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Electromagnetic Source Imaging in Presurgical Evaluation of Children with Drug-Resistant Epilepsy
Published on: September 20, 2024
Clinical predictors of intractable childhood epilepsy
Aithala Gururaj1, Laszlo Sztriha, Joseph Hertecant
1Department of Paediatrics, Faculty Perubatan, Universiti Teknologi MARA, Shah Alam, Selangor, Malaysia. g.aithala@gmail.com
Insights
Pediatric intractable epilepsy is linked to early onset, frequent seizures, neonatal seizures, developmental delay, and neurological deficits. Conversely, few early seizures and no neurological deficits suggest a better prognosis for childhood epilepsy.
Area of Science:
- Pediatric Neurology
- Epileptology
- Clinical Neuroscience
Background:
- Medically intractable epilepsy poses significant challenges in pediatric care.
- Identifying factors predicting treatment resistance is crucial for effective management.
- Understanding these factors aids in developing targeted therapeutic strategies for children.
Purpose of the Study:
- To identify clinical, electroencephalographic, and radiological predictors of medically intractable seizures in children.
- To compare factors associated with intractable epilepsy versus drug-responsive epilepsy in a pediatric cohort.
- To investigate the prevalence and characteristics of intractable epilepsy in the Al Ain Medical District, UAE.
Main Methods:
- Prospective case-control study design.
- Inclusion of children referred to pediatric neurology and neurodevelopmental clinics.
- Comparison between children with intractable epilepsy and those seizure-free for at least two years.
Main Results:
- Children with intractable epilepsy were more likely to have onset before one year of age, high seizure frequency, a history of neonatal seizures, developmental delay, status epilepticus, neurological deficits, and abnormal brain imaging.
- Symptomatic localization-related epilepsy was more prevalent in the intractable epilepsy group.
- Factors such as early onset, seizure frequency, neonatal seizures, developmental delay, neurological deficits, and abnormal imaging are significant indicators of intractable epilepsy.
Conclusions:
- Children presenting with idiopathic epilepsy syndromes (localization-related and generalized) with fewer seizures at onset and no neurological deficits generally have a better prognosis.
- Early identification of risk factors can guide prognosis and treatment planning for pediatric epilepsy.
- This study provides valuable insights into epilepsy management in the UAE population.
Objective:
This study aimed to determine the clinical, electroencephalographic, and radiological factors associated with medically intractable seizures in children in the Al Ain Medical District in the United Arab Emirates.
Methods:
This work used a prospective case-control study of children referred to pediatric neurology and neurodevelopmental clinics at Tawam and Al Ain University Hospitals.
Results:
There were 55 children with intractable epilepsy; their data were compared with 50 children who responded well to antiepileptic drugs and who were seizure-free for at least 2 years. Onset <1 year of age, a high seizure frequency at onset, positive history of neonatal seizures, developmental delay and status epilepticus, neurological deficits, and abnormal brain imaging results were found to be significantly more common in the study group. Symptomatic localization-related epilepsy was more common in children in this group than in the control group.
Conclusion:
Our study suggests that children who present with idiopathic localization-related and generalized epilepsy syndromes with few seizures at onset and with no neurological deficits tend to have a relatively good prognosis.
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