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Coagulopathy after hemorrhagic traumatic brain injury, an observational study of the incidence and prognosis

BACKGROUND: Traumatic brain injury is associated with high rates of mortality and morbidity. Trauma patients with a coagulopathy have a 10-fold increased mortality risk compared to patients without a coagulopathy. The aim of this study was to identify the incidence of coagulopathy and relate early c...

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Autores principales: van Gent, Jort A. N., van Essen, Thomas A., Bos, Mettine H. A., Cannegieter, Suzanne C., van Dijck, Jeroen T. J. M., Peul, Wilco C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6982633/
https://www.ncbi.nlm.nih.gov/pubmed/31741112
http://dx.doi.org/10.1007/s00701-019-04111-z
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author van Gent, Jort A. N.
van Essen, Thomas A.
Bos, Mettine H. A.
Cannegieter, Suzanne C.
van Dijck, Jeroen T. J. M.
Peul, Wilco C.
author_facet van Gent, Jort A. N.
van Essen, Thomas A.
Bos, Mettine H. A.
Cannegieter, Suzanne C.
van Dijck, Jeroen T. J. M.
Peul, Wilco C.
author_sort van Gent, Jort A. N.
collection PubMed
description BACKGROUND: Traumatic brain injury is associated with high rates of mortality and morbidity. Trauma patients with a coagulopathy have a 10-fold increased mortality risk compared to patients without a coagulopathy. The aim of this study was to identify the incidence of coagulopathy and relate early coagulopathy to clinical outcome in patients with traumatic intracranial hemorrhages. METHODS: Between September 2015 and December 2016, 108 consecutive cranial trauma patients with traumatic intracranial hemorrhages were included in this study. To assess the relationship between patients with a coagulopathy and outcome, a chi-squared test was performed. RESULTS: A total of 29 out of the 108 patients (27%) with a traumatic intracranial hemorrhage developed a coagulopathy within 72 h after admission. Overall, a total of 22 patients (20%) died after admission of which ten were coagulopathic at emergency department presentation. Early coagulopathy in patients with traumatic brain injury is associated with progression of hemorrhagic injury (odds ratio 2.4 (95% confidence interval 0.8–8.0)), surgical intervention (odds ratio 2.8 (95% confidence interval 0.87–9.35)), and increased in-hospital mortality (odds ratio 23.06 (95% confidence interval 5.5–95.9)). CONCLUSION: Patients who sustained a traumatic intracranial hemorrhage remained at risk for developing a coagulopathy until 72 h after trauma. Patients who developed a coagulopathy had a worse clinical outcome than patients who did not develop a coagulopathy.
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spelling pubmed-69826332020-02-06 Coagulopathy after hemorrhagic traumatic brain injury, an observational study of the incidence and prognosis van Gent, Jort A. N. van Essen, Thomas A. Bos, Mettine H. A. Cannegieter, Suzanne C. van Dijck, Jeroen T. J. M. Peul, Wilco C. Acta Neurochir (Wien) Original Article - Brain trauma BACKGROUND: Traumatic brain injury is associated with high rates of mortality and morbidity. Trauma patients with a coagulopathy have a 10-fold increased mortality risk compared to patients without a coagulopathy. The aim of this study was to identify the incidence of coagulopathy and relate early coagulopathy to clinical outcome in patients with traumatic intracranial hemorrhages. METHODS: Between September 2015 and December 2016, 108 consecutive cranial trauma patients with traumatic intracranial hemorrhages were included in this study. To assess the relationship between patients with a coagulopathy and outcome, a chi-squared test was performed. RESULTS: A total of 29 out of the 108 patients (27%) with a traumatic intracranial hemorrhage developed a coagulopathy within 72 h after admission. Overall, a total of 22 patients (20%) died after admission of which ten were coagulopathic at emergency department presentation. Early coagulopathy in patients with traumatic brain injury is associated with progression of hemorrhagic injury (odds ratio 2.4 (95% confidence interval 0.8–8.0)), surgical intervention (odds ratio 2.8 (95% confidence interval 0.87–9.35)), and increased in-hospital mortality (odds ratio 23.06 (95% confidence interval 5.5–95.9)). CONCLUSION: Patients who sustained a traumatic intracranial hemorrhage remained at risk for developing a coagulopathy until 72 h after trauma. Patients who developed a coagulopathy had a worse clinical outcome than patients who did not develop a coagulopathy. Springer Vienna 2019-11-18 2020 /pmc/articles/PMC6982633/ /pubmed/31741112 http://dx.doi.org/10.1007/s00701-019-04111-z Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article - Brain trauma
van Gent, Jort A. N.
van Essen, Thomas A.
Bos, Mettine H. A.
Cannegieter, Suzanne C.
van Dijck, Jeroen T. J. M.
Peul, Wilco C.
Coagulopathy after hemorrhagic traumatic brain injury, an observational study of the incidence and prognosis
title Coagulopathy after hemorrhagic traumatic brain injury, an observational study of the incidence and prognosis
title_full Coagulopathy after hemorrhagic traumatic brain injury, an observational study of the incidence and prognosis
title_fullStr Coagulopathy after hemorrhagic traumatic brain injury, an observational study of the incidence and prognosis
title_full_unstemmed Coagulopathy after hemorrhagic traumatic brain injury, an observational study of the incidence and prognosis
title_short Coagulopathy after hemorrhagic traumatic brain injury, an observational study of the incidence and prognosis
title_sort coagulopathy after hemorrhagic traumatic brain injury, an observational study of the incidence and prognosis
topic Original Article - Brain trauma
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6982633/
https://www.ncbi.nlm.nih.gov/pubmed/31741112
http://dx.doi.org/10.1007/s00701-019-04111-z
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