266.1 🎓 醫孞生版

266.1.0.1 📌 䞀頁重點

266.1.0.1.1 Spectrum
266.1.0.1.1.1 Premature Ventricular Contractions (PVCs)
  • Ectopic ventricular beats
  • Usually benign in healthy
  • Frequent / multifocal / R-on-T can be precursor to VT/VF
  • Treatment: usually none; β-blocker if symptomatic; ablation if frequent + symptomatic + LV dysfunction (PVC-induced cardiomyopathy)
266.1.0.1.1.2 Non-Sustained VT (NSVT)
  • ≥ 3 consecutive ventricular beats
  • < 30 seconds
  • Often asymptomatic
  • Significance varies by clinical context
266.1.0.1.1.3 Sustained VT
  • 30 seconds duration OR hemodynamic compromise

  • Monomorphic (uniform QRS) vs polymorphic (varying QRS — usually ischemic)
  • Wide QRS > 120 ms typically
  • AV dissociation possible
266.1.0.1.1.4 Ventricular Fibrillation (VF)
  • Chaotic, no organized complexes
  • No effective cardiac output → cardiac arrest
  • Treatment: immediate defibrillation
266.1.0.1.1.5 Torsades de Pointes
  • Polymorphic VT with QT prolongation
  • “Twisting around baseline” appearance
  • Acquired (drugs, electrolyte) or congenital LQTS
  • Treatment: magnesium IV + isoproterenol or pacing + cause correction; defibrillation if sustained
266.1.0.1.2 Sudden Cardiac Death (SCD)
266.1.0.1.2.1 Definition
  • Death within 1 hour of symptom onset
  • ~ 50% of cardiovascular deaths
  • ~ 7-9 million deaths/yr globally
266.1.0.1.2.2 Causes
  • Ischemia + MI (60-80%)
  • Structural heart disease (cardiomyopathy, HF)
  • Channelopathies (LQTS, Brugada, CPVT, idiopathic VF)
  • Commotio cordis (chest trauma during specific repolarization phase)
  • Inflammatory (myocarditis)
  • Aortic dissection / rupture
  • PE
266.1.0.1.2.3 Survival
  • Witnessed arrest with bystander CPR + AED — survival 30-50%
  • Unwitnessed: < 10%
266.1.0.1.3 Implantable Cardioverter Defibrillator (ICD)
266.1.0.1.3.1 Secondary Prevention (Class I)
  • Survivors of cardiac arrest from VF/VT (no reversible cause)
  • Sustained hemodynamically unstable VT
  • Sustained VT + structural heart disease
266.1.0.1.3.2 Primary Prevention (Class I/IIa)
  • HFrEF EF ≀ 35% + NYHA II-III on optimal medical therapy (≥ 3 months) — MADIT-II, SCD-HeFT
  • HCM with risk factors (family hx SCD, syncope, NSVT, LVH ≥ 30 mm, abnormal BP response, late gadolinium enhancement)
  • Symptomatic LQTS + recurrent syncope despite β-blocker
  • Brugada syndrome with prior cardiac arrest or syncope
  • ARVC with high-risk features
  • CPVT with recurrent VT despite β-blocker
  • HFpEF + EF 35-50% + NSVT + inducible VT on EP study (some indications)
266.1.0.1.3.3 ICD Technology
  • Transvenous ICD: traditional; lead through subclavian to RV
  • Subcutaneous ICD (S-ICD): lead under skin (no transvenous lead); cannot pace
  • Wearable cardioverter defibrillator (LifeVest): external; bridge to ICD or recovery
266.1.0.1.4 Acute Management
266.1.0.1.4.1 Pulseless VT / VF
  • Immediate defibrillation (200 J biphasic)
  • CPR
  • Epinephrine 1 mg IV q3-5 min
  • Amiodarone 300 mg IV bolus (for refractory)
  • Lidocaine alternative
  • Treat reversible causes (Hs and Ts)
266.1.0.1.4.2 Sustained VT with Pulse
  • Stable: amiodarone IV, procainamide IV, lidocaine IV
  • Unstable: synchronized cardioversion 100-200 J
  • Magnesium for torsades
266.1.0.1.4.3 Polymorphic VT / Torsades
  • Magnesium 2 g IV bolus + correct electrolytes (K, Ca)
  • Withhold offending drugs
  • Isoproterenol or temporary pacing for bradycardia-related
  • Cardioversion / defibrillation if sustained / hemodynamically unstable
266.1.0.1.4.4 Acute Long QT (Torsades)
  • Stop offending drugs
  • Correct K + Mg + Ca
  • Mag IV
  • Isoproterenol or pacing if bradycardic
266.1.0.1.5 Channelopathies + Inherited Arrhythmia Syndromes
266.1.0.1.5.1 Long QT Syndrome (LQTS)
  • Congenital types: LQT1 (KCNQ1), LQT2 (KCNH2), LQT3 (SCN5A) — most common
  • Romano-Ward (autosomal dominant)
  • Jervell-Lange-Nielsen (autosomal recessive + deafness)
  • Triggers: exercise (LQT1), startle/loud noise (LQT2), sleep/rest (LQT3)
  • Treatment:
    • β-blockers (first-line, except LQT3 — caution; some mexiletine + propranolol)
    • ICD if recurrent syncope/cardiac arrest despite β-blocker
    • Avoid QT-prolonging drugs
266.1.0.1.5.2 Brugada Syndrome
  • ST elevation V1-V3 (Type 1 = coved; Type 2 = saddle-back)
  • SCN5A mutations
  • Risk of VF + SCD
  • Treatment:
    • ICD for symptomatic or family hx SCD
    • Quinidine for storms
    • Avoid drugs that unmask Brugada (sodium channel blockers, propofol, others)
    • Avoid fever
266.1.0.1.5.3 Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)
  • Plakophilin-2, desmoplakin, other mutations
  • Fibrofatty replacement of RV
  • Risk of VT + SCD
  • Treatment:
    • ICD
    • Exercise restriction
    • Antiarrhythmic drugs
    • β-blockers
266.1.0.1.5.4 Catecholaminergic Polymorphic VT (CPVT)
  • RYR2 mutations
  • Exercise-induced bidirectional VT
  • Treatment:
    • β-blockers (nadolol typically)
    • Flecainide (calcium handling)
    • ICD if symptomatic despite drugs
    • Exercise restriction
    • Left cardiac sympathetic denervation for refractory
266.1.0.1.5.5 Hypertrophic Cardiomyopathy (HCM)
  • See Ch 270
  • Sudden cardiac death = leading cause of death in HCM
  • Risk factors: family history SCD, syncope, NSVT, LVH ≥ 30 mm, abnormal BP response, late gadolinium enhancement on MRI
  • ICD for high-risk
266.1.0.1.6 Catheter Ablation for VT
  • Substrate-based mapping (scar from MI primarily)
  • Idiopathic VT (RVOT origin most common, also LVOT, fascicular)
  • Sustained monomorphic VT not responding to drugs
  • Recurrent VT despite ICD shocks (ICD shock reduction)
  • VT storm (refractory recurrent VT)
266.1.0.1.7 Familial Screening for SCD
  • First-degree relatives of SCD victims
  • ECG + echo + cardiac MRI + family history + genetic testing
  • Channelopathies: family-based genetic + ECG screening

