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Use of troponin assay after electrical injuries: a 15-year multicentre retrospective cohort in emergency departments
BACKGROUND: Patients with electrical injury are considered to be at risk of cardiac arrhythmia. Assessing the risk of developing a major adverse cardiac event (MACE) is the cornerstone of patient management. The aim of this study was to assess the performance of initial troponin and troponin rise to...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474711/ https://www.ncbi.nlm.nih.gov/pubmed/34565432 http://dx.doi.org/10.1186/s13049-021-00955-6 |
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author | Delphine, Douillet Stéphanie, Kalwant Yara, Amro Benjamin, Gicquel Idriss, Arnaudet Dominique, Savary Quentin, Le Bastard François, Javaudin |
author_facet | Delphine, Douillet Stéphanie, Kalwant Yara, Amro Benjamin, Gicquel Idriss, Arnaudet Dominique, Savary Quentin, Le Bastard François, Javaudin |
author_sort | Delphine, Douillet |
collection | PubMed |
description | BACKGROUND: Patients with electrical injury are considered to be at risk of cardiac arrhythmia. Assessing the risk of developing a major adverse cardiac event (MACE) is the cornerstone of patient management. The aim of this study was to assess the performance of initial troponin and troponin rise to predict Major Adverse Cardiac Events (MACEs) in all patients with electrical injuries admitted to the Emergency Department. METHODS: This is a multicentre retrospective study in which consecutive patients with electrical injuries admitted to the Emergency Departments (ED) (adult and paediatric) of five French Hospitals were included between 2005 and 2019. The threshold for troponin elevation is based on the European Society of Cardiology guidelines for patients presenting without persistent ST segment elevation. The primary endpoint was the rate of MACE. RESULTS: A total of 785 included patients were admitted to ED with a first diagnosis of electrical injury during the study period. Troponin assays were performed in 533 patients (67.9%), including 465 of 663 adults (70.1%) and 68 of 122 children (55.7%) and 17/533 (3.2%) of patients had an initial elevated troponin. If none of the clinical criteria for MACE were present (i.e., previous known heart disease, exposure to a high voltage of ≥ 1000 Volts, initial loss of consciousness, or an abnormal initial ECG), this defined a low-risk subgroup (n = 573, 76.0%) that could be safely discharged. The initial positive troponin assay had a sensitivity of 83.3 (95% CI 35.9–99.6%), a specificity of 97.7 (95% CI 96.1–98.8%), a positive likelihood ratio 36.6 (95% CI 18.8–71.1%) and a negative predictive value of 99.9 (95% CI 99.2–99.9%) in predicting a MACE. CONCLUSIONS: Troponin assay appears to be a predictive marker of MACE risk and should be considered in high-risk patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13049-021-00955-6. |
format | Online Article Text |
id | pubmed-8474711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84747112021-09-28 Use of troponin assay after electrical injuries: a 15-year multicentre retrospective cohort in emergency departments Delphine, Douillet Stéphanie, Kalwant Yara, Amro Benjamin, Gicquel Idriss, Arnaudet Dominique, Savary Quentin, Le Bastard François, Javaudin Scand J Trauma Resusc Emerg Med Original Research BACKGROUND: Patients with electrical injury are considered to be at risk of cardiac arrhythmia. Assessing the risk of developing a major adverse cardiac event (MACE) is the cornerstone of patient management. The aim of this study was to assess the performance of initial troponin and troponin rise to predict Major Adverse Cardiac Events (MACEs) in all patients with electrical injuries admitted to the Emergency Department. METHODS: This is a multicentre retrospective study in which consecutive patients with electrical injuries admitted to the Emergency Departments (ED) (adult and paediatric) of five French Hospitals were included between 2005 and 2019. The threshold for troponin elevation is based on the European Society of Cardiology guidelines for patients presenting without persistent ST segment elevation. The primary endpoint was the rate of MACE. RESULTS: A total of 785 included patients were admitted to ED with a first diagnosis of electrical injury during the study period. Troponin assays were performed in 533 patients (67.9%), including 465 of 663 adults (70.1%) and 68 of 122 children (55.7%) and 17/533 (3.2%) of patients had an initial elevated troponin. If none of the clinical criteria for MACE were present (i.e., previous known heart disease, exposure to a high voltage of ≥ 1000 Volts, initial loss of consciousness, or an abnormal initial ECG), this defined a low-risk subgroup (n = 573, 76.0%) that could be safely discharged. The initial positive troponin assay had a sensitivity of 83.3 (95% CI 35.9–99.6%), a specificity of 97.7 (95% CI 96.1–98.8%), a positive likelihood ratio 36.6 (95% CI 18.8–71.1%) and a negative predictive value of 99.9 (95% CI 99.2–99.9%) in predicting a MACE. CONCLUSIONS: Troponin assay appears to be a predictive marker of MACE risk and should be considered in high-risk patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13049-021-00955-6. BioMed Central 2021-09-26 /pmc/articles/PMC8474711/ /pubmed/34565432 http://dx.doi.org/10.1186/s13049-021-00955-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Original Research Delphine, Douillet Stéphanie, Kalwant Yara, Amro Benjamin, Gicquel Idriss, Arnaudet Dominique, Savary Quentin, Le Bastard François, Javaudin Use of troponin assay after electrical injuries: a 15-year multicentre retrospective cohort in emergency departments |
title | Use of troponin assay after electrical injuries: a 15-year multicentre retrospective cohort in emergency departments |
title_full | Use of troponin assay after electrical injuries: a 15-year multicentre retrospective cohort in emergency departments |
title_fullStr | Use of troponin assay after electrical injuries: a 15-year multicentre retrospective cohort in emergency departments |
title_full_unstemmed | Use of troponin assay after electrical injuries: a 15-year multicentre retrospective cohort in emergency departments |
title_short | Use of troponin assay after electrical injuries: a 15-year multicentre retrospective cohort in emergency departments |
title_sort | use of troponin assay after electrical injuries: a 15-year multicentre retrospective cohort in emergency departments |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474711/ https://www.ncbi.nlm.nih.gov/pubmed/34565432 http://dx.doi.org/10.1186/s13049-021-00955-6 |
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