What is the comparison between procainamide and lidocaine for converting ventricular tachycardia (VT) with a pulse?

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: December 20, 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.

Procainamide vs Lidocaine for Converting VT with a Pulse

Procainamide is superior to lidocaine for converting hemodynamically stable ventricular tachycardia with a pulse, demonstrating significantly higher conversion rates (80% vs 21%) in head-to-head comparison. 1

Evidence-Based Comparison

Efficacy Data

Procainamide demonstrates markedly superior conversion rates compared to lidocaine:

  • In the definitive randomized trial, procainamide (10 mg/kg) terminated VT in 12 of 15 patients (80%) versus lidocaine (1.5 mg/kg) which terminated only 3 of 14 patients (21%), p<0.01 1
  • When analyzing total VT episodes, procainamide converted 20 of 26 episodes (77%) compared to lidocaine's 4 of 15 episodes (27%), p<0.01 1
  • Procainamide successfully terminated 8 of 11 VTs that failed to respond to lidocaine, while lidocaine only terminated 1 of 1 VT that failed procainamide 1
  • International consensus guidelines confirm lidocaine was less effective than procainamide (LOE 2) in terminating VT 2

Guideline Recommendations

Current guidelines clearly favor procainamide for stable monomorphic VT:

  • Procainamide is recommended for patients with hemodynamically stable monomorphic VT who do not have severe congestive heart failure or acute myocardial infarction 2
  • Lidocaine is considered second-line antiarrhythmic therapy for monomorphic VT, with conversion effectiveness of only approximately 20% 2, 3
  • The 2010 International Consensus explicitly states procainamide demonstrated improved reversion rates over lidocaine in hemodynamically stable monomorphic VT 2

Clinical Algorithm for Drug Selection

Choose Procainamide When:

  • Patient has hemodynamically stable monomorphic VT with pulse 2
  • No severe congestive heart failure present 2
  • No acute myocardial infarction in progress 2
  • Normal renal function (procainamide requires dose adjustment in renal insufficiency) 2

Choose Lidocaine When:

  • VT occurs in the setting of acute myocardial infarction 2
  • Procainamide is contraindicated 2
  • Patient has severe heart failure (procainamide has negative inotropic effects) 2
  • Rapid administration needed (lidocaine bolus faster than procainamide infusion) 2

Immediate Cardioversion Instead When:

  • Patient is hemodynamically unstable (hypotension, altered mental status, chest pain, heart failure) 4, 5
  • Systolic blood pressure ≤90 mmHg 5

Dosing Regimens

Procainamide Dosing:

  • Loading infusion: 10-15 mg/kg (500-1250 mg) at 20-50 mg/min 2
  • Alternative: 10 mg/kg at 100 mg/min 1
  • Maintenance infusion: 1-4 mg/min 2
  • Stop infusion if: arrhythmia suppressed, hypotension develops, QRS widens >50%, or maximum dose reached 2

Lidocaine Dosing:

  • Initial bolus: 1.0-1.5 mg/kg (75-100 mg) 2
  • Additional boluses: 0.5-0.75 mg/kg every 5-10 minutes up to total 3 mg/kg 2
  • Maintenance infusion: 1-4 mg/min (30-50 mcg/kg/min) 2

Critical Safety Considerations

Procainamide Warnings:

  • May cause proarrhythmia including torsades de pointes 2
  • Hypotension and negative inotropic effects require monitoring 2
  • Reduce dose in renal insufficiency due to NAPA accumulation 2
  • Significantly prolongs QRS width and QT interval 1
  • Contraindicated in severe heart failure 2

Lidocaine Warnings:

  • Volume of distribution and clearance reduced in heart failure 2
  • Reduce infusion rate in elderly, heart failure, or hepatic dysfunction 4
  • Generally well tolerated except in shock states 2
  • Monitor for CNS toxicity (confusion, seizures) 5

Mechanism of Superior Efficacy

Procainamide's superior performance relates to its electrophysiologic effects:

  • Procainamide significantly prolongs effective refractory period of ventricle, HV interval, and QRS duration 6
  • Lidocaine does not significantly affect these parameters 6
  • Procainamide's Class Ia sodium channel blockade with intermediate kinetics provides more sustained antiarrhythmic effect 2
  • Procainamide's metabolite NAPA adds Class III antiarrhythmic activity 2

Common Pitfalls to Avoid

  • Do not use lidocaine as first-line for stable VT outside the acute MI setting—procainamide is more effective 2, 1
  • Do not give procainamide in severe heart failure or acute MI—use amiodarone instead 2
  • Do not delay cardioversion if patient becomes hemodynamically unstable during drug infusion 4, 5
  • Do not use verapamil or diltiazem for wide-complex tachycardia—may precipitate cardiovascular collapse 5
  • Do not ignore renal function when dosing procainamide—NAPA accumulation increases torsades risk 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Treatment for Ventricular Tachycardia Storm

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Cardiac Arrhythmia Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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.