Sudden Cardiac Death Flashcards
Best available predictor of sudden death risk
Severe LV dysfx w/ reduced EF
Inhospital cardiac arrest px w HF are more likely to have what cardiac rhythms as initial documented cardiac arrest?
V fib
CHF px w NHYA class IV (sx at rest) are more likely to die of pump failure than sudden cardiac death. TRUE or FALSE?
TRUE. NYHA II & III px are at higher risk of cardiac death than pump failure
Unexplained LVH w nondilated ventricular chambers
Hypertrophic cardiomyopathy
Most common cardiovascular cause of sudden cardiac death in young athletes
Hypertrophic cardiomyopathy
Recommended tx for individuals w prior documented cardiac arrest, 1st deg relative who has sudden cardiac death, unexplained episodes of syncope
Implantable cardioverter-defibrillator
Implantable cardioverter-defibrillator is also recommended for px with max LV wall thickness >/= ___mm
30
Hereditary form of cardiac muscle disease characterized by R-sided HF, vent arrhythmias of RV origin, syncope and sudden cardiac death.
Arrthythmogenic RV cardiomyopathy
ECG findings of arrthythmogenic RV cardiomyopathy
T-wave inversion in the right precordial leads V1-3
Most freq coronary artery anomaly assoc w sudden cardiac death
Anomalous origin of the L coronary artery (from pulmonary artery syndrome)
Greatest risk of sudden cardiac death w congenital heart dse exists in those w ___ lesions
L heart obstructive
VHD that causes effort-induced dyspnea, myocardial ischemia and ventricular arrhythmias
Hemodynamically severe aortic stenosis
Murmur in severe aortic stenosis
Harsh, late-peaking systolic murmur at the upper R sternal border w radiation to the neck
Diffuse degenerative disease of heart’s electrical generation and conduction system
Sick sinus syndrome
Idiopathic slerodegenration of AV node and bundle branches
Lenegre’s disease
Invasion of conduction system by fibrosis or calcification
Lev’s disease
Hereditary channelopathy characterized by sudden cardiac death occuring out of hospital in young men during sleep or at rest w/o premonitory sx or anatomic abnormality
Sudden arrhythmic death syndrome
Disease caused by mutations in genes that encode the proteins responsible for interacting w Na, K, Ca ion channels within the heart
Ion channel disease
Syndrome w ECG finding of a prominent J-wave w characteristic downsloping ST elevation in V1-3; common in SE asia termed as “bangungut” in Phils
Brugada syndrome
Syndrome characterized by prominent, notch-like J wave on the QRS downslope ff by upsloping ST elevation; commonly w reciprocal ST depression in aVR
Early repolarization syndrome
Syndrome w prolongation of QTc, syncope and sudden cardiac arrest caused by torsades de pointes and Vfib
Long QT syndrome
Normal QT interval limits (in seconds)
0.35 to 0.44 sec
Short QT syndrome can be secondary to SIRS, myocardial ischemia, increased vagal tone, acidosis and what electrolyte abnormalities?
Hypercalcemia
Hyperkalemia
Genetic disorder involving defective myocardial cellular calcium handling; characterized by stress-related/ exercise-induced ventricular tachy
Cathecholaminergic polymorphic ventricular tachycardia