What is the drug of choice for stable antidromic atrioventricular reentrant tachycardia (AVRT) associated with Wolff-Parkinson-White (WPW) syndrome?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: October 27, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Drug of Choice for Stable Antidromic AVRT in WPW Syndrome

For stable antidromic atrioventricular reentrant tachycardia (AVRT) associated with Wolff-Parkinson-White (WPW) syndrome, ibutilide, procainamide, or flecainide are the preferred pharmacological agents as they effectively slow conduction through the accessory pathway. 1, 2

Pharmacological Management Algorithm

First-line agents:

  • Ibutilide (IV): Recommended as first-line therapy for stable patients with antidromic AVRT due to its ability to slow conduction through the accessory pathway 1, 2
  • Procainamide (IV): Equally effective first-line option that slows conduction through the accessory pathway and can terminate the tachyarrhythmia 1, 2
  • Flecainide (IV): Alternative first-line agent that effectively slows accessory pathway conduction 1, 2

Second-line agents:

  • Propafenone: Class IC antiarrhythmic that reduces conduction and increases the effective refractory period of the accessory pathway in both directions 3, 4
  • Disopyramide or Quinidine: Class IA antiarrhythmics that may be considered if first-line agents are unavailable or ineffective 1, 2

Critical Contraindications

  • AVOID AV nodal blocking agents in patients with WPW and antidromic AVRT as they can paradoxically increase conduction through the accessory pathway, potentially precipitating ventricular fibrillation 1, 2
  • Specifically contraindicated medications include:
    • Beta-blockers 1, 2
    • Calcium channel blockers (diltiazem, verapamil) 1, 2
    • Digoxin 1, 2
    • Adenosine (should be used with extreme caution as it may precipitate atrial fibrillation with rapid ventricular response) 1

Mechanism of Action

  • Ibutilide, procainamide, and flecainide work by slowing conduction through the accessory pathway, which is the critical component in antidromic AVRT 1
  • In antidromic AVRT, the accessory pathway serves as the antegrade limb of the circuit while the AV node serves as the retrograde limb 5
  • These agents increase the refractory period of the accessory pathway, thereby interrupting the reentrant circuit 3, 4

Special Considerations

  • Antidromic AVRT is rare, occurring in less than 5% of patients with WPW syndrome clinically and is inducible in less than 10% of WPW cases in electrophysiology studies 5
  • If pharmacological therapy fails or the patient becomes hemodynamically unstable, synchronized cardioversion is recommended 1
  • After acute management, catheter ablation of the accessory pathway should be considered as definitive treatment, with success rates >95% in experienced centers 1, 2

Monitoring and Follow-up

  • Even after successful acute treatment, patients should be evaluated for definitive management with catheter ablation 2
  • Patients with WPW syndrome who have experienced antidromic AVRT are at risk for recurrent episodes and potentially life-threatening arrhythmias 1
  • Risk factors for sudden cardiac death in WPW include shortest pre-excited R-R interval <250 ms during atrial fibrillation, multiple accessory pathways, and history of symptomatic tachycardia 1

Remember that while pharmacological therapy can effectively terminate acute episodes of antidromic AVRT, catheter ablation remains the definitive treatment of choice for symptomatic patients with WPW syndrome 1, 2, 6.

References

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.