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Reduced serum cholinesterase is an independent risk factor for all-cause mortality in the pediatric intensive care unit

OBJECTIVE: Our aim was to assess the relationship between serum cholinesterase levels at intensive care unit admission and all-cause mortality in the pediatric intensive care unit. METHODS: We used the pediatric intensive care unit database (a large pediatric intensive care database in China from 20...

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Autores principales: Yue, Chaoyan, Zhang, Chunyi, Ying, Chunmei, Jiang, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730412/
https://www.ncbi.nlm.nih.gov/pubmed/36505241
http://dx.doi.org/10.3389/fnut.2022.809449
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author Yue, Chaoyan
Zhang, Chunyi
Ying, Chunmei
Jiang, Hua
author_facet Yue, Chaoyan
Zhang, Chunyi
Ying, Chunmei
Jiang, Hua
author_sort Yue, Chaoyan
collection PubMed
description OBJECTIVE: Our aim was to assess the relationship between serum cholinesterase levels at intensive care unit admission and all-cause mortality in the pediatric intensive care unit. METHODS: We used the pediatric intensive care unit database (a large pediatric intensive care database in China from 2010 to 2018) to conduct a retrospective analysis to evaluate the serum cholinesterase levels at intensive care unit admission of 11,751 critically ill children enrolled to the intensive care unit. We analyzed the association between serum cholinesterase and all-cause mortality. Adjusted smoothing spline plots, subgroup analysis and segmented multivariate logistic regression analysis were conducted to estimate the relative risk between proportional risk between serum cholinesterase and death. RESULTS: Of the 11,751 children, 703 (5.98%) died in hospital. After adjusting for confounders, there was a negative association between serum cholinesterase and the risk of death in pediatric intensive care unit. For every 1,000 U/L increase in serum cholinesterase, the risk of death was reduced by 16% (adjusted OR = 0.84, 95% CI: 0.79, 0.89). The results of sensitivity analysis showed that in different stratified analyses (age, intensive care unit category, albumin, alanine aminotransferase, creatinine, neutrophils), the effect of serum cholinesterase on all-cause mortality remained stable. CONCLUSION: After adjusting for inflammation, nutrition, and liver function factors, cholinesterase reduction is still an independent risk factor for pediatric intensive care unit all-cause mortality.
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spelling pubmed-97304122022-12-09 Reduced serum cholinesterase is an independent risk factor for all-cause mortality in the pediatric intensive care unit Yue, Chaoyan Zhang, Chunyi Ying, Chunmei Jiang, Hua Front Nutr Nutrition OBJECTIVE: Our aim was to assess the relationship between serum cholinesterase levels at intensive care unit admission and all-cause mortality in the pediatric intensive care unit. METHODS: We used the pediatric intensive care unit database (a large pediatric intensive care database in China from 2010 to 2018) to conduct a retrospective analysis to evaluate the serum cholinesterase levels at intensive care unit admission of 11,751 critically ill children enrolled to the intensive care unit. We analyzed the association between serum cholinesterase and all-cause mortality. Adjusted smoothing spline plots, subgroup analysis and segmented multivariate logistic regression analysis were conducted to estimate the relative risk between proportional risk between serum cholinesterase and death. RESULTS: Of the 11,751 children, 703 (5.98%) died in hospital. After adjusting for confounders, there was a negative association between serum cholinesterase and the risk of death in pediatric intensive care unit. For every 1,000 U/L increase in serum cholinesterase, the risk of death was reduced by 16% (adjusted OR = 0.84, 95% CI: 0.79, 0.89). The results of sensitivity analysis showed that in different stratified analyses (age, intensive care unit category, albumin, alanine aminotransferase, creatinine, neutrophils), the effect of serum cholinesterase on all-cause mortality remained stable. CONCLUSION: After adjusting for inflammation, nutrition, and liver function factors, cholinesterase reduction is still an independent risk factor for pediatric intensive care unit all-cause mortality. Frontiers Media S.A. 2022-11-24 /pmc/articles/PMC9730412/ /pubmed/36505241 http://dx.doi.org/10.3389/fnut.2022.809449 Text en Copyright © 2022 Yue, Zhang, Ying and Jiang. 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
Yue, Chaoyan
Zhang, Chunyi
Ying, Chunmei
Jiang, Hua
Reduced serum cholinesterase is an independent risk factor for all-cause mortality in the pediatric intensive care unit
title Reduced serum cholinesterase is an independent risk factor for all-cause mortality in the pediatric intensive care unit
title_full Reduced serum cholinesterase is an independent risk factor for all-cause mortality in the pediatric intensive care unit
title_fullStr Reduced serum cholinesterase is an independent risk factor for all-cause mortality in the pediatric intensive care unit
title_full_unstemmed Reduced serum cholinesterase is an independent risk factor for all-cause mortality in the pediatric intensive care unit
title_short Reduced serum cholinesterase is an independent risk factor for all-cause mortality in the pediatric intensive care unit
title_sort reduced serum cholinesterase is an independent risk factor for all-cause mortality in the pediatric intensive care unit
topic Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730412/
https://www.ncbi.nlm.nih.gov/pubmed/36505241
http://dx.doi.org/10.3389/fnut.2022.809449
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