Cardiomyopathy Flashcards

1
Q

what are the causes of dilated cardiomyopathy

A

idiopathic 50%

genetic

alclcohol

infective

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2
Q

what inheritance pattern is seen in dilated cardiomyopathy resulting from a genetic cause

A

autosomal dominant 25%

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3
Q

what are the clinical features of dilated cardiomyopathy

A

asymptomatic

heart failure symptoms

arrhythmia (AF or sudden cardiac death due to VF)

thromboembolism

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4
Q

what would you see on examination of a patient with dilated cardiomyopathy

A

displaced apex beat

S3 and S4 gallop

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5
Q

how would you broadly manage dilated cardiomyopathhy

A
  1. Manage heart failure symptoms
    - beta blockers and ACEi
    - loop and thiazide diuretics
  2. Treat any identifiable cause
  3. Prevent any complications
    - consider anti-arrhythmics
    - heart transplantation
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6
Q

what is hypertrophic cardiomyopathy characterised by

A

asymmetrical LB hypertrophy with impaired diastolic filling

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7
Q

what type of cardiomyopathy is most commonly associated with sudden cardiac death in the under 35s

A

hypertrophic cardiomyopathy

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8
Q

what causes hypertrophic cardiomyopathy

A

genetics - autosomal dominant

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9
Q

what are the two types of hypertrophic cardiomyopathy

A

Obstructive (hypertrophic obstructive cardiomyopathy - HOCM) - involves narrowing of the ventricular outflow tract due to a thickened interventricular septum

non obstructive

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10
Q

what are the clinical features of hypertrophic cardiomyopathy

A

most asymptomatic

present similarly to aortic stenosis eg.

  • angina
  • dyspnoea
  • pre-syncope/syncope
  • sudden death

AF

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11
Q

what is the most common arrhythmia seen in hypertrophic cardiomyopathy

A

AF

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12
Q

what would you see on clinical examination of a patient with hypertrophic cardiomyopathy

A
  • jerky pulse
  • palpable LV hypertrophy
  • double impulse at apex
  • pansystolic murmur
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13
Q

what changes on ECG would you see in hypertrophic cardiomyopathy

A

LV hypertrophy

T wave inversion

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14
Q

what drug is CI in hypertrophic cardiomyopathy

A

digoxin

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15
Q

how do you manage hypertrophic cardiomyopathy

A

initially use beta-blockers and rate limiting calcium channel blockers (verapamil)

surgical myectomy is the treatment of choice for those who do not respond to medical therapy

Alcohol ablation/HF treatment/heart transplant

Prevent complications - anti-arryhthmics, ICD

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16
Q

describe the epidemiology of restrictive cardiomyopathy

A

common in developing countries, equal gender preponderance

17
Q

what is restrictive cardiomyopathy

A

contraction of atria against stiff non-dilated ventricles with near normal systolic function

18
Q

what are the causes of restrictive cardiomyopathy (and the most common)

A

most common - amyloidosis

sarcoidosis
metastases + radiotherapy

19
Q

how do you detect amyloidosis on microscopy

A

congo red stain

20
Q

what are the clinical features of restrictive cardiomyopathy

A

often presents with symptoms of congestive HF

21
Q

how does Takotsubos present

A

brought on by stressful situations

symptoms and signs mimic MI but patients have non-obstructive coronary artery