Cargando…

Nutritional Management of Intestinal Failure due to Short Bowel Syndrome in Children

Background: The most common cause of intestinal failure (IF) in childhood remains short bowel syndrome (SBS), where bowel mass is significantly reduced due to a congenital atresia or resection and parenteral nutrition (PN) needed. Home PN has improved outcome and quality of life, but the long-term t...

Descripción completa

Detalles Bibliográficos
Autores principales: Puoti, Maria Giovanna, Köglmeier, Jutta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823779/
https://www.ncbi.nlm.nih.gov/pubmed/36615720
http://dx.doi.org/10.3390/nu15010062
_version_ 1784866245175148544
author Puoti, Maria Giovanna
Köglmeier, Jutta
author_facet Puoti, Maria Giovanna
Köglmeier, Jutta
author_sort Puoti, Maria Giovanna
collection PubMed
description Background: The most common cause of intestinal failure (IF) in childhood remains short bowel syndrome (SBS), where bowel mass is significantly reduced due to a congenital atresia or resection and parenteral nutrition (PN) needed. Home PN has improved outcome and quality of life, but the long-term therapeutic goal is to achieve enteral autonomy whilst avoiding long term complications. This paper is aimed at discussing nutritional strategies available to clinicians caring for these patients. Methods: A literature search was performed from 1992 to 2022 using Pubmed, MEDLINE and Cochrane Database of Systematic Reviews, and recent guidelines were reviewed. In the absence of evidence, recommendations reflect the authors’ expert opinion. Results: Consensus on the best possible way of feeding children with IF-SBS is lacking and practice varies widely between centres. Feeding should commence as soon as possible following surgery. Oral feeding is the preferred route and breast milk (BM) the first milk of choice in infants. Donor BM, standard preterm or term formula are alternatives in the absence of maternal BM. Extensively hydrolysed or amino acid-based feeds are used when these are not tolerated. Solids should be introduced as soon as clinically appropriate. Children are encouraged to eat by mouth and experience different tastes and textures to avoid oral aversion. Aggressive weaning of PN and tube (over-) feeding are now discouraged. Conclusions: To date, uniform agreement on the optimal type of feed, timing of food introduction and feeding regime used is lacking and great difference in practice remains. There is need for more research to establish common treatment protocols.
format Online
Article
Text
id pubmed-9823779
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-98237792023-01-08 Nutritional Management of Intestinal Failure due to Short Bowel Syndrome in Children Puoti, Maria Giovanna Köglmeier, Jutta Nutrients Review Background: The most common cause of intestinal failure (IF) in childhood remains short bowel syndrome (SBS), where bowel mass is significantly reduced due to a congenital atresia or resection and parenteral nutrition (PN) needed. Home PN has improved outcome and quality of life, but the long-term therapeutic goal is to achieve enteral autonomy whilst avoiding long term complications. This paper is aimed at discussing nutritional strategies available to clinicians caring for these patients. Methods: A literature search was performed from 1992 to 2022 using Pubmed, MEDLINE and Cochrane Database of Systematic Reviews, and recent guidelines were reviewed. In the absence of evidence, recommendations reflect the authors’ expert opinion. Results: Consensus on the best possible way of feeding children with IF-SBS is lacking and practice varies widely between centres. Feeding should commence as soon as possible following surgery. Oral feeding is the preferred route and breast milk (BM) the first milk of choice in infants. Donor BM, standard preterm or term formula are alternatives in the absence of maternal BM. Extensively hydrolysed or amino acid-based feeds are used when these are not tolerated. Solids should be introduced as soon as clinically appropriate. Children are encouraged to eat by mouth and experience different tastes and textures to avoid oral aversion. Aggressive weaning of PN and tube (over-) feeding are now discouraged. Conclusions: To date, uniform agreement on the optimal type of feed, timing of food introduction and feeding regime used is lacking and great difference in practice remains. There is need for more research to establish common treatment protocols. MDPI 2022-12-23 /pmc/articles/PMC9823779/ /pubmed/36615720 http://dx.doi.org/10.3390/nu15010062 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Puoti, Maria Giovanna
Köglmeier, Jutta
Nutritional Management of Intestinal Failure due to Short Bowel Syndrome in Children
title Nutritional Management of Intestinal Failure due to Short Bowel Syndrome in Children
title_full Nutritional Management of Intestinal Failure due to Short Bowel Syndrome in Children
title_fullStr Nutritional Management of Intestinal Failure due to Short Bowel Syndrome in Children
title_full_unstemmed Nutritional Management of Intestinal Failure due to Short Bowel Syndrome in Children
title_short Nutritional Management of Intestinal Failure due to Short Bowel Syndrome in Children
title_sort nutritional management of intestinal failure due to short bowel syndrome in children
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823779/
https://www.ncbi.nlm.nih.gov/pubmed/36615720
http://dx.doi.org/10.3390/nu15010062
work_keys_str_mv AT puotimariagiovanna nutritionalmanagementofintestinalfailureduetoshortbowelsyndromeinchildren
AT koglmeierjutta nutritionalmanagementofintestinalfailureduetoshortbowelsyndromeinchildren