Paroxysmal non-epileptic events in children: a retrospective study over a period of 10 years
A M Bye1, D J Kok, F T Ferenschild
1Department of Neurology, Sydney Children's Hospital, Randwick, New South Wales, Australia. A.Bye@unsw.edu.au
Insights
Video electroencephalogram (EEG) monitoring accurately diagnoses paroxysmal non-epileptic events in children. This study identified common non-epileptic events and their characteristics, aiding differential diagnosis.
Area of Science:
- Pediatric Neurology
- Clinical Neurophysiology
Background:
- Paroxysmal non-epileptic events (PNEs) in children can mimic epileptic seizures, leading to diagnostic challenges.
- Accurate differentiation is crucial for appropriate management and treatment.
Purpose of the Study:
- To determine the frequency, nature, and clinical characteristics of PNEs in children.
- To evaluate the utility of video electroencephalogram (EEG) monitoring in diagnosing PNEs.
Main Methods:
- Retrospective analysis of 666 children aged 2 weeks to 17 years undergoing video EEG monitoring over a 10-year period.
- Review of telemetry files, medical charts, video recordings, and record sheets.
Main Results:
- 285 children had confirmed non-epileptic events; 269 had epileptic events; 112 had no events recorded.
- Common PNE subgroups included staring spells (34%), sleep phenomena (15%), arousals (13%), motor tics (11%), and shuddering (7%).
- Developmental delay was noted in 43% of children with PNEs, and 40% had a co-existing epilepsy diagnosis. An epileptiform interictal EEG was observed in 24% of the total sample.
Conclusions:
- PNEs can be misdiagnosed, especially in children with developmental delay, epilepsy, or epileptiform EEG findings.
- Video EEG monitoring is highly effective, achieving a specific diagnosis in 96% of PNE cases.
Objective:
To determine the frequency, nature and clinical characteristics of paroxysmal non-epileptic events in children diagnosed by video electroencephalogram (EEG) monitoring at a tertiary referral centre.
Methodology:
A retrospective study of children with paroxysmal non-epileptic events, aged 2 weeks to 17 years inclusive was undertaken. The study group consisted of children who had video EEG monitoring during a 10-year period (1988-99). Telemetry files, medical charts, events recorded on video and record sheets were reviewed.
Results:
A total of 666 children were analysed, 269 had epileptic events recorded, 285 had non-epileptic events and 112 had no events recorded. In children with non-epileptic events, 43% were developmentally delayed, 25% had an abnormal neurological examination and 40% had epilepsy. In the study sample an epileptiform interictal EEG was common (24%). The major subgroups of non-epileptic events were: staring (34%), sleep phenomena - benign sleep myoclonus (15%), arousals (13%), motor tics (11%) and shuddering (7%). Developmental delay (57%) was common in children who presented with staring spells. A diagnosis of a specific non-epileptic event was reached in 96% of cases.
Conclusion:
Paroxysmal non-epileptic events can cause diagnostic confusion, particularly in children with developmental delay, epilepsy or an epileptiform EEG. Accurate diagnosis can be reached in the majority of cases using video EEG monitoring.
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