# Oral anticoagulant reversal and mortality in trauma patients: a multicentre propensity score–matched cohort study

**Authors:** Elodie Lang, Marion Gautier, Jean-Luc Hanouz, Fanny Vardon, Vincent Legros, Gary Duclos, Florent Hericher, Gerard Audibert, Delphine Huet-Garrigue, Paer-Sélim Abback, Benjamin Popoff, Olivier Duranteau, Samy Figueiredo, Pierre-Antoine Allain, Thomas Botrel, Jean Pasqueron, Anne Godier

PMC · DOI: 10.1016/j.eclinm.2025.103577 · 2025-10-16

## TL;DR

This study finds that preinjury use of oral anticoagulants increases trauma mortality, but following guidelines to reverse their effects can significantly reduce this risk without causing more blood clots.

## Contribution

The study demonstrates that guideline-concordant reversal of oral anticoagulants reduces trauma mortality without increasing thrombotic risk, emphasizing the need for systematic implementation of reversal strategies.

## Key findings

- Preinjury oral anticoagulant therapy is independently associated with increased trauma mortality, particularly with vitamin K antagonists.
- Guideline-concordant reversal of anticoagulants significantly reduces mortality at both day 1 and day 7 post-trauma.
- There is no significant association between anticoagulant reversal and thrombotic complications.

## Abstract

Oral anticoagulant (OAC) therapy increases bleeding risk but its impact on trauma outcomes and the benefit of reversal remains uncertain. This study aimed to evaluate 1/the effect of preinjury OAC therapy on trauma mortality and 2/the protective role of OAC reversal and its associated thrombotic risk.

We conducted an observational study using a prospective multicenter trauma registry between January 2012 and December 2023. OAC-treated patients were matched with non-OAC-treated patients using a propensity score. Univariable and multivariable logistic regressions assessed associations between OAC therapy and day 1 and day 7 mortality. The effect of guideline-concordant OAC reversal was evaluated. Thrombotic complications were recorded.

Of the 27,426 trauma patients, 3% were OAC-treated. They were older, had more comorbidities, and experienced higher mortality. After matching (n = 2196), OAC therapy remained independently associated with increased mortality (day 1: OR 2·21, 95% CI [1·41–3·43]; day 7: OR 2·06, [1·41–3·00]), with greater risk from vitamin K antagonists (VKA) than direct oral anticoagulants (DOAC). Guideline-concordant OAC reversal, achieved only in 21% of cases, independently reduced mortality at day 1 (OR 0·10, 95% CI [0·03–0·31], p < 0·01) and day 7 (OR 0·51, 95% CI [0·22–0·97], p < 0·01). No significant association was found between reversal and thrombotic complications.

Preinjury OAC therapy substantially increased trauma mortality, particularly with VKA. Guideline-concordant reversal was associated with reduced mortality in both VKA- and DOAC-treated patients without excess thrombotic risk but remains underused. These findings emphasise the urgent need for systematic implementation of reversal strategies in OAC-treated trauma patients.

The Traumabase registry is funded by several Regional Health Agencies (Agences Régionales de Santé, ARS): ARS Île-de-France, ARS Occitanie, ARS Grand Est, 10.13039/501100014160ARS Hauts-de-France, and ARS Auvergne-Rhône-Alpes. The registry is also funded by the French Road Safety Observatory—Road Safety Delegation Service (Observatoire National Interministériel de la Sécurité Routière—Délégation à la Sécurité Routière).

## Full-text entities

- **Diseases:** trauma (MESH:D014947), Thrombotic (MESH:D013927), bleeding (MESH:D006470)
- **Chemicals:** DOAC (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12554126/full.md

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Source: https://tomesphere.com/paper/PMC12554126