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Complex partial status epilepticus in children with epilepsy
Kenichi Kikumoto1, Harumi Yoshinaga, Katsuhiro Kobayashi
1Department of Child Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Okayama 700-8558, Japan. kkikumoto@mac.com
Insights
Diagnosing complex partial status epilepticus (CPSE) in children requires careful observation of subtle symptoms and EEG findings. This study clarifies CPSE characteristics in pediatric epilepsy patients.
Area of Science:
- Pediatric Neurology
- Epileptology
- Clinical Neurophysiology
Background:
- Complex partial status epilepticus (CPSE) is frequently underdiagnosed in pediatric populations.
- Understanding the nuances of CPSE presentation in children is crucial for timely diagnosis and management.
Purpose of the Study:
- To elucidate the clinical characteristics and underlying pathophysiology of CPSE in children with epilepsy.
- To improve diagnostic accuracy for CPSE in pediatric patients.
Main Methods:
- Retrospective review of medical records and electroencephalograms (EEGs) from 17 children diagnosed with CPSE.
- Analysis of clinical symptoms, EEG patterns (ictal and postictal), and estimated epileptogenic zones.
Main Results:
- CPSE was diagnosed in children aged 3 months to 17 years, often associated with various epilepsy types.
- Subtle symptoms (autonomic disturbances, altered consciousness) were prominent in many CPSE episodes, sometimes with minor or major motor elements.
- Ictal EEG patterns varied, including spike-dominant and spike/high-voltage slow wave mixes, even with subtle clinical signs. Epileptogenic zones showed variability, with a majority not originating from the temporal lobe.
Conclusions:
- Accurate diagnosis of CPSE in children necessitates close monitoring of subtle clinical symptoms and mild convulsive elements.
- Integration of ictal EEG findings is essential for diagnosing CPSE, especially when clinical presentation is ambiguous.
Purpose:
Complex partial status epilepticus (CPSE) is often under-diagnosed, especially in children. The aim of this study was to clarify the characteristics and pathophysiology of CPSE in children with epilepsy.
Subjects And Methods:
We retrospectively reviewed the medical records and EEGs of 17 children with epilepsy who were diagnosed as having CPSE by ictal or postictal EEGs to investigate clinical and EEG features.
Results:
The ages at diagnosis of CPSE ranged from 3 months to 17 years. At the time of diagnosis of CPSE, 13 patients had symptomatic localization-related epilepsy, two had epilepsy with continuous spike-waves during slow wave sleep, and each patient had cryptogenic localization-related epilepsy and idiopathic localization-related epilepsy. Only subtle symptoms including autonomic ones associated with disturbance of consciousness were the main clinical features in 12 of 44 CPSE episodes. Another 22 episodes showed minor focal motor elements, and the other 10 had major convulsive phase during or immediately before CPSE. Ictal EEGs of CPSE were divided into three types according to the degree of high-voltage slow waves (HVS) and spike components. Ictal EEGs could show spike-dominant or spike and HVS mixed patterns even if patients showed only subtle symptoms. The epileptogenic areas estimated by the ictal or postictal EEGs showed variability with only two cases of temporal origin.
Conclusion:
The close observation of clinical symptoms such as various subtle symptoms and/or mild convulsive elements and ictal EEGs are absolutely needed for the diagnosis of CPSE in children.
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