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Risk factors for status epilepticus in children with symptomatic epilepsy
G Novak1, J Maytal, A Alshansky
1Division of Neurology, Schneider Children's Hospital, New Hyde Park, NY 11040, USA.
Insights
Identifying risk factors for status epilepticus (SE) in children with symptomatic epilepsy is crucial. Focal background EEG abnormalities, partial seizures with secondary generalization, first seizure as SE, and neuroimaging abnormalities independently predict higher SE risk.
Area of Science:
- Pediatric Neurology
- Epileptology
Background:
- Status epilepticus (SE) is a neurological emergency in children.
- Identifying risk factors for SE in children with symptomatic epilepsy is essential for targeted prevention and management.
Purpose of the Study:
- To determine independent risk factors for status epilepticus (SE) in children with symptomatic epilepsy.
Main Methods:
- Retrospective case-control study.
- Matched 44 children with symptomatic epilepsy and SE to 88 controls without SE.
- Reviewed medical records for clinical and EEG data, and neuroimaging findings.
Main Results:
- Four independent predictors of SE risk were identified: focal background EEG abnormalities (OR=6.51), partial seizures with secondary generalization (OR=4.61), first seizure as SE (OR=3.99), and generalized neuroimaging abnormalities (OR=2.85).
- No significant differences were found in epilepsy etiology, age at onset, polypharmacy, or subtherapeutic antiepileptic drug levels.
- A trend suggested increased phenobarbital use in SE patients (p=0.057).
Conclusions:
- Focal background EEG abnormalities, partial seizures with secondary generalization, initial seizure as SE, and generalized neuroimaging abnormalities are significant independent predictors of SE risk in children with symptomatic epilepsy.
- These findings aid in identifying high-risk children who may benefit from closer monitoring and tailored treatment strategies.
Abstract:
The purpose of this study was to determine risk factors for status epilepticus (SE) in children with symptomatic epilepsy through a retrospective case-control study. Patients (44 children with a prior diagnosis of symptomatic epilepsy experiencing one or more episodes of SE between January 1, 1991, and June 1, 1995) were matched for age at follow-up to controls (88 children with symptomatic epilepsy without SE during that interval) and medical records were reviewed. Patients and controls did not differ in etiology or in age at epilepsy onset (1 year 5 months [SD, 2 years 3 months] versus 1 year 3 months [SD, 1 year 5 months]). Univariate analysis revealed significant associations between SE and several factors, including history of a first seizure as SE, partial epilepsy, partial seizures with secondary generalization, focal paroxysmal abnormalities and focal background abnormalities on EEG, and generalized abnormalities on neuroimaging. Groups did not differ in the proportion of patients on polypharmacy or with subtherapeutic serum antiepileptic drug levels, but there was a trend for greater use of phenobarbital in patients (57% versus 38%, odds ratio (OR) = 2.6, p = 0.057). With multiple logistic regression, four factors emerged as independent predictors of SE risk: focal background EEG abnormalities (OR = 6.51, p = 0.0005), partial seizures with secondary generalization (OR = 4.61, p = 0.0021), first seizure as SE (OR = 3.99, p = 0.034), and generalized abnormalities on neuroimaging (OR = 2.85, p = 0.034). These four factors are indicators of a higher risk of SE in children with symptomatic epilepsy.