Cardiomyopathy Flashcards

1
Q

What are the four main types of cardiomyopathy?

A
  • Hypertrophic,
  • Dilated (most common)
  • Restrictive,
  • Arrhythmogenic
    Can also be classficied as priamry, secondary or mixed.
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2
Q

What are some causes of dilated cardiomyopathy?

A
  • Idiopathic (most common)
  • Alcohol or cocaine
  • Myocarditis: Coxsackie B virus, HIV, diphtheria, chagas disease
  • IHD, hypertension
  • Wet beriberi: Thiamine deficiency
  • Peripartum (more common in obese patients),
  • Doxorubicin
  • Infiltrative (haemochromatosis, amyloidosis and sarcoidosis)
  • Thyrotoxicosis
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3
Q

What are the signs and symptoms of dilated cardiomyopathy?

A

Symptoms related to heart failure - Exertional dyspnoea, orthopnea, PND, peripheral oedema.
Common signs - displaced apex beat, S3 gallop rhythm, systolic murmur (regurgitation of AV valves) and balloon appearance of heart of X ray.

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4
Q

What are the causes of restrictive cardiomyopathy

A
  • Familial non-infiltrative cardiomyopathy
  • Infiltrative: Amyloidosis, sarcoidosis, Gaucher disease (lipid accumulation), Hurler syndrome or fatty infiltration.
  • Storage: Haemochromatosis, fabry disease
  • Others: Diabetic cardiomyopathy, scleroderma, Loeffler’s syndrome (hyperesosinophilic syndrome), radiation or chemotherapy
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5
Q

What are the signs and symptoms of restrictive cardiomyopathy?

A
  • Similar to heart failure and constrictive pericarditis.
  • RV failure symptoms due to reduced venous return.
  • Commonly have Af
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6
Q

What is arrhythmogenic right ventricular cardiomyopathy?

A

It is caused by fatty fibrous material replacing the myocardium. Caused by genetic defect in desmosomes. It causes palpitations, syncope and sudden cardiac death

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7
Q

What is Takotsubo cardiomyopathy?

A

Apical ballooning of the myocardium usually triggered by extreme stress.
Suspect in patients with trop positive chest pain and history of significant stressor. DO ECHO

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8
Q

What are some neuromuscular conditions which cause cardiomyopathy?

A
  • Fredreich’s ataxia,
  • Duchenne-becker muscular dystrophy,
  • Myotonic dystrophy
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9
Q

What is hypertrophic obstructive cardiomyopathy and its features

A
  • Autosomal dominant condition which causes mutation in gene encoding beta-myosin heave chain protein or myosin binding protein C.
  • It results in diastolic dysfunction, left ventricular hypertrophy and decreased cardiac output
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10
Q

What are the signs and symptoms of HOCM?

A

Often asymptomatic but can present with:
- Exertional dyspnoea, angina, syncope (typically following exercise as subaortic hypertrophy of ventricular septum results in function aortic stenosis),
- Sudden death most commonly due to ventricular arrhythmias
- Heart failure
- Systolic murmurs,
- Jerky pulse

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11
Q

What is HOCM associated with?

A

Friedrich’s ataxia and Woldd-Parkinson White syndrome

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12
Q

What are the ECHO findings for HOCM

A

MR SAM ASH - definitive diagnosis
- Mitral Regurgitation
- Systolic Anterior Motion of mitral valve leaflets.
- Asymmetrical septal hypertrophy

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13
Q

What is the management of HOCM?

A

ABCDE
- Amiodarone,
- Beta blockers or verapamil for symptoms
- Cardioverter defibrillator
- Dual chamber pacemaker
- Endocarditis prophylaxis

Avoid ACE inhibitors and nitriates as it can worsen things

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14
Q

What drugs should be avoided in HOCM

A

Nitrates, ace inhibitors and ionotrophes

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15
Q

What is WPW?

A

Arrhythmia caused by congenital accessory pathway leading to atrio-ventricular re-entry tachycardia

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16
Q

What are the ECG findings of WPW?

A

Short PR interval
Wide QRS with slurred upstroke (delta wave)
Left axis deviation (if right sided pathway)
Right axis deviation (if left sided pathway)