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Published on: April 5, 2011
Convulsive status epilepticus in children
1Florence Miller Neuropediatric Unit, Shaare Zedek Hospital, Jerusalem, Israel.
Insights
Pediatric status epilepticus (SE) is common, but outcomes have improved significantly. Most children, especially those without prior neurological issues, experience favorable prognoses with rare long-term effects.
Area of Science:
- Pediatric Neurology
- Epileptology
- Clinical Pediatrics
Background:
- Status epilepticus (SE) is a common neurological emergency in infants and children.
- Children with pre-existing neurological abnormalities are at higher risk.
- Over 90% of pediatric SE cases are convulsive and generalized.
Purpose of the Study:
- To review the epidemiology, etiology, and outcomes of status epilepticus in children.
- To assess the impact of SE on neurological sequelae and recurrence risk.
- To highlight recent trends in pediatric SE morbidity and mortality.
Main Methods:
- Review of recent pediatric series on status epilepticus.
- Analysis of SE etiology, including idiopathic, febrile, and symptomatic causes.
- Evaluation of mortality rates, neurological sequelae, and recurrence risks based on patient history and SE type.
Main Results:
- Pediatric SE mortality has declined to 3-10%, primarily in cases with severe CNS insults or progressive disorders.
- Neurological sequelae are rare in children with idiopathic or febrile SE.
- Recurrence risk is high (approx. 50%) in neurologically abnormal children but low in normal children.
Conclusions:
- The prognosis for pediatric status epilepticus is generally favorable, particularly in neurologically normal children.
- Advances in therapy and the immature brain's resilience contribute to positive outcomes.
- Understanding risk factors is crucial for managing SE and preventing recurrence in pediatric populations.
Abstract:
Status epilepticus (SE) occurs most commonly in infancy and childhood. Children with prior neurological abnormalities are most susceptible. More than 90% of cases are convulsive and the majority are generalized. SE may occur in the setting of an acute illness, in patients with established epilepsy or as a first unprovoked seizure. The etiology can be classified as idiopathic, remote symptomatic, febrile, acute symptomatic, or associated with a progressive encephalopathy. The morbidity and mortality of status have dramatically declined in recent years. Overall mortality in recent pediatric series was 3-10%, with almost all fatalities associated with acute central nervous system insults or progressive neurologic disorders. Neurological sequelae in children with idiopathic or febrile status are rare. Neurologically normal children with SE as their first unprovoked seizure have the same risk of experiencing subsequent seizures of any type as children who present with a brief first seizure. The risk of recurrent episodes of convulsive SE approaches 50% in neurologically abnormal children but is very low in neurologically normal children. The favorable outcome of SE in children may be related to advances in therapy and to the resistance of the immature brain to damage from seizures.
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