Key result
Severe malaria anemia linked to ~18% higher absolute prevalence of prolonged QTc vs uncomplicated malaria.
Why the study?
Severe malaria anemia is a major cause of childhood heart failure and may cause myocardial damage detectable by ECG and elevated troponin T levels.
Do children with severe malaria anemia have more ECG changes and higher cTnT levels compared to those with uncomplicated malaria without anemia?
Case-Control (n=83)
Do children with severe malaria anemia have more ECG changes and higher cTnT levels compared to those with uncomplicated malaria without anemia?
Absolute Event Rate: 23% vs 5%
p-value: p=0.027
Children with severe malaria anemia have a higher prevalence of prolonged QTc compared to those with uncomplicated malaria, but similar troponin T levels, suggesting increased arrhythmia risk without necessarily greater myocardial injury.
May signal arrhythmia risk in pediatric severe malaria anemia; hypothesis-generating, needs prospective confirmation before practice change.
BACKGROUND: Severe malaria anemia is a major cause of childhood heart failure in malaria endemic countries. The resulting hypoxic-ischemic injuries may cause myocardial damage detectable by electrocardiogram (ECG) and elevated troponin T (cTnT) levels. OBJECTIVE: Evaluate the ECG changes and cTnT levels in children with severe malaria anemia compared with those who had uncomplicated malaria without anemia. METHODS: Consecutive children with severe malaria anemia were recruited as subjects while controls were age- and gender-matched children with uncomplicated malaria without anemia. ECG findings, cTnT levels, and the proportion of children with elevated cTnT were compared between subjects and controls. RESULTS: There were 43 subjects with a mean age of 25.7 ± 22.9 months. Controls were forty children; mean age was 31.2 ± 20.0 months. All the subjects and 10 (25.0%) controls had ECG abnormalities. Five (11.6%) subjects and no control had ST segment changes, P = 0.06. Twenty-three percent of subjects compared to 5% of the controls had prolonged QTc, P = 0.027. Median cTnT of subjects (131.8 ng/L) was not significantly higher than the 85.9 ng/L of controls, P = 0.99. The median cTnT of subjects that died 208.9 ng/L was higher than in survivors 99.6 ng/L, P = 0.51. CONCLUSION: Prolonged QTc was more prevalent in children with severe malaria anemia compared to those without anemia, suggesting that children with severe malaria anemia were more prone to arrhythmias. The median cTnT value in the subjects was not significantly lower than that in controls, suggesting that children with severe malaria anemia are not prone to myocardial injury any more than those with uncomplicated malaria without anemia.
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Sadoh et al. (2016) conducted a case-control in Severe malaria anemia (n=83). Severe malaria anemia vs. Uncomplicated malaria without anemia was evaluated on Prolonged QTc (p=0.027). Severe malaria anemia was associated with a higher prevalence of prolonged QTc compared to uncomplicated malaria without anemia (23% vs 5%, P=0.027).
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