Malaria Coinfections in Febrile Pediatric Inpatients: A Hospital-Based Study From Ghana
Benedikt Hogan1,2, Daniel Eibach1, Ralf Krumkamp1,2
1Department of Infectious Disease Epidemiology, Bernhard Nocht Institute for Tropical Medicine Hamburg, Germany.
Insights
Malaria is a leading cause of childhood illness in sub-Saharan Africa. Lower malaria parasite densities in Ghanaian children correlate with increased risk of other serious infections, suggesting parasite levels can guide diagnosis and treatment.
Area of Science:
- Pediatrics
- Infectious Diseases
- Tropical Medicine
Background:
- Malaria remains a significant cause of childhood morbidity and mortality in sub-Saharan Africa, despite epidemiological shifts.
- Understanding the causes of febrile illness in hospitalized children is crucial for effective public health strategies.
Purpose of the Study:
- To describe the causes of febrile illness in hospitalized children in Ghana.
- To determine the burden of malaria coinfections and their association with parasite densities.
Main Methods:
- Prospective study of children (≥30 days to ≤15 years) with fever (≥38.0°C) admitted to a primary hospital in Ghana.
- Diagnosis of malaria parasitemia and screening for bacterial, viral, and parasitic pathogens in blood, stool, urine, respiratory, and cerebrospinal fluid.
- Calculation of associations between Plasmodium parasite densities and other detected pathogens.
Main Results:
- Plasmodium parasitemia was the predominant diagnosis (59%) in 1238 enrolled children.
- Other common diagnoses included lower respiratory tract infections (34%), urinary tract infections (18%), gastrointestinal infections (17%), and invasive bloodstream infections (5%).
- Lower Plasmodium parasite densities were associated with increased frequency of lower respiratory tract, gastrointestinal, and bloodstream infections.
Conclusions:
- In hospitalized children, higher malaria parasite densities are inversely correlated with the likelihood of nonmalarial comorbidities.
- Malaria parasite densities serve as an important indicator for the probability of coinfection.
- Parasite density can inform decisions regarding antimicrobial medication in febrile children.
Background:
The epidemiology of pediatric febrile illness is shifting in sub-Saharan Africa, but malaria remains a major cause of childhood morbidity and mortality. The present study describes causes of febrile illness in hospitalized children in Ghana and aims to determine the burden of malaria coinfections and their association with parasite densities.
Methods:
In a prospective study, children (aged ≥30 days and ≤15 years) with fever ≥38.0°C were recruited after admission to the pediatric ward of a primary hospital in Ghana. Malaria parasitemia was determined and blood, stool, urine, respiratory, and cerebrospinal fluid specimens were screened for parasitic, bacterial, and viral pathogens. Associations of Plasmodium densities with other pathogens were calculated.
Results:
From November 2013 to April 2015, 1238 children were enrolled from 4169 admissions. A clinical/microbiological diagnosis could be made in 1109/1238 (90%) patients, with Plasmodium parasitemia (n = 728/1238 [59%]) being predominant. This was followed by lower respiratory tract infections/pneumonia (n = 411/1238 [34%]; among detected pathogens most frequently Streptococcus pneumoniae, n = 192/299 [64%]), urinary tract infections (n = 218/1238 [18%]; Escherichia coli, n = 21/32 [66%]), gastrointestinal infections (n = 210 [17%]; rotavirus, n = 32/97 [33%]), and invasive bloodstream infections (n = 62 [5%]; Salmonella species, n = 47 [76%]). In Plasmodium-infected children the frequency of lower respiratory tract, gastrointestinal, and bloodstream infections increased with decreasing parasite densities.
Conclusions:
In a hospital setting, the likelihood of comorbidity with a nonmalarial disease is inversely correlated with increasing blood levels of malaria parasites. Hence, parasite densities provide important information as an indicator for the probability of coinfection, in particular to guide antimicrobial medication.
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