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Following Severe Pediatric Malaria, Epilepsy Screening Is Needed Even Among Children Without Coma: Findings From a Prospective Cohort Study

delete2026-07-10
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PRE
AI
A
Archana A. Patel
S
Shaida Nishat
R
Rasesh B. Joshi
S
Suzanna Mwanza
J
Joseph Kasolo
A
Angela Masempela
T
Thelma Musakanya
T
Tina Mwale
V
Violet Nambeye
R
Rosemary Nyirongo
R
Ruth G. Tembo
N
Nicole O’Brien
K
Karl B. Seydel
C
Christopher Cortina
B
Bo Zhang
M
Maitreyi Mazumdar
A
Alexander Rotenberg
G
Gretchen L. Birbeck
DOI:10.1177/11795735261467520delete
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Abstract

Abstract

En 中文
<jats:sec> <jats:title>Background</jats:title> <jats:p>Severe pediatric malaria with neurological presentation has a spectrum of severity, from frank coma (Cerebral Malaria (CM)) to impaired consciousness and/or complex seizures without coma (malaria with central nervous system signs, CNS-M). Approximately 9-16% of pediatric CM survivors develop post-malaria epilepsy (PME), but rates after CNS-M are understudied.</jats:p> </jats:sec> <jats:sec> <jats:title>Objective</jats:title> <jats:p>Determine PME rates following severe pediatric malaria with neurologic signs, with and without coma (CM and CNS-M).</jats:p> </jats:sec> <jats:sec> <jats:title>Design</jats:title> <jats:p>Prospective cohort study.</jats:p> </jats:sec> <jats:sec> <jats:title>Methods</jats:title> <jats:p>Children 6 months-11 years who presented to a district level hospital in Zambia with CM or CNS-M between Nov 2021-June 2024 were enrolled. Children were excluded for pre-existing epilepsy or alternative explanation for acute neurologic symptoms. Primary outcome was PME at 1 year. Important covariates included coma, age, pre-illness neurodevelopment, acute hospitalization data, acute and follow-up EEG, and 1-year neurodevelopmental outcomes. Acute, 1-, 6-, and 12-month data were collected. EEGs were analyzed with conventional and quantitative methods. PME was determined by standardized screening and physician review using ILAE criteria.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>141 children met inclusion criteria, 48 had CM, 93 CNS-M. CNS-M children were younger (mean 40.8 vs. 54.3 months, p=0.005) and male predominant (64.8% vs. 43.8%, p=0.006). 18.4% of the cohort developed PME, with no significant incidence difference between CNS-M (20.4%) and CM (14.6%) groups, p=0.495. Focal epilepsy was more common in CNS-M 78.9% vs. CM 28.6% (p=0.028). There were no differences in qualitative EEG findings. Quantitative EEG measures demonstrated more severe and prolonged cortical dysfunction in CM (p&lt;0.01).</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusions</jats:title> <jats:p>CNS-M presentation was twice as frequent as CM at this district hospital. Quantitative EEG supports CM as a more severe acute illness, but PME developed in 15-20% of children within one year regardless of malarial coma. These findings suggest that severe malaria with neurologic involvement-regardless of coma during acute presentation-has significant secondary epilepsy risk.</jats:p> </jats:sec>

Journal

J
Journal of Central Nervous System Disease
IF:
2.8
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57
Citations:
709

Organization

C
chipata central hospital
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N
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M
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