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Factors Associated with the Development of Coagulopathy after Open Traumatic Brain Injury

Background: The incidence of coagulopathy after open traumatic brain injury (TBI) is high. Coagulopathy can aggravate intracranial hemorrhage and further increase morbidity and mortality. The purpose of this study was to determine the clinical characteristics of coagulopathy after open TBI and its r...

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Autores principales: Chen, Yuhui, Tian, Jun, Chi, Bin, Zhang, Shangming, Wei, Liangfeng, Wang, Shousen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745860/
https://www.ncbi.nlm.nih.gov/pubmed/35011926
http://dx.doi.org/10.3390/jcm11010185
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author Chen, Yuhui
Tian, Jun
Chi, Bin
Zhang, Shangming
Wei, Liangfeng
Wang, Shousen
author_facet Chen, Yuhui
Tian, Jun
Chi, Bin
Zhang, Shangming
Wei, Liangfeng
Wang, Shousen
author_sort Chen, Yuhui
collection PubMed
description Background: The incidence of coagulopathy after open traumatic brain injury (TBI) is high. Coagulopathy can aggravate intracranial hemorrhage and further increase morbidity and mortality. The purpose of this study was to determine the clinical characteristics of coagulopathy after open TBI and its relationship with the prognosis. Methods: This study retrospectively evaluated patients with isolated open TBI from December 2018 to December 2020. Coagulopathy was defined as international normalized ratio (INR) > 1.2, activated thromboplastin time (APTT) > 35 s, or platelet count <100,000/μL. We compared the relationship between the clinical, radiological, and laboratory parameters of patients with and without coagulopathy, and the outcome at discharge. Logistic regression analysis was used to evaluate the risk factors associated with coagulopathy. We then compared the effects of treatment with and without TXA in open TBI patients with coagulopathy. Results: A total of 132 patients were included in the study; 46 patients developed coagulopathy. Patients with coagulopathy had significantly lower platelet levels (170.5 × 10(9)/L vs. 216.5 × 10(9)/L, p < 0.001), and significantly higher INR (1.14 vs. 1.02, p < 0.001) and APTT (30.5 s vs. 24.5 s, p < 0.001) compared to those with no coagulopathy. A Low Glasgow Coma Scale (GCS) score, high neutrophil/lymphocyte ratio (NLR), low platelet/lymphocyte ratio (PLR), and hyperglycemia at admission were significantly associated with the occurrence of coagulopathy. Conclusions: Coagulopathy often occurs after open TBI. Patients with a low GCS score, high NLR, low PLR, and hyperglycemia at admission are at greater risk of coagulopathy, and therefore of poor prognosis. The efficacy of TXA in open TBI patients with coagulopathy is unclear. In addition, these findings demonstrate that PLR may be a novel indicator for predicting coagulopathy.
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spelling pubmed-87458602022-01-11 Factors Associated with the Development of Coagulopathy after Open Traumatic Brain Injury Chen, Yuhui Tian, Jun Chi, Bin Zhang, Shangming Wei, Liangfeng Wang, Shousen J Clin Med Article Background: The incidence of coagulopathy after open traumatic brain injury (TBI) is high. Coagulopathy can aggravate intracranial hemorrhage and further increase morbidity and mortality. The purpose of this study was to determine the clinical characteristics of coagulopathy after open TBI and its relationship with the prognosis. Methods: This study retrospectively evaluated patients with isolated open TBI from December 2018 to December 2020. Coagulopathy was defined as international normalized ratio (INR) > 1.2, activated thromboplastin time (APTT) > 35 s, or platelet count <100,000/μL. We compared the relationship between the clinical, radiological, and laboratory parameters of patients with and without coagulopathy, and the outcome at discharge. Logistic regression analysis was used to evaluate the risk factors associated with coagulopathy. We then compared the effects of treatment with and without TXA in open TBI patients with coagulopathy. Results: A total of 132 patients were included in the study; 46 patients developed coagulopathy. Patients with coagulopathy had significantly lower platelet levels (170.5 × 10(9)/L vs. 216.5 × 10(9)/L, p < 0.001), and significantly higher INR (1.14 vs. 1.02, p < 0.001) and APTT (30.5 s vs. 24.5 s, p < 0.001) compared to those with no coagulopathy. A Low Glasgow Coma Scale (GCS) score, high neutrophil/lymphocyte ratio (NLR), low platelet/lymphocyte ratio (PLR), and hyperglycemia at admission were significantly associated with the occurrence of coagulopathy. Conclusions: Coagulopathy often occurs after open TBI. Patients with a low GCS score, high NLR, low PLR, and hyperglycemia at admission are at greater risk of coagulopathy, and therefore of poor prognosis. The efficacy of TXA in open TBI patients with coagulopathy is unclear. In addition, these findings demonstrate that PLR may be a novel indicator for predicting coagulopathy. MDPI 2021-12-30 /pmc/articles/PMC8745860/ /pubmed/35011926 http://dx.doi.org/10.3390/jcm11010185 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chen, Yuhui
Tian, Jun
Chi, Bin
Zhang, Shangming
Wei, Liangfeng
Wang, Shousen
Factors Associated with the Development of Coagulopathy after Open Traumatic Brain Injury
title Factors Associated with the Development of Coagulopathy after Open Traumatic Brain Injury
title_full Factors Associated with the Development of Coagulopathy after Open Traumatic Brain Injury
title_fullStr Factors Associated with the Development of Coagulopathy after Open Traumatic Brain Injury
title_full_unstemmed Factors Associated with the Development of Coagulopathy after Open Traumatic Brain Injury
title_short Factors Associated with the Development of Coagulopathy after Open Traumatic Brain Injury
title_sort factors associated with the development of coagulopathy after open traumatic brain injury
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745860/
https://www.ncbi.nlm.nih.gov/pubmed/35011926
http://dx.doi.org/10.3390/jcm11010185
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