HF/ Cardiomyopathy Flashcards
headaches/fatigue
OSA tx
Central apnea
sleep apnea
CPAP
optimize volume and GDMT
rapidly progressive HF, may be in refractory shock+ ventricular arrhythmias+ h/o autoimmune d/o in young, previously healthy person
endomyocardial biopsy to eval for giant cell myocarditis
VAD complications
Bleeding, stroke, driveline infection, RV dysfunction, and device failure/thrombosis
myocarditis presentation
long term
mild dyspnea or chest pain that resolves spontaneously to arrhythmias and cardiogenic shock dilated cardiomyopathy (DCM) with heart failure
restrictive cardiomyopathy (amyloid, infiltrative, inflammatory, and endomyocardial processes) hemochromatosis, myocarditis, tachy CM, peripartum CM, takotsubo
biventricular HF, severely elevated BNP, low voltage, biatrial enlargement dilated CM (increased EDV, decreased EF, and increased eccentric myocardial mass)
myocarditis treatment
standard HF therapy, no immunosupression
Heart block/ ventricular arrhythmias + cardiomyopathy
lyme disease
chagas ECG
chagas echo
right bundle branch block, left anterior fascicular block, and atrioventricular block
ventricular dysfunction, segmental wall motion abnormalities, and apical aneurysms
hypersensitivity myocarditis
diagnosis
temporal association b/w onset of HF and new med
biopsy
chemo (anthracyclines, HER2 antagonists, and TKI therapy) induced cardiomyopathy definition
decrease in global EF/ more severe in septum
CHF signs and symptoms
LVEF drop of ≤5-55% with signs/symptoms
LVEF drop of ≤10-55% with signs/symptoms
MUGA is equivalent to echo
pulm htn in HFpEF
related to elevated left heart filling pressures
treat BP, diurese, control ventricular rate
hypotension in patients with obstructive CM
Avoid increasing contractility (will increase gradient and reduce output)
Choose agents that increase afterload (phenylephrine), alpha agonists)
excitation-contraction coupling
calcium enters cell-> calcium released from SR-> binds to troponin C-> displaces tropomyosin-> cross bridge formation
greatest risk factors for HF
hypertension and CAD
lifetime risk for development of HF at age 40
1 in 5
ICD in HCM
personal history of sudden cardiac death (SCD), ventricular fibrillation, or hemodynamically significant VT, first-degree relative with SCD, maximum wall thickness >30 mm, and one or more recent syncopal episodes, hypotension with exercise
HFpEF facts
50% of HF, as fatal as HFrEF
female, older, and hypertensive
prevalence increasing
torsemide> furosemide because
better oral bioavailability
switch if lasix is not working
Risk factors for anthracycline CM
lifetime dose, intravenous bolus admin, higher single doses, h/o of mediastinal radiation, use of other cardiotoxic agents such as cyclophosphamide, trastuzumab, and paclitaxel, female, underlying cardiovascular disease, extremes of age, increased time since therapy completion, prechemo EF <50%
most common viruses to cause myocarditis in the West
parvovirus B19 and HHV-6
spironolactone for HFpEF
TOPCAT, neutral
subgroup analysis in North American patients positive, but jury is still out
hypertensive acute heart failure
use vasodilators: nitroglycerin, isosorbide mononitrate, isosorbide dinitrate, and sodium nitroprusside, captopril?
Brockenbrough sign (HOCM)
post PVC increased contractility-> interventricular septum to anterior leaflet of mitral valve-> obstruction -> stroke volume and aortic pulse pressure falls
Post PVC
increased contractility and increased preload-> increased pressure gradient
in AS, subaortic membrane, and HOCM
Inotropy for palliation
end stage HF
continuous, intermittent has not been studied
Cardiac transplant or VAD-> continuous inotropy if not a candidate for others
preservation of the base and a large segment of apical ballooning, severely elevated BNP
treatment
takotsubo
ACEI/ BB
peripartum cardiomyopathy + severely reduced EF
anticoagulation, avoid preg
renal dysfunction in acute HF
venous congestion (hypervolemia without shock), low renal perfusion (cardiogenic shock), and dysfunctional autoregulation of the kidney