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The edition · Neurology

Epilepsy on a DOAC: the choice of antiseizure drug was linked to clot, bleed and death risks

A target-trial emulation in 9,529 adults found levetiracetam, valproate and enzyme inducers each carried distinct risks against lamotrigine or lacosamide. Plus a neutral tirofiban trial in branch atheromatous stroke, timing of antiseizure drug withdrawal, and a generic lamotrigine supplement.

The edition in brief

In 9,529 adults with epilepsy taking a direct oral anticoagulant, a target-trial emulation using international electronic health records compared antiseizure monotherapies with lamotrigine or lacosamide. Levetiracetam was associated with more thromboembolic events (HR 1.98) and higher mortality (HR 1.60); strong enzyme inducers with more thromboembolism (HR 1.55) but less major bleeding; valproate with higher mortality (HR 1.49) and more intracranial bleeding (HR 3.01). These are observational associations, but they support favouring lamotrigine or lacosamide when choosing a new antiseizure drug for someone on a DOAC. In the STRATEGY trial of 970 Chinese patients with branch atheromatous disease stroke, adding 24 hours of intravenous tirofiban to aspirin did not reduce early neurological deterioration or new stroke (17.1% vs 19.6%; HR 0.88, 95% CI 0.65–1.19). A meta-analysis of 22 studies found relapse after antiseizure drug withdrawal was more likely with less than five years of seizure freedom (RR 1.49). The FDA recorded a supplement to a generic lamotrigine application on 15 October; no detail of the change is given. The pearl covers lamotrigine titration and its interaction with valproate.

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