Cardiomyopathy, Myocarditis + Pericarditis Flashcards
Dilated cardiomyopathy
A structural and functional description where the ventricular function is impaired
How can dilated cardiomyopathy occur?
- Primary problem
- End result of pathological injury to myocardium
Excluding ischaemia and valvular causes, what is the aetiology of dilated cardiomyopathy?
- Genetic and familial ( SCN5A gene, Muscular dystrophy)
- Inflammatory (infectious, autoimmune, postpartum)
- Toxic (drugs, exogenous chemicals, endocrine)
- Injury (cell loss, scar replacement)
What is the pathological change in dilated cardiomyopathy?
- Can be 1 but often all chambers are dilated and therefore functionally impaired
- Thrombosis isn’t uncommon
What are the symptoms of dilated cardiomyopathy?
- Progressive and slow onset
- Dyspnoea
- Fatigue
- Orthopnoes
- PND
- Ankle swelling
- Weight gain of fluid overload
- Cough
PMH of dilated cardiomyopathy
- Systemic illness
- Travel
- HT
- Vascular disease
- Thyroid
- Neuromuscular disease
SH of dilated cardiomyopathy
- Alcohol
- Job
What would be found on examination of dilated cardiomyopathy?
- Poor superficial perfusion
- Thready pulse
- Irregular pulse if in AF
- SOB at rest
- Narrow pulse pressure
- JVP elevated +/- TR waves
- Displace apex beat
- S3 and S4
- MR murmur
- Pulmonary oedema
- Pleural effusion
- Ankle oedema
- Sacral oedema
- Ascites
- Hepatomegaly
What investigations should be carried out for dilated cardiomyopathy?
- Repeated ECG noting LBBB if present
- CXR
- N terminal pro Brain Natriuretic peptide
- Bloods
- ECHO
- CMRI
- Coronary angiogram
- Biopsy
What are the general measures in treating dilated cardiomyopathy?
- Correct anaemia
- Remove exacerbating factors
- Correct endocrine disturbances
- Advise on fluid and salt intake
- Manage weight
- HF nurse referral
What are the specific treatments for dilated cardiomyopathy?
-ACE inhibitors, ATII blockers, diuretics
-B-blockers
-Spironolactone
-Anticoagulants
-SCD risk assessment
Cardiac transplant
What is the prognosis of dilated cardiomyopathy?
Generally poor and often influenced by the causes where known
Restrictive and infiltrative cardiomyopathy.
Less common than dilated, describes the physiology of filling and myocyte relaxation capacity, the systolic function may or may not be impaired
What is the aetiology of restrictive and infiltrative cardiomyopathy?
- Non infiltrative (Familial forms of HCM, Scleroderma, Diabetic, pseudoxanthoma elasticum)
- Infiltrative (Amyloid, Sarcoid)
- Storage diseases (haemochromatosis, Fabry disease)
- Endomyocardial (Fibrosis, carcinoid, radiation, drug effects)
What is the pathology of restrictive and infiltrative cardiomyopathy?
- The inability to fill a ventricle whose wall has reduced compliance.
- relaxation of the ventricular wall us an active process that needs functioning intact myocytes
What are the investigations carried out for restrictive and infiltrative cardiomyopathy?
-Repeated ECG noting LBBB and other conduction defects
-CXR
-N terminal pro Brain Natriuretic peptide
-Blood (sarcoid, hemochromatosis)
-Auto antibodies for sclerotic CT disease
-Amyloid needs non cardiac biopsy
-Fabry: low plasma alpha galactosidase A activity
-ECHO
CMRI
-Biopsy
What are the specific treatment measures for restrictive and infiltrative cardiomyopathy?
- Limited diuretic use as low filling pressures
- B-blockers, limited ACEI use
- Anticoagulants
- SCD risk assessment
- Cardiac transplant
What is the prognosis for restrictive and infiltrative cardiomyopathy?
Poor unless reversible
What is the morphological description of hypertrophic cardiomyopathy?
Impaired relaxation is a common feature and systolic function is usually adequate albeit with some functional abnormality
Why does hypertrophic cardiomyopathy have a relatively high prevalence?
- Genetic basis
- Sarcomere gene defect
- Autosomal dominant
- Variable expression and incomplete penetrance
What is the pathology of hypertrophic cardiomyopathy?
- Myocyte hypertrophy and disarray
- Can be genarlised or segmental wall thickness
- Can be apical, septal or generalised
- Impaired relaxation so behaves in as restrictive manner
- If septal hypertrophy this coupled with mitral valve defect lead to LVOT obstruction
What are the symptoms of hypertrophic cardiomyopathy?
-Asymptomatic
-Fatigue
-Dyspnoea
-Anginal like chest pain
-Exertional pre-syncope
Syncope related to arrhythmias or LVOT obstruction
What can be found on examination of hypertrophic cardiomyopathy?
- Can be nothing
- Notched pulse pattern
- Irregular pulse if in AF or ectopy
- Double impulse over apex
- Thrills and murmurs
- LVOT murmur will increase with Valsalva and decrease with squatting
- JVP will be raised in very restrictive filling
What are the investigations for hypertrophic cardiomyopathy?
- ECG (often abnormal but can be normal)
- ECHO
- CMRI
- Risk stratification for SCD, may need ICD
- Holters repeatedly