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Published on: June 8, 2017
Persistent neurocognitive impairments associated with severe falciparum malaria in Kenyan children
J A Carter1, V Mung'ala-Odera, B G R Neville
1Centre for International Child Health, Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK. j.carter@ich.ucl.ac.uk
Insights
Severe malaria can cause long-lasting neurocognitive impairments in children, impacting their development years later. Early identification and ongoing support are crucial for affected children.
Area of Science:
- Pediatric Neurology
- Infectious Diseases
- Neurodevelopmental Disorders
Background:
- Severe falciparum malaria can lead to persistent neurocognitive impairments.
- A subgroup of children exhibits particularly poor neurocognitive outcomes following severe malaria.
Purpose of the Study:
- To characterize the specific neurocognitive impairments in children with a history of severe malaria.
- To identify factors associated with persistent deficits in this vulnerable population.
Main Methods:
- Recruited three groups of children: cerebral malaria (CM), malaria with seizures (M/S), and unexposed controls.
- Conducted comprehensive developmental assessments on 487 children up to nine years post-illness.
- Classified impairments using standard definitions.
Main Results:
- 24% of CM and M/S groups showed impairments versus 10% of controls.
- CM was linked to a higher rate of multiple impairments.
- Impairments at discharge predicted increased mortality risk within the first year.
Conclusions:
- Neurocognitive impairments persist for up to nine years after severe malaria.
- Deficits may become more apparent with increased cognitive demands.
- Neurological status at discharge is a poor predictor; follow-up and multidisciplinary support are essential.
Objectives:
There is little information on the characteristics of persisting impairments associated with severe forms of falciparum malaria. Previous work has suggested the existence of a group of children with particularly poor performance on neurocognitive assessments in the context of average group performance. The aim of this study was to provide a detailed characterisation of impairments in this subgroup.
Methods:
Three groups of children were recruited: children admitted up to nine years earlier with cerebral malaria (CM) (n = 152), malaria and complicated seizures (M/S) (n = 156), or those unexposed to either condition (n = 179). Each child underwent a series of developmental assessments. Standard definitions were used to classify impairment.
Results:
Twenty-four percent of the CM and M/S groups had at least one impairment in the major domains assessed in the study, compared with 10% of the unexposed group. CM was associated with a higher proportion of multiple impairments and an increased risk of mortality in the first year after recovery in those identified with impairments on discharge.
Conclusions:
After severe malaria, some children have neurocognitive impairments that are evident as long as nine years later. Impairments may become more evident as children progress and face more complex cognitive and linguistic demands, socially and educationally. The child's neurological status at discharge was not a good predictor of later neurocognitive impairment. This highlights the importance of follow up for children with severe malaria and the involvement of therapists and educators in the provision of services for this population.
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