Cardiomyopathy Flashcards

1
Q

Disease of the heart muscle where the heart is structurally and functionally abnormal

A

Cardiomyopathy

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2
Q

What are three viruses that can cause viral myocarditis?

A

Coxsackie group B, Parvo B19, and adenovirus

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3
Q

Immune mediated and leads to myocyte loss and fibrosis

A

Viral Myocarditis

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4
Q

Viral myocarditis is usually self limited but some progress to

A

Dilated cardiomyopathy

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5
Q

Toxins such as chronic alcohol ingestion or chemotherapeutic agents can cause

A

Dilated cardiomyopathy

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6
Q

Causes oxidative stress, cell apoptosis, decreases myocardial protein synthesis

A

Chronic Alcohol ingestion

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7
Q

Anthracyclines are chemotherapeutic agents that can cause

A

Dilated Cardiomyopathy

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8
Q

Heart Failure toward the end of pregnancy or in months after delivery wihtout any identifiable cause

A

Peri-partum CM

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9
Q

Impaired VEGF signaling and altered prolactin processing are causes of

A

Peripartum CM

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10
Q

Up to 50% of cardiomyopathies are likely

A

Familial

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11
Q

We want to use diuretics, ACEI/ARB, beta-blockers, and aldosterone antagonists to treat

A

Dilated cardiomyopathies

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12
Q

with a DCM that has a LVEF less than 35%, treat w/

A

AICD

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13
Q

If we have a DCM w/ LBBB and a QRS greater than 120 ms, treat w/

A

CRT

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14
Q

Autosomal dominant condition w/ variable penetrance

-Characterized by myocardial disarray

A

Hypertrophic Cardiomyopathy (HCM)

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15
Q

Due to mutation in one of several sarcomeric genes such as Beta-myosin heavy chain, cardiac troponins, and myosin binding protein

A

HCM

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16
Q

Characterized by asymetric LVH and normal to hyperdynamic LVEF

-Most common cause of SCD in athletes

A

HCM

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17
Q

Clinically presents w/ DOE/SOB and angina

A

HCM

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18
Q

Which type of murmur is seen in HCM?

A

S4

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19
Q

If HCM has an LVOT obstruction than we will see a systolic diamond shaped murmur from LPSB and an

A

Apical holocystoli murmur from MR

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20
Q

EKG will show LVH, LAE, and Q waves (in inferior and lateral leads)

A

HCM

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21
Q

Increased dynamic obstruction after anextrasystolic beat

A

Brockenbrough-Braunwald Sign

22
Q

We can use beta blockers to treat

23
Q

Which Ca2+ channel blocker can be used to treat HCM?

24
Q

What is a class IA anti-arrhythmic that is used to treat HCM?

A

Disopyramide

25
Reduces contractility which reduces obstruction in HCM which then decreases O2 demand
Disopyramide
26
Disopyramide decreaes HR which increases
Diastolic Filling Time
27
For HCM with a wall thickness of gretaer than 30mm, we want to treat w/
AICD
28
Characteried by ventricular muscle stiffness leading to diastolic dysfunction
Restrictive Cardiomyopathy
29
Do not need thick walls for diagnosis (Although most will have increased wall thickness) -Normal-near normal LVEF except in late stages
Restrictive Cardiomyopathy
30
Restrictive cardiomyopathy results from
Scarring/fibrosis or infiltration
31
The most common cause of restrictive cardiomyopathy is
Amyloidosis
32
Extracellular deposit of amyloid fibrils -misfolded insoluble protein with a beta-pleated sheet configuration
Amyloidosis
33
Igg light chain produced by clonal population of plasma cells in bone marrow
AL amyloid
34
Mutations in gene encoding TTR lead to misfolding and deposition of amyloids -Autosomal dominant
Familial Systemic Amyloidosis (FAP)
35
Clincially presents w/ peripheral neuropathy and autonomic dysfunction
FAP
36
Due to breakdown of normal TTR (non-mutated) -Almost always limited to the heart
Senile Systemic Amyloidosis (SSA)
37
Commonly presents w/ Carpal tunnel syndrome
SSA
38
Caused by a misfolding of ANP - only seen on autopsy - Mostly elderly women
Isolated Atrial Amyloidosis
39
Usually occurs in setting of chronic inflammation -Breakdown of inflammatory protein serum amyloid A
Secondary Amyloiosis
40
The major target of secondary amyloidosis is the
Kidney
41
Fabry's disease, Myxoedematous cardiomyopthy, an haemochromatosis are conditions that may mimic
Amyloid Heart Disease
42
In RCM we see increased muscle stiffness which causes
Decreased compliance
43
We see both right and left sided volume overload w/
RCM
44
The decrease cavity size seen in RCM causes decreases in
SV and CO
45
Increased JVD with inspiration
Kussmaul sign
46
Kussmaul sign is seen w/
RCM
47
Genetic disorder where the RV free wall is replaced by fibro-fatty tissue
Arrhythmogenic RV cardiomyopathy
48
Shows RV dysfunction, dilation, and akinesis
Arrhythmogenic RV cardiomyopathy
49
Arrested development of myocardial compaction during fetal growth -Autosomal dominant/X-linked recessive
LV non-compliance
50
Characterized by deep intra-trabecular recesses
LV non-compaction
51
Also known as Takotsubo CM, broken heart syndrome
Stress-induced cardiomyopathy