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Seizures in children with primary brain tumors: incidence and long-term outcome
Raja B Khan1, Daniel L Hunt, Frederick A Boop
1Department of Radiological Sciences, St. Jude Children's Research Hospital, Memphis, TN 38105-2794, USA. raja.khan@stjude.org
Insights
Seizures in children with brain tumors can often be controlled, but specific factors like neurological deficits and EEG abnormalities predict poor outcomes. Further research into gabapentin as an initial anti-epileptic drug is warranted.
Area of Science:
- Pediatric Neurology
- Neuro-oncology
- Epileptology
Background:
- Brain tumors are a significant cause of seizures in children.
- Understanding seizure incidence and outcomes is crucial for effective management.
- Identifying risk factors for poor seizure control is essential for improving patient care.
Purpose of the Study:
- To determine the incidence and long-term outcomes of seizures associated with brain tumors in pediatric patients.
- To identify predictors of adverse seizure outcomes in this population.
Main Methods:
- Retrospective analysis of medical records for children with brain tumors and seizures at a single institution.
- Characterization of seizure status for six months prior to follow-up.
- Multivariate analysis to identify independent predictors of uncontrolled seizures.
Main Results:
- 157 children with a median follow-up of 3.3 years were analyzed.
- Seizures were controlled in 65% of children; 17% had intractable seizures.
- Neurological deficits, T2 peri-cavity hyperintensity, and EEG slow waves independently predicted uncontrolled seizures.
Conclusions:
- Focal neurological deficits, T2 peri-cavity hyperintensity, and EEG slow waves are key predictors of poor seizure control in pediatric brain tumor patients.
- While most brain tumor-related seizures can be managed, these factors indicate a higher risk.
- Prospective studies on gabapentin as a first-line anti-epileptic drug are recommended.
Purpose:
To estimate the incidence and long-term outcome of brain tumor related seizures in children and to identify risk factors for adverse seizure outcome.
Methods:
Analysis of medical records of children treated for brain tumor and seizures in a single institution. Children were identified from hospital database and neurology clinic records. Seizure status was characterized for the 6 months prior to most recent follow-up.
Results:
Median follow-up after first seizure of the 157 analyzed children was 3.3 years. Tumor location was supratentorial in 81% and posterior fossa in 19%. Initial anti-epileptic drugs were phenytoin (n=52), carbamazepine (n=38), phenobarbital (n=14), gabapentin (n=31), or others (n=22). Seizures were controlled in 65% of the children and uncontrolled in 35% (17% intractable). Gabapentin showed a trend toward better seizure control (p=0.06). Neurologic deficit, T2 peri-cavity hyperintensity, and EEG slow waves were independently predictive of uncontrolled seizures by multivariate analysis.
Conclusions:
T2 peri-cavity hyperintensity, focal neurologic deficits, and EEG slow waves predict poor seizure control in children with brain tumors. Seizures can be controlled in most patients with brain tumors. Gabapentin use as first anti-epileptic drug needs to be studied prospectively.
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