# Coagulopathy, injury severity and bleeding progression but not prior antiplatelet and anticoagulation therapies drive prognosis in patients with moderate to severe traumatic brain injury

**Authors:** Franziska Lieschke, Daniel T. Marggrander, Konstantin D. Kohlhase, Daniel Touma, Jan Hendrik Schaefer, Sarah C. Reitz, Juergen Konczalla, Cora R. Schindler, Christian Grefkes, Ferdinand O. Bohmann

PMC · DOI: 10.3389/fneur.2025.1592583 · 2025-07-09

## TL;DR

This study finds that coagulopathy and injury severity, not prior antiplatelet or anticoagulant use, most strongly affect outcomes in traumatic brain injury patients.

## Contribution

The study identifies key predictors of poor outcomes in TBI patients, challenging the role of prior antihemostatic therapies.

## Key findings

- Coagulopathy, injury severity, and bleeding progression predict poor functional outcomes in TBI patients.
- Prior antiplatelet or anticoagulant use is linked to worse mRS scores and higher mortality.
- Tranexamic acid use does not improve outcomes despite being given to more severely injured patients.

## Abstract

Antiplatelet and anticoagulant therapies complicate the management and outcomes of traumatic brain injury (TBI) patients. This study evaluates clinical profiles and short-term outcomes focusing on prior antihemostatic therapy and tranexamic acid (TXA) use.

We analyzed TBI patients admitted to University Hospital Frankfurt (2018–2021), assessing demographics, injury characteristics, clinical course, and short-term outcomes. The primary endpoint was hemorrhage progression; secondary endpoints included the modified Rankin Scale (mRS) at discharge, mortality and thromboembolic complications. Regression models identified predictors of functional outcome and mortality.

Among 218 patients (median age 70 years, 35% female, median GCS at admission 7), 44% had prior antiplatelet or anticoagulation therapy. These patients were older, had higher pre-injury mRS scores, and more often sustained TBIs from falls. While hemorrhage progression was similar, they had worse mRS scores (p = 0.02) and higher mortality (p = 0.002). Coagulopathy (OR 1.11, CI 1.07–1.16, p < 0.001), injury severity (OR 2.25, CI 1.51–3.41, p < 0.001), and bleeding progression (OR 2.23, CI 1.48–3.41, p < 0.001) predicted poor functional outcomes. TXA was more often given to younger, severely injured patients but did not impact outcome.

This study underscores the need for tailored therapeutic approaches to improve survival and functional recovery in patients with pre-injury antiplatelet and anticoagulant therapies.

## Linked entities

- **Chemicals:** tranexamic acid (PubChem CID 5526)
- **Diseases:** traumatic brain injury (MONDO:0858950)

## Full-text entities

- **Diseases:** thromboembolic (MESH:D013923), Coagulopathy (MESH:D001778), injury (MESH:D014947), TBI (MESH:D000070642), bleeding (MESH:D006470)
- **Chemicals:** TXA (MESH:D014148)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12283275/full.md

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Source: https://tomesphere.com/paper/PMC12283275