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Childhood Absence Epilepsy with Coexisting Centrotemporal Spikes: Frequency, Electroclinical Course and Prognosis
Maria Augusta Montenegro1, Shifteh Sattar2, Mark Nespeca2
1Department of Neurosciences, Rady Children Hospital, University of California San Diego, United States; Yale University, Department of Pediatrics / Neurology.
Insights
Centrotemporal spikes occur in 9% of childhood absence epilepsy (CAE) patients. Seizures are well-controlled with medication, and outcomes are excellent, even if EEG spikes persist.
Area of Science:
- Neurology
- Pediatric Epilepsy
- Clinical Neurophysiology
Background:
- Childhood absence epilepsy (CAE) is a common epilepsy syndrome in children.
- The presence of centrotemporal spikes in CAE is not well-characterized.
- Understanding this EEG finding's impact on CAE course and prognosis is crucial.
Purpose of the Study:
- To determine the frequency of centrotemporal spikes in CAE patients.
- To evaluate the electroclinical course and prognosis of CAE with centrotemporal spikes.
- To investigate the relationship between EEG findings and treatment response.
Main Methods:
- Retrospective chart review of patients diagnosed with CAE.
- Inclusion criteria: seizure onset < 10 years old.
- Exclusion criteria: developmental delay, abnormal EEG background, atypical seizures, or other epilepsy types.
Main Results:
- 276 patients with CAE were analyzed; 9% exhibited centrotemporal spikes.
- Absence seizures were controlled in all patients treated with antiseizure medication (ASM).
- Generalized epileptiform discharges remitted in 95.5% with ASM, but centrotemporal spikes persisted in 59%.
Conclusions:
- Centrotemporal spikes are an EEG trait in 9% of CAE patients, not indicative of focal seizures.
- Excellent seizure control and prognosis are achieved with ASM, irrespective of persistent centrotemporal spikes.
- Remission of generalized discharges correlates with ASM treatment, highlighting effective management strategies.
Objective:
The objective of this study was to evaluate the frequency, electroclinical course and prognosis of patients with CAE that also present with centrotemporal spikes.
Methods:
This was a retrospective study based on chart review. Patients with diagnosis of CAE and seizure onset < 10 years-old were included. Patients with developmental delay, abnormal EEG background, atypical absence, generalized tonic-clonic, myoclonic or eyelid myoclonic seizures were excluded.
Results:
276 patients with CAE were included; 25 (9%) had at least one EEG showing centrotemporal spikes. Age of absence seizure onset ranged from 3 to 10 years-old (mean = 6 years-old). Absence seizures were controlled in all patients treated with antiseizure medication (ASM). CAE evolved to other type of idiopathic generalized epilepsy in four (16%) patients. No patient had generalized tonic-clonic seizures, except those with evolution to other type of idiopathic generalized epilepsy. No patient had focal seizures. Remission of the generalized epileptiform discharges correlated with ASM treatment in 95.5% of the patients, whereas centrotemporal epileptiform discharges persisted in 59%. Follow-up ranged from 1 to 16 years (mean = 6 years; median = 6 years).
Conclusion:
Centrotemporal spikes were identified in 9% of patients with CAE. Focal seizures were not seen, suggesting that it reflects an EEG trait. Remission of the generalized epileptiform discharges correlates with ASM treatment and seizure outcome is excellent, despite persistence of centrotemporal spikes.
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