Multimodality Imaging in Apical Hypertrophic Cardiomyopathy: Can Echocardiography Learn from Cardiac Magnetic
Francesco Mangini1, Massimo Grimaldi1, Francesco Spinelli2
1Cardiology Department, General Regional Hospital F. Miulli, 70021 Acquaviva delle Fonti, Italy.
Apical hypertrophic cardiomyopathy diagnosis benefits from complementary roles of echocardiography and cardiac magnetic resonance imaging. Cardiac MRI is the reference standard, while echocardiography offers real-time dynamic assessment and identifies obstructive gradients.
Area of Science:
- Cardiology
- Medical Imaging
Background:
- Apical hypertrophic cardiomyopathy (AHC) is an under-recognized variant of hypertrophic cardiomyopathy.
- It is characterized by predominant thickening of the left ventricle's apical segments.
Purpose of the Study:
- To review the diagnostic roles and complementary nature of echocardiography and cardiac magnetic resonance imaging (CMR) in AHC.
- To highlight how CMR can refine echocardiographic practice for AHC diagnosis.
Main Methods:
- Review of echocardiography and CMR in diagnosing and assessing apical hypertrophic cardiomyopathy.
- Comparison of the strengths and limitations of each imaging modality for AHC.
Main Results:
- Transthoracic echocardiography is the first-line imaging technique but may underestimate apical involvement.
- Cardiac MRI is the reference standard for defining apical morphology, quantifying hypertrophy, and tissue characterization.
- Echocardiography excels in real-time cardiac dynamics and identifying subtle obstructive gradients.
Conclusions:
- Echocardiography and CMR have complementary roles in diagnosing and managing AHC.
- CMR provides a research platform for developing new echocardiographic criteria for AHC.
- Methodological and conceptual benefits can be derived from integrating CMR findings into echocardiographic practice for AHC.
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