• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/22

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

22 Cards in this Set

  • Front
  • Back
what is the pathophys of cardiomyopathy?
either systolic dysfunction - due to an abnormality of ventricular emptying, secondary to impaired contractility - dilated cardiomyopathy

or diastolic dysfunction - due to an abnormality of diastolic relaxation - hypertrophic cardiomyopathy
what's the difference between cardiomyopathy and HF
cardiomyopathy is a Dx based on a test (or pathology) whereas HF is a clinical Dx
What are the consequences of increased LA pressure?

What are the symptoms?
hydrostatic forces push fluid into the pulmonary interstitium, fluid fills the alveoli

SOBOE
orthopnea
PND

this is LSHF
What are the consequences of increased RA pressure?

What are the symptoms?
hydrostatic forces push fluid into peripheral interstitium (overwhelm the lymphatics ability to remove excess fluid)

edema
ascities
weight gain
elevated JVP
what are the classifications of cardiomyopathies?
1. Dilated cardiomyopathy
2. Hypertrophy cardiomyopathy
3. Restrcitive cardiomyopathy
4. Arrhythmogenic right ventricular cardiomyopathy/dysplasia
5. Unclassified cardiomyopathies
Causes of DCM?
viruses
gene mutations
EtOH
thyroid disease
Toxic medications
pregoness

most often idiopathic
findings of DCM?
whole heart dilation
impaired systolic function
functional atrioventricular regurgitation is common
prone to arryhthmias
Physical exam findings of DCM
decreased CO:
tachy
decreased BP
pulsus alternans
pulmonary venous congestion
crackles, pleural effusions
precordial exam
laterally displaced apex
S3, MR
systemic congestion:
increased JVP, increased liver size
ascities, peripheral edema
Dx studies for DCM?
CXR: enlarged cardiac silhouette, vascular redistribution, interstitial edema, pleural effusions
EKG
B/W: TSH, ANA, RF, iron, LFTs
echo
wall motion study
cardiac cath
CXR: enlarged cardiac silhouette, vascular redistribution, interstitial edema, pleural effusions
EKG
B/W: TSH, ANA, RF, iron, LFTs
echo
wall motion study
cardiac cath
treatment and prognosis of DCM?
Prognosis 5 year survival 20-60%

treatment (2 categories)
- reduce mortality
ACEi
BB
+/- aldosterone anatagonist
+/- ICD
+/- bi-ventricular pacemaker
- improve symptoms
diuretics
+/- dig
+/- nitrate
Causes of HOCM
most common genetic CV disorder
other causes - severe uncontrolled HTN, AS, athlete's heart, fabry's, metabolic disorders
HOCM variants
Asymmetric septal hypertrophy without obstruction
Asymmetric septal hypertrophy with obstruction
symmetric hypertrophy concentric
apical hypertrophy
clinical manifestations of HOCM
asymptomatic - ECG or echo
symptomatic - dyspnea
angina
fatigue, pre-syncope, syncope
Pathophys of HOCM
Diastolic dysfunction due to:
- increased LV cavity stiffness
hypertrophy
fibrosis
- impaired relaxation
ischemia - supply demand mismatch
abnormal Ca metabolism
abnormal LV loading
HOCM findings on exam
bisferens pulse
S4
murmur of outflow obstruction
MR
what maneuvers can be done to help differentiate the murmur of HOCM and AS?

How do they work?
valsava or standing (decrease preload and afterload) making the murmur of HOCM louder and the murmur of AS quieter
squatting (increases preload and afterload) making the murmur of HOCM quieter and the murmur of AS louder
management of HOCM
investigations:
EKG, ECHO
Medical
BB
CCB
LVOT obstruction
alcohol spetal ablation
myomectomy
if high risk for ventricular rhythms - ICD
risk factors for SCD
family Hx
gene mutations prone to SCD
aborted SCD
syncope
abnormal BP response to exercise
non-sustained VT
LV septal thickness > 30 mm
restrictive cardiomyopathy pathophys
non-dilated ventricles with severe impairment of LV filling
diastolic function impaired with normal systolic function
results in high LV filling pressures

hard to differentiate from constrictive pericarditis
major causes of restrictive cardiomyopathy

and what is the great thing about restrictive cardiomyopathy
amyloidosis, sarcoidosis, fabry's disease

it's rare outside of the tropics
clinical manifestations of restrictive cardiomyopathy
symptoms of right and left heart failure
- fatigue, dyspnea, peripheral edema
management of restrictive cardiomyopathy
treat underlying cause