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Global Characterisation of Coagulopathy in Isolated Traumatic Brain Injury (iTBI): A CENTER-TBI Analysis

Abstract:
Background - Trauma-induced coagulopathy in patients with traumatic brain injury (TBI) is associated with high rates of complications, unfavourable outcomes and mortality. The mechanism of the development of TBI-associated coagulopathy is poorly understood. Methods - This analysis, embedded in the prospective, multi-centred, observational Collaborative European NeuroTrauma Effectiveness Research in Traumatic Brain Injury (CENTER-TBI) study, aimed to characterise the coagulopathy of TBI. Emphasis was placed on the acute phase following TBI, primary on subgroups of patients with abnormal coagulation profile within 4 h of admission, and the impact of pre-injury anticoagulant and/or antiplatelet therapy. In order to minimise confounding factors, patients with isolated TBI (iTBI) (n = 598) were selected for this analysis. Results - Haemostatic disorders were observed in approximately 20% of iTBI patients. In a subgroup analysis, patients with pre-injury anticoagulant and/or antiplatelet therapy had a twice exacerbated coagulation profile as likely as those without premedication. This was in turn associated with increased rates of mortality and unfavourable outcome post-injury. A multivariate analysis of iTBI patients without pre-injury anticoagulant therapy identified several independent risk factors for coagulopathy which were present at hospital admission. Glasgow Coma Scale (GCS) less than or equal to 8, base excess (BE) less than or equal to − 6, hypothermia and hypotension increased risk significantly. Conclusion - Consideration of these factors enables early prediction and risk stratification of acute coagulopathy after TBI, thus guiding clinical management
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1007/s12028-020-01151-7

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Role:
Author
ORCID:
0000-0003-4885-0832
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Role:
Author
ORCID:
0000-0001-9782-7255


Publisher:
Springer
Journal:
Neurocritical Care More from this journal
Volume:
35
Issue:
1
Pages:
184-196
Publication date:
2020-12-11
DOI:
EISSN:
1556-0961
ISSN:
1541-6933


Language:
English
Keywords:
Pubs id:
1148840
Local pid:
pubs:1148840
Source identifiers:
W3110934237
Deposit date:
2026-02-12
ARK identifier:
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