Antiarrhythmic Therapy

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General Principles

Vaughan-Williams Classification

Categorizes agents based on primary electrophysiological mechanism of action.Pasted image 20260619215059.png

Class Mechanism of Action Examples
I Sodium channel blockade; slows depolarization
IA (Moderate) Prolongs action potential Procainamide, Quinidine, Disopyramide
IB (Weak) Shortens repolarization Lidocaine, Mexiletine, Phenytoin
IC (Strong) Markedly slows conduction Flecainide, Propafenone
II Beta-adrenergic receptor blockade; suppresses sympathetic activity Propranolol, Atenolol, Esmolol, Nadolol
III Potassium channel blockade; prolongs action potential & refractoriness Amiodarone, Sotalol, Dofetilide, Ibutilide
IV Calcium channel blockade; slows AV node conduction Verapamil, Diltiazem
V (Misc) Variable mechanisms (AV node blockade, Na+/K+ ATPase inhibition) Adenosine, Digoxin, Magnesium

Specific Pharmacologic Agents & Dosing Profiles

Class I: Sodium Channel Blockers

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Procainamide (Class IA)

Lidocaine (Class IB)

Flecainide (Class IC)

Class II: Beta-Blockers

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Propranolol

Esmolol

Class III: Potassium Channel Blockers

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Amiodarone

Sotalol

Class IV: Calcium Channel Blockers

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Verapamil

Class V: Miscellaneous

Adenosine

Digoxin

Clinical Management by Arrhythmia Type

Narrow QRS Tachycardias

Wide QRS Tachycardias (Ventricular Tachycardia)

Fetal Arrhythmia Management

Maternal transplacental administration required. Medication doses higher than standard adult arrhythmia management due to altered maternal pharmacokinetics (increased blood volume, altered gastric emptying, heightened renal clearance). Direct fetal intramuscular or umbilical vein injection reserved for severe, refractory hydropic cases.

Adverse Effects and Therapeutic Monitoring

Drug Key Adverse Effects Drug Interactions Therapeutic Level
Amiodarone Thyroid dysfunction, pulmonary fibrosis, hepatotoxicity, prolonged QTc, blue skin. Increases levels of digoxin, warfarin, flecainide, phenytoin. 0.5–2.5 mg/L (correlation poor).
Flecainide Proarrhythmia, negative inotropy, QRS widening. Milk inhibits absorption in infants. Amiodarone increases toxicity. 0.2–1.0 mcg/mL.
Procainamide SLE-like syndrome, QRS/QTc prolongation, hypotension. Cimetidine/Amiodarone increase levels. Procainamide: 4–10 mcg/mL. Combined (w/ NAPA): 10–30 mcg/mL.
Lidocaine CNS toxicity (seizures, coma), paresthesias. Cimetidine, propranolol increase toxicity. 1.5–5.0 mcg/mL.
Digoxin AV block, PR prolongation, visual disturbances, vomiting. Quinidine, amiodarone, verapamil increase levels. 0.8–2.0 ng/mL.
Sotalol Torsades de pointes, severe bradycardia, QTc prolongation. Avoid concurrent QT prolonging drugs. N/A