ASE’s Comprehensive Echocardiography

Right Ventricle in Dilated Cardiomyopathy

Dilated cardiomyopathy (DCM) encompasses a wide range of conditions in which the primary disorder is the enlargement of the ventricular chambers with normal left ventricular (LV) wall thickness, which ultimately leads to reduced LV contractile function and symptoms of heart…

Echocardiographic Assessment of Myocarditis

Myocarditis is a pathophysiological condition defined as infiltration of the myocardium by inflammatory cells with associated degenerative and necrotic changes not typical of ischemic injury. In severe cases, myocarditis is characterized by a rapid onset of heart failure symptoms. Although…

Apical Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is a primary disease of cardiac muscle characterized by a hypertrophied, nondilated left ventricle unassociated with other cardiac diseases that can reasonably account for the magnitude of hypertrophy present. The distribution of left ventricular hypertrophy (LVH), the…

Hypertrophic Cardiomyopathy: Screening of Relatives

Acknowledgment The authors would acknowledge Dr. Maithri Siriwardena, who was a coauthor of this chapter in the second edition of the textbook. Hypertrophic cardiomyopathy (HCM) is a common genetic cardiac disorder. The prevalence of overt HCM (using the threshold of…

Hypertrophic Cardiomyopathy: Assessment of Therapy

Acknowledgment The authors acknowledge Dr. Paul Szmitko, who was the first author of this chapter in the second edition of the textbook. Dynamic left ventricular outflow tract obstruction (LVOTO) is an important clinical feature of hypertrophic cardiomyopathy (HCM). Resting or…