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Published on: May 16, 2019
Direct Oral Anticoagulants and Concomitant Anti-seizure Medications: A Retrospective, Case-Control Study in a
Eugenia Rota1, Paolo Immovilli2, Irene Pappalardo3
1The Neurology Unit, San Giacomo Hospital, ASL Alessandria, Novi Ligure, Italy.
Direct oral anticoagulants (DOACs) combined with anti-seizure medications (ASMs) like valproic acid (VPA) or levetiracetam (LEV) showed no increased risk of bleeding or clotting events in real-world use. Epilepsy patients on DOACs and ASMs had similar outcomes to those on DOACs alone.
Area of Science:
- Pharmacology
- Neurology
- Clinical Medicine
Background:
- Direct oral anticoagulants (DOACs) are increasingly prescribed for patients with epilepsy on anti-seizure medications (ASMs).
- Guidelines recommend caution due to potential pharmacologic interactions, but clinical evidence is limited.
- Real-world data on the safety and efficacy of DOAC-ASM co-therapy is scarce.
Purpose of the Study:
- To assess the frequency of ischemic/hemorrhagic events and epileptic seizures in patients using DOAC-ASM co-therapy.
- To compare outcomes of DOAC-ASM co-therapy with DOAC monotherapy and ASM monotherapy.
- To evaluate the clinical relevance of potential drug interactions between DOACs and ASMs.
Main Methods:
- A retrospective case-control study design.
- Inclusion of 124 patients on concomitant DOAC and ASM (valproic acid or levetiracetam) therapy for at least 6 months.
- Comparison with age- and gender-matched DOAC-control and ASM-control groups using data from electronic health records.
Main Results:
- The DOAC-ASM co-therapy group experienced 1.6% ischemic and 1.6% major hemorrhagic events.
- The DOAC-control group had 3.2% ischemic events and no hemorrhagic events.
- No statistically significant differences were found in ischemic/hemorrhagic events between the co-therapy and DOAC-control groups, nor in seizure recurrence rates compared to the ASM-control group.
Conclusions:
- Concomitant use of levetiracetam or valproic acid with DOACs did not significantly increase the risk of adverse events in a real-world clinical setting.
- Findings suggest that DOACs can be safely co-administered with these specific ASMs.
- Further research with larger sample sizes is warranted to confirm these results.
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