Cardiomyopathies and Cardiac Infections Flashcards
Non-ischemic Cardiomyopathies
- Dilated cardiomyopathy (DCM)
- Restrictive cardiomyopathy (RCM)
- Hypertrophic cardiomyopathy (HCM)
- Arrhythmogenic right ventricular
cardiomyopathy - Unclassified cardiomyopathies (ex.
Takotsubo)
Ischemic cardiomyopathies
- An enlarged heart caused by
CAD - Usually accompanied by HF
*IDIOPATHIC
Dilated Cardiomyopathy
Most Common
- Significant dilation of ventricles
Without hypertrophy
poor systolic function (EF < 40%) - Elevated systolic & diastolic volumes in the
ventricles - Structural changes cause
Less blood being ejected
More blood remaining in ventricles
Lead to HF - Valve dysfunction (regurgitation)
From an overstretched ventricle
DCM
D = DILATED
D = Distended heart muscle
You have decreased cardiac output
Which means decreased O2
Most common of all the cardiomyopathies
Inherited – 30-50% genetically linked
Idiopathic – 20-30%
Other causes: pregnancy, heavy alcohol use, viral infections, chemo treatment, HTN, persistent tachycardia, etc.…
RESTRICTIVE CARDIOMYOPATHY
R = Rock hard muscle (think of it like a brick wall)
R = Rigid & thick
Least common type of cardiomyopathy
Can be either inherited or acquired
Causes: infiltrative disease, storage disease, non-infiltrative disease, endomyocardial
HYPERTROPHIC CARDIOMYOPAHTY
Autosomal dominant
Passed down through genes
- 1 parent = 50% chance of getting
H = huge heart muscle
Means less blood in
- Decreased cardiac output
- Decreased O2 to body
Most common cause of SCD (sudden cardiac death) in young competitive athletes
ARVC (ARRYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY
Inherited
Uncommon
Starts in the right ventricle
TAKOTSUBO CARDIOMYOPATHY “BROKEN HEART SYNDROME”
Stress induced
Mimics ACS
More common in women than men
Cardiac catheterization to diagnose