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Ischemic cerebrovascular events in patients with Chagas cardiomyopathy: a prospective follow-up study
Maria Carmo P Nunes1, Marcia M Barbosa, Antônio Luiz P Ribeiro
1School of Medicine, Federal University of Minas Gerais, and ECOCENTER, Hospital Socor, Belo Horizonte, MG, Brazil. mcarmo@waymail.com.br
Insights
In Chagas cardiomyopathy patients, low left ventricular ejection fraction increases the risk of ischemic cerebrovascular events (ICE). This study identifies key predictors for ICE in this population.
Area of Science:
- Cardiology
- Neurology
- Infectious Diseases
Background:
- Chagas disease cardiomyopathy is a prevalent form of dilated cardiomyopathy globally.
- It is a significant cause of stroke in Latin America.
- The long-term risk of ischemic cerebrovascular events (ICE) and its link to left ventricular (LV) dysfunction require further investigation.
Purpose of the Study:
- To determine the incidence of ICE in patients with Chagas cardiomyopathy.
- To evaluate the impact of LV ejection fraction on the risk of ICE.
Main Methods:
- Prospective enrollment of 213 Chagas disease patients with LV systolic dysfunction.
- Anticoagulation use was guided by clinical indications.
- Cox proportional-hazards analysis was used to assess risk factors for ICE.
Main Results:
- The overall incidence of ICE was 2.67 events per 100 patient-years over a mean follow-up of 36 months.
- Independent risk factors for ICE included reduced LV ejection fraction (HR 0.95) and increased indexed left atrial volume (HR 1.04).
- Patients with LV ejection fraction ≤35% had a 3.41-fold increased risk of ICE.
Conclusions:
- The annual incidence of ICE in Chagas cardiomyopathy patients is relatively low.
- LV ejection fraction and indexed left atrial volume are independently associated with ICE risk in this cohort.
Background:
Chagas disease cardiomyopathy is a common form of dilated cardiomyopathy worldwide, and an important cause of stroke in Latin America. The long-term cumulative risk of ischemic cerebrovascular event (ICE) and its relation to left ventricular (LV) dysfunction have not been determined. The aims of this study were to describe the incidence and to evaluate the effect of LV ejection fraction on the risk for ICE in patients with Chagas cardiomyopathy.
Methods:
A total of 213 consecutive patients with Chagas disease and LV systolic dysfunction, 131 males, mean age 48+/-12 years, were prospectively enrolled. The use of anticoagulation was based on clinical indications. The end point was ICE, which included fatal or nonfatal stroke and transient ischemic attack. Risk factors for events were assessed by Cox proportional-hazards analysis.
Results:
Mean follow-up was 36 months; 69 patients died and seven underwent cardiac transplantation. The overall incidence of ICE was 2.67 events per 100 patient/years. Independent risk factors for ICE included LV ejection fraction (HR 0.95, 95% CI 0.91 to 0.99, p=0.009) and left atrial volume corrected for body surface area (HR 1.04, 95% CI 1.01 to 1.07, p=0.007), which persisted after adjustment for anticoagulation use. Patients with ejection fractions
Conclusions:
In patients with Chagas cardiomyopathy, the annual incidence of ICE is low. Left ventricular ejection fraction and indexed left atrial volume appear to be independently associated with these events.
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