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Do we need new prokinetics to reduce enteral feeding intolerance during critical illness?
Gastrointestinal feeding intolerance and critical illness-associated gastric motility dysfunction are common. Although recent guidelines recommend not interrupting gastric feeding when gastric residual volume (GRV) is lower than 500 mL or to completely abandon measurement of GRV, it may seem that th...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5035451/ https://www.ncbi.nlm.nih.gov/pubmed/27663648 http://dx.doi.org/10.1186/s13054-016-1466-3 |
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author | van Zanten, Arthur Raymond Hubert |
author_facet | van Zanten, Arthur Raymond Hubert |
author_sort | van Zanten, Arthur Raymond Hubert |
collection | PubMed |
description | Gastrointestinal feeding intolerance and critical illness-associated gastric motility dysfunction are common. Although recent guidelines recommend not interrupting gastric feeding when gastric residual volume (GRV) is lower than 500 mL or to completely abandon measurement of GRV, it may seem that the relevance of prokinetics is reduced. In patients at risk for aspiration and in multimodal strategies to enhance feeding performance, however, use of prokinetics is still advocated. Metoclopramide and erythromycin are commonly used promotility agents, although with relevant side effects. Potential targets for new agents and early study results are addressed. |
format | Online Article Text |
id | pubmed-5035451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50354512016-09-29 Do we need new prokinetics to reduce enteral feeding intolerance during critical illness? van Zanten, Arthur Raymond Hubert Crit Care Editorial Gastrointestinal feeding intolerance and critical illness-associated gastric motility dysfunction are common. Although recent guidelines recommend not interrupting gastric feeding when gastric residual volume (GRV) is lower than 500 mL or to completely abandon measurement of GRV, it may seem that the relevance of prokinetics is reduced. In patients at risk for aspiration and in multimodal strategies to enhance feeding performance, however, use of prokinetics is still advocated. Metoclopramide and erythromycin are commonly used promotility agents, although with relevant side effects. Potential targets for new agents and early study results are addressed. BioMed Central 2016-09-24 /pmc/articles/PMC5035451/ /pubmed/27663648 http://dx.doi.org/10.1186/s13054-016-1466-3 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Editorial van Zanten, Arthur Raymond Hubert Do we need new prokinetics to reduce enteral feeding intolerance during critical illness? |
title | Do we need new prokinetics to reduce enteral feeding intolerance during critical illness? |
title_full | Do we need new prokinetics to reduce enteral feeding intolerance during critical illness? |
title_fullStr | Do we need new prokinetics to reduce enteral feeding intolerance during critical illness? |
title_full_unstemmed | Do we need new prokinetics to reduce enteral feeding intolerance during critical illness? |
title_short | Do we need new prokinetics to reduce enteral feeding intolerance during critical illness? |
title_sort | do we need new prokinetics to reduce enteral feeding intolerance during critical illness? |
topic | Editorial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5035451/ https://www.ncbi.nlm.nih.gov/pubmed/27663648 http://dx.doi.org/10.1186/s13054-016-1466-3 |
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