Increased prevalence of epilepsy associated with severe falciparum malaria in children
Julie A Carter1, Brian G R Neville, Steven White
1Neurosciences Unit, Institute of Child Health, The Wolfson Centre, London, United Kingdom. j.carter@ich.ucl.ac.uk
Insights
Children with a history of severe malaria, including cerebral malaria or complicated seizures, have a higher risk of developing epilepsy. This study quantifies the increased prevalence of epilepsy in these pediatric populations.
Area of Science:
- Pediatric neurology
- Infectious diseases
- Epidemiology
Background:
- Seizures are common in severe malaria, potentially leading to epilepsy.
- The link between falciparum malaria and epilepsy requires further investigation.
Purpose of the Study:
- To determine the prevalence and characteristics of epilepsy in children with a history of severe malaria.
- To compare epilepsy rates between children with cerebral malaria, malaria with complicated seizures, and unexposed children.
Main Methods:
- Epilepsy history was obtained from parents of 487 children (aged 6-9 years).
- Children were categorized into cerebral malaria (CM), malaria/complicated seizures (M/S), or unexposed groups.
- Electroencephalogram (EEG) was performed, and epilepsy status (active, inactive, none) was determined.
Main Results:
- Epilepsy prevalence was higher in children with prior CM (9.2%) and M/S (11.5%) compared to unexposed (2.2%).
- Tonic-clonic seizures were most common, followed by focal to bilateral tonic-clonic seizures.
- EEG abnormalities were present in 26% of active epilepsy cases at initial assessment.
Conclusions:
- Children with CM or M/S show an increased risk of epilepsy.
- Epilepsy prevalence linked to CM is comparable to other severe encephalopathies.
- Epilepsy prevalence associated with M/S is more than double that of complicated febrile seizures.
Purpose:
Multiple, prolonged, generalized, or focal seizures are common in children with severe malaria, with or without coma. In other contexts, such seizures have been associated with the development of epilepsy. The relation between falciparum malaria and epilepsy is undetermined; thus we measured the prevalence and characteristics of epilepsy in children with a history of severe malaria.
Methods:
We took a detailed epilepsy history from the parents of 487 children (aged 6-9 years) to compare the prevalence of epilepsy between three exposure groups: children with a history of cerebral malaria (CM), malaria and complicated seizures (M/S), or those unexposed to either complication. Each child had an EEG and was classified as having active, inactive, or no epilepsy.
Results:
An increased prevalence of epilepsy was seen in children previously admitted with CM [9.2%; OR, 4.4; 95% confidence interval (CI), 1.4-13.7] or M/S (11.5%; OR, 6.1; 95% CI, 2.0-18.3) compared with the unexposed group (2.2%). The most commonly reported seizure types were tonic-clonic (42%), focal becoming secondarily generalized (16%), and both (21%). Twenty-six percent of the active epilepsy group initially had EEG abnormalities.
Conclusions:
These results suggest that children exposed to CM or M/S have an increased propensity for epilepsy relative to children unexposed to these complications. The prevalence of epilepsy associated with CM is similar to that reported after other severe encephalopathies. The prevalence associated with M/S is more than twice that reported after complicated febrile seizures.
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