Myocardial Disease Flashcards

1
Q

outline the pathologies in myocardial disease

A
  • myocarditis
  • cardiomyopathy
    • restrictive
    • dilated
    • HOCM
  • Cardiac myxoma
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2
Q

HOCM: Epidemiology

A

most common cause of sudden death in young

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3
Q

HOCM: pathophysiology

A

LV outflow tract obstruction from asymmetrical LVH, especially involving the septum

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4
Q

HOCM: aetiology

A
  • 50% genetic - autosomal dominant
    • B-myosin heavy chain mutation commonest
  • rest - sporadic

important to ask about history of sudden death!!!

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5
Q

HOCM: symptoms

A
  • often asymptomatic
  • dyspnoea
  • angina
  • exertional syncope
  • palpitations
  • sudden death
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6
Q

HOCM: signs?

A
  • jerky pulse
  • double apex beat
  • ejection systolic murmur at LLSE
    • gets louder w valsalva, decreses on squatting
  • S4
  • JVP- prominent a wave
  • may impair mitral valve closure thus causing regurgitation
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7
Q

HOCM: associations?

A
  • friederich’s ataxia
  • WPW
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8
Q

HOCM: Ix

A
  • ECG
    • LVH
    • Q waves
    • ventricular ectopics or other arrhythmias
  • ECHO- MR SAM ASH
    • MR
    • SAM- systolic anterior motion of anterior mitral valve leaflet
    • ASH- asymmetrical septal hypertrophy
  • exercise test +/- holter to quantify risk
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9
Q

HOCM: Rx

A
  • medical
    • -ve inotropes
    1. beta blockers
    2. verapamil
    • anti-arrhythmics
      • amiodarone
    • anticoagulate if AF or emboli
  • surgical
    • septal myomectomy
  • consider ICD
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10
Q

Restrictive Cardiomyopathy: pathology

A

stiff, rigid ventricles lead to impaired diastolic filling

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11
Q

Restrictive Cardiomyopathy: aetiology

mnemonic

A

miSSHAPEN–> consider infiltrative diseases

Sarcoidosis

Systemic sclerosis

Haemochromatosis

Amyloidosis

Primary: endomyocardial fibrosis

Eosinophilia

Neoplasia: carcinoid

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12
Q

Restrictive Cardiomyopathy: clinical features?

A

as constrictive pericarditis

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13
Q

Restrictive Cardiomyopathy: diagnosis?

A

catheterisation

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14
Q

Restrictive Cardiomyopathy: Rx

A

treat cause

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15
Q

Dilated Cardiomyopathy: pathophysiology

A

global ventricular dilatation

  • dilated heart leading to predominantly systolic dysfunction
  • LV more dilated than RV
  • eccentric hypertrophy seen

dilatation=thinning+expanding

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16
Q

Dilated Cardiomyopathy: aetiology?

A

30% hereditary

DILATE

Dystrophy; muscular, myotonic

Infection: myocarditis /Idiopathic

Late pregnancy: peri/post partum

Autoimmune: SLE

Toxins: Doxorubicin, cyclophosphamide

Endocrine: thyrotoxicosis

17
Q

Dilated Cardiomyopathy: presentation

A
  • LVF & RVF
  • arrythmias
  • stretching of chambers may result in MR/TR
18
Q

Dilated Cardiomyopathy: signs

A
  • raised JVP
  • S3
  • displaced apex
  • reduced BP
19
Q

Dilated Cardiomyopathy: Ix

A
  • ECG
    • T wave inversion
  • CXR
    • balloon appearance of heart
  • Echo
    • globally dilated heart
  • catheter + biopsy
    • myocardial fibre disarray
20
Q

Dilated Cardiomyopathy: Rx

A
  • bed rest
  • diuretics, ACEI, digoxin, anticoagulation
  • non-medical
    • biventricular pacing
    • ICD
  • surgical
    • heart transplant
21
Q

Cardiac Myxoma: what is it?

A

rare, benign cardiac tumour that usually arises in LA

22
Q

Cardiac Myxoma: epidemiology

A
  • F>M
  • 3rd-6th deciles
23
Q

Cardiac Myxoma: clinical features

A
  • fever
  • SOB
  • wt loss
  • syncope
24
Q

Cardiac Myxoma: signs

A
  • clubbing
  • loud 1st heart sound
  • loud 3rd heart sound
25
Q

Cardiac Myxoma: Ix

A
  • Echo
  • raised ESR
26
Q

Cardiac Myxoma: Rx

A

surgical excision