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Aneurysmal Subarachnoid Hemorrhage in Hospitalized Patients on Anticoagulants-A Two Center Matched Case-Control Study
Michael Veldeman1,2, Tobias Rossmann1,3, Miriam Weiss2,4
1Department of Neurosurgery, University of Helsinki and Helsinki University Hospital, 00260 Helsinki, Finland.
Insights
Direct oral anticoagulants (DOAC) and vitamin K antagonists (VKA) did not worsen outcomes in patients with subarachnoid hemorrhage (SAH). This study found no increased severity or poor clinical outcomes associated with these anticoagulants in SAH patients.
Area of Science:
- Neurology
- Cardiology
- Pharmacology
Background:
- Direct oral anticoagulants (DOAC) and vitamin K antagonists (VKA) are increasingly used for thromboembolism prevention.
- Their impact on patients with aneurysmal subarachnoid hemorrhage (SAH) requires investigation.
Purpose of the Study:
- To assess the effect of prior DOAC and VKA treatment on SAH severity and patient outcomes.
- To compare outcomes of anticoagulant-treated SAH patients with matched controls.
Main Methods:
- Retrospective analysis of consecutive SAH patients from two university hospitals.
- Comparison of DOAC- and VKA-treated patients with age- and sex-matched SAH controls.
- Assessment of SAH severity using modified Fisher grading and outcomes via Glasgow Outcome Scale at 6 months.
Main Results:
- Nine patients were on DOAC and 15 on VKA at the time of aneurysm rupture, matched with controls.
- No significant difference in poor-grade SAH (WFNS4-5) between DOAC/VKA groups and controls.
- Neither DOAC nor VKA treatment was independently associated with unfavorable outcomes (GOS 1-3) at 12 months.
Conclusions:
- Iatrogenic coagulopathy from DOAC or VKA was not linked to increased SAH severity.
- Prior DOAC or VKA treatment did not correlate with worse clinical outcomes in hospitalized SAH patients.
Abstract:
Objective-Direct oral anticoagulants (DOAC) are replacing vitamin K antagonists (VKA) for the prevention of ischemic stroke and venous thromboembolism. We set out to assess the effect of prior treatment with DOAC and VKA in patients with aneurysmal subarachnoid hemorrhage (SAH). Methods-Consecutive SAH patients treated at two (Aachen, Germany and Helsinki, Finland) university hospitals were considered for inclusion. To assess the association between anticoagulant treatments on SAH severity measure by modified Fisher grading (mFisher) and outcome as measured by the Glasgow outcome scale (GOS, 6 months), DOAC- and VKA-treated patients were compared against age- and sex-matched SAH controls without anticoagulants. Results-During the inclusion timeframes, 964 SAH patients were treated in both centers. At the time point of aneurysm rupture, nine patients (0.93%) were on DOAC treatment, and 15 (1.6%) patients were on VKA. These were matched to 34 and 55 SAH age- and sex-matched controls, re-spectively. Overall, 55.6% of DOAC-treated patients suffered poor-grade (WFNS4-5) SAH compared to 38.2% among their respective controls (p = 0.35); 53.3% of patients on VKA suffered poor-grade SAH compared to 36.4% in their respective controls (p = 0.23). Neither treatment with DOAC (aOR 2.70, 95%CI 0.30 to 24.23; p = 0.38), nor VKA (aOR 2.78, 95%CI 0.63 to 12.23; p = 0.18) were inde-pendently associated with unfavorable outcome (GOS1-3) after 12 months. Conclusions-Iatrogenic coagulopathy caused by DOAC or VKA was not associated with more severe radiological or clinical subarachnoid hemorrhage or worse clinical outcome in hospitalized SAH patients.
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