Restrictive cardiomyopathy
Background
- Muscle is stiff from fibrosis or infiltrating process (e.g. amyloidosis, hemochromatosis)
- Form of diastolic dysfunction (difficulty filling); ventricular endocardial thickening or myocardial infiltration-->high filling pressures, impaired diastolic filling-->mitral and/or tricuspid regurgitation--> venous pulmonary hypertension
- Ventricular EF typically normal, though systolic function may deteriorate in absence of compensatory hypertrophy
- If nodal/conduction tissues affected by infiltrative/fibrotic process, may cause SA or AV block
- Must distinguish from constrictive pericarditis
Clinical features
Differential Diagnosis
Restrictive cardiomyopathy etiology DDX
- Idiopathic
- Familial non=infiltrative disease
- Infiltrative disease (amyloidosis, sarcoidosis, Gaucher, Hurler)
- Storage diseases (hemochromatosis, Fabry, glycogen/lysosomal storage diseases)
- Diabetes
- Scleroderma
- Endomyocardial fibrosis (hypereosinophilic syndrome, medication toxicity)
- Radiation, chemotherapy (doxorubicin)
- Metastatic disease, carcinoid syndrome
Evaluation
- Consider if CHF but no evidence of cardiomegaly or systolic dysfunction
- ECG
- Typically nonspecific ST/TW abnormalities
- Other features may include low voltage, pathologic Q waves, LVH, AV block
showing ST-segment and T-wave abnormalities
- CXR- heart typically normally sized, though can be enlarged in advanced stages of some underlying disease processes
- Echocardiography
- Normal LVEF
- Elevated LV filling pressures, impaired longitudinal contraction
- +/- dilated atria, myocardial hypertrophy
- Definitive diagnosis may require MRI, catheterization, biopsy
Management
- Symptom-directed
- Diuretics for edema or pulmonary vascular congestion
- Caution as cardiac output preload dependant
- Caution with afterload reduction as may cause profound hypotension
- Treat arrhythmias
- Avoid digoxin in amyloidosis as sensitivity to dig-induced arrhythmias common
- Diuretics for edema or pulmonary vascular congestion
See Also
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