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Risk and causes of death in children with a seizure disorder
Victoria Nesbitt1, Martin Kirkpatrick, Gale Pearson
1Institute of Ageing and Health, Newcastle University, Newcastle upon Tyne, UK.
Insights
Childhood epilepsy increases death risk, primarily in those with neurodevelopmental disorders. The risk of sudden unexplained death in children with idiopathic epilepsy is very low.
Area of Science:
- Pediatric Neurology
- Epileptology
- Public Health
Background:
- Epilepsy is a common childhood neurological disorder.
- Understanding mortality patterns in pediatric epilepsy is crucial for risk assessment and management.
- Previous studies have varied in scope and population.
Purpose of the Study:
- To determine the incidence and causes of death in children with epilepsy.
- To evaluate the role of seizure disorders in pediatric mortality.
- To compare sudden unexplained death rates in children with and without epilepsy.
Main Methods:
- Retrospective analysis of clinical and death certificate data.
- Inclusion of two UK population-based samples of children (1 month to 18 years) with epilepsy.
- Largest reported series of pediatric epilepsy deaths (n=265).
Main Results:
- Seizure disorders were not the primary cause of death in approximately two-thirds of cases.
- Unexplained death rates ranged from 7.3% to 9.7%, exclusively in children with symptomatic epilepsy.
- No unexplained deaths occurred in children with idiopathic epilepsy.
- Acute symptomatic seizures were implicated in the final illness of 4% of deaths.
Conclusions:
- Childhood epilepsy is linked to higher mortality, mainly in those with co-occurring neurodevelopmental disorders.
- The risk of unexpected, unexplained death in pediatric idiopathic epilepsy is minimal.
- Risk stratification should consider underlying epilepsy etiology and associated conditions.
Aim:
To describe the frequency and causes of death in children with epilepsy, ascertain the contribution of seizure disorder to cause of death, and compare with rates of sudden unexplained death in children without epilepsy.
Method:
This study was a retrospective review of clinical and death certificate records. It examined two UK population-based samples of deaths in children with epilepsy from 1 month to 18 years, together comprising the largest reported series of deaths in children with epilepsy (n=265).
Results:
In approximately two-thirds, the death was not due to the seizure disorder. Rates of unexplained death were similar in the two samples at 7.3% and 9.7%: all were in children with symptomatic or presumed symptomatic epilepsy. There were no unexplained deaths in the children with idiopathic epilepsy. Four per cent of the deaths were of children experiencing acute symptomatic seizures as part of their final illness. The risk of unexpected, unexplained death in children with idiopathic epilepsy is not more than 65 per 100,000 child-years.
Interpretation:
Epilepsy is associated with an increased risk of death in childhood but this risk is almost entirely confined to those with an associated neurodevelopmental disorder. The risk of unexpected, unexplained death in children with idiopathic epilepsy is extremely small.
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