cardiomyopathy Flashcards

1
Q

Define cardiomyopathy?

A

A group of diseases in which the myocardium becomes structurally and functionally abnormal

  • In the absence of coronary artery disease, valvular disease and congenital heart disease
  • It can affect young people
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2
Q

what is the difference between primary and secondary cardiomyopathy?

A

primary- confined to myocardium

secondary- part of systemic disease

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3
Q

what are the 3 types of cardiomyopathy>

A

Dilated – ventricle dilated, thin walls, reduced ventricular pressure

Hypertrophic – muscle hypertrophies inwards, more rigid, obstruction etc.

Restrictive – basically the same amount of muscle but it’s rigid and doesn’t pump as well as normal

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4
Q

describe the history for cardiomyopathy

A

Symptoms of HF:

  • SOB on exertion
  • Fainting
  • Fatigue

Sudden death often 1st presentation

Family history

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5
Q

what is seen on examination in cardiomyopathy?

A
  • Respiratory crackles
  • Murmurs
  • S3, S4
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6
Q

outline the investigations for cardiomyopathy?

A

No single diagnostic test for all types

ECHO

Can also do bloods, BNP, CXR, ECG, cardiac catheterisation, stress test

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7
Q

outline the pathophysiology of dilated cardiomyopathy?

A

Ventricles enlarge and become dilated.

Walls thin and weaken -> can’t contract effectively.

Think of the Law of Laplace: increased radius leads to reduced ventricular pressure

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8
Q

what are the risk factors for dilated cardiomyopathy?

A

Alcohol, post-viral, haemochromatosis, genetic

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9
Q

outline the presentation of dilated cardiomyopathy?

A

Signs and symptoms of HF

Displaced apex beat, TR/MR murmur, S3

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10
Q

what are the investigations for dilated cardiomyopathy?

A

Globular heart on CXR, dilated ventricle on Echo

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11
Q

outline the pathophysiology of hypertrophic cardiomyopathy?

A
  • H for Hench – muscle thickens inwards.
  • Increased stiffness of the muscle affects pumping.
  • Thickened muscle disrupts electrical conduction and causes arrythmia.
  • Hypertrophic Obstructive Cardiomyopathy (HOCM) = thickened ventricle obstructs the outflow of blood.
  • 50% is familial (autosomal dominant)
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12
Q

what are the symptoms of hypertrophic cardiomyopathy?

A

Usually asymptomatic

Sudden cardiac death is often the 1stpresentation

Angina, dyspnoea on exertion, palpitations, syncope

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13
Q

what are the signs of hypertrophic cardiomyopathy?

A

Ejection systolic murmur

Jerky carotid pulse

Double apex beat but NOT DISPLACED

S4

LVH by voltage criteria

  • Deep S in V1/2
  • Tall R in V5/6
  • S in V1 + R in V5 or V6 ≥ 7 large squares
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14
Q

what are the investigations for hypertrophic cardiomyopathy?

A

ECG: Q waves, left axis deviation, signs of left ventricular hypertrophy

Echo: ventricular hypertrophy (asymmetrical septal hypertrophy

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15
Q

Outline the pathophysiology of restrictive cardiomyopathy?

A

R for Rigid – ventricles become abnormally rigid and lose flexibility.

Impaired ventricular filling during diastole.

Reduced preload -> reduced blood flow + backing up of blood.

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16
Q

what are the causes of restrictive cardiomyopathy?

A

Sarcoidosis, amyloidosis, haemochromatosis (the infiltrative ”osis” diseases)

Familial

Idiopathic

Rarer than dilated or hypertrophic cardiomyopathy

17
Q

what are the symptoms of restricive cardiomyopathy?

A

Asymptomatic or HF symptoms

18
Q

what are the signs of restricive cardiomyopathy?

A

RHF signs: raised JVP, S3, ascites and oedema, hepatomegaly

Kussmaul’s sign = paradoxical rise in JVP during inspiration

19
Q

what is Arrhythmogenic Right Ventricular Cardiomyopathy?

A
  • Progressive fatty and fibrous replacement of the ventricular myocardium
  • Inherited (autosomal dominant)
20
Q

what is Takotsubo Cardiomyopathy

A
  • Sudden temporary weakening of heart muscle after a significant stressor
  • ”Broken heart syndrome”