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Comparison of outcome between Chagas cardiomyopathy and idiopathic dilated cardiomyopathy
Amanda Pires Barbosa1, Augusto Cardinalli Neto, Ana Paula Otaviano
1Hospital de Base de São José do Rio Preto, São José do Rio Preto, SP, Brazil. amandapbarbosa@yahoo.com.br
Insights
Patients with Chagas cardiomyopathy face worse outcomes than those with idiopathic dilated cardiomyopathy, even with modern heart failure treatments. This study highlights the critical need for targeted therapies for Chagas cardiomyopathy patients.
Area of Science:
- Cardiology
- Infectious Diseases
- Public Health
Background:
- Chagas cardiomyopathy outcomes are poorly understood compared to idiopathic dilated cardiomyopathy.
- Contemporary data on Chagas cardiomyopathy prognosis is limited.
Purpose of the Study:
- To compare the prognosis of Chagas cardiomyopathy patients with chronic systolic heart failure to those with idiopathic dilated cardiomyopathy.
- Evaluate outcomes in the current era of heart failure management.
Main Methods:
- Prospective follow-up of 352 patients (246 Chagas cardiomyopathy, 106 idiopathic dilated cardiomyopathy) from 2000-2008.
- All patients received standard contemporary medical therapy for heart failure.
Main Results:
- Chagas cardiomyopathy etiology (HR=3.29) and digoxin use (HR=3.17) were associated with increased mortality.
- Beta-blocker therapy (HR=0.39) was associated with decreased mortality.
- Survival probabilities at 49 months were 41% for Chagas cardiomyopathy vs. 82% for idiopathic dilated cardiomyopathy (p<0.005).
Conclusions:
- Patients with Chagas cardiomyopathy exhibit a poorer prognosis than those with idiopathic dilated cardiomyopathy.
- Current heart failure therapies do not fully mitigate the adverse outcomes in Chagas cardiomyopathy.
- Further research into specific treatments for Chagas cardiomyopathy is warranted.
Background:
Little is known about the outcome of patients with Chagas cardiomyopathy in comparison to that of patients with idiopathic dilated cardiomyopathy in the contemporary era.
Objective:
To compare the outcome of chagasic patients with chronic systolic heart failure secondary to Chagas cardiomyopathy with that observed in patients with IDC in the contemporary era.
Methods:
A total of 352 patients (246 with Chagas cardiomyopathy, 106 with idiopathic dilated cardiomyopathy) prospectively followed at our Institution from January, 2000 to January, 2008 were included. All patients received standard contemporary medical therapy.
Results:
In Cox proportional hazards model multivariate analysis, digoxin use (Hazard Ratio=3.17; 95% Confidence Interval 1.62 to 6.18; p=0.001), need of inotropic support (Hazard Ratio=2.08; 95% Confidence Interval 1.43 to 3.02; p<0.005), left ventricular ejection fraction (Hazard Ratio=0.97; 95% Confidence Interval 0.95 to 0.99; p<0.005), and Chagas cardiomyopathy etiology (Hazard Ratio=3.29; 95% Confidence Interval 1.89 to 5.73; p<0.005) were positively associated with mortality, whereas beta-blocker therapy (Hazard Ratio=0.39; 95% Confidence Interval 0.26 to 0.56; p<0.005) was negatively associated with mortality. Survival probability for patients with Chagas cardiomyopathy at 8, 24, and 49 months was 83%, 61%, and 41%, respectively, and for patients with idiopathic dilated cardiomyopathy 97%, 92%, and 82%, respectively (p<0.005).
Conclusion:
In the current era of heart failure therapy, patients with Chagas cardiomyopathy have a poorer outcome in comparison to patients with idiopathic dilated cardiomyopathy.
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Imbalances in Cardiac Output
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