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Loading dose of quinine in African children with cerebral malaria
M van der Torn1, P E Thuma, G F Mabeza
1Division of Hematology and Oncology, George Washington University Medical Center, Washington, DC, USA.
Insights
A loading dose of quinine may improve outcomes for children with cerebral malaria, leading to faster recovery from coma and fever. While not statistically significant, trends suggest lower mortality and higher hemoglobin levels with this treatment approach.
Area of Science:
- Tropical Medicine
- Pediatric Infectious Diseases
- Malariology
Background:
- Cerebral malaria is a severe complication of Plasmodium falciparum infection, often leading to rapid mortality.
- Early and effective treatment is crucial, as many deaths occur within 48 hours of hospital admission.
- The standard treatment regimen for quinine may be insufficient in the critical early hours.
Purpose of the Study:
- To evaluate the impact of a quinine loading dose on clinical outcomes in children with cerebral malaria.
- To investigate the association between serum iron levels and mortality in pediatric cerebral malaria.
- To assess the effect of quinine loading dose on recovery time, parasite clearance, and fever resolution.
Main Methods:
- Retrospective review of clinical and laboratory data for 113 children diagnosed with cerebral malaria.
- Comparison of outcomes between children who received a standard quinine dose and those who received an initial loading dose (20 mg/kg) followed by maintenance doses (10 mg/kg every 8 hours).
- Analysis of serum iron levels, transferrin saturation, mortality, coma recovery, parasite clearance, fever duration, and hemoglobin levels.
Main Results:
- Elevated serum iron levels, indicated by transferrin saturation, were significantly associated with increased mortality.
- Children receiving a quinine loading dose demonstrated faster recovery from coma and more rapid clearance of parasitemia and fever.
- Trends suggested lower mortality and higher hemoglobin levels in the loading dose group, though these did not reach statistical significance.
Conclusions:
- A quinine loading dose appears beneficial for improving clinical recovery in pediatric cerebral malaria patients.
- High serum iron levels are a critical risk factor for mortality in cerebral malaria.
- Further prospective studies are warranted to confirm the mortality benefit of quinine loading doses in this population.
Abstract:
The majority of deaths from cerebral malaria occur within 48 h after admission to hospital. Because of the possibility of inadequate treatment within this period, the use of a loading dose of quinine has been proposed. We reviewed clinical and laboratory data for 113 children with cerebral malaria, who were treated with intravenous quinine, 10 mg/kg every 8 h, at Macha Mission Hospital in rural Zambia. In 1990-1991, 39 children were not given a loading dose of quinine while, in 1992-1993, 74 children received a loading dose of 20 mg/kg. Elevated serum iron levels, as reflected in transferrin saturation, were strongly associated with higher mortality. A loading dose of quinine was associated with faster recovery from coma and enhanced clearance of parasitaemia and fever. The loading dose was also associated with trends to lower mortality and higher haemoglobin levels, but these differences were not statistically significant.
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Malaria
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