Why the study?
Knowledge gaps remain in the pathogenesis of Chagas cardiomyopathy nearly a century after its discovery, with persistent challenges in diagnosis and treatment.
This review highlights the ongoing knowledge gaps in the pathogenesis, diagnosis, and treatment of Chagas cardiomyopathy, emphasizing the need for etiology-specific therapies.
Persistent gaps in Chagas cardiomyopathy pathogenesis knowledge warrant further study; leaves open optimal diagnostic and treatment strategies.
and remains one of the most neglected tropical diseases despite being a significant contributor to morbidity and mortality in both endemic regions of Latin America and non-endemic countries like the United States. Since its discovery almost a century ago, knowledge gaps still exist in the mechanisms involved in the pathogenesis of Chagas cardiomyopathy, and numerous challenges exist in its diagnosis and treatment. This article reviews the main pathogenetic mechanisms involved in the progression of Chagas cardiomyopathy, which has been proposed as a result of years of research. It also emphasizes the challenges involved in the diagnosis of the asymptomatic indeterminate phase and has focused on several diagnostic techniques, including echocardiography, electrocardiogram (ECG), magnetic resonance imaging (MRI), and nuclear imaging in diagnosing symptomatic Chagas cardiomyopathy. In this article, we have also provided a brief overview of the current treatment of Chagas cardiomyopathy, which is not etiology-specific but instead derived from the knowledge acquired from the treatment of other cardiomyopathies.
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Veluswami et al. (2024) studied this question.
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