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Bartonella quintana, an Unrecognized Cause of Infective Endocarditis in Children in Ethiopia
Insights
Bartonella quintana endocarditis is rarely seen in children but is a significant cause of culture-negative endocarditis in Ethiopian children with heart defects. Diagnosis requires specific testing for this bacterial infection.
Area of Science:
- Infectious Diseases
- Pediatrics
- Cardiology
Background:
- Bartonella quintana endocarditis is a known cause of culture-negative endocarditis in adults.
- This infection is rarely reported in pediatric populations.
- Ethiopia presents a unique demographic for studying endemic infectious diseases.
Observation:
- Five pediatric patients (7-16 years) from Ethiopia with congenital heart defects and endocarditis were studied.
- Four cases were confirmed as Bartonella quintana infections; one involved an undetermined Bartonella species.
- Patients were often afebrile and oligosymptomatic, despite some experiencing heart failure.
Findings:
- Diagnosis was confirmed via echocardiography, elevated Bartonella IgG titers, and Bartonella quintana DNA detection in vegetations.
- Elevated erythrocyte sedimentation rate was noted, while C-reactive protein levels were normal or slightly elevated.
- Embolic events occurred in two patients, highlighting the systemic potential of the infection.
Implications:
- Bartonella quintana may be an underrecognized cause of native valve endocarditis in Ethiopian children with heart defects.
- Clinicians should consider Bartonella quintana in culture-negative endocarditis cases, especially in individuals from or with travel history to East Africa.
- Increased awareness and diagnostic pursuit are crucial for timely management of pediatric Bartonella endocarditis in endemic regions.
Abstract:
Bartonella quintana endocarditis, a common cause of culture-negative endocarditis in adults, has rarely been reported in children. We describe 5 patients 7-16 years of age from Ethiopia with heart defects and endocarditis; 4 cases were caused by infection with B. quintana and 1 by Bartonella of undetermined species. All 5 patients were afebrile and oligosymptomatic, although 3 had heart failure. C-reactive protein was normal or slightly elevated, and erythrocyte sedimentation rate was high. The diagnosis was confirmed by echocardiographic demonstration of vegetations, the presence of high Bartonella IgG titers, and identification of B. quintana DNA in excised vegetations. Embolic events were diagnosed in 2 patients. Our data suggest that B. quintana is not an uncommon cause of native valve endocarditis in children in Ethiopia with heart defects and that possible B. quintana infection should be suspected and pursued among residents of and immigrants from East Africa, including Ethiopia, with culture-negative endocarditis.
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