Cardiomyopathy Flashcards

1
Q

What is cardiomyopathy?

A

The heart muscle becomes thick, enlarged or rigid causing the heart to become weaker as the disease progresses

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2
Q

What is hypertrophic cardiomyopathy?

A

LV outflow obstruction from the asymmetric septal hypertrophy
- leading cause of sudden cardiac death in the young

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3
Q

Prevalence of hypertrophic cardiomyopathy

A
0.2%
Autosomal dominant inheritance (50%)
- 70% have mutations in genes encoding for beta-myosin, alpha-tropomysin and troponin -t
Presents at any age 
Family history of sudden death
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4
Q

Signs and symptoms of hypertrophic cardiomyopathy

A
Sudden death 
Angina 
Dyspnoea 
Palpitations
Syncope 
Heart failure 
Jerky pulse
Alpha wave in JVP
Double apex beat
Systolic thrill at lower left sternal edge 
Harsh ejection systolic murmur
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5
Q

What investigations are required in ?hypertrophic cardiomyopathy

A

ECG
Echo
MRI
Cardiac catheterisation - assess severity of gradient, coronary artery disease or mitral regurgitation

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6
Q

What would you expect to see on ECG in hypertrophic cardiomyopathy

A
LVH
Progressive T-wave inversion 
Deep waves - inferior and lateral leads
AF
Wolff-Parkinson-White syndrome
Ventricular ectopies 
VT
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7
Q

What would you expect to see on echo in hypertrophic cardiomyopathy

A

Asymmetrical septal hypertrophy
Small LV cavity with hypercontractile posterior wall
Midsystole aortic valve closure
Systolic anterior movement of mitral valve

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8
Q

What is the pharmacological treatment for hypertrophic cardiomyopathy

A

Beta-blockers or verapamil - for symptoms (decreased ventricular contractility)
Amiodarone - arrhythmia
Anticoagulate any AF

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9
Q

What is the surgical treatment for hypertrophic cardiomyopathy

A

Septal myomectomy - decreases LV outflow tract gradient

Implantable defibrillator

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10
Q

What are the poor prognostic factors affecting mortality in hypertrophic cardiomyopathy

A

Age less than 14
Family history
Syncope at presentation

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11
Q

What is dilated cardiomyopathy

A

Dilated, flabby heart of an unknown cause

- thin walls, less muscle, weaker contractions

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12
Q

What are conditions are associated with developing dilated cardiomyopathy

A
Alcohol abuse 
Hypertension 
Chemotherapeutics - doxorubicin 
Haemochromatosis 
Thyrotoxicosis
Duchenne's muscle dystrophy 
Congenital - X-linked
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13
Q

What are the signs and symptoms of dilated cardiomyopathy

A
Fatigue
Dyspnoea
Pulmonary oedema 
Right ventricular failure 
Emboli/AF
Ventricular tachycardia 
Tachycardia 
Hypotension
Increased JVP
Displaced and diffuse apex
Mitral regurgitation/Tricuspid regurgitation 
S3 gallop
Pleural effusion 
Hepatosplenomeagly 
Oedema 
Jaundice 
Ascites
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14
Q

What investigations are required in ?dilated cardiomyopathy

A
Bloods - BNP (hyponatraemia poor prognostic factor)
CXR
- cardiomeagly and pulmonary oedema 
ECG
Echo
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15
Q

What changes would you expect to see on ECG and echo in dilated cardiomyopathy

A
ECG
- increased heart rate 
- non-specific T-wave changes 
- poor R-wave progression 
Echo
- globally dilated hypokinetic heart 
- low ejection fraction 
- look for MR/TR 
- mural thrombus
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16
Q

Treatment for dilated cardiomyopathy

A
Bed rest
Diuretics
Beta-blockers
Anticoagulation - AF
Biventricular pacing 
Intra-coronary device 
LVADs - left ventricular assist device 
Transplant
17
Q

What is restrictive cardiomyopathy

A

Stiffened, but unthickened ventricle walls

  • lack of stretch restricts ventricular filling
  • decreased stroke volume
18
Q

What are the causes of restrictive cardiomyopathy

A

Idiopathic
Amyloidosis - familial amyloid cardiomyopathy
Haemochromatosis
Sarcoidosis - granulmoa’s form in the heart tissue
Endomyocardial fibrosis

19
Q

How does restrictive cardiomyopathy present

A

Right heart failure and increased JVP
Hepatomeagly
Oedema
Ascites

20
Q

How is restrictive cardiomyopathy diagnosed

A

Echo
MRI
Cardiac catheterisation - low amplitude QRS

21
Q

How is restrictive cardiomyopathy treated?

A

Treat the cause
e.g. venesection for haemochromatosis
Transplant