Literature DB >> 21895617

Nutritional outcome in children with severe generalized recessive dystrophic epidermolysis bullosa: a short- and long-term evaluation of gastrostomy and enteral feeding.

V Colomb1, E Bourdon-Lannoy, C Lambe, F Sauvat, S Hadj Rabia, D Teillac, Y De Prost, C Bodemer.   

Abstract

BACKGROUND: Generalized recessive dystrophic epidermolysis bullosa (RDEB) is often complicated by high nutritional difficulties with risks of malnutrition.
OBJECTIVES: To provide information regarding the benefits of enteral feeding by gastrostomy (GTF), energy and protein requirements, tolerance, growth and pubertal development in children with RDEB.
METHODS: Twenty-four patients were referred over a 7-year period in a retrospective study. Gastrostomy placement was decided in patients unable to feed orally and/or presenting loss in weight and height of at least 1 SD compared with their best growth level, despite regular nutritional advice. Weight and height were expressed as Z-scores. Catch-up growth following GTF onset was studied.
RESULTS: Gastrostomies were performed in 11 children (aged 9·0±5·8years), and one young man aged 18years. The body weight Z-score was -2·3±1·0, height Z-score 1·1±1·1, weight-for-height was 81±11% and height-for-age 95± 4%. At onset, GTF provided 74±21% and 180±81% of the recommended dietary allowance (RDA) for energy and proteins, respectively. At study update (53±20months), GTF provided 91±29% and 205±100% of RDA for energy and proteins, respectively. Weight-for-height reached 92±15% and height-for-age 98±5%. A normal puberty was obtained when GT was performed before the age of 10years. Skin was not improved.
CONCLUSION: Malnutrition was observed in 50% of the children with generalized RDEB. Protein and energy needs are particularly high. GTF is well tolerated and helps with catch-up growth and puberty. It must be considered before malnutrition onset, and, if necessary, before puberty.
© 2011 The Authors. BJD © 2011 British Association of Dermatologists.

Entities:  

Mesh:

Year:  2012        PMID: 21895617     DOI: 10.1111/j.1365-2133.2011.10592.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  8 in total

Review 1.  [Hereditary epidermolysis bullosa in school children and adolescents. Clinical picture and interdisciplinary management].

Authors:  H Ott; C Eich; K Schriek; B Ludwikowski
Journal:  Hautarzt       Date:  2016-04       Impact factor: 0.751

Review 2.  Novel and emerging therapies in the treatment of recessive dystrophic epidermolysis bullosa.

Authors:  Ellie Rashidghamat; John A McGrath
Journal:  Intractable Rare Dis Res       Date:  2017-02

3.  Corneal Changes and Strategies to Improve Survival of Hypomorphic Collagen VII-Deficient Mice for the Study of Ocular Dystrophic Epidermolysis Bullosa.

Authors:  Vicki M Chen; Karrie Southwell; Erin Huynh; Stefanie Gavett; Lauren Richey; Michael Esmail
Journal:  Comp Med       Date:  2022-02-07       Impact factor: 1.565

Review 4.  Nutritional aspects of children and adolescents with epidermolysis bullosa: literature review.

Authors:  Ana Paula Caio Zidorio; Eliane Said Dutra; Dryelle Oliveira Dias Leão; Izelda Maria Carvalho Costa
Journal:  An Bras Dermatol       Date:  2015 Mar-Apr       Impact factor: 1.896

Review 5.  A systematic literature review of the disease burden in patients with recessive dystrophic epidermolysis bullosa.

Authors:  Jean Yuh Tang; M Peter Marinkovich; Eleanor Lucas; Emily Gorell; Albert Chiou; Ying Lu; Jodie Gillon; Dipen Patel; Dan Rudin
Journal:  Orphanet J Rare Dis       Date:  2021-04-13       Impact factor: 4.123

Review 6.  Supporting sexuality for people living with epidermolysis bullosa: clinical practice guidelines.

Authors:  Alex King; Humphrey Hanley; Mark Popenhagen; Florencia Perez; Kerry Thompson; Diana Purvis; Nora Garcia; Ida Steinlein; Mia Werkentoft; Matthew Lightfoot; Michelle Lahat; Kalsoom Begum; Julio Tanabe
Journal:  Orphanet J Rare Dis       Date:  2021-01-06       Impact factor: 4.123

7.  Epidermolysis Bullosa in children: the central role of the pediatrician.

Authors:  Maria Rosaria Marchili; Giulia Spina; Marco Roversi; Cristina Mascolo; Elisabetta Pentimalli; Marialuisa Corbeddu; Andrea Diociaiuti; Maya El Hachem; Alberto Villani
Journal:  Orphanet J Rare Dis       Date:  2022-04-04       Impact factor: 4.123

Review 8.  Multicentre consensus recommendations for skin care in inherited epidermolysis bullosa.

Authors:  May El Hachem; Giovanna Zambruno; Eva Bourdon-Lanoy; Annalisa Ciasulli; Christiane Buisson; Smail Hadj-Rabia; Andrea Diociaiuti; Carolina F Gouveia; Angela Hernández-Martín; Raul de Lucas Laguna; Mateja Dolenc-Voljč; Gianluca Tadini; Guglielmo Salvatori; Cristiana De Ranieri; Stephanie Leclerc-Mercier; Christine Bodemer
Journal:  Orphanet J Rare Dis       Date:  2014-05-20       Impact factor: 4.123

  8 in total

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