Cardiomyopathy Flashcards

1
Q

Cardiomyopathy

A

Any condition leading to an abnormally functional morphological abnormal myocardium

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2
Q

3 Cardiomyopathies

A

Dilated
Restrictive
Hypertrophic

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3
Q

How do most cardiomyopathies present?

A

Like heart failure

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4
Q

Best diagnostic modality for cardiomyopathy

A

ECHO!!!

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5
Q

Systolic dysfunction

A

Can’t contract the ventricles and empty them like we used to - ventricles pump harder - going to eventually have diatolic dysfunction

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6
Q

Diastolic dysfunction

A

LV can’t stretch - Ventricle made of glass

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7
Q

Myocarditis

A

Infectious or non-infectious process leads to necrosis. May lead to dilated cardiomyopathy

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8
Q

Two main mechanisms of cardiomyopathy

A

Autoimmune or infectious

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9
Q

Acute phase of myocarditis

A

Substernal, pleuritic chest pain
First 2 weeks
Fever

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10
Q

Chronic phase of myocarditis

A

Autoimmune - after the first two weeks

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11
Q

4 infectious causes of myocarditis

A

Adenovirus
COVID-19
Coxsackie virus
Cytomegalovirus

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12
Q

3 noninfectious causes of myocarditis

A

Alcohol
Cocaine
Anthracyclines

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13
Q

Myocarditis presentation

A

Acute febrile illness
SOB, Pleural chest pain, may present with HF, arrhythmias
No hx of heart problems

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14
Q

Best position to hear pericardial friction rub

A

Leaning forward

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15
Q

Four Initial tests for myocarditis

A

EKG - Sinus tachy, dysrhythmia, ST-T changes
Cardiac biomarkers - Elevated troponins (may have to cath)
CXR - Enlarged cardiac silloette
Increased/Reduced uptake of dye on cardiac MRI

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16
Q

Only true way to diagnose myocarditis -gold standard

A

A heart biopsy - only get if it will change presentation - patient decompensating rapidly and we have no idea what is going on

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17
Q

NSAIDs and IHD

A

NOT indicated

18
Q

Dilated cardiomyopathy

A

Big, dilated left ventricle with low ejection fraction, #1 reason for a heart transplant
Systolic dysfunction

19
Q

Presentation of dilated cardiomyopathy on PE

A

Valvular disorders
Arrhythmias
Pulsus alternans d/t limited emptying
S3 gallop
HF symptoms

20
Q

Etiologies of dilated cardiomyopathy

A

Pregnancy - usually go back to baseline
Lyme
Chagas
Alcohol
AF, SVT, AVNRT

21
Q

DCM etiolology mneumonic

A

Alcohol
Beri beri
Coxsackie
Cocaine
Chagas
Doxirubicin toxicity

22
Q

Diagnosis for DCM

A

Echo and BNP/pro-BMP

23
Q

Treatment for DCM

A

CHF management
Heart Transplant
Defibrillator

24
Q

Restrictive cardiomyopathy

A

Fibrosis leading to a DIASTOLIC dysfunction
Bi-atrial enlargement

25
6 Etiologies of restrictive cardiomyopathy
Amyloidosis Sarcoidosis Hemochromatosis Fabry disease Radiation Fatty infiltration
26
Diagnosis and treatment for restrictive cardiomyopathy
Echo or MRI, may consider Biopsy Treat HF and Underlying cause
27
Hypertrophic cardiomyopathy
Typically a genetic issue Septal buildup of myocytes - block the aortic valve Worse with exercise, standing, valsalva DIASTOLIC dysfunction
28
Presentation of hypertrophic cardiomyopathy
Fatigue, chest pain, aortic stenosis like murmur - worse with valsalva, better with squatting Sudden death
29
Diagnostics of hypertrophic cardiomyopathy
LVH on EKG ECHO with LV wall over 1.5 cm thick
30
Management of hypertrophic CM non invasive
Activity restriction BB or Verapamil Avoid diuretics or vasodilators
31
Invasive management of hypertrophic cardiomyopathy
Septal myectomy or alcohol septal ablation
32
Screening of HTCM
Screen first degree relatives - annual echo until 20, then Q5 years
33
MCC of HF in US
Ischemic cardiomyopathy
34
Ischemic cardiomyopathy
Characterized by systolic dysfunction Presentation - CHF Usually LV dysfunction Regional wall abnormality on Echo - akinetic
35
Management of ischemic cardiomyopathy
Nuclear viability scan for hibernation Revascularization Manage CHF ICD/Wearable defibrillator
36
Arrhythmogenic right ventricular cardiomyopathy
RV free wall myocardium is replaced by fibrous/fatty tissue Sudden death in YAs More common in europe
37
Left ventricular noncompaction
Congenital - CHF, etc. at birth Heart wall looks like spongy bone Usually need a heart transplant
38
Stress induced/Takutsobu Cardiomyopathy
Broken heart syndrome STEMI in the absence of CAD Due to an intense psychological stressor
39
MC patient for stress induced cardiomyopathy
Postmenopausal women
40
Diagnosis and tx for stress induced cardiomyopathy
LV apical ballooning!!! on echo or LV angiography Almost all patients recover in a few weeks - BB for 1 year
41
Key sign for stress induced cardiomyopathy
LV apical ballooning