# Prevalence and risk factors of gross neurologic deficits in children after severe malaria: A systematic review and meta-analysis

**Authors:** Allen Eva Okullo, Simple Ouma, Chandy C. John, Michael Boele van Hensbroek, Kevin Ouma Ojiambo, Caroline Otike, Alison Annet Kinengyere, Andrea L. Conroy, Moses Ocan, Ekwaro A. Obuku, Richard Idro, Alejandro Torrado Pacheco, Bashir Sajo Mienda, Bashir Sajo Mienda

PMC · DOI: 10.1371/journal.pone.0333258 · PLOS One · 2026-03-17

## TL;DR

This study finds that children with cerebral malaria in Sub-Saharan Africa are more likely to have severe neurological issues after recovery compared to those with other severe malaria forms.

## Contribution

The study provides a global meta-analysis of gross neurologic deficits in children with severe malaria, identifying regional and clinical risk factors.

## Key findings

- Gross neurologic deficits occurred in 15.2% of children with cerebral malaria at hospital discharge.
- Children in Sub-Saharan Africa had higher prevalence of deficits compared to East Asia & Pacific.
- Risk factors included coma duration, convulsions, hypoglycaemia, and acute kidney injury.

## Abstract

Children with severe malaria may develop gross neurologic deficit(s). We conducted a systematic review on the prevalence and risk factors of gross neurologic deficits after childhood severe malaria.

The systematic review was conducted following PRISMA guidelines. Article search was conducted in MEDLINE, EMBASE, Web of Science, and Global Index Medicus. Studies included reported on prevalence and/or risk factors of gross neurologic deficits after severe malaria in children. Risk of bias analysis and heterogeneity assessment were performed using ROBINS tool and I2-statistic, respectively. Data analysis was done using quantitative synthesis in R ver4.5.0 software, and narrative synthesis.

41 studies from 16 countries in Sub-Saharan Africa and Asia comprising 11,635 children were included in the analysis. Gross neurologic deficits included motor, movement, sensory, and speech impairments. 31 studies included prevalence of gross neurologic deficits at hospital discharge (cerebral malaria (CM), n = 26, broader forms of severe malaria, n = 5). Prevalence of deficits at hospital discharge in children with CM was 15.2% (95%CI: 11.5–18.8) (I2 = 89.1%), compared to 2.4% (95%CI: 2.0–2.8) (I2 = 36.6%) in children with broader forms of severe malaria. Prevalence of deficits in CM decreased from 15.2% to 5.7% (95%CI: 1.2–10.2) (I2 = 79.2%) after 12 months follow-up. At regional level, Sub-Saharan Africa had a prevalence of 14.2% (95%CI: 10.5–17.9) (I2 = 94.9%) compared to East Asia & Pacific at 2.3% (95%CI: 0.8–3.8) (I2 = 0.0%) and South Asia at 6.1% (95%CI: 0.0–14.8) (I2 = 0.0%). Risk factors for gross neurologic deficits included profound coma, coma lasting ≥48 hours, multiple convulsions, hypoglycaemia, and acute kidney injury.

Gross neurologic deficits are more prevalent in children in Sub-Saharan Africa with CM compared to severe malaria in general, and a number of clinical factors in children with CM increase the risk. Interventions by clinicians should target children with CM at highest risk during admission.

## Linked entities

- **Diseases:** malaria (MONDO:0005136), cerebral malaria (MONDO:0005625)

## Full-text entities

- **Diseases:** malaria (MESH:D008288), epilepsies (MESH:D004827), brain injury (MESH:D001930), CM (MESH:D016779), dystonia (MESH:D004421), hypertonia (MESH:D009122), malnutrition (MESH:D044342), hypotonia (MESH:D009123), sensory deficit (MESH:D012678), metabolic acidosis (MESH:D000138), anaemia (MESH:D000743), impairments (MESH:D060825), development problems (MESH:D002658), injury (MESH:D014947), neurologic sequelae (MESH:D009422), delayed speech (MESH:D007805), visual or hearing (MESH:D006311), neurological complication (MESH:D002493), paresis (MESH:D010291), aphasia (MESH:D001037), CND (MESH:C535376), cortical blindness (MESH:D019575), neurologic damage (MESH:D020196), motor and movement deficits (MESH:D009069), plegia (MESH:D010243), neurologic function (MESH:D003291), visual impairment (MESH:D014786), deafness (MESH:D003638), motor, movement, sensory, and speech impairments (MESH:D013064), intracranial hypertension (MESH:D019586), Ataxia (MESH:D001259), acute kidney injury (MESH:D058186), squint (MESH:D013285), SMA (MESH:D014897), herniation (MESH:D004677), coma (MESH:D003128), cranial nerve palsies (MESH:D003389), impaired hearing (MESH:D034381), neuronal injury (MESH:D009410), spasticity (MESH:D009128), Convulsions (MESH:D012640), hypoglycemia (MESH:D007003), attention (MESH:D001289), tremors (MESH:D014202), dyspraxia (MESH:D001072), Severe (MESH:D045169), GND (MESH:D009461)
- **Chemicals:** oxygen (MESH:D010100), artesunate (MESH:D000077332), SM (MESH:D012493), PONE-D-25-49673 (-), urea nitrogen (MESH:C530477), Artemether (MESH:D000077549), quinine (MESH:D011803), quinolinic acid (MESH:D017378), creatinine (MESH:D003404), nitrogen (MESH:D009584), urea (MESH:D014508), chloroquine (MESH:D002738)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12994846/full.md

## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC12994846/full.md

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Source: https://tomesphere.com/paper/PMC12994846