Sudden Cardiac Death and Sudden Cardiac Arrest Flashcards
What are the etiologies of SCD/SCA?
90% are from primary myocardial process and 10% from primary electrical process
What are some channelmyopathies?
Long/Short QT Syndrome
Brugada Syndrome
Catecholaminergic polymorphic VT
What are some primary electrical processes associated with SCA/SCD?
Channelmyopathies, acquired LQTS, WPW syndrome, Commotio Cordis
Hypertrophic Cardiomyopathy etiology
Genetic disease that results in LVH
HCM symptoms
Chest pain, dyspnea, syncope
EKG signs of HCM
Deep and narrow Q waves in lateral (common) and inferior leads.
Signs of LVH
Apical variant shows deeply inverted T waves in precordial leads.
Etiology of Arrhythmogenic Right Ventricular Dysplasia (ARVD)
Fibrofatty replacement of myocardium. Most common in RV and may result in reentrant paroxysmal VT. A fib common. Can lead to RV failure.
EKG of ARVD
Epsilon wave
S wave upstroke of 55ms in V1-V3
QRS >110ms V1-V3
T wave inversion V1-V3
Brugada Syndrome Etiology
Heart appears normal. Associated with polymorphic VT and VF. High chance of a-fib. Defective Na+ cardiac channels.
Brugada Syndrome EKG
pseudo-RBBB and persistent ST elevation in V1-V2. There is type 1: ST elevation >2mm, downsloping ST segment, inverted T wave.
Type 2: ST elevation >2mm, “saddle-back” ST-T wave config. Upright/biphasic T wave.
Catecholaminergic Polymorphic VT (CPVT) etiology
Recurrent PVT brought on by exercise or emotional stress in the absence of structural heart disease. Defective handling of Ca2+ channels by sarcoplasmic reticulum.