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Long-term prognosis in childhood epilepsy: survival and seizure prognosis
Insights
Children with active epilepsy had their prognosis assessed over 12 years. Neurodevelopmental deficits, frequent, and varied seizures negatively impacted long-term seizure remission in pediatric epilepsy patients.
Area of Science:
- Pediatric Neurology
- Epileptology
- Clinical Epidemiology
Background:
- Active epilepsy in children presents a significant challenge for long-term management and prognosis.
- Understanding prognostic factors is crucial for effective clinical intervention and patient counseling.
Purpose of the Study:
- To investigate the long-term prognosis of childhood-onset active epilepsy.
- To identify clinical factors influencing seizure remission and mortality over a 12-year period.
Main Methods:
- A cohort of 194 children (0-19 years) with active epilepsy in Sweden was initially investigated.
- A follow-up study was conducted 12 years later to assess outcomes, including mortality and seizure status.
- Clinical and psychometric data, including signs of neurodeficit and seizure characteristics, were analyzed.
Main Results:
- Eleven out of 194 children died within the 12-year follow-up period; 8 of these had signs of neurodeficit.
- Long-standing seizure remission was achieved in 124 children (64%).
- Negative prognostic factors included neurodeficit, frequent seizures, and multiple seizure types, associated with >80% persistent epilepsy.
- Children without neurodeficit and with infrequent seizures had an excellent prognosis, with only 11% active epilepsy after 12 years.
Conclusions:
- Neurodevelopmental status and seizure characteristics are critical determinants of long-term epilepsy outcomes in children.
- The annual remission rate was stable at approximately 13% for children without neurodeficit but declined significantly over time for those with neurodeficit.
- Early identification of negative prognostic factors can guide management strategies for pediatric epilepsy patients.
Abstract:
All children aged 0-19 years who had active epilepsy in a defined Swedish population were traced and given a clinical and psychometric investigation. Twelve years later, a follow-up study was carried out. Eleven of the 194 children had died, 8 of whom had had signs of neurodeficit, i.e., abnormal neurology and/or mental retardation. A long-standing remission of seizures occurred in 124 of the 194 children. Signs of neurodeficit, frequent seizures, and many types of seizures were negative prognostic factors. The presence of all these factors carried a bad prognosis, seizures persisting during 12 years in greater than 80%. For those who were mentally and neurologically normal and had low seizure frequency, prognosis was excellent, only 11% still having active epilepsy after 12 years. A study of the annual remission rate showed that each year approximately 13% of the children without neurodeficit had remission from epilepsy the next year. This rate appeared to be stable over the 12 years studied. Among those children with neurodeficit, the annual remission rate was high only during the first years after onset, later falling to 3% a year.
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