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Pediatric delirium is associated with increased brain injury marker levels in cardiac surgery patients

Despite global consensus on the importance of screening pediatric delirium, correlations between pediatric delirium during acute brain injury and adult delirium are unclear. Therefore, we hypothesized that similar pediatric biomarkers reflect acute brain injury as in adult delirium. We observed pedi...

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Autores principales: Matsuishi, Yujiro, Hoshino, Haruhiko, Enomoto, Yuki, Shimojo, Nobutake, Matsubara, Muneaki, Kato, Hideyuki, Mathis, Bryan J., Morita, Kojiro, Hiramatsu, Yuji, Inoue, Yoshiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636141/
https://www.ncbi.nlm.nih.gov/pubmed/36333387
http://dx.doi.org/10.1038/s41598-022-22702-2
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author Matsuishi, Yujiro
Hoshino, Haruhiko
Enomoto, Yuki
Shimojo, Nobutake
Matsubara, Muneaki
Kato, Hideyuki
Mathis, Bryan J.
Morita, Kojiro
Hiramatsu, Yuji
Inoue, Yoshiaki
author_facet Matsuishi, Yujiro
Hoshino, Haruhiko
Enomoto, Yuki
Shimojo, Nobutake
Matsubara, Muneaki
Kato, Hideyuki
Mathis, Bryan J.
Morita, Kojiro
Hiramatsu, Yuji
Inoue, Yoshiaki
author_sort Matsuishi, Yujiro
collection PubMed
description Despite global consensus on the importance of screening pediatric delirium, correlations between pediatric delirium during acute brain injury and adult delirium are unclear. Therefore, we hypothesized that similar pediatric biomarkers reflect acute brain injury as in adult delirium. We observed pediatric cardiac surgery patients from neonatal age to 18 years, who were admitted to our pediatric intensive care unit after cardiovascular operations between October 2019 to June 2020, up to post-operative day 3 (4 days total). We recorded age, sex, risk score (Risk Adjustment in Congenital Heart Surgery [RACHS-1]), midazolam/dexmedetomidine/fentanyl dosage, and pediatric Sequential Organ Failure Assessment (pSOFA). Richmond Agitation-Sedation Scale (RASS), Cornell Assessment of Pediatric Delirium (CAPD), Face, Leg, Activity, Consolability (FLACC) behavioral scale, and Withdrawal Assessment Tool (WAT-1) scales were used and serum sampling for neuron specific enolase (NSE) was conducted. Consciousness status was considered hierarchical (coma > delirium > normal) and associations between conscious status and NSE were conducted by hierarchical Bayesian modeling. We analyzed 134 data points from 40 patients (median age 12 months). In the multi-regression model, NSE was positively associated with coma [posterior odds ratio (OR) = 1.1, 95% credible interval (CrI) 1.01–1.19] while pSOFA [posterior OR = 1.63, 95% CrI 1.17–2.5], midazolam [posterior OR = 1.02, 95% CrI 1.01–1.04], and dexmedetomidine [posterior OR = 9.52, 95% CrI 1.02–108.85] were also associated. We also evaluated consciousness state probability at each NSE concentration and confirmed both that consciousness was hierarchically sorted and CAPD scores were also associated with NSE [posterior OR = 1.32, 95% CrI 1.09–1.58]. “Eye contact” (r = 0.55) was the most correlated component with NSE within the pain, withdrawal syndrome, and PD items. PD within the hierarchy of consciousness (coma, delirium, normal) and CAPD scores are associated with brain injury marker levels. Using pediatric delirium assessment tools for monitoring brain injury, especially eye contact, is a reliable method for observing PD.
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spelling pubmed-96361412022-11-06 Pediatric delirium is associated with increased brain injury marker levels in cardiac surgery patients Matsuishi, Yujiro Hoshino, Haruhiko Enomoto, Yuki Shimojo, Nobutake Matsubara, Muneaki Kato, Hideyuki Mathis, Bryan J. Morita, Kojiro Hiramatsu, Yuji Inoue, Yoshiaki Sci Rep Article Despite global consensus on the importance of screening pediatric delirium, correlations between pediatric delirium during acute brain injury and adult delirium are unclear. Therefore, we hypothesized that similar pediatric biomarkers reflect acute brain injury as in adult delirium. We observed pediatric cardiac surgery patients from neonatal age to 18 years, who were admitted to our pediatric intensive care unit after cardiovascular operations between October 2019 to June 2020, up to post-operative day 3 (4 days total). We recorded age, sex, risk score (Risk Adjustment in Congenital Heart Surgery [RACHS-1]), midazolam/dexmedetomidine/fentanyl dosage, and pediatric Sequential Organ Failure Assessment (pSOFA). Richmond Agitation-Sedation Scale (RASS), Cornell Assessment of Pediatric Delirium (CAPD), Face, Leg, Activity, Consolability (FLACC) behavioral scale, and Withdrawal Assessment Tool (WAT-1) scales were used and serum sampling for neuron specific enolase (NSE) was conducted. Consciousness status was considered hierarchical (coma > delirium > normal) and associations between conscious status and NSE were conducted by hierarchical Bayesian modeling. We analyzed 134 data points from 40 patients (median age 12 months). In the multi-regression model, NSE was positively associated with coma [posterior odds ratio (OR) = 1.1, 95% credible interval (CrI) 1.01–1.19] while pSOFA [posterior OR = 1.63, 95% CrI 1.17–2.5], midazolam [posterior OR = 1.02, 95% CrI 1.01–1.04], and dexmedetomidine [posterior OR = 9.52, 95% CrI 1.02–108.85] were also associated. We also evaluated consciousness state probability at each NSE concentration and confirmed both that consciousness was hierarchically sorted and CAPD scores were also associated with NSE [posterior OR = 1.32, 95% CrI 1.09–1.58]. “Eye contact” (r = 0.55) was the most correlated component with NSE within the pain, withdrawal syndrome, and PD items. PD within the hierarchy of consciousness (coma, delirium, normal) and CAPD scores are associated with brain injury marker levels. Using pediatric delirium assessment tools for monitoring brain injury, especially eye contact, is a reliable method for observing PD. Nature Publishing Group UK 2022-11-04 /pmc/articles/PMC9636141/ /pubmed/36333387 http://dx.doi.org/10.1038/s41598-022-22702-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Matsuishi, Yujiro
Hoshino, Haruhiko
Enomoto, Yuki
Shimojo, Nobutake
Matsubara, Muneaki
Kato, Hideyuki
Mathis, Bryan J.
Morita, Kojiro
Hiramatsu, Yuji
Inoue, Yoshiaki
Pediatric delirium is associated with increased brain injury marker levels in cardiac surgery patients
title Pediatric delirium is associated with increased brain injury marker levels in cardiac surgery patients
title_full Pediatric delirium is associated with increased brain injury marker levels in cardiac surgery patients
title_fullStr Pediatric delirium is associated with increased brain injury marker levels in cardiac surgery patients
title_full_unstemmed Pediatric delirium is associated with increased brain injury marker levels in cardiac surgery patients
title_short Pediatric delirium is associated with increased brain injury marker levels in cardiac surgery patients
title_sort pediatric delirium is associated with increased brain injury marker levels in cardiac surgery patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636141/
https://www.ncbi.nlm.nih.gov/pubmed/36333387
http://dx.doi.org/10.1038/s41598-022-22702-2
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