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Electrographic seizures after convulsive status epilepticus in children and young adults: a retrospective multicenter
Iván Sánchez Fernández1, Nicholas S Abend2, Daniel H Arndt3
1Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA; Department of Child Neurology, Hospital Sant Joan de Déu, Universidad de Barcelona, Barcelona, Spain.
Insights
One-third of children with convulsive status epilepticus (CSE) experienced electrographic seizures, with some having seizures not visible clinically. Prior epilepsy diagnosis and epileptiform discharges predict these seizures.
Area of Science:
- Pediatric Neurology
- Epileptology
- Clinical Neurophysiology
Background:
- Convulsive status epilepticus (CSE) is a medical emergency in children.
- The occurrence and predictors of electrographic seizures following CSE are not well-defined.
Purpose of the Study:
- To determine the prevalence and characteristics of electrographic seizures after CSE in children.
- To identify predictors and clinical outcomes associated with post-CSE electrographic seizures.
Main Methods:
- Multicenter retrospective study involving children aged 1 month to 21 years.
- Continuous electroencephalographic (EEG) monitoring was performed after CSE.
- Clinical and EEG data were analyzed to identify electrographic seizures and associated factors.
Main Results:
- Electrographic seizures occurred in 33% of 98 children following CSE.
- Electrographic-only seizures were present in 34.4% of those with electrographic seizures.
- Predictors included a prior epilepsy diagnosis (P=.029) and interictal epileptiform discharges (P<.0005).
- Children with electrographic seizures had longer PICU stays (9.5 vs 2 days, P=.0001).
Conclusions:
- Approximately one-third of children with CSE develop electrographic seizures, some without clinical manifestations.
- A history of epilepsy and interictal epileptiform discharges are significant risk factors.
- The findings highlight the importance of continuous EEG monitoring in children post-CSE.
Objective:
To describe the prevalence, characteristics, and predictors of electrographic seizures after convulsive status epilepticus (CSE).
Study Design:
This was a multicenter retrospective study in which we describe clinical and electroencephalographic (EEG) features of children (1 month to 21 years) with CSE who underwent continuous EEG monitoring.
Results:
Ninety-eight children (53 males) with CSE (median age of 5 years) underwent subsequent continuous EEG monitoring after CSE. Electrographic seizures (with or without clinical correlate) were identified in 32 subjects (33%). Eleven subjects (34.4%) had electrographic-only seizures, 17 subjects (53.1%) had electroclinical seizures, and 4 subjects (12.5%) had an unknown clinical correlate. Of the 32 subjects with electrographic seizures, 15 subjects (46.9%) had electrographic status epilepticus. Factors associated with the occurrence of electrographic seizures after CSE were a previous diagnosis of epilepsy (P = .029) and the presence of interictal epileptiform discharges (P < .0005). The median (p25-p75) duration of stay in the pediatric intensive care unit was longer for children with electrographic seizures than for children without electrographic seizures (9.5 [3-22.5] vs 2 [2-5] days, Wilcoxon test, Z = 3.916, P = .0001). Four children (4.1%) died before leaving the hospital, and we could not identify a relationship between death and the presence or absence of electrographic seizures.
Conclusions:
After CSE, one-third of children who underwent EEG monitoring experienced electrographic seizures, and among these, one-third experienced entirely electrographic-only seizures. A previous diagnosis of epilepsy and the presence of interictal epileptiform discharges were risk factors for electrographic seizures.
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