Cardiomyopathies - The Big Three
- Overview: Diseases of the heart muscle leading to impaired cardiac function.
| Feature | Dilated (DCM) | Hypertrophic (HCM) | Restrictive (RCM) |
|---|---|---|---|
| Systolic/Diastolic | Systolic Dysfunction | Diastolic Dysfunction | Diastolic Dysfunction |
| EF | ↓↓ (< 40%) | Normal or ↑ | Normal |
| Ventricle | Dilated, thin wall | Thickened wall | Rigid, non-dilated |
| Key Cause | Idiopathic, Alcohol | Genetic (AD) | Amyloidosis, Sarcoid |
| Heart Sounds | S3 Gallop | S4 Gallop | S3 Gallop |
⭐ HCM Murmur: Murmur intensity decreases with maneuvers that ↑ preload/afterload (e.g., squatting, handgrip).

Dilated Cardiomyopathy - Stretched & Weak
- Pathophysiology: Impaired contractility (systolic dysfunction) → ↓ ejection fraction (<40%) → ventricular dilation. Most common cardiomyopathy.
- Etiologies: Mostly idiopathic. 📌 ABCCCD
- Alcohol (reversible)
- Beriberi (wet), Bug (Chagas disease)
- Cocaine, Coxsackie B
- Chemotherapy (Doxorubicin)
- Dystrophy (muscular)
- Clinical: S3 gallop, mitral/tricuspid regurgitation, balloon-like heart on CXR.
- Diagnosis: Echo is key → shows LV dilation & ↓ EF.
⭐ Reversible Causes: Key reversible causes include alcohol toxicity, thyroid dysfunction, and tachycardia-induced cardiomyopathy. Always consider these in new-onset HF.

Hypertrophic Cardiomyopathy - Thick & Obstructed
- Etiology: Autosomal dominant mutation in sarcomere protein genes (e.g., MYH7, MYBPC3).
- Pathophysiology: Asymmetric left ventricular hypertrophy (LVH), particularly the septum, leading to dynamic LV outflow tract (LVOT) obstruction and severe diastolic dysfunction.
- Clinical: Exertional dyspnea, angina, and syncope. Major cause of sudden cardiac death in young athletes.
- Auscultation: Harsh crescendo-decrescendo systolic murmur at the left sternal border.
⭐ Exam Favorite: Maneuvers that decrease LV cavity size (↓ preload) like Valsalva or standing, worsen the obstruction and increase the murmur. Maneuvers that increase LV cavity size (↑ preload/afterload) like squatting or handgrip, decrease the murmur.
- Dx: Echocardiogram shows septal wall thickness > 15 mm.
- Rx: β-blockers, verapamil. Avoid preload-reducing agents (diuretics, nitrates).
Restrictive Cardiomyopathy - Stiff & Stubborn
- Pathophysiology: Rigid, non-compliant ventricles lead to impaired diastolic filling and bi-atrial enlargement, with preserved systolic function initially.
- Etiology: Primarily infiltrative diseases.
- Amyloidosis: Most common cause; associated with multiple myeloma, chronic inflammation.
- Sarcoidosis: Non-caseating granulomas infiltrate the myocardium.
- Hemochromatosis: Iron deposition.
- Clinical: Resembles constrictive pericarditis. Predominantly right-sided HF symptoms (JVD, peripheral edema, ascites). Kussmaul's sign (paradoxical ↑JVP with inspiration) may be present.
- Diagnosis:
- ECG: Low-voltage QRS complexes.
- Echocardiogram: Thickened ventricular walls, sparkling "granular" appearance in amyloidosis.
⭐ Exam Favorite: The combination of low voltage on ECG despite thickened myocardium on echo is a classic finding for cardiac amyloidosis.

High‑Yield Points - ⚡ Biggest Takeaways
- Dilated cardiomyopathy, the most common form, presents with systolic dysfunction and is often idiopathic or due to alcohol abuse.
- Hypertrophic cardiomyopathy is an autosomal dominant condition causing diastolic dysfunction; its murmur increases with Valsalva.
- Restrictive cardiomyopathy results from infiltrative diseases like amyloidosis or sarcoidosis, leading to diastolic dysfunction.
- Arrhythmogenic RV cardiomyopathy involves fibrofatty infiltration of the right ventricle, causing arrhythmias.
- Takotsubo cardiomyopathy ("broken-heart syndrome") is a stress-induced, reversible apical ballooning.
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