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Long-term Survival Following Heart Transplantation for Chagas Versus Non-Chagas Cardiomyopathy: A Single-center
Jefferson L Vieira1, Maria G V Sobral1, Francisco Y Macedo2
1Heart Failure Division, Hospital de Messejana Dr Carlos Alberto Studart, Fortaleza, Ceará, Brazil.
Insights
Heart transplant survival is similar for patients with Chagas cardiomyopathy (CC) and other heart failure causes. However, survival improvements over time benefit most patients, excluding those with CC, highlighting a need for further research.
Area of Science:
- Cardiology
- Transplantation Medicine
- Infectious Diseases
Background:
- Limited data exists on long-term survival after heart transplantation (HT) for patients with Chagas cardiomyopathy (CC).
- Understanding post-HT outcomes in CC is crucial for improving patient management and prognosis.
Purpose of the Study:
- To evaluate and compare post-heart transplant survival in patients with Chagas cardiomyopathy versus other etiologies of heart failure.
- To analyze survival trends across different eras of heart transplantation.
Main Methods:
- Retrospective cohort study of 376 adult heart transplant recipients (1997-2019).
- Patients categorized by heart failure etiology: Chagas cardiomyopathy (n=66), nonischemic cardiomyopathy (n=214), ischemic cardiomyopathy (n=96).
- Analysis stratified by heart transplant era: early (1997-2009), recent (2010-2014), and current (2015-2019).
Main Results:
- Post-HT survival rates at 1, 5, and 10 years were comparable across etiological groups.
- Overall 1-year survival improved significantly from 70% in early eras to 80% in the current era.
- Time-related survival improvements were observed in non-CC patients but not in CC patients after adjustment for covariates.
Conclusions:
- Posttransplant survival is comparable between Chagas cardiomyopathy and other heart failure etiologies.
- While overall heart transplant survival has improved, this progress has not extended to patients with Chagas cardiomyopathy.
- Emphasizes the need for dedicated research, policy development, and a collaborative registry for heart transplantation in Chagas cardiomyopathy.
Abstract:
Data on post-heart transplant (HT) survival of patients with Chagas cardiomyopathy (CC) are scarce. We sought to evaluate post-HT survival in patients with CC as compared with other causes of heart failure across different eras of HT.
Methods:
We conducted a retrospective, cohort study of 376 adult HT recipients between October 1997 and November 2019. Participants were classified according to the etiology of heart failure as CC (N = 66), nonischemic cardiomyopathy (N = 214), and ischemic cardiomyopathy (N = 96), and according to the era of HT as early (1997-2009), recent (2010-2014), and current era (2015-2019).
Results:
After a mean follow-up of 5.0 y (0-20.5 y), post-HT survival rates at 1, 5, and 10 y were comparable between groups. One-y survival improved from 70% in the early eras to 80% in the current era (hazard ratio [HR], 0.63; 95% confidence interval [CI], 0.41-0.97; P = 0.034). After adjustment for sex, age, and mechanical circulatory support, time-related improvement in survival was observed only in patients without CC (HR, 0.54; 95% CI, 0.32-0.91; P = 0.019) but not in those with CC (HR, 0.99; 95% CI, 0.36-2.73; P = 0.98). Causes of death were similar between patients with CC and the other etiological subgroups.
Conclusions:
Posttransplant survival is comparable between patients with CC, nonischemic cardiomyopathy, and ischemic cardiomyopathy. Although survival has improved significantly over years for most HT recipients, it has remained unchanged for those with Chagas disease. These trends underscore the importance of scientific research, policy discussions and a collaborative registry of heart transplantation in Chagas cardiomyopathy.
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