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Status epilepticus in children with epilepsy: Dutch study of epilepsy in childhood
Hans Stroink1, Ada T Geerts1, Cees A Van Donselaar1
1Department of Neurology, St. Elisabeth Hospital and TweeSteden Hospital, TilburgDepartment of Pediatric Neurology, Erasmus MC/Sophia Children's Hospital, RotterdamDepartment of Neurology, Medical Center Rijnmond-South, RotterdamDepartment of Pediatric Neurology, University Medical Center, UtrechtDepartment of Pediatric Neurology, University Medical Center, GroningenDepartment of Pediatric Neurology, Juliana Children's Hospital, The Hague, The Netherlands.
Insights
Status epilepticus (SE) in children with epilepsy does not significantly worsen outcomes or mortality. However, SE indicates underlying disease severity and is linked to poorer prognosis, especially when occurring after initial diagnosis.
Area of Science:
- Pediatric Neurology
- Epileptology
- Clinical Neuroscience
Background:
- Status epilepticus (SE) is a critical neurological emergency.
- Understanding the long-term course and outcomes of epilepsy following SE in children is crucial for prognosis.
- The presenting sign or occurrence during the course of epilepsy may influence outcomes.
Purpose of the Study:
- To investigate the course and outcome of epilepsy in children who experienced status epilepticus (SE).
- To compare outcomes for children with SE as a presenting sign versus those with SE after epilepsy diagnosis.
- To identify factors influencing prognosis in pediatric epilepsy with SE.
Main Methods:
- Prospective follow-up of 494 children (1 month–15 years) with newly diagnosed epilepsy for 5 years.
- Analysis of outcomes, including terminal remission and intractable epilepsy, for children with and without SE.
- Identification of independent factors associated with SE at presentation and during the course of epilepsy.
Main Results:
- Of 494 children, 47 experienced SE; 41 had SE at diagnosis, with 32 experiencing it as their first seizure.
- Terminal remission at 5 years was not significantly worse for children with SE at presentation (31.7% vs. 21.2%).
- SE recurrence occurred in 32% of children with SE at diagnosis; children with SE after diagnosis had a worse prognosis.
Conclusions:
- While SE at presentation doesn't significantly worsen epilepsy outcomes or mortality, it indicates underlying disease severity.
- Children experiencing SE during their epilepsy course face a worse prognosis and higher SE recurrence rates.
- Etiology and epilepsy type are key prognostic factors, with SE often being an indicator of disease severity.
Purpose:
To study course and outcome of epilepsy in children having had a status epilepticus (SE) as the presenting sign or after the diagnosis.
Methods:
A total of 494 children with newly diagnosed epilepsy, aged 1 month through 15 years, were followed prospectively for 5 years.
Results:
A total of 47 Children had SE. Forty-one of them had SE when epilepsy was diagnosed. For 32 (78%), SE was the first seizure. SE recurred in 13 out of 41 (32%). Terminal remission at 5 years (TR5) was not significantly worse for these 41 children: 31.7% had a TR5 <1 year versus 21.2% of 447 children without SE. They were not more often intractable. Five out of six children with first SE after diagnosis had a TR5 <1 year. Mortality was not significantly increased for children with SE. Independent factors associated with SE at presentation were remote symptomatic and cryptogenic etiology, and a history of febrile convulsions. Children with first SE after inclusion more often had symptomatic etiology.
Conclusions:
Although we find a trend for shorter TR5 in children with SE at presentation, outcome and mortality are not significantly worse. Etiology is an important factor for prognosis. Children with SE during the course of their epilepsy have a worse prognosis and a high recurrence rate of SE. This outcome is not due to the SE itself, but related to the etiology and type of epilepsy. The occurrence of SE is just an indicator of the severity of the disease.
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