cardiomyopathy Flashcards

1
Q

What is the most common form of cardiomyopathy?

A

Dilated cardiomyopathy (DCM)

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2
Q

What happens in dilated cardiomyopathy?

A

Dilated left ventricle without hypertrophy and systolic dysfunction
Diminished contractile elements
Diffuse necrosis of myocardial cells

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3
Q

what are the symptoms of dilated cardiomyopathy

A

Poor systolic function (low EF)
Increasing end-diastolic pressure
Increasing pulmonary and systemic venous pressures
Altered valve function (usually regurgitation)
Thrombi formation

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4
Q

what do you avoid for dilated cardiomyopathy

A

verapamil

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5
Q

what causes hypertrophic cardiomyopathy

A

A rare autosomal dominant condition

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6
Q

what is the surveillance for someone with a family history of hypertrophic cardiomyopathy

A

12-18 years of age: echocardiogram every year
18-70 years of age: echocardiogram every 5 years

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7
Q

when does the thickening of hypertrophic cardiomyopathy

A

Begins during early adolescence and stops when growth is finished

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8
Q

What are the symptoms of hypertrophic cardiomyopathy?

A

High EF, smaller ventricular cavities, takes longer for the ventricles to relax after systole

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9
Q

what are the clinical manifestations of hypertrophic cardiomyopathy

A

Cardiac arrest, sustained vtach and vfib, angina, syncope, palpitations, and left heart failure
Higher EF: small amount of blood but the muscle is stronger

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10
Q

What is a nonsurgical septal reduction therapy

A

alcohol septal ablation

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11
Q

what should patients with hypertrophic cardiomyopathy avoid?

A

dehydration and diuretics

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12
Q

what is the cause of restrictive or constrictive cardiomyopathy

A

Diastolic dysfunction caused by rigid ventricular walls that impair diastolic filling and ventricular stretch

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13
Q

What are the symptoms of restrictive or constrictive cardiomyopathy?

A

Right sided heart failure, decreased ventricular filling, decreased CO

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14
Q

what should patients with restrictive or constrictive cardiomyopathy avoid

A

nifedipine

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15
Q

what causes arrhythmogenic right ventricular cardiomyopathy

A

Much of the right ventricle is replaced by a chaotic mix of heart muscle, fibrous tissue, and fat
Right ventricle dilates and develops poor contractility

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16
Q

what is a symptom of arrythmogenic right ventricular cardiomyopathy

A

Arrhythmia, ventricular tachycardia

17
Q

How would blood relatives of a patient with arrhythmogenic right ventricular cardiomyopathy be monitored?

A

12 lead ECG, Holter monitor, and echocardiography

18
Q

How would the ECG of an arrhythmogenic right ventricular cardiomyopathy present?

A

Epsilon wave”: slow RV, and flipped Ts in V2-V3

19
Q

What cardiomyopathy causes sudden death among young athletes?

A

Arrhythmogenic right ventricular cardiomyopathy

20
Q

who is most likely to have cardiomyopathy

A

African Americans and older adults

21
Q

what are the surgical management methods for cardiomyopathy: Left ventricular assist devices (LVAD)

A

Short term, to get them to transplant, or for those who can’t get transplant

22
Q

what are the surgical management methods for cardiomyopathy: Intra aortic balloon pump

A

Only done for about 1 week while waiting for transplant
Deflated during systole; inflated during diastole
Reduces afterload
Increases myocardial perfusion

23
Q

what are the surgical management methods for cardiomyopathy: heart transplant

A

Needs to be done within 4 hours of harvest → time is a factor
Immunosuppressants to reduce rejection

24
Q

what are the surgical management methods for cardiomyopathy: total artificial hearts

A

replace both ventricles