Can flecainide cause bradycardia?

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Last updated: October 25, 2025View editorial policy

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Flecainide and Bradycardia

Yes, flecainide can cause bradycardia as a known adverse effect, particularly sinus bradycardia and various degrees of atrioventricular block. 1, 2

Mechanism and Cardiac Conduction Effects

  • Flecainide is a class IC antiarrhythmic drug that primarily blocks sodium channels, affecting cardiac conduction by prolonging PR, QRS, and QT intervals 2
  • It slows cardiac conduction in most patients, with PR interval increases averaging about 25% (0.04 seconds) and