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Procainamide

Procainamide

Procainamide is an important antiarrhythmic medication used in pediatric emergency medicine to manage various cardiac arrhythmias. It is classified as a Class IA antiarrhythmic agent according to the Vaughan Williams classification.

  • Generic Name: Procainamide
  • Brand Names: Pronestyl, Procan SR
  • Drug Class: Class IA antiarrhythmic
  • Available Forms: Injectable solution, oral tablets, extended-release capsules

Mechanism of Action

Procainamide exerts its antiarrhythmic effects through multiple mechanisms:

  • Sodium channel blockade: Decreases the rate of rise of the action potential (phase 0)
  • Potassium channel blockade: Prolongs the effective refractory period and action potential duration
  • Anticholinergic effects: Increases AV node conduction and decreases automaticity of the SA node
  • Decreases membrane responsiveness and excitability in ventricular and atrial tissue
  • Slows conduction velocity, particularly in ischemic or depolarized tissues

Indications

In pediatric emergency medicine, procainamide is used for:

  • Treatment of sustained ventricular tachycardia with a pulse
  • Management of supraventricular tachycardias (SVT) refractory to adenosine
  • Conversion of atrial fibrillation or atrial flutter to sinus rhythm
  • Treatment of hemodynamically stable wide-complex tachycardias of unknown origin
  • Management of accelerated idioventricular rhythm
  • Suppression of premature ventricular contractions (PVCs)
  • Treatment of Wolff-Parkinson-White syndrome with rapid conduction over an accessory pathway

Dosage and Administration

Dosing in pediatrics should be carefully calculated based on the child's weight and clinical situation:

  • Loading dose (IV):
    • 10-15 mg/kg (maximum 100 mg/dose)
    • Administer over 30-60 minutes
    • May repeat every 5-10 minutes up to a maximum total dose of 15 mg/kg or 500 mg, whichever is lower
  • Maintenance infusion:
    • 20-80 mcg/kg/minute
    • Titrate to effect and monitor ECG continuously
  • Oral dosing (if transitioning to oral therapy):
    • 15-50 mg/kg/day divided into doses every 4-6 hours
    • Maximum daily dose: 4 g/day

Adverse Effects

Procainamide can cause several side effects, including:

  • Cardiovascular:
    • QT interval prolongation (risk of Torsades de Pointes)
    • Hypotension (especially with rapid IV administration)
    • Bradycardia or heart block
    • Paradoxical tachyarrhythmias
  • Gastrointestinal:
    • Nausea and vomiting
    • Anorexia
    • Diarrhea
  • Central Nervous System:
    • Dizziness
    • Confusion
    • Psychosis (rare)
  • Hematologic:
    • Agranulocytosis (rare but serious)
    • Neutropenia
  • Immunologic:
    • Lupus-like syndrome (with prolonged use)
    • Myasthenia-like syndrome

Precautions and Considerations

  • ECG monitoring: Continuous ECG monitoring is essential during administration
  • QT prolongation: Use with caution in patients with pre-existing QT prolongation or those on other QT-prolonging medications
  • Renal impairment: Dose adjustment is necessary in patients with renal dysfunction
  • Hepatic impairment: Use with caution; may need dose adjustment
  • Electrolyte imbalances: Correct hypokalemia and hypomagnesemia before administration
  • Myasthenia gravis: May exacerbate symptoms
  • Proarrhythmic potential: Can paradoxically worsen arrhythmias in some cases
  • Drug interactions: Be aware of interactions with other antiarrhythmics and QT-prolonging drugs
  • Conversion to oral therapy: Consider N-acetylprocainamide (NAPA) levels when transitioning to oral dosing


Further Reading
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