(Part 1) Sudden cardiac death and sport cardiology: multimodality imaging in cardiomyopathies
Feb 6, 2024
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Dr. Harald Jorstad and Dr. Maria Sanz de la Garza discuss the role of imaging in diagnosing cardiomyopathies and coronary artery disease, and the challenges in evaluating athletes. They highlight the use of echocardiography and CMR for diagnosis, identification of pathological features, and differentiation between cardiomyopathies. The evaluation of myocardial patterns, including diastolic function and hypertrophy mechanical dispersion, is also explored.
Imaging techniques like echocardiography and CMR play a vital role in assessing cardiomyopathies, providing accurate diagnoses, risk stratification, and prognosis assessment.
CMR complements echocardiography in evaluating hypertrophic left ventricular hypertrophy and fibrosis, which are important factors for predicting arrhythmic events.
Deep dives
Imaging Challenges in Athletes and Cardiomyopathies
Imaging plays a critical role in the prevention and assessment of sudden cardiac death in athletes and individuals with cardiomyopathies. Echocardiography is commonly used for initial evaluation, assessing myocardial contractility and providing important diagnostic information. CMR (cardiac magnetic resonance) is considered the gold standard for assessing ventricular function and volume, providing specific characterization and identification of potential fibrosis. Hypertrophic left ventricular hypertrophy, dilation of ventricles, and the differentiation between arrhythmogenic cardiomyopathy and physiological adaptations are common clinical scenarios. Imaging techniques, such as speckle tracking analysis and tissue Doppler imaging, help evaluate these conditions, providing more accurate diagnoses, risk stratification, and prognosis assessment.
Assessing Hypertrophic Left Ventricular Hypertrophy
Echocardiography is crucial for assessing hypertrophic left ventricular hypertrophy (HCM). It helps identify the gray zone between physiological adaptations and pathological hypertrophy, using parameters like diastolic dysfunction and speckle tracking echocardiography to evaluate mechanical dispersion and ventricular contractility. CMR complements echocardiography by providing more accurate evaluations of hypertrophy, fibrosis, and higher-risk factors. CMR is also essential for risk stratification, as it can assess ventricular gradient and hypertrophy grades, providing prognostic implications. Presence of fibrosis, evaluated through CMR, indicates a higher risk of developing arrhythmic events.
Differentiating Dilated Ventricles and Arrhythmogenic Cardiomyopathy
The imaging assessment of dilated ventricles in athletes involves evaluating left ventricular (LV) systolic function, abnormal diastolic function, and mechanical dispersion using echocardiography. CMR plays a vital role in determining the etiology and prognosis of dilated cardiomyopathies (DCM). Different patterns observed through CMR, such as subepicardial reticular pattern, myocarditis-associated patterns, and mesocardiac LGE pattern, provide valuable diagnostic and prognostic insights. Differentiating between arrhythmogenic right ventricular cardiomyopathy (ARVC) and physiological adaptations requires careful evaluation of RV dilation and systolic function in athletes, along with specific CMR assessments. Overall, multimodality imaging is crucial for accurate differentiation, risk stratification, and adequate follow-up in athletes and patients with cardiomyopathies.
With Harald Jorstad, Amsterdam UMC - The Netherlands and Maria Sanz de la Garza, Hospital Clinic Barcelona, Barcelona - Spain.
In the first of two podcasts, Dr Harald Jorstad (Amsterdam UMC, the Netherlands) joins Dr Maria Sanz de la Garza (Hospital Clínic de Barcelona, Barcelona, Spain) to discuss the role of imaging for the prevention of sudden cardiac death with a focus on multimodality imaging in cardiomyopathies.
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