Cardiomyopathy Flashcards
Cardiomyopathy
Group of diseases that directly affect myocardial structures or function;
heart can’t function right way because shape/structures change & can’t function the way it should
Primary
idiopathic
Only involves heart muscle, other heart structures unaffected
Secondary
Known cause and is secondary to another disease process
Dilated Cardiomyopathy
Most common type
Most common reason patients need heart transplant
Thinned muscle wall, can’t pump effectively and get blood out to organs as it’s supposed to
Can be left or right sided, but most often we see left
Dilated Cardiomyopathy SxS
S/S HF Fatigue SOB, dyspnea, orthopnea, dry cough Abdominal bloating, anorexia Dysrhythmia, heart murmur Edema Right side (HF symptoms): Hepatomegaly JVD
Dilated C/ Causes
Often follows infectious myocarditis
Cardiotoxic agents: alcohol, cocaine, chemo agents
CAD, pregnancy, HTN, valve disease
Dilated C. Complications
Leads to heart failure in 25-40% of cases
Dilated. C Diagnostics
Patient history and exclusion of other causes for HF
Echocardiography: basis for majority of Dx
Lab: elevated BNP in presence of HF
Heart catheterization
Ejection fraction (might see 20%, normal is 55)
Dilated C. Drug Therapy
To control HF (contractility, preload, afterload):
Nitrates and diuretics: decrease preload
ACE inhibitors: decrease afterload
Beta blockers and aldosterone antagonists control neuro-hormonal stimulation
Antidysrhythmics
Anticoagulants
Dobutamine (dobutrex) (IV inotrope) and milrinone (Primacor): continuous IV, increase contractility
Dilated C. Interprofessional Care
Control HF: increase contractility, decrease preload and afterload
Activity:
Reduced physical activity during period of decompensation
Cardiac rehab program to increase exercise tolerance
Diet:
Sodium restriction
Small frequent meals during liver congestion
Increased nutrition (prevent chacexia)
Vitamins; no alcohol
Dilated C. Surgical Therapies
Ventricular assist device (VAD): allow heart to recover, bridge to transplant
Implantable defibrillators
Cardiac transplantation – 50% of heart transplants are to treat dilated cardiomyopathy
If not candidate for cardiac transplant, they can have a permanent VAD placed
Hypertrophic Cardiomyopathy
Massive ventricular hypertrophy
Rapid forceful contractions of the L ventricle
Impaired relaxation (diastole)
Obstruction to aortic outflow (not always present)
Thickened septum and ventricular wall
Impaired ventricular filling because the ventricle is noncompliant and unable to relax; can get in the way of ejection as well
Hypertrophic C. Causes
Familial (genetic basis)
Idiopathic
Sporadic occurrence
Autosomal dominant trait causing encoding of cardiac sarcomere
- Note: this is the disease process that causes sudden cardiac death in young athletes; usually the first sign that they have it
Aggravating Factors of Hypertrophic C.
Increase contractility (exercise, + inotropes)
Increased HR (exercise, fever, increased CO)
Deecreased preload (hypovolemia, sepsis, fluid shifts)
Loss of atrial kick (atrial fibrillation, ventricular arrhythmias)
*Arrhythmias may occur and cause sudden death!
SxS Hypertrophic C
Sudden death from arrhythmias may be first sign Exertional dyspnea Fatigue Angina Syncope