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Epilepsy in rural Ugandan children: seizure pattern, age of onset and associated findings
1Springview Cottage, More Hall Lane, Bolsterstone, Sheffield, UK. maureen.duggan1@btinternet.com
Insights
Childhood epilepsy prevalence in Uganda is 2.04‰, with generalized tonic-clonic seizures most common. Early-onset complex partial seizures may be linked to malaria, suggesting community-based epilepsy management is crucial.
Area of Science:
- Pediatric Neurology
- Epidemiology
- Global Health
Background:
- Hospital-based data limits understanding of childhood epilepsy in sub-Saharan Africa.
- A community-based approach is needed for epilepsy management integration in Uganda.
- This study surveyed children in Rukungiri District to inform program development.
Purpose of the Study:
- To determine the prevalence and seizure types of epilepsy in children under 18 in Rukungiri District, Uganda.
- To identify factors associated with epilepsy in this population.
- To provide data for integrating epilepsy management into community health programs.
Main Methods:
- An outreach method was used, assessing children with recurrent seizures at 19 sites.
- Clinical diagnosis, including seizure type, was made for 440 children under 18.
- Neurological and developmental assessments were conducted.
Main Results:
- The age-specific prevalence of epilepsy in children under 15 was 2.04‰.
- Generalized tonic-clonic seizures accounted for 53% of cases, followed by complex partial seizures (CPS) at 27%.
- Cerebral palsy was associated with CPS, and 50.2% of seizures began in infancy.
Conclusions:
- Epilepsy prevalence in Ugandan children is similar to that in Gambian children.
- Early-onset CPS in Uganda may be linked to malaria, similar to findings in Kenya.
- These findings support the need for community-based epilepsy care and further research into malaria's role.
Introduction:
Much information on childhood epilepsy in sub Saharan Africa is hospital based. A survey was considered necessary before integrating epilepsy management into a Ugandan community programme.
Method:
Using an 'outreach' method, children with recurrent seizures were offered assessment at 19 sites in Rukungiri District. A brief history and neurological and developmental assessment was carried out on each child. A clinical diagnosis of epilepsy, including seizure type, was given to 440 of 618 children <18 years with 178 exclusions.
Results:
The age-specific prevalence of epilepsy in children < 15 years was 2.04‰ (95% CI 1.94‰ to 2.24 ‰) based on 395 cases in an <15 years population of 193,126. Percentage distribution by seizure type was:-generalised tonic-clonic (53%), complex partial seizures CPS (27%), simple partial and miscellaneous seizures (6% each), with some diagnostic overlap between seizure types. Cerebral palsy, evident or evolving, was most strongly associated with CPS. A positive perinatal or infantile history was noted in 12 and 6% respectively, and 50.2% of seizures began in infancy.
Conclusions:
The prevalence of epilepsy is similar in Gambian children. The high contribution from early-onset CPS, resembles Kenyan reports of malaria-associated CPS, suggesting a causal association with malaria.
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