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22 Cards in this Set

  • Front
  • Back

Types of STRUCTURAL cardiomyopathies

-dilation (60%)


w/ or w/o systolic dysfunction



-hypertrophic (5%)


w/ or w/o obbstruction



-restrictive diastolic (lusitropic) dysfunction (35%)

Clinical presentation of cardiomyopathy

-fxn limitation (reduced exertional capacity)


-fatigue


-orthopnea


-dependent edema


-anorexia


-sleep disturbance

Key findings for a DILATED cardiomyopathy

-jugular venous distention> 8 cm


-S3 at apex (volume overloaded ventricle)


-ant chest wall heave (enlarged heart)


-laterally displaced PMI


-basilar pulmonary rales (congestion/fluid)


-hepatomegaly/peripheral edema (R sided congestion)

Key findings for a RESTRICTIVE cardiomyopathy (stiff heart, higher contractile fxn)

-jugular venous distention when decompensated


-S4 at apex (stiff heart)


-PMI normal (at mid-clavicular line)


-basilar pulmonary rales


-peripheral edema



(normal size heart= no heaves)



Key findings for a HYPERTROPHIC cardiomyopathy


(abnormal thickened myocardium, due to genetics)

-S4 at apex


-systolic murmur in 2nd parasternal interspace (in obstructive hypertrophy)


-hyperdynamic precordium


-PMI normal


-bifid carotid upstroke


Primary causes of Dilated cardiomyopathy

-familoial genetics


-RV arrhythmogenic dysplasia


-muscular dystrophy (Duchenne's)

Secondary causes of Dilated cardiomyopathy

-ischemia


-infection (viruses (any), HIV)


-valvular heart disease (aortic or mitral insuffic)


-toxins (ETOH, anthracyclines, antiretrovirals)


-endocrinoopathy (DM, hypothyroidism)


-post-partum


-CT disorders (SLE, RA)



(anything that doesn't get resolved eventually leads to dilated cardiomyopathy= final common pathway)

Mycocardial dysfunction leads to what 4 main pathophysiologies?

-fluid retention


-tachycardia


-inc afterload


-remodeling



(all failed attempts to inc fxn)

Causes of RESTRICTIVE cardiomyopathy

-infiltrative diseases (sarcoidosis, tuberculosis(


-endomyocardial fibrosis


-early myocardial ischemic scarring


-CT disease

Causes of HYPERTROPHIC cardiomyopathy

*obstructive cardiomyopathy (HOC):


-genetic somatic dominant w /variable penetrance


-most common in young athletes



*non-obstructive hypertrophy:


-diffuse myopathy w/ diastolic dysfunction & normal systolic fxn

Dx for cardiomyopathy

-history & physical exam (esp ask about supplements)


-ECG


-lab eval


-CXR


-stress test


-angiography

What can an ECG reveal?

-presence of ischemia


-conduction system dysfxn (BBB)


-rhythm disturbance



*normal ECG = little value

Stress testing is ONLY for what pts?

stable pts w/o hypertrophic obstructive cardimyopathy

Therapy for cardiomyopathy (tx steps)

1. determine baseline functional capacity & resolve fluid overload (diuresis)


2. address/fix acute reversible factors (hypertension, ischemia, anemia, fever, uncontrolled DM)


3. investigate w/ tests


4. investigate cause of pathology (lab eval)

Objective therapy for dilated cardiomyopathy

1. diuresis


2. reduce preload


3. reduce afterload


4. augment contractility


-maintain sinus rhythm


-device therapy

Objective therapy for restrictive cardiomyopathy

1. diuresis



-no meds to relax


-maintain sinus rhythm

Objective therapy for hypertrophic cardiomyopathy

1. beta-blocker or Ca2+ blocker (slow contractility)



- defibrillator in high risk pts


-septal ablaction/excision (remove obstruction)


(do NOT use diuresis)


Drugs that reduce preload

diuresis


nitrates


salt/fluid restriction


spironolactone


morphine (acutely)

Drugs that reduce afterload

-ACE inhibitors


-angiotensin receptor blockers


-Hydralazine


-Digoxin (does not reduce mortality)


-infusion therapy (only in hospital- dobutamine, milrinone, amrinone


-beta-blockers (carvedelol, bucindolol, metoprolol)


ACE inhibitors & beta blockers have the greatest combined ability to reduce mortality in __________

dilated cardiomyopathy

what mechanical interventions can be used in patients who are waiting for a heart transplant?

-intra-arotic balloon counterpulstation (IABP)


-Left ventricular assist device (LVAD)

What test is the most important to identify whether cardiomyopathy is stiff (restricted) or dilated?

echocardiograph