266.1.0.2 1⃣ PVCs (Premature Ventricular Contractions)

266.1.0.2.1 Background
  • Ectopic ventricular beats
  • Common (40% of adults on Holter)
  • Usually benign in healthy
266.1.0.2.2 Causes
  • Idiopathic (most)
  • Caffeine, alcohol, stress, fatigue
  • Ischemia
  • Electrolytes (hypokalemia, hypomagnesemia)
  • Drugs (digoxin, antiarrhythmics, stimulants)
  • Hyperthyroidism
  • Structural heart disease
266.1.0.2.3 When to Worry
  • Symptomatic (palpitations, presyncope)
  • Frequent (> 10,000 / 24 hr or > 10% PVC burden) → may cause LV dysfunction (PVC-induced cardiomyopathy)
  • Multifocal
  • R-on-T phenomenon
  • Couplets / triplets / NSVT
  • Structural heart disease
  • Family history SCD
266.1.0.2.4 Workup
  • ECG
  • Holter / event monitor (quantify burden)
  • Echo (rule out structural)
  • Stress test (rule out ischemia)
  • Cardiac MRI if suspicion structural
266.1.0.2.5 Treatment
  • Asymptomatic + benign: no treatment
  • Symptomatic: β-blocker, calcium channel blocker
  • PVC-induced cardiomyopathy: catheter ablation
  • Idiopathic PVCs from RVOT/LVOT: catheter ablation curative
  • Avoid triggers (caffeine, stimulants)

266.1.0.3 2⃣ Sustained VT

266.1.0.3.1 Categories
266.1.0.3.1.1 Monomorphic VT
  • Uniform QRS morphology
  • Usually from re-entry circuit around scar (post-MI)
  • More common in patients with ischemic cardiomyopathy
  • Can also occur from non-ischemic cardiomyopathy
266.1.0.3.1.2 Polymorphic VT
  • Varying QRS morphology
  • Torsades de pointes if QT prolonged
  • Acute ischemia (often)
  • Hypokalemia, hypomagnesemia
  • Drug-induced LQTS
266.1.0.3.1.3 Idiopathic VT
  • Outflow tract VT (RVOT, LVOT) — usually monomorphic
  • Fascicular VT (left posterior fascicle, verapamil-sensitive)
  • Generally good prognosis
  • Catheter ablation often curative
266.1.0.3.2 Wide-Complex Tachycardia Differential
266.1.0.3.2.1 Diagnosis Approach (Brugada Algorithm)
  1. Absence of RS in all precordial leads → VT
  2. R to S interval > 100 ms in any precordial lead → VT
  3. AV dissociation → VT
  4. Morphology criteria → VT vs aberrant SVT
266.1.0.3.3 Features Favoring VT (vs Aberrant SVT)
  • Older age, structural heart disease, prior MI
  • AV dissociation
  • Capture / fusion beats
  • Wide QRS (> 140 ms)
  • Concordant precordial pattern
  • Northwest axis (-90 to -180)
266.1.0.3.4 Treatment
266.1.0.3.4.1 Stable Sustained VT
  • Procainamide IV (PROCAMIO trial — first choice over amiodarone)
  • Amiodarone IV (alternative)
  • Lidocaine IV (alternative; if ischemic)
  • Cardioversion if drug failure
266.1.0.3.4.2 Unstable Sustained VT
  • Synchronized cardioversion (100-200 J biphasic)
  • Treat ischemia if cause
266.1.0.3.4.3 Refractory / Recurrent
  • Beta-blocker (IV β-blocker; esmolol, propranolol — for sympathetic storm)
  • Catheter ablation
  • ECMO bridge if refractory
266.1.0.3.5 Reversible Causes (Hs and Ts)
266.1.0.3.5.1 Hs
  • Hypoxia
  • Hypovolemia
  • Hydrogen (acidosis)
  • Hyper/Hypokalemia
  • Hypothermia
266.1.0.3.5.2 Ts
  • Tension pneumothorax
  • Tamponade
  • Toxins
  • Thrombosis (PE, MI)
  • Trauma

266.1.0.4 3⃣ Ventricular Fibrillation (VF) + Cardiac Arrest

266.1.0.4.1 Background
  • Chaotic ventricular electrical activity
  • No cardiac output
  • Lethal within minutes without intervention
  • Most common cause of SCD
266.1.0.4.2 Causes
  • Acute ischemia + MI (most common in adults)
  • Cardiomyopathy (HCM, DCM, ARVC)
  • LV dysfunction (severe HFrEF)
  • Channelopathies (LQTS, Brugada, CPVT)
  • Electrolyte abnormalities (hypokalemia)
  • Drug overdose / toxic
  • Commotio cordis (chest trauma during specific repolarization)
  • Post-cardiac surgery
  • Severe HF / shock
266.1.0.4.3 Initial Response
  • Immediate defibrillation (200 J biphasic)
  • High-quality CPR
  • Identify + treat reversible causes
  • Hospital admission post-resuscitation
266.1.0.4.4 Post-Cardiac Arrest Care
  • Targeted temperature management (33-36°C × 24 hr — controversial; some recommendation for fever avoidance only)
  • Hemodynamic optimization
  • Neurologic prognostication (delayed 72+ hours)
  • Coronary angiography + PCI for suspected ischemic cause
  • ICD post-discharge in survivors without reversible cause

266.1.0.5 4⃣ Torsades de Pointes

266.1.0.5.1 Background
  • Polymorphic VT with QT prolongation
  • “Twisting around baseline” appearance
  • Often self-terminates but can degenerate to VF
266.1.0.5.2 Causes
266.1.0.5.2.1 Congenital LQTS
  • LQT1 (KCNQ1), LQT2 (KCNH2), LQT3 (SCN5A) most common
266.1.0.5.2.2 Acquired Long QT
  • Drugs:
    • Antiarrhythmics (Ia, III): quinidine, sotalol, ibutilide, dofetilide, amiodarone (less often)
    • Antibiotics: macrolides, FQ
    • Antifungals: fluconazole, voriconazole
    • Antipsychotics: haloperidol, clozapine, ziprasidone, others
    • Antidepressants: TCAs, citalopram, escitalopram
    • Methadone
    • Ondansetron
    • Cisapride (withdrawn)
    • Other: cocaine, alcohol (some)
  • Electrolytes: hypokalemia, hypomagnesemia, hypocalcemia
  • Bradycardia
  • MI / cardiac ischemia
  • CNS event (stroke, hemorrhage)
  • Hypothyroidism
266.1.0.5.3 Management
  • Stop offending drugs (if acquired)
  • Magnesium IV 2 g (1st-line)
  • Correct electrolytes (K, Ca, Mg)
  • Isoproterenol (increases HR, shortens QT)
  • Temporary pacing (overdrive bradycardia)
  • Lidocaine (alternative)
  • Defibrillation if hemodynamically unstable / sustained

266.1.0.6 5⃣ ICD (Implantable Cardioverter Defibrillator)

266.1.0.6.1 Components
  • Generator (under chest wall)
  • Lead(s) to right ventricle (transvenous ICD)
  • Subcutaneous ICD has lead under skin (no transvenous)
266.1.0.6.2 Functions
  • Continuous monitoring
  • Detect VT/VF
  • Anti-tachycardia pacing (ATP) for VT — painless, often effective
  • Shock for sustained VT or VF
  • Pacing function (backup bradycardia)
266.1.0.6.3 Primary Prevention Indications
266.1.0.6.3.1 HFrEF
  • EF ≀ 35% + NYHA II-III on optimal medical therapy ≥ 3 months
  • EF ≀ 30% + NYHA I (some indications)
  • Ischemic + non-ischemic cardiomyopathy
  • MADIT-II, SCD-HeFT trials
266.1.0.6.3.2 HCM
  • Family history SCD < 50 yr
  • Recent unexplained syncope
  • NSVT on Holter
  • LV wall thickness ≥ 30 mm
  • Abnormal BP response to exercise
  • Extensive late gadolinium enhancement on CMR
266.1.0.6.3.3 Channelopathies
  • LQTS: recurrent syncope / cardiac arrest despite β-blockers
  • Brugada: cardiac arrest, syncope, family hx SCD
  • CPVT: recurrent syncope despite β-blocker / flecainide
  • ARVC: high-risk features
  • Short QT: cardiac arrest
266.1.0.6.4 Secondary Prevention
  • Survivors of cardiac arrest (no reversible cause)
  • Sustained hemodynamically unstable VT
  • Sustained VT + structural heart disease
266.1.0.6.5 Complications
  • Inappropriate shocks (sinus tachycardia, AF, oversensing) — distressing
  • Lead failure
  • Infection
  • Battery depletion (5-10 yr)
266.1.0.6.6 Innovations
266.1.0.6.6.1 Subcutaneous ICD (S-ICD)
  • No transvenous lead
  • Useful in young patients, anatomic issues
  • Cannot pace (anti-tachycardia pacing)
266.1.0.6.6.2 Wearable Cardioverter Defibrillator (LifeVest)
  • External vest
  • Bridge to ICD or recovery
  • Post-MI (early period)
  • New HF until reassessment
266.1.0.6.6.3 Subcutaneous + Leadless Innovation
  • Newer technology emerging
  • Combined leadless pacemaker + ICD (in development)
266.1.0.6.7 Decision-Making
  • Patient preference essential
  • Quality of life vs longevity
  • Life expectancy
  • Comorbidities
  • Shock anxiety
  • Driving restrictions (varies by jurisdiction)

266.1.0.7 6⃣ Catheter Ablation for VT

266.1.0.7.1 Indications
  • Sustained monomorphic VT (especially scar-mediated, post-MI)
  • Idiopathic VT (RVOT, LVOT, fascicular)
  • Recurrent VT despite ICD shocks (reduces shocks)
  • VT storm (refractory recurrent)
  • VT in non-ischemic cardiomyopathy
266.1.0.7.2 Technique
  • 3D mapping (CARTO, EnSite)
  • Substrate ablation (scar)
  • Endocardial + epicardial approach
  • Hemodynamic support during mapping (impella, ECMO) for tolerable
266.1.0.7.3 Success Rates
  • Idiopathic VT: 80-90% single-procedure success
  • Scar-mediated VT: 60-80%
  • Multiple procedures sometimes needed
266.1.0.7.4 Risks
  • Cardiac perforation / tamponade
  • Stroke
  • Procedural mortality 1-3%
  • Recurrence common