Cardiomyopathy & Myocarditis Flashcards

1
Q

Is hyoertrophic cardiomyopathy more of a systolic or a diastolic dysfunction?

A

diastolic. LV outflow obstruction

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2
Q

What is SAM?

A

systolic anterior motion of the mitral valve. mitral valve gets stuck in the aortic valve and causes outflow obstruction.

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3
Q

What causes a systolic murmur to get louder (in HCM)? What causes it to get softer?

A
  • standing/valsalva

- squatting

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4
Q

Of the primary cardiomyopathies, which are genetic, which are acquired, and which are mixed?

A

genetic- HCM
Mixed- Dilated CM, restrictive CM
Acquired- inflammatory (myocarditis)

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5
Q

Describe clinical presentation and possible outcomes of acute myocarditis?

A
  • acute inflammation (usually viral)
  • often affects young adults

With low EF and HF there is high mortality. Some recover, others develop chronic dilated cardiomyopathy.

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6
Q

myocardial dilation is often accompanied by what?

A

compensatory hypertrophy.

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7
Q

dilated cardiomyopathy pathophysiology.

A

decreased CO leads to activation of the renin-angiotensin-aldosterone system– causes increase in BP. AT-II causes endothelial dysfunction and prothrombotic effects.
Also, sympathetic nervous system is activated–release of norepinephrine is associated with ventricular remodeling (bad).

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8
Q

thinking about the pathophys from the last card which drugs would you want to give to someone with dilated cardiomyopathy?

A

ACE-inhibitors, angiotensin II receptor blockers (ARBs), and
Beta-blockers (decrease sympathetic tone)

ACE and Beta especially. They are helpful for improving function and reversing remodeling.

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9
Q

On clinical presentation, people with dilated cardiomyopathy present with symptoms of what?

A

heart failure. volume overload, dypnea, orthopnea, PND, edema etc..

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10
Q

what might happen to the atria in left ventricular hypertrophy?

A

left atrial enlargement

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11
Q

Higher levels of what biomarker is indicative of a worse prognosis in dilated CM?

A

brain natriuretic peptide (BNP)

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12
Q

hypertrophic CM causes myocyte ______

A

disarray

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13
Q

dilated CM has _____ hypertrophy while hypertrophic CM has ______ hypertrophy.

A

concentric (sarcomeres added in parallel)

eccentric (sarcomeres added in series)

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14
Q

What is the most frequent symptom on exertion of HCM?

A

dyspnea

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15
Q

Why might people with HCM have anginal chest pain?

A

very thick heart walls, decreased blood flow there.

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16
Q

what is the study of choice for HCM and what does it usually reveal?

A

septal hypertrophy on echocardiogram

17
Q

What are some important treatment procedures of HCM?

A
surgical myomectomy (cut out some of the heart)
alcohol ablation (kills some heart cells)
18
Q

What are the hallmarks of restrictive cardiomyopathy?

A

amyloidosis (cardiac amyloid) and sarcoidosis (systemic disorders)

19
Q

HCM has a good or bad contractility?

A

good. pumps like a beast

20
Q

What is ARVC and common presentation?

A

arrythmogenic Right ventricular cardiomyopathy- there is progressive replacement of the myocardium with fibrofatty tissue. Get dilated cardiomyopathy (RV or LV) and can get sudden death in young and middle aged pats.

21
Q

What is important for diagnosing HCM?

A

ECG- LV hypertropy, LA enlargement