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Updated: Jan 26, 2026

Robotic-Guided Stereoelectroencephalography for Invasive Epilepsy Monitoring
Published on: June 13, 2025
Insights
Childhood neurocognitive impairment in epilepsy significantly increases mortality risk over 50 years. Lower cognitive function also reduces the likelihood of achieving complete seizure remission.
Area of Science:
- Neurology
- Pediatrics
- Epilepsy Research
Background:
- Childhood-onset epilepsy can have long-term consequences beyond seizures.
- Neurocognitive function is a critical aspect of development and long-term outcomes.
Purpose of the Study:
- To investigate the association between childhood neurocognitive impairment and long-term mortality.
- To examine the relationship between childhood neurocognitive status and complete seizure remission over 50 years.
Main Methods:
- A population-based cohort of 245 individuals with childhood-onset epilepsy was followed for up to 50 years.
- Neurocognition was assessed using IQ scores and functional criteria before age 18.
- Mortality and 10-year terminal seizure remission were analyzed using Cox regression.
Main Results:
- 49% had normal childhood neurocognition, 51% had impairment.
- Mortality was significantly higher in those with impaired neurocognition (44%) compared to normal (13%).
- Increased neurocognitive impairment correlated with higher mortality risk and lower rates of seizure remission.
Conclusions:
- Severity of childhood neurocognitive impairment is directly associated with increased long-term mortality risk.
- Impaired neurocognition in childhood epilepsy is linked to a reduced chance of achieving complete seizure remission.
- Normal neurocognition does not preclude premature death or guarantee seizure remission in all individuals.
Abstract:
Neurocognition in Childhood Epilepsy: Impact on Mortality and Complete Seizure Remission 50 Years Later Sillanpää M, Saarinen MM, Karrasch M, Schmidt D, Hermann BP. Epilepsia. 2019;60(1):131-138. doi:10.1111/epi.14606. Epub 2018 Nov 22.
Objective:
To study associations of the severity of impairment in childhood neurocognition (NC) with long-term mortality and complete seizure remission.
Methods:
A population-based cohort of 245 subjects with childhood-onset epilepsy was followed up for 50 years (median = 45, range = 2-50). Childhood NC before age 18 years was assessed as a combination of formal intelligence quotient scores and functional criteria (school achievement, working history, and psychoneurological development). Impaired NC was categorized with respect to definitions of intellectual functioning in International Classification of Diseases, Tenth Revision (R41.83, F70-F73). The outcome variables, defined as all-cause mortality and 10-year terminal remission with the 5 past years off medication (10YTR), were analyzed with Cox regression models.
Results:
Of the 245 subjects, 119 (49%) had normal childhood NC, whereas 126 (51%) had various degrees of neurocognitive impairment. During the 50-year observation period, 71 (29%) of the subjects died, 13% of those with normal and 44% of those with impaired NC. The hazard of death increased gradually in line with more impaired cognition, reaching significance in moderate, severe, and profound impairment versus normal NC (hazard ratio [Bonferroni corrected 95% confidence interval] = 3.3 [1.2-9.2], 4.2 [1.2-14.2], and 5.5 [2.4-12.3], respectively). The chance for 10YTR was highest among subjects with normal NC (61%), whereas none of those with profound impairment reached 10YTR. In the intermediate categories, the chance was, however, not directly related to the increasing severity of impairment.
Significance:
The severity of neurocognitive impairment during childhood shows a parallel increase in the risk of death. In comparison with normal NC, subjects with lower childhood NC are less likely to enter seizure remission. However, normal NC does not guarantee complete remission or prevent premature death in some individuals with childhood-onset epilepsy.
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