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_MS2 Cardio > 8/7- Cardiomyopathies > Flashcards

8/7- Cardiomyopathies Flashcards

1
Q

What is cardiomyopathy?

A

Genetic or acquired primary disease of the myocardium

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2
Q

What are the different subtypes of cardiomyopathy?

A
  • Dilated
  • Hypertrophic
  • Restrictive
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3
Q

What is the equation for ejection fraction?

What is a normal value

A

EF = SV/EDV x 100%

EF is about 50-75%

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4
Q

What is dilated cardiomyopathy (DCM)?

  • Which chambers affected
  • Progressive?
  • Arrhythmias
  • Consequences
A

Ventricular dilation and impaired systolic function: congestive heart failure

  • 1 or both ventricles are affected (more often L or both; rarely R alone)
  • Generally progressive
  • Atrial and ventricular arrhythmias are common
  • Sudden death may occur at any age
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5
Q

What is the main problem in dilated cardiomyopathy as opposed to hypertrophic and restrictive?

A

Dilated involves decreased systolic function and ejection fraction while hypertrophic and restrictive have more problems with diastole since stiffer ventricles are harder to fill

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6
Q

What are some (potentially reversible) causes of dilated cardiomyopathy?

A

- Alcohol

- Ischemia

- Hypertension

  • Cocaine
  • Medications
  • Endocrine
  • Nutritional
  • Electrolyte imbalance
  • Iron (hemachromatosis or congenital anemias)
  • Tachycardia
  • Sleep apnea
  • Infections (Chagas/viral)
  • Autoimmune
  • Sarcoidosis

**Most common causes

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7
Q

What is the pathophysiology behind alcohol causing ___ cardiomyopathy? Reversible or irreversible?

A

Alcohol -> DCM

  • Associated with heavy, prolonged use
  • Often evident as asymptomatic LV dysfunction
  • Direct toxic effects of alcohol and nutritional deficiencies; in addition to a higher than expected incidence of HTN

**Potentially reversible after alcohol abstinence!**

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8
Q

What is the pathophysiology behind ischemia causing ___ cardiomyopathy? Reversible or irreversible?

A

Ischemia -> DCM

  • Revascularization restores function in chronically ischemic (hibernating) myocardium

Practical implication:

  • Coronary angiography or stress testing is recommended in most pts presenting with dilated cardiomyopathy to exclude or confirm CAD as a possible etiology

(b/c it is potentially treatable)

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9
Q

What are some (irreversible) causes of DCM?

A
  • Idipoathic
  • Post MI Scarring
  • Familial
  • HIV

**Differentiate between hibernation and scarring**

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10
Q

What may cause hypertrophic cardiomyopathy (HCM)? Characterstics? Involves what?

A

Genetic disease

  • Autosomal dominant
  • Involves sarcomere
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11
Q

What are the different phenotypes of HCM?

A

There are numerous phenotypes of HCM

  • Obstructive
  • Non-obstructive
  • Regional
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12
Q

What physical characteristics are seen in HCM?

  • Problem with what function of the heart?
  • Arrhythmias?
  • Consequences?
A
  • Thick walls and filling abnormalities
  • Arrhythmias common
  • Sudden death at a younger age
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13
Q

What does this show?

A

Apical HCM

  • Hypertrophy mainly at ventricular apex
  • Classic T wave inversions on EKG
  • “Yamaguchi syndrome”
  • Thought to be a more benign variant of HCM
  • Not too much trouble with ventricle emptying (since apex is mainly affected), but may become symptomatic in later stages
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14
Q

What does this show?

A

Asymmetric septal hypertrophy (ASH/IHSS)

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15
Q

Characteristics of HCM: SAM (systolic anterior motion) and LVOT (left ventricular outflow tract) obstruction

A
  • Altered left ventricle geometry
  • Abnormal mitral valve pathology: long anterior MV leaflet

- Venturi effect: systolic anterior motion of the mitral leaflet: SAM (if leaflet flows through restricted area, turbulence increases but pressure decreases, sucking leaflet towards the septum where it may hit and transiently stop blood)

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16
Q

What is this showing?

A

SAM and LVOT (with HCM?)

  • Very mosaic pattern is turbulence created in obstruction in LVOT
  • Left ventricular pressure must increase significantly to push blood through this obstruction
17
Q

Pressure characteristics of HCM with SAM and LVOT?

A
  • Higher ventricular pressure proximal to the LVOT compared to the aortic valve
  • May help differentiate from aortic stenosis???
18
Q

What are some clinical manifestations of HCM?

A

Symptoms are common; there is impaired filling of the heart

- Dyspnea

- Chest pain

- (Pre)syncope

- Outflow obstruction:at rest or with exertion only

- Arrhythmias

  • Fatigue
  • Edema
  • Normal systolic function
  • Mitral insufficiency

Dyspnea, palpitations, syncope, chest pain in about 30-50%

19
Q

What is the natural history of HCM?

A

Bimodal:

  • Early developing during puberty
  • Later evident age > 60 yo

Annual mortality is about 2% (4-6% during adolescence)

  • Most deaths are sudden: ventricular arrhythmias (may start as SVT); exertional

Endocarditis

20
Q

What is restrictive CM (RCM)?

A
  • Non-dilated ventriclewith normal wall thickness (or increased) and systolic function
  • Dilated atria
  • Myocardium is rigid; ventricles fill at high pressures only (diastolic dysfunction)
21
Q

Causes of restrictive CM?

A

- Idiopathic

  • Amyloidosis
  • Sarcoidosis
  • Hemochromatosis (often dilated CMP)
  • Radiation
  • Hypereosinophilic syndrome
  • Endomyocardial Fibrosis
  • Chloroquine therapy
22
Q

How does restrictive CM present?

A

Any age

Dyspnea and edema most common!

  • High venous pressures

—Elevated jugular venous pressures

—Pulmonary venous congestion

Later: fatigue, weakness with low CO

23
Q

Comparison of cardiomyopathies in terms of LVEF, WTH, LVEDV, and LA size

A
24
Q

Anatomy of cardiomyopathies

A

Congestive

  • Dilated LV
  • Decreased systolic function

Restrictive and hypertrophic

  • Normal LV size
  • Normal or increased systolic function
  • Decreased diastolic function
25
Q

Clinical presentations of cardiomyopathies

A

Dilated: Systolic CHF

Hypertrophic: Diastolic CHF

  • Angina
  • Syncope
  • SCD (sudden cardiac death)

Restrictive: Diastolic CHF

  • CHB (complete heart block)
26
Q

What are some physical findings in dilated cardiomyopathy?

A
  • Left ventricular or biventricular CHF
  • Decreased S1, weak pulses (low SV)
  • S3 gallop +/- S4 gallop
  • MR and TR holosystolic murmurs
  • Pulsus alternans
27
Q

What are some physical findings in hypertrophic cardiomyopathy?

A
  • Spike and Dome or Bisferiens arterial pulse
  • Bifid apical impulse

Dynamic auscultation:

  • Paradoxical A2-P2 split: late A2
  • Systolic murmurs at apex/LSB
  • Louder and longer murmur with maneuvers that decrease EDV or increase systolic function

- Stand/Valsalva: increased

- Squat: decreased

28
Q

What are some things that can be done to decrease LVEDV in dynamic auscultation? What cardiomyopathy is being assessed?

A

Decrease LVEDV by:

  • Standing
  • Valsalva

Done in dynamic auscultation of HCM

  • Increase LVOT obstruction and murmur
29
Q

What are some things that can be done to increase LVEDV in dynamic auscultation? What cardiomyopathy is being assessed?

A

Increase LVEDV by:

  • Leg elevation
  • Squatting

Done in dynamic auscultation of HCM:

  • Decrease LVOT obstruction and murmur
30
Q

What is the Brockenbrough-Morro-Braunwald phenomenon?

A

Decreased pulse in the beat that follows an ectopic beat

  • Greater LVOT obstruction due to greater contractility
  • Anything causing a more forceful contraction worsens the obstruction (lowers the stroke volume)
31
Q

What are some physical findings in RCM?

A

Exam:

  • Right sided failure (elevated JVP, hepatomegaly, ascites, and edema out of proportion to L heart failure)
  • Mitral and Triscuspid insufficiency
  • Rapid filling sound (S3 gallop)
32
Q

What is seen on the ECG in cardiomyopathies?

A

Congestive: LBBB, low voltage

Hypertrophic: Severe LVH, pathologic Q waves, WPW

Restrictive: low voltage, heart blocks

33
Q

Which one of the following groups of CMs is predominantly associated with systolic heart failure with decreased ejection fraction?

A. Hypertrophic CMP

B. Dilated CMP

C. Restirictive CMP

D. None of the above

A

Which one of the following groups of CMs is predominantly associated with systolic heart failure with decreased ejection fraction?

A. Hypertrophic CMP

B. Dilated CMP

C. Restirictive CMP

D. None of the above

34
Q

Which one of the following causes of DCM is NOT potentially reversible?

A. Alcoholic cardiomyopathy

B. Ischemic CMP with hibernating myocardium

C. Hypothyroidism associated CMP

D. CMP due to post MI scarring

A

Which one of the following causes of DCM is NOT potentially reversible?

A. Alcoholic cardiomyopathy

B. Ischemic CMP with hibernating myocardium

C. Hypothyroidism associated CMP

D. CMP due to post MI scarring

35
Q

Which one is true about the murmur of LVOT obstruction hypertrophic CMP?

A. Best heard in the axillary are

B. Becomes softer with Valsalva

C. Becomes louder with standing

D. Becomes louder with leg elevation

A

Which one is true about the murmur of LVOT obstruction hypertrophic CMP?

A. Best heard in the axillary are

B. Becomes softer with Valsalva

C. Becomes louder with standing

D. Becomes louder with leg elevation

36
Q

Which type of cardiomyopathy suggested by normal size LV, normal wall thickness, normal LV systolic fct and very large atria?

A. Dilated CMP

B. Hypertrophic

C. Restrictive

D. All of the above

A

Which type of cardiomyopathy suggested by normal size LV, normal wall thickness, normal LV systolic fct and very large atria?

A. Dilated CMP

B. Hypertrophic

C. Restrictive

D. All of the above

37
Q

All are true about – phenomenon except:

  1. Occurs in hypertrophic CMP
  2. Decreased pulse (weaker in the beat the t follows an ectopic beat)
  3. Increased pulse (stronger) in the beat that follows an ectopic beat
  4. Related to dynamic chang….
A

All are true about – phenomenon except:

  1. Occurs in hypertrophic CMP
  2. Decreased pulse (weaker in the beat the t follows an ectopic beat)

3. Increased pulse (stronger) in the beat that follows an ectopic beat

  1. Related to dynamic chang….
38
Q

Treatment in cardiomyopathies?

A

_MS2 Cardio (35 decks)

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