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Plasma glutamine concentration after intensive care unit discharge: an observational study
INTRODUCTION: Low plasma glutamine concentration at ICU admission is associated with unfavorable outcomes. The prediction of plasma glutamine concentration after ICU discharge on outcomes has not been characterized. In the recent Scandinavian Glutamine Trial, a survival advantage was seen with gluta...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4300616/ https://www.ncbi.nlm.nih.gov/pubmed/25488701 http://dx.doi.org/10.1186/s13054-014-0677-8 |
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author | Smedberg, Marie Grass, Johanna Nordmark Pettersson, Linn Norberg, Åke Rooyackers, Olav Wernerman, Jan |
author_facet | Smedberg, Marie Grass, Johanna Nordmark Pettersson, Linn Norberg, Åke Rooyackers, Olav Wernerman, Jan |
author_sort | Smedberg, Marie |
collection | PubMed |
description | INTRODUCTION: Low plasma glutamine concentration at ICU admission is associated with unfavorable outcomes. The prediction of plasma glutamine concentration after ICU discharge on outcomes has not been characterized. In the recent Scandinavian Glutamine Trial, a survival advantage was seen with glutamine supplementation as long as patients stayed in the ICU. It was therefore hypothesized that the glutamine level may drop at ICU discharge, indicative of a sustained glutamine deficiency, which may be related to outcome. METHODS: Fully fed ICU patients intravenously supplemented with glutamine for >3 days were studied at ICU discharge and post ICU. In study A, plasma glutamine level was followed every 5 to 7 days post ICU of the remaining hospital stay and compared to the level on the day of ICU discharge (n = 63). In study B, plasma glutamine level 24 to 72 hours after ICU discharge was related to 12-month all-cause mortality (n = 100). RESULTS: Post-ICU plasma glutamine levels were within normal range and were not found to be predictive for mortality outcome. Plasma glutamine level at discharge, on the other hand, was within normal limits but higher in nonsurvivors. In addition, it was adding prediction value to discharge SOFA scores for post-ICU mortality. CONCLUSIONS: Post-ICU glutamine levels are not indicative of glutamine depletion. The relation between plasma glutamine concentration and glutamine availability during critical illness is not well understood, and needs to be studied further to define the possible role for glutamine supplementation. |
format | Online Article Text |
id | pubmed-4300616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43006162015-01-22 Plasma glutamine concentration after intensive care unit discharge: an observational study Smedberg, Marie Grass, Johanna Nordmark Pettersson, Linn Norberg, Åke Rooyackers, Olav Wernerman, Jan Crit Care Research INTRODUCTION: Low plasma glutamine concentration at ICU admission is associated with unfavorable outcomes. The prediction of plasma glutamine concentration after ICU discharge on outcomes has not been characterized. In the recent Scandinavian Glutamine Trial, a survival advantage was seen with glutamine supplementation as long as patients stayed in the ICU. It was therefore hypothesized that the glutamine level may drop at ICU discharge, indicative of a sustained glutamine deficiency, which may be related to outcome. METHODS: Fully fed ICU patients intravenously supplemented with glutamine for >3 days were studied at ICU discharge and post ICU. In study A, plasma glutamine level was followed every 5 to 7 days post ICU of the remaining hospital stay and compared to the level on the day of ICU discharge (n = 63). In study B, plasma glutamine level 24 to 72 hours after ICU discharge was related to 12-month all-cause mortality (n = 100). RESULTS: Post-ICU plasma glutamine levels were within normal range and were not found to be predictive for mortality outcome. Plasma glutamine level at discharge, on the other hand, was within normal limits but higher in nonsurvivors. In addition, it was adding prediction value to discharge SOFA scores for post-ICU mortality. CONCLUSIONS: Post-ICU glutamine levels are not indicative of glutamine depletion. The relation between plasma glutamine concentration and glutamine availability during critical illness is not well understood, and needs to be studied further to define the possible role for glutamine supplementation. BioMed Central 2014-12-09 2014 /pmc/articles/PMC4300616/ /pubmed/25488701 http://dx.doi.org/10.1186/s13054-014-0677-8 Text en © Smedberg et al.; licensee BioMed Central. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 | Research Smedberg, Marie Grass, Johanna Nordmark Pettersson, Linn Norberg, Åke Rooyackers, Olav Wernerman, Jan Plasma glutamine concentration after intensive care unit discharge: an observational study |
title | Plasma glutamine concentration after intensive care unit discharge: an observational study |
title_full | Plasma glutamine concentration after intensive care unit discharge: an observational study |
title_fullStr | Plasma glutamine concentration after intensive care unit discharge: an observational study |
title_full_unstemmed | Plasma glutamine concentration after intensive care unit discharge: an observational study |
title_short | Plasma glutamine concentration after intensive care unit discharge: an observational study |
title_sort | plasma glutamine concentration after intensive care unit discharge: an observational study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4300616/ https://www.ncbi.nlm.nih.gov/pubmed/25488701 http://dx.doi.org/10.1186/s13054-014-0677-8 |
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