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Updated: Feb 5, 2026

Assessment of Cerebral Lateralization in Children using Functional Transcranial Doppler Ultrasound fTCD
Published on: September 27, 2010
Transcranial Doppler Ultrasonography Provides Insights into Neurovascular Changes in Children with Cerebral Malaria
Nicole Fortier O'Brien1, Tshimanga Mutatshi Taty2, Melissa Moore-Clingenpeel3
1Department of Pediatrics, Division of Critical Care Medicine, Nationwide Children's Hospital, The Ohio State University, Columbus, OH.
Insights
Cerebral malaria in children causes diverse neurovascular changes, including hyperemia and low flow, impacting outcomes. Transcranial Doppler ultrasound (TCD) can identify these patterns to guide targeted therapies.
Area of Science:
- Pediatric Neurology
- Vascular Biology
- Infectious Diseases
Background:
- Cerebral malaria is a severe complication of Plasmodium falciparum infection in children.
- Neurovascular dysfunction plays a critical role in the pathophysiology and outcomes of cerebral malaria.
- Understanding these changes is crucial for developing effective treatments.
Purpose of the Study:
- To evaluate neurovascular changes in pediatric patients with cerebral malaria using transcranial Doppler ultrasound (TCD).
- To correlate specific TCD-identified neurovascular phenotypes with clinical outcomes, including mortality and neurologic sequelae.
- To explore the potential of TCD as a tool for guiding individualized adjunctive therapies.
Main Methods:
- Daily TCD examinations were performed on African children with cerebral malaria from enrollment through hospital day 8, discharge, or death.
- Neurologic outcomes were assessed two weeks post-enrollment.
- Comparison patients without cerebral malaria underwent TCD to establish a baseline.
Main Results:
- Distinct TCD phenotypes were observed in children with cerebral malaria, including hyperemia (26%), low flow (28%), microvascular obstruction (22%), and vasospasm (13%).
- Impaired cerebral autoregulation was common (80%) but improved over time.
- Children with vasospasm had higher rates of sequelae, while those with low flow had higher mortality. Autoregulation differed significantly between those with and without normal neurologic outcomes.
Conclusions:
- Specific neurovascular phenotypes identified by TCD in pediatric cerebral malaria are associated with distinct clinical outcomes.
- TCD can differentiate patient groups, suggesting its utility in tailoring treatments.
- Further validation of TCD-based phenotypic grouping may enable personalized adjunctive therapies to mitigate injury mechanisms in cerebral malaria.
Objective:
To evaluate neurovascular changes in pediatric patients with cerebral malaria.
Study Design:
African children with cerebral malaria were enrolled and underwent daily transcranial Doppler ultrasound (TCD) examinations through hospital day 8, discharge, or death. Neurologic outcomes were assessed 2 weeks after enrollment.
Results:
In total, 160 children with cerebral malaria and 155 comparison patients were included. In patients with cerebral malaria, TCD flow changes characterized as hyperemia were seen in 42 (26%), low flow in 46 (28%), microvascular obstruction in 35 (22%), cerebral vasospasm in 21 (13%), and isolated posterior hyperemia in 7 (4%). Most had a single neurovascular phenotype observed throughout participation. Among comparison patients, 76% had normal TCD findings (P < .001). Impaired autoregulation was present in 80% of cases (transient hyperemic response ratio 1.01 ± 0.03) but improved through day 4 (1.1 ± 0.02, P = .014). Overall mortality was 24% (n = 39). Neurologic deficits were evident in 21% of survivors. Children meeting criteria for vasospasm were most likely to survive with sequelae, and children meeting criteria for low flow were most likely to die. Autoregulation was better in children with a normal neurologic outcome (1.09, 95% CI 1.06-1.12) than in others (0.98, 95% CI 0.95-1) (P ≤ .001).
Conclusions:
Several distinct changes in TCD measurements were identified in children with cerebral malaria that permitted phenotypic grouping. Groups had distinct associations with neurologic outcomes. Validation of pathogenic mechanisms associated with each phenotype may aid in developing TCD as a portable, easy-to-use tool to help guide targeted adjunctive therapy in cerebral malaria aimed at causative mechanisms of injury on an individual level.
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