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Published on: May 16, 2013
Pediatric cerebral malaria in Accra, Ghana
C Wolf-Gould1, L Osei, J O Commey
1Department of Medicine, Yale School of Medicine, New Haven, CT 06510.
Insights
Diagnosing pediatric cerebral malaria is challenging, with the Glasgow coma scale proving more effective than parasite levels for predicting hospital stay. Autopsy-confirmed cases sometimes lacked detectable parasites.
Area of Science:
- Tropical Medicine
- Pediatric Infectious Diseases
- Clinical Diagnostics
Background:
- Cerebral malaria diagnosis and treatment efficacy are poorly understood globally.
- Accurate diagnostic and prognostic tools for pediatric cerebral malaria are needed.
Purpose of the Study:
- To evaluate the diagnostic and prognostic utility of the Glasgow coma scale (GCS) and parasitaemia levels in pediatric cerebral malaria.
- To assess the accuracy of initial clinical diagnosis and the response to antimalarial treatment.
Main Methods:
- Retrospective evaluation of 31 pediatric patients with suspected cerebral malaria at Korle Bu Hospital, Ghana.
- Analysis of clinical data, including initial diagnosis confirmation rates, Glasgow coma scale scores, and blood parasitaemia levels.
- Correlation of GCS and parasitaemia with length of hospital stay and treatment outcomes.
Main Results:
- Only 65% of initial cerebral malaria diagnoses were confirmed; 16% were reclassified (pneumonia, meningitis, encephalitis).
- Initial Glasgow coma score (mean 10.4) was a stronger predictor of hospital stay (r=0.66) than initial parasitaemia (mean 10^4.6 parasites/mm3, r=0.17).
- Parasitaemia fluctuated or rose in 33% of patients despite therapy; high parasitaemia correlated with deep coma when assessed longitudinally. Deaths occurred in patients with negative blood smears but autopsy-confirmed cerebral malaria.
Conclusions:
- Clinical diagnosis of pediatric cerebral malaria has limitations, necessitating further investigation.
- The Glasgow coma scale is a valuable prognostic index in pediatric cerebral malaria.
- Diagnostic challenges and treatment responses highlight the need for improved management strategies, especially in cases with negative blood smears.
Abstract:
Characteristics of pediatric cerebral malaria, including specificity of clinical diagnosis, efficacy of antimalarial regimens, and the influence of drug resistance remain poorly defined in many parts of the world. The utility of the Glasgow coma scale and quantitative assessment of parasitaemia levels as diagnostic and prognostic indices in cerebral malaria were determined in this study. Thirty-one pediatric patients with admission diagnoses of cerebral malaria in the emergency ward at Korle Bu Hospital, Accra, Ghana were evaluated. Mean age was 4.8 years. The initial diagnosis of malaria was confirmed in 65 per cent of patients; 16 per cent ultimately received another diagnosis including pneumonia, meningitis or encephalitis. In 19 per cent the diagnoses were inconclusive. Mean initial blood parasitaemia level was 10(4.6) parasites per mm3, and mean initial Glasgow coma score was 10.4. The initial Glasgow score was a better predictor of length of stay (Pearson correlation coefficient r = 0.66) than initial parasitaemia level (r = 0.17). For most treated patients parasitaemia levels decreased a mean of 1.3 logs per day of therapy; however, in 33 per cent parasitaemia continued to rise or fluctuate. High parasitaemia levels were associated with deep levels of coma, but only when both parameters were assessed throughout the hospital stay. Both deaths in this series occurred in patients who had persistently negative blood smears for malaria parasites, but showed autopsy findings consistent with cerebral malaria.
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