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Published on: April 21, 2017
Epilepsy in hemiplegic cerebral palsy due to perinatal arterial ischaemic stroke
Jithangi Wanigasinghe1, Susan M Reid, Mark T Mackay
1University of Colombo, Lady Ridgeway Hospital, Sri Lanka.
Insights
Epilepsy affects over half of children with hemiplegic cerebral palsy (CP) from perinatal arterial ischaemic stroke (AIS). However, most achieve seizure remission within ten years, indicating a good prognosis.
Area of Science:
- Neurology
- Pediatrics
- Epileptology
Background:
- Hemiplegic cerebral palsy (CP) in children can stem from perinatal arterial ischaemic stroke (AIS).
- Epilepsy is a common comorbidity in this population, impacting neurological outcomes.
- Understanding epilepsy's characteristics in this specific CP subgroup is crucial for management.
Observation:
- This study analyzed 63 children with hemiplegic CP due to perinatal AIS.
- Epilepsy developed in 54% of participants, with term delivery and severe motor impairment as risk factors.
- Initial seizures included spasms, focal, or myoclonic types, often with Rolandic or occipital origins.
Findings:
- Children with hemiplegic CP and AIS show a high incidence of epilepsy (54%).
- Despite initial seizures, 85% achieved remission within 10 years.
- Many exhibited features consistent with idiopathic partial epilepsy on EEG.
Implications:
- The prognosis for seizure control in children with hemiplegic CP due to AIS is generally favorable.
- Clinical and electroencephalographic findings may resemble idiopathic epilepsy, guiding treatment approaches.
- Further research into specific epilepsy syndromes within this population is warranted.
Aim:
The aim of this study was to describe the frequency, risk factors, manifestations, and outcome of epilepsy in children with hemiplegic cerebral palsy (CP) due to perinatal arterial ischaemic stroke (AIS).
Method:
The study group comprised 63 participants (41 males, 22 females) from a population-based CP register whose brain imaging showed perinatal AIS. Information collected included occurrence of neonatal seizures, family history of epilepsy, motor function and epilepsy onset, treatment, and outcome. Electroclinical findings were classified according to seizure semiology, seizure type, and epilepsy syndrome.
Results:
Mean age of participants at the time of study was 10 years 6 months (SD 4 y 7 mo, range 4-20 y). Gross Motor Function Classification System levels I and II were reported in 96% of participants, and Manual Ability Classification System levels I and II were reported in 79% of children. Thirty-four children (54%) developed epilepsy. Term delivery and more severe motor impairment were associated with epilepsy, but neonatal seizures and family history of epilepsy were not. Initial seizures were epileptic spasms, focal seizures, or myoclonic seizures. Focal seizure semiology suggested Rolandic or occipital seizure origin in the majority of children. Focal epileptic discharges in children with focal seizures had features of idiopathic partial epilepsy. Only 15% of children had active epilepsy 10 years after onset.
Interpretation:
Despite a high incidence of epilepsy in children with hemiplegic CP due to AIS, the prognosis for seizure remission is good. Many children have clinical features, electroencephalography findings, and remission typical of idiopathic partial epilepsy.
Related Concept Videos
Ischemic Stroke l: Introduction
Epilepsy ll: Types
Seizures: Classification
Seizures are typically classified into two main categories: focal and generalized seizures.
Focal Seizures
Focal seizures originate from specific regions of the brain. These seizures are further sub-classified into two types:
Ischemic Stroke ll: Pathophysiology
Seizures l: Introduction
Hemorrhagic Stroke l: Introduction

