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Clinical Characteristics and Outcomes of Chagas Disease in the United States: A Multicenter Retrospective Analysis
Andrés F Henao-Martínez1, Christian Olivo-Freites2, Nelson I Agudelo Higuita3,4
1Division of Infectious Diseases, Department of Medicine, University of Colorado Denver, Aurora, Colorado.
Insights
Chagas disease impacts 300,000 in the U.S. Chronic Chagas cardiomyopathy presents significant risks for arrhythmias, stroke, and mortality, underscoring the need for early screening and treatment.
Area of Science:
- Infectious Diseases
- Cardiology
- Epidemiology
Background:
- Chagas disease affects 300,000 individuals in the U.S.
- Clinical characteristics and outcomes of chronic Chagas disease require further investigation.
- Understanding disease progression is vital for patient management.
Purpose of the Study:
- To evaluate clinical characteristics and outcomes of chronic Chagas disease in a U.S. multicenter network.
- To assess the risk of cardiomyopathy and other complications in different forms of Chagas disease.
- To determine the prevalence of Chagas disease and treatment patterns in the U.S.
Main Methods:
- Retrospective cohort study using the TriNetX research network.
- Identified patients with dual-positive Trypanosoma cruzi IgG serology.
- Captured clinical outcomes for up to 5 years of follow-up.
Main Results:
- Identified 429 patients with positive Chagas serology (2.2% of tested).
- Cardiomyopathy risk was 1.3% annually in the indeterminate form; CCC showed annual risks of 1.6% for arrhythmias and 0.8% for stroke.
- CCC yearly mortality was 2.7%, hospitalization 17.1%; only 13 patients received antitrypanosomal therapy.
Conclusions:
- Chronic Chagas cardiomyopathy imposes a substantial burden with increased morbidity and mortality.
- Screening for Chagas disease in at-risk populations in the U.S. is crucial.
- Limited antitrypanosomal treatment documented, highlighting a gap in care.
Abstract:
Chagas disease affects approximately 300,000 patients in the United States. We evaluated a multicenter U.S.-based network to obtain clinical characteristics and outcomes of chronic Chagas disease by disease forms. This was a U.S.-based, multicenter, population-based, retrospective cohort study. We queried TriNetX, a global research network, to identify patients with dual-positive IgG serology for Trypanosoma cruzi. We captured outcomes of interest for up to 5 years. We found 429 patients with evidence of dual-positive T. cruzi IgG out of 19,831 patients with an available test result from 31 U.S. medical centers. The positive proportion for those tested was 2.2%, up to 4.6% among Hispanics. We found a prevalence of a positive Chagas serology of 0.02% among Hispanics. Cardiomyopathy risk reached an annual rate of 1.3% during the initial 5 years of follow-up among patients with the indeterminate form. We found no new events for pulmonary embolism, sudden death, or left ventricular aneurysms at 5 years. Annual risks for arrhythmias and stroke for chronic Chagas cardiomyopathy (CCC) were 1.6% and 0.8%, respectively. The yearly mortality and hospitalization rates for CCC were 2.7% and 17.1%, respectively. Only 13 patients had a documented antitrypanosomal therapy course within 6 months after diagnosis. Of those receiving treatment, 10 patients received benznidazole and three nifurtimox. Chagas disease screening in patients from endemic areas living in the United States remains crucial. Chronic Chagas cardiomyopathy carries a considerable disease burden, translating into increased morbidity and mortality and an enlarging medical health service utilization.
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