3.8 Review

Chagas heart disease: An overview of diagnosis, manifestations, treatment, and care

Journal

WORLD JOURNAL OF CARDIOLOGY
Volume 13, Issue 12, Pages 654-675

Publisher

BAISHIDENG PUBLISHING GROUP INC
DOI: 10.4330/wjc.v13.i12.654

Keywords

Chagas disease; Diagnosis; Treatment; Heart failure; Arrhythmia; Stroke

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Chagas heart disease, caused by Trypanosoma cruzi, affects around 30% of patients. It is classified into four stages based on criteria including ECG, echocardiogram, and clinical findings. CHD presents with various clinical manifestations, with sudden cardiac death, heart failure, and stroke being the main complications. Sudden cardiac death is the most common cause of death in CHD patients, followed by heart failure and stroke.
Chagas heart disease (CHD) affects approximately 30% of patients chronically infected with the protozoa Trypanosoma cruzi. CHD is classified into four stages of increasing severity according to electrocardiographic, echocardiographic, and clinical criteria. CHD presents with a myriad of clinical manifestations, but its main complications are sudden cardiac death, heart failure, and stroke. Importantly, CHD has a higher incidence of sudden cardiac death and stroke than most other cardiopathies, and patients with CHD complicated by heart failure have a higher mortality than patients with heart failure caused by other etiologies. Among patients with CHD, approximately 90% of deaths can be attributed to complications of Chagas disease. Sudden cardiac death is the most common cause of death (55%-60%), followed by heart failure (25%-30%) and stroke (10%-15%). The high morbimortality and the unique characteristics of CHD demand an individualized approach according to the stage of the disease and associated complications the patient presents with. Therefore, the management of CHD is challenging, and in this review, we present the most updated available data to help clinicians and cardiologists in the care of these patients. We describe the clinical manifestations, diagnosis and classification criteria, risk stratification, and approach to the different clinical aspects of CHD using diagnostic tools and pharmacological and non-pharmacological treatments.

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