Literature DB >> 9862831

Percutaneous endoscopic gastrostomy feeding in patients with cystic fibrosis.

S G Williams1, F Ashworth, A McAlweenie, S Poole, M E Hodson, D Westaby.   

Abstract

BACKGROUND: Malnutrition is a common management problem in patients with cystic fibrosis (CF). Various approaches to supplemental nutrition by both parenteral and enteral routes have been used. AIM: To analyse the efficacy and acceptability of supplemental overnight feeding using a percutaneous endoscopic gastrostomy (PEG) in patients with CF. PATIENTS: 53 patients with CF (43 adults; age >17 years) with severe pulmonary disease.
METHODS: The technical success and complications of PEG insertion were documented together with changes in nutritional and pulmonary status of the cohort.
RESULTS: PEG tubes were successfully inserted in all patients, with immediate complications (respiratory depression) in two (4%) and late complications in 13 (25%). Feeding was well tolerated by 50/51 (98%) of the cohort during a mean (SEM) follow up of 14.5 (2.1) months. The adult cohort had a significant increase in weight and body mass index at six months which was maintained at 12 months. Serum albumin concentration remained stable at six months but had fallen by 12 months, although the differences were not statistically significant. These results were reflected in the paediatric cohort. Pulmonary function in those followed up for one year had apparently stabilised, but the number of admissions to hospital over the year before and the year after PEG did not change. Half of the cohort were accepted for heart-lung/lung transplantation, the improvement in nutritional status being a prerequisite for this.
CONCLUSION: Supplemental PEG tube feeding is well tolerated and results in a significant improvement in nutritional status and an apparent stabilisation of pulmonary function in severely malnourished CF patients with advanced pulmonary disease

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Year:  1999        PMID: 9862831      PMCID: PMC1760069          DOI: 10.1136/gut.44.1.87

Source DB:  PubMed          Journal:  Gut        ISSN: 0017-5749            Impact factor:   23.059


  18 in total

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  7 in total

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Authors:  J W Puntis
Journal:  Arch Dis Child       Date:  2001-04       Impact factor: 3.791

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Authors:  Wael El-Matary
Journal:  Can J Gastroenterol       Date:  2008-12       Impact factor: 3.522

3.  Nutritional outcomes following gastrostomy in children with cystic fibrosis.

Authors:  Gia M Bradley; Kathryn A Carson; Amanda R Leonard; Peter J Mogayzel; Maria Oliva-Hemker
Journal:  Pediatr Pulmonol       Date:  2012-02-01

4.  Administration of CREON® pancrelipase pellets via gastrostomy tube is feasible with no loss of gastric resistance or lipase activity: an in vitro study.

Authors:  George Shlieout; Andreas Koerner; Mario Maffert; Kristin Forssmann; Steven Caras
Journal:  Clin Drug Investig       Date:  2011       Impact factor: 2.859

Review 5.  Maintenance of nutritional status in patients with cystic fibrosis: new and emerging therapies.

Authors:  Daina Kalnins; Michael Wilschanski
Journal:  Drug Des Devel Ther       Date:  2012-06-20       Impact factor: 4.162

6.  Exercise capacity following a percutaneous endoscopic gastrostomy in a young female with cystic fibrosis: a case report.

Authors:  Owen W Tomlinson; Alan R Barker; Patrick J Oades; Craig A Williams
Journal:  Physiol Rep       Date:  2016-08-22

7.  Brazilian Guidelines for Nutrition in Cystic Fibrosis.

Authors:  Lenycia de Cassya Lopes Neri; Miriam Isabel Souza Dos Santos Simon; Valéria Laguna Salomão Ambrósio; Eliana Barbosa; Monique Ferreira Garcia; Juliana Ferreira Mauri; Renata Rodrigues Guirau; Mirella Aparecida Neves; Carolina de Azevedo Pedrosa Cunha; Marcelo Coelho Nogueira; Anna Carolina Di Creddo Alves; Jocemara Gurmini; Maria de Fatima Servidoni; Matias Epifanio; Rodrigo Athanazio
Journal:  Einstein (Sao Paulo)       Date:  2022-04-01
  7 in total

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