Cardiomyopathy Flashcards
What is dilated cardiomyopathy?
The most common cardiomyopathy, in which heart muscle becomes thin and stretched out
What are the causes of dilated cardiomyopathy?
Idiopathic
Genetic
- Duchenne Muscular Dystrophy
- Haemochromatosis
Infection
- Chagas disease
Alcohol
Drugs
Wet Beriberi/B1 deficiency
Peripartum cardiomyopathy
Secondary
- HTN
- Valve disease
How does dilated cardiomyopathy present?
Fatigue
Dyspnoea
Cough
Weight gain
Auscultation
- Pansystolic murmur
- S3
- Gallop
Arrythmia/palpitations
Progress to HF
What investigations are used in dilated cardiomyopathy diagnosis?
CXR
- Dilated heart
ECHO
- Dilated left ventricle
- No regional wall motion abnormalities
- Decreased left ventricular ejection fraction
Biopsy
- Visably stretched fibres
ECG
- LBBB
>BNP
FBC
- Polycythaemia
How is dilated cardiomyopathy managed?
Reduce strain on heart
- Diuretic
- ACEI
Increase contractility
- Digoxin
Anticoagulation
- Warfarin
Left Ventricular Assist Device (LVAD)/mechanical pump
Heart transplant
What is restrictive/infiltrative cardiomyopathy?
Condition in which the heart muscle becomes restricted, meaning stiffened and less compliant
What are the causes of restrictive cardiomyopathy?
Amyloidosis
Sarcoidosis
Haemochromatosis
Genetics
Fibrosis
Diabetes
Radiation
Loffler Syndrome/eosinophils accumulationin
Fabry’s Disease
What is Fabry’s disease?
Rare genetic disease in which there is a deficiency of the enzyme alpha-galactosidase A (a-Gal A) that causes a build up of a type of fat called globotriaosylceramide (Gb3, or GL-3) in the body
How does restrictive cardiomyopathy present?
Dyspnoea
Cough
Angina
Progresses to HF
Auscultation
- Audible S3/4
Hepatomegaly
What investigations are used for restrictive cardiomyopathy diagnosis?
ECG
- Small QRS
Biopsy
- Visible sarcoid/amyloidosis
MRI
ECHO
- Fibrosis
CXR
>Fe
- Haemochromatosis
What is the management for restrictive cardiomyopathy?
Treat underlying cause
- Removing excess iron
Reduce strain on heart
- B Blockers
- ACEI
- Diuretics
Anti-coagulation/thrombus prophylaxis
- Warfarin
Implantable Cardioverter Defibrillator (ICD)
Heart transplant
What is hypertrophic/obstructive cardiomyopathy?
Autosomal dominant genetic mutation in proteins that code for sacromeres, causing hypertrophy and left ventricular outflow obstruction, known as the most common genetic heart condition and common cause of sudden death in young athletes
How does obstructive cardiomyopathy present?
Can be asymptomatic
Dyspnoea, angina, dizziness,
Syncope
Palpitations, arrythmias
Auscultation
- Pansystolic murmur, mitral regurgitation
- S4, ventricular hypertrophy
Notched pulse/pulse bisferins
Jerky pulse
Displeaced apex beat, hypertrophy
What investigations are used in obstructive cardiomyopathy diagnosis?
ECG
- LV hypertrophy
CXR
- Cardiomegaly
CMR
- Asymmetric septal hypertrophy and systolic anterior movement (SAM) of the anterior leaflet of mitral valve
ECHO
Genetic Analysis
MRI
What are the complications of obstructive cardiomyopathy?
Mitral regurgitation
Pulmonary oedema
Arrythmias
Ischaemia
Sudden death