Cardiomypathy, Infectious, inflammatory Cardiac Disorders

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25 Terms

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What is cardiomyopathy?
A disease of the heart muscle associated with cardiac dysfunction, classified by structural and functional abnormalities.
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List the five classifications of cardiomyopathy.
Dilated cardiomyopathy, hypertrophic cardiomyopathy, restrictive/constrictive cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy/dysplasia, and unclassified cardiomyopathy.
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What is the most common form of cardiomyopathy?
Dilated cardiomyopathy (DCM).
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What is Ischemic cardiomyopathy?
An enlarging heart caused by coronary artery disease, usually accompanied by heart failure.
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What are primary cardiomyopathies focused on?
Primarily on the heart muscle itself, including genetic, nongenetic, and acquired conditions.
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What electrolyte is majorly involved in cardiomyopathy?
Sodium.
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Describe the pathophysiology of dilated cardiomyopathy (DCM).
Characterized by significant ventricular dilation without simultaneous hypertrophy leading to poor systolic function and decreased ejection fraction.
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What are the symptoms commonly experienced by a patient with heart failure due to cardiomyopathy?
PND, cough, orthopnea, peripheral edema, nausea, chest pain, palpitations, dizziness, and syncope.
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What is hypertrophic cardiomyopathy (HCM)?
An autosomal dominant condition that leads to increased heart muscle size and mass, often resulting in life-threatening arrhythmias.
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What common screening methods are used for HCM?
12-lead ECG, physical examination, and echocardiograms.
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What is the leading cause of sudden death in young athletes?
Hypertrophic cardiomyopathy (HCM).
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What is the major complication associated with HCM?
Obstruction of the left ventricular outflow tract (LVOT), which can lead to syncope and heart failure.
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What is restrictive cardiomyopathy (RCM)?
A form of cardiomyopathy characterized by rigid ventricular walls that impair diastolic filling.
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What are common causes of restrictive cardiomyopathy?
Infiltrative diseases, storage diseases, noninfiltrative diseases, and endomyocardial diseases.
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What is arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D)?
An inherited muscle disease that leads to progression of the myocardium being replaced by fibrous scar and adipose tissue.
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What are the common diagnostic tools for ARVC/D?
ECG, echocardiogram, cardiac MRI, and family history.
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What is the primary indicator for performing a heart transplant?
Severe heart failure symptoms that are uncontrolled by medical therapy.
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What role do ventricular assist devices (VADs) play in heart failure management?
Provide mechanical support for the heart in patients with end-stage heart failure or who are awaiting heart transplantation.
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What is infective endocarditis?
A microbial infection of the heart's endocardium with a high mortality rate, typically occurring in those with prosthetic heart valves or defects.
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What symptoms are associated with infective endocarditis?
Fever, heart murmur, and petechiae clusters on the body.
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How is myocarditis characterized?
An inflammatory process affecting the myocardium, potentially leading to heart dilation and thrombi.
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What is the most characteristic symptom of pericarditis?
Chest pain, particularly that worsens with deep inspiration or when lying down.
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What is the primary method for diagnosing pericarditis?
History, signs and symptoms, echocardiogram.
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What are the potential complications of pericarditis?
Fluid accumulation leading to cardiac tamponade.
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What treatment options are often prescribed for pericarditis?
NSAIDs for pain relief, corticosteroids, colchicine, and possible pericardiocentesis.