Electrographic Seizures and Predictors of Epilepsy after Pediatric Arteriovenous Malformation Rupture

Julia S Keenan1, Dana B Harrar2, Claire Har1

  • 1Division of Epilepsy and Neurophysiology, Children's National Hospital, Washington, DC; Department of Neurology, Children's National Hospital, Washington, DC.

The Journal of Pediatrics
|September 29, 2024
PubMed

Insights

Electroencephalogram (EEG)-confirmed seizures are infrequent after arteriovenous malformation (AVM) rupture causing intracerebral hemorrhage (ICH). However, patients experiencing remote seizures (over 30 days post-rupture) face a higher risk of developing epilepsy.

Area of Science:

  • Neurology
  • Neurosurgery
  • Pediatric Intensive Care

Background:

  • Intracerebral hemorrhage (ICH) resulting from arteriovenous malformation (AVM) rupture can lead to seizures and epilepsy.
  • Predicting epilepsy development in these patients is crucial for timely intervention.

Purpose of the Study:

  • To identify clinical and electroencephalogram (EEG) predictors of epilepsy in pediatric patients following ICH due to AVM rupture.
  • To determine the incidence of electrographic seizures and epilepsy development in this cohort.

Main Methods:

  • Retrospective review of pediatric patients with ICH secondary to AVM rupture over 11 years.
  • Analysis of clinical variables, seizure types (acute, subacute, remote), and EEG findings.
  • Assessment of outcomes including mortality and epilepsy development post-discharge.

Main Results:

  • Sixteen percent of patients developed epilepsy, with a median diagnosis time of 1.34 years post-rupture.
  • Remote seizures (occurring >30 days after AVM rupture) were significantly associated with epilepsy development (P < .001).
  • Acute symptomatic seizures (<7 days post-rupture) did not predict epilepsy (P = .16).

Conclusions:

  • EEG-confirmed seizures are uncommon but can indicate a high seizure burden in patients with ICH secondary to AVM rupture.
  • The occurrence of remote seizures is a key predictor for the subsequent development of epilepsy in this population.
Abstract