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The Association Between Vitamin E Deficiency and Critically Ill Children With Sepsis and Septic Shock
Background: Literature is scarce on the assessment of vitamin E status in septic children. We aim to investigate the prevalence of vitamin E deficiency in critically ill children with sepsis and septic shock and its association with clinical features and outcomes. Methods: We compared serum vitamin...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241937/ https://www.ncbi.nlm.nih.gov/pubmed/34222298 http://dx.doi.org/10.3389/fnut.2021.648442 |
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author | Dang, Hongxing Li, Jing Liu, Chengjun Xu, Feng |
author_facet | Dang, Hongxing Li, Jing Liu, Chengjun Xu, Feng |
author_sort | Dang, Hongxing |
collection | PubMed |
description | Background: Literature is scarce on the assessment of vitamin E status in septic children. We aim to investigate the prevalence of vitamin E deficiency in critically ill children with sepsis and septic shock and its association with clinical features and outcomes. Methods: We compared serum vitamin E status between the confirmed or suspected infection and no infection groups, the sepsis shock and no sepsis shock groups upon pediatric intensive care unit admission. Clinical characteristics were compared in subgroup patients with and without vitamin E deficiency. The association between vitamin E deficiency and septic shock were evaluated using univariate and multivariable methods. Results: 182 critically ill children with confirmed or suspected infection and 114 without infection were enrolled. The incidence of vitamin E deficiency was 30.2% in the infection group and 61.9% in the septic shock subgroup (P < 0.001). Thirty-days mortality in critically ill children with vitamin E deficiency was significantly higher than that without vitamin E deficiency (27.3 vs. 14.2%, P < 0.05). Vitamin E levels were inversely associated with higher pediatric risk of mortality (r = − 0.238, P = 0.001) and cardiovascular sequential organ failure assessment (r = −0.249, p < 0.001) scores in critically ill children with infection. In multivariable logistic regression, vitamin E deficiency showed an independent effect on septic shock (adjusted OR: 6.749, 95%CI: 2.449–18.60, P < 0.001). Conclusion: Vitamin E deficiency is highly prevalent in critically ill children with sepsis and contributed to the septic shock. |
format | Online Article Text |
id | pubmed-8241937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82419372021-07-01 The Association Between Vitamin E Deficiency and Critically Ill Children With Sepsis and Septic Shock Dang, Hongxing Li, Jing Liu, Chengjun Xu, Feng Front Nutr Nutrition Background: Literature is scarce on the assessment of vitamin E status in septic children. We aim to investigate the prevalence of vitamin E deficiency in critically ill children with sepsis and septic shock and its association with clinical features and outcomes. Methods: We compared serum vitamin E status between the confirmed or suspected infection and no infection groups, the sepsis shock and no sepsis shock groups upon pediatric intensive care unit admission. Clinical characteristics were compared in subgroup patients with and without vitamin E deficiency. The association between vitamin E deficiency and septic shock were evaluated using univariate and multivariable methods. Results: 182 critically ill children with confirmed or suspected infection and 114 without infection were enrolled. The incidence of vitamin E deficiency was 30.2% in the infection group and 61.9% in the septic shock subgroup (P < 0.001). Thirty-days mortality in critically ill children with vitamin E deficiency was significantly higher than that without vitamin E deficiency (27.3 vs. 14.2%, P < 0.05). Vitamin E levels were inversely associated with higher pediatric risk of mortality (r = − 0.238, P = 0.001) and cardiovascular sequential organ failure assessment (r = −0.249, p < 0.001) scores in critically ill children with infection. In multivariable logistic regression, vitamin E deficiency showed an independent effect on septic shock (adjusted OR: 6.749, 95%CI: 2.449–18.60, P < 0.001). Conclusion: Vitamin E deficiency is highly prevalent in critically ill children with sepsis and contributed to the septic shock. Frontiers Media S.A. 2021-06-16 /pmc/articles/PMC8241937/ /pubmed/34222298 http://dx.doi.org/10.3389/fnut.2021.648442 Text en Copyright © 2021 Dang, Li, Liu and Xu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Nutrition Dang, Hongxing Li, Jing Liu, Chengjun Xu, Feng The Association Between Vitamin E Deficiency and Critically Ill Children With Sepsis and Septic Shock |
title | The Association Between Vitamin E Deficiency and Critically Ill Children With Sepsis and Septic Shock |
title_full | The Association Between Vitamin E Deficiency and Critically Ill Children With Sepsis and Septic Shock |
title_fullStr | The Association Between Vitamin E Deficiency and Critically Ill Children With Sepsis and Septic Shock |
title_full_unstemmed | The Association Between Vitamin E Deficiency and Critically Ill Children With Sepsis and Septic Shock |
title_short | The Association Between Vitamin E Deficiency and Critically Ill Children With Sepsis and Septic Shock |
title_sort | association between vitamin e deficiency and critically ill children with sepsis and septic shock |
topic | Nutrition |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241937/ https://www.ncbi.nlm.nih.gov/pubmed/34222298 http://dx.doi.org/10.3389/fnut.2021.648442 |
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