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Age-dependent thrombin generation predicts 30-day mortality and symptomatic thromboembolism after multiple trauma

Trauma-induced coagulopathy (TIC) is a risk factor for death and is associated with deviations in thrombin generation. TIC prevalence and thrombin levels increase with age. We assayed in vivo and ex vivo thrombin generation in injured patients (n = 418) to specifically investigate how age impacts th...

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Autores principales: Lesbo, Maj, Hviid, Claus V. B., Brink, Ole, Juul, Svend, Borris, Lars C., Hvas, Anne-Mette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9886925/
https://www.ncbi.nlm.nih.gov/pubmed/36717730
http://dx.doi.org/10.1038/s41598-023-28474-7
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author Lesbo, Maj
Hviid, Claus V. B.
Brink, Ole
Juul, Svend
Borris, Lars C.
Hvas, Anne-Mette
author_facet Lesbo, Maj
Hviid, Claus V. B.
Brink, Ole
Juul, Svend
Borris, Lars C.
Hvas, Anne-Mette
author_sort Lesbo, Maj
collection PubMed
description Trauma-induced coagulopathy (TIC) is a risk factor for death and is associated with deviations in thrombin generation. TIC prevalence and thrombin levels increase with age. We assayed in vivo and ex vivo thrombin generation in injured patients (n = 418) to specifically investigate how age impacts thrombin generation in trauma and to address the prognostic ability of thrombin generation. Biomarkers of thrombin generation were elevated in young (< 40 years) and older (≥ 40 years) trauma patients. In vivo thrombin generation was associated with Injury Severity Score (ISS) and this association was stronger in young than older patients. In vivo thrombin generation decreased faster after trauma in the young than the older patients. Across age groups, in vivo thrombin generation separated patients dying/surviving within 30 days at a level comparable to the ISS score (AUC 0.80 vs. 0.82, p > 0.76). In vivo and ex vivo thrombin generation also predicted development of thromboembolic events within the first 30 days after the trauma (AUC 0.70–0.84). In conclusion, younger trauma patients mount a stronger and more dynamic in vivo thrombin response than older patients. Across age groups, in vivo thrombin generation has a strong ability to predict death and/or thromboembolic events 30 days after injury.
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spelling pubmed-98869252023-02-01 Age-dependent thrombin generation predicts 30-day mortality and symptomatic thromboembolism after multiple trauma Lesbo, Maj Hviid, Claus V. B. Brink, Ole Juul, Svend Borris, Lars C. Hvas, Anne-Mette Sci Rep Article Trauma-induced coagulopathy (TIC) is a risk factor for death and is associated with deviations in thrombin generation. TIC prevalence and thrombin levels increase with age. We assayed in vivo and ex vivo thrombin generation in injured patients (n = 418) to specifically investigate how age impacts thrombin generation in trauma and to address the prognostic ability of thrombin generation. Biomarkers of thrombin generation were elevated in young (< 40 years) and older (≥ 40 years) trauma patients. In vivo thrombin generation was associated with Injury Severity Score (ISS) and this association was stronger in young than older patients. In vivo thrombin generation decreased faster after trauma in the young than the older patients. Across age groups, in vivo thrombin generation separated patients dying/surviving within 30 days at a level comparable to the ISS score (AUC 0.80 vs. 0.82, p > 0.76). In vivo and ex vivo thrombin generation also predicted development of thromboembolic events within the first 30 days after the trauma (AUC 0.70–0.84). In conclusion, younger trauma patients mount a stronger and more dynamic in vivo thrombin response than older patients. Across age groups, in vivo thrombin generation has a strong ability to predict death and/or thromboembolic events 30 days after injury. Nature Publishing Group UK 2023-01-30 /pmc/articles/PMC9886925/ /pubmed/36717730 http://dx.doi.org/10.1038/s41598-023-28474-7 Text en © The Author(s) 2023 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
Lesbo, Maj
Hviid, Claus V. B.
Brink, Ole
Juul, Svend
Borris, Lars C.
Hvas, Anne-Mette
Age-dependent thrombin generation predicts 30-day mortality and symptomatic thromboembolism after multiple trauma
title Age-dependent thrombin generation predicts 30-day mortality and symptomatic thromboembolism after multiple trauma
title_full Age-dependent thrombin generation predicts 30-day mortality and symptomatic thromboembolism after multiple trauma
title_fullStr Age-dependent thrombin generation predicts 30-day mortality and symptomatic thromboembolism after multiple trauma
title_full_unstemmed Age-dependent thrombin generation predicts 30-day mortality and symptomatic thromboembolism after multiple trauma
title_short Age-dependent thrombin generation predicts 30-day mortality and symptomatic thromboembolism after multiple trauma
title_sort age-dependent thrombin generation predicts 30-day mortality and symptomatic thromboembolism after multiple trauma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9886925/
https://www.ncbi.nlm.nih.gov/pubmed/36717730
http://dx.doi.org/10.1038/s41598-023-28474-7
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