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Serum phosphate is not an early predictor of neurocognitive outcomes in acute carbon monoxide poisoning patients
OBJECTIVE: Carbon monoxide (CO) poisoning causes brain injury by hypoxia and inflammatory mechanisms. Hypoxic conditions result in increased serum phosphate concentration due to loss of polarity of the cell membrane, changes in membrane fluidity, and consequent destruction of phospholipids in the ce...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society of Emergency Medicine
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10090729/ https://www.ncbi.nlm.nih.gov/pubmed/36174973 http://dx.doi.org/10.15441/ceem.22.299 |
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author | Lee, Yuseon Kim, Sung Hwa Cha, Yong Sung |
author_facet | Lee, Yuseon Kim, Sung Hwa Cha, Yong Sung |
author_sort | Lee, Yuseon |
collection | PubMed |
description | OBJECTIVE: Carbon monoxide (CO) poisoning causes brain injury by hypoxia and inflammatory mechanisms. Hypoxic conditions result in increased serum phosphate concentration due to loss of polarity of the cell membrane, changes in membrane fluidity, and consequent destruction of phospholipids in the cell membrane. This study aimed to evaluate whether serum phosphate measured in the emergency department (ED) can serve as an early predictor of neurocognitive sequelae 1 month after acute CO poisoning. METHODS: We included patients ≥16 years with acute CO poisoning from a cohort who were treated at a single tertiary academic hospital in Wonju, Korea, between January 2006 and May 2021. Neurocognitive outcome was assessed using the Global Deterioration Scale score; patients were classified into favorable (1–3 points) or poor (4–7 points) neurocognitive outcome groups based on this score. These two groups were compared before and after propensity score matching. RESULTS: Data from 888 patients were analyzed. Seven hundred seventy-one patients (86.8%) were assigned to the favorable outcome group and 117 patients (13.2%) to the poor outcome group. Patients with a poor outcome had a higher mean serum phosphate level than those with a favorable outcome (3.9 mg/dL vs. 3.5 mg/dL, P=0.001). Propensity score matching yielded 85 matched patient pairs. After matching, serum phosphate level in the ED was not significantly different between the favorable and poor outcome groups (3.9 vs. 3.7 mg/dL, P=0.349). CONCLUSION: Serum phosphate level measured in the ED did not predict poor neurocognitive outcomes 1 month after CO poisoning. |
format | Online Article Text |
id | pubmed-10090729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Korean Society of Emergency Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-100907292023-04-13 Serum phosphate is not an early predictor of neurocognitive outcomes in acute carbon monoxide poisoning patients Lee, Yuseon Kim, Sung Hwa Cha, Yong Sung Clin Exp Emerg Med Original Article OBJECTIVE: Carbon monoxide (CO) poisoning causes brain injury by hypoxia and inflammatory mechanisms. Hypoxic conditions result in increased serum phosphate concentration due to loss of polarity of the cell membrane, changes in membrane fluidity, and consequent destruction of phospholipids in the cell membrane. This study aimed to evaluate whether serum phosphate measured in the emergency department (ED) can serve as an early predictor of neurocognitive sequelae 1 month after acute CO poisoning. METHODS: We included patients ≥16 years with acute CO poisoning from a cohort who were treated at a single tertiary academic hospital in Wonju, Korea, between January 2006 and May 2021. Neurocognitive outcome was assessed using the Global Deterioration Scale score; patients were classified into favorable (1–3 points) or poor (4–7 points) neurocognitive outcome groups based on this score. These two groups were compared before and after propensity score matching. RESULTS: Data from 888 patients were analyzed. Seven hundred seventy-one patients (86.8%) were assigned to the favorable outcome group and 117 patients (13.2%) to the poor outcome group. Patients with a poor outcome had a higher mean serum phosphate level than those with a favorable outcome (3.9 mg/dL vs. 3.5 mg/dL, P=0.001). Propensity score matching yielded 85 matched patient pairs. After matching, serum phosphate level in the ED was not significantly different between the favorable and poor outcome groups (3.9 vs. 3.7 mg/dL, P=0.349). CONCLUSION: Serum phosphate level measured in the ED did not predict poor neurocognitive outcomes 1 month after CO poisoning. The Korean Society of Emergency Medicine 2022-09-30 /pmc/articles/PMC10090729/ /pubmed/36174973 http://dx.doi.org/10.15441/ceem.22.299 Text en Copyright © 2023 The Korean Society of Emergency Medicine https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ). |
spellingShingle | Original Article Lee, Yuseon Kim, Sung Hwa Cha, Yong Sung Serum phosphate is not an early predictor of neurocognitive outcomes in acute carbon monoxide poisoning patients |
title | Serum phosphate is not an early predictor of neurocognitive outcomes in acute carbon monoxide poisoning patients |
title_full | Serum phosphate is not an early predictor of neurocognitive outcomes in acute carbon monoxide poisoning patients |
title_fullStr | Serum phosphate is not an early predictor of neurocognitive outcomes in acute carbon monoxide poisoning patients |
title_full_unstemmed | Serum phosphate is not an early predictor of neurocognitive outcomes in acute carbon monoxide poisoning patients |
title_short | Serum phosphate is not an early predictor of neurocognitive outcomes in acute carbon monoxide poisoning patients |
title_sort | serum phosphate is not an early predictor of neurocognitive outcomes in acute carbon monoxide poisoning patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10090729/ https://www.ncbi.nlm.nih.gov/pubmed/36174973 http://dx.doi.org/10.15441/ceem.22.299 |
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