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Cardiomyopathy a heart muscle disease associated with cardiac dysfunction. It is classified according to the structure and functional abnormalities of the heart muscle.
Dilated Cardiomyopathy -Occurs more in men and African Americans -Significant dilation of the ventricles without increased muscle wall thickness. -Ventricles have elevated systolic and diastolic volumes but a decrease in ejection fraction.
Causes of dilated cardiomyopathy Major cause - heavy alcohol intake or viral infection.
Dilated cardiomyopathy signs and symptoms (left-sided heart failure) fatigue dysrhythmias ventricular dilation impairment of systolic function atrial enlargement stasis of blood in the left ventricle
Hypertrophic Cardiomyopathy autosomal dominant condition (rare). The heart muscle asymmetrically increases in size and mass, especially along the septum. HCM may be obstructive or nonobstructive.
Hypertrophic obstructive cardiomyopathy If the increased septal size causes misalignment of the papillary muscles of the left ventricle the septum and the mitral valve can obstruct blood flow from the left ventricle.
Hypertrophic cardiomyopathy signs and symptoms -dyspnea -fatigue -angina -syncope -sudden death syndrome
Restrictive cardiomyopathy is characterized by diastolic dysfunction caused by rigid ventricular walls that impair diastolic filling and ventricular stretch. Systolic funcition is usually normal. Least common cardiomyopathy. The cause is idiopathic.
Restrictive cardiomyopathy signs and symptoms (right sided heart failure) -dypnea -non-productive cough -chest pain (angina) -fatigue Most clients are asymptomatic until late adolescence or early adulthood.
Arrhythmogenic right ventricular cardiomyopathy occurs when the right ventricle is progressively infiltrated and replaced with fibrous scar and adipose tissue.
Cardiomyopathy clinical manifestations -dyspnea on exertion -c/o fatigue -cough especially with exertion -orthopnea (which may lead to misdiagnosis of pneumonia or bronchitis) -chest pain -palpitations -dizziness -syncope on exertion -fluid retention -peripheral edema -nausea
Diagnosis of cardiomyopathy Patient history, by ruling out MI as a cause for heart failure, the echocardiogram is the most helpful diagnostic tool because the structure and function of the ventricles can be observed
Cardiac catherization used to rule out CAD as a causitive factor
Chest x-ray will reveal an enlargement of the heart and possibly pulmonary congestion
Endomyocardial biopsy may be performed to analyze the myocardial tissue cells to identify fibrous tissue and infiltrates that may have caused the cardiomyopathy
Medical management of cardiomyopathy is directed toward determining and managing possible underlying or precipitating causes
Correct the heart failure medications, low sodium diet, and exercise (this is difficult because of the fatigue and dyspnea on exertion)/rest (patients can't lie down they try to rest in a high fowlers or in a recliner). Fluid limitation of 1.5 to 2 liters per day.
Correct the dysrhythmias with medications and an implanted cardiac defibrillator
Prophylatic treatment of infective endocarditis antibiotics, rest, and antipyretics
Prophylatic treatment of stasis of the blood in the left ventricle systemic anticoagulation to prevent thromboembolic events due to the stasis of blood in the left ventricle
Created by: shellic
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