Antiarrhythmic Drugs in Pediatrics

Antiarrhythmic Drugs in Pediatrics

Key Points

  • Antiarrhythmic medications are used to treat and prevent cardiac arrhythmias in children
  • Choice of drug depends on the type of arrhythmia, age of patient, and underlying cardiac condition
  • Careful monitoring is essential due to potential proarrhythmic effects
  • Vaughan Williams classification system helps organize these drugs based on mechanism of action

Mechanism of Action

Antiarrhythmic drugs work by modifying the electrical conduction system of the heart through various mechanisms:

  • Sodium channel blockade
  • Beta-adrenergic blockade
  • Potassium channel blockade
  • Calcium channel blockade

Classification of Antiarrhythmic Drugs

Class I (Sodium Channel Blockers)

Class IA

  • Quinidine
    • Use: SVT, AF, VT
    • Side effects: QT prolongation, GI disturbance
  • Procainamide
    • Use: SVT, VT
    • Monitoring: QT interval, ANA levels

Class IB

  • Lidocaine
    • Use: Ventricular arrhythmias
    • Advantage: Short half-life, minimal hemodynamic effects

Class IC

  • Flecainide
    • Use: SVT, especially in structurally normal hearts
    • Contraindication: Structural heart disease

Class II (Beta Blockers)

  • Propranolol
    • Use: SVT, Long QT syndrome
    • Dosing: Start low, titrate based on response
  • Esmolol
    • Use: Acute arrhythmias
    • Advantage: Ultra-short acting, IV administration

Class III (Potassium Channel Blockers)

  • Amiodarone
    • Use: Life-threatening arrhythmias
    • Major considerations: Long-term toxicity
  • Sotalol
    • Use: SVT, VT
    • Monitoring: QT interval essential

Class IV (Calcium Channel Blockers)

  • Verapamil
    • Use: SVT in older children
    • Caution: Avoid in infants

Clinical Applications

Supraventricular Tachycardia (SVT)

  • First-line: Adenosine
  • Maintenance: Beta blockers, flecainide
  • Refractory cases: Amiodarone, sotalol

Ventricular Tachycardia (VT)

  • Acute: Lidocaine, amiodarone
  • Chronic: Beta blockers, sotalol
  • Special considerations for channelopathies

Long QT Syndrome

  • Beta blockers are mainstay
  • Avoid QT-prolonging agents
  • Consider mexiletine in specific genotypes

Dosing & Administration

Common Pediatric Doses

Amiodarone

  • Loading: 5-10 mg/kg IV over 30-60 minutes
  • Maintenance: 5-15 mg/kg/day divided q8-24h
  • Maximum: 1200 mg/day

Propranolol

  • Initial: 0.5-1 mg/kg/day divided q6-8h
  • Titrate to: 2-4 mg/kg/day
  • Maximum: 16 mg/kg/day

Flecainide

  • Initial: 2-3 mg/kg/day divided q8-12h
  • Maximum: 150-200 mg/day
  • Target serum level: 200-1000 ng/mL

Monitoring & Precautions

General Monitoring Parameters

  • ECG monitoring
    • QT interval
    • PR interval
    • QRS duration
  • Drug levels when applicable
  • Organ function
    • Liver function tests
    • Thyroid function
    • Renal function

Drug-Specific Monitoring

  • Amiodarone
    • Thyroid function every 3-6 months
    • Liver enzymes every 6 months
    • Annual ophthalmologic exam
    • Chest X-ray baseline and annually
  • Flecainide
    • ECG monitoring for QRS widening
    • Drug levels

Special Populations

  • Neonates: Careful with dosing and monitoring
  • Renal impairment: Dose adjustment needed
  • Genetic variants: Consider pharmacogenetic testing


Further Reading
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