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Vocabulary-style flashcards covering definitions of key cardiology terms from the lecture notes.
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Dilated cardiomyopathy (DCM)
A cardiomyopathy characterized by dilation of all heart chambers with impaired global systolic function.
Hypertrophic cardiomyopathy (HCM/HOCM)
A cardiomyopathy with thickened myocardium causing dynamic LV outflow tract obstruction, often with a small LV cavity.
Systolic anterior motion (SAM) of the mitral valve
Anterior movement of the mitral valve leaflets into the LVOT during systole, contributing to obstruction.
Asymmetric septal hypertrophy (ASH)
Uneven thickening of the interventricular septum, typical in HOCM.
Small LV cavity
Reduced left ventricular cavity size often seen with HOCM due to septal hypertrophy.
Increased septal thickness
Marked thickening of the interventricular septum, characteristic of HCM.
B-notch (M-mode aortic valve sign)
A notch on the aortic valve M-mode trace seen in HOCM, indicating obstruction.
Mid-systolic notching (aortic valve)
Notch in the aortic valve trace during mid-systole; not a hallmark sign of HOCM.
Mid-systolic notching (pulmonary valve)
Not typically associated with hypertrophic cardiomyopathy as seen on M-mode.
Ground-glass/speckled IVS appearance
Speckled or ground-glass look of the interventricular septum on 2D echo, often seen in restrictive/infiltrative cardiomyopathies.
Interventricular septum (IVS) speckling
A speckled myocardial appearance on imaging associated with infiltrative diseases.
Myocardium
The muscular middle layer of the heart responsible for contraction; affected in cardiomyopathies.
LVOT gradient
Dynamic pressure gradient across the left ventricular outflow tract caused by obstruction.
Systolic high-velocity, late-peaking CW Doppler signal
Doppler pattern indicative of LVOT obstruction, common in HOCM.
A dip (M-mode finding)
A dip in the M-mode trace associated with increased left ventricular end-diastolic pressure.
HOCM in pregnancy
Hypertrophic obstructive cardiomyopathy that may present or worsen during pregnancy due to hemodynamic changes.
Sarcoidosis
Multisystem granulomatous disease; cardiac involvement can cause heart failure and dysrhythmias.
Amyloidosis
Extracellular deposition of amyloid protein causing stiff, restrictive cardiomyopathy and sometimes pericardial effusion.
Hemochromatosis
Iron overload disorder that can cause cardiomyopathy through iron deposition in the heart.
Implantable cardioverter defibrillator (ICD)
Device used to prevent sudden cardiac death by terminating malignant arrhythmias.
Restrictive/infiltrative cardiomyopathy
Diastolic dysfunction with stiff ventricles; may resemble constrictive pericarditis.
Alcohol as a cause of dilated cardiomyopathy
Alcohol abuse can lead to dilated cardiomyopathy.
Viral infection as a cause of dilated cardiomyopathy
Viral myocarditis can result in dilated cardiomyopathy.
Chemotherapy as a cause of dilated cardiomyopathy
Certain chemotherapeutic agents can cause dilated cardiomyopathy.
All of the above (alcohol, viral, chemotherapy) as DCM etiology
All listed factors can contribute to dilated cardiomyopathy.
Beta blockers
First-line pharmacologic therapy to reduce LVOT obstruction and symptoms in HOCM.
Calcium channel blockers
Medications used to reduce LVOT obstruction and symptoms in HOCM (e.g., verapamil, diltiazem).
Digitalis
Not recommended as a primary therapy for hypertrophic obstructive cardiomyopathy (HOCM).
Amiodarone
Antiarrhythmic that may be used in HOCM for rhythm control in select cases.
Incomplete closure of mitral valve (MV)
MR due to annular dilation or MV dysfunction, seen in dilated cardiomyopathy.
Chagas disease
Parasitic infection (Trypanosoma cruzi) causing cardiomyopathy.
Pompe’s disease
Glycogen storage disease type II; causes early-life cardiomyopathy with glycogen accumulation.
Idiopathic hypertrophic subaortic cardiomyopathy (IHSCM)
Another name for idiopathic hypertrophic cardiomyopathy (HOCM).
Noncompaction cardiomyopathy
Cardiomyopathy with persistent intramyocardial trabeculations and sinusoids in the left ventricle.
Endomyocardial fibrosis
Fibrosis of the endomyocardium; primary cause is hypereosinophilia in many cases.
Fractional shortening (FS)
Systolic function index; FS < 25% indicates reduced systolic function, typical of DCM.
E-point septal separation (EPSS)
Measurement used to assess systolic function; EPSS >7 mm suggests reduced systolic function.
TEI index (Myocardial performance index)
An index combining systolic and diastolic function to evaluate overall cardiac performance.
Parietal and visceral layers of the pericardium
Two layers that make up the pericardium; inflammation here defines pericarditis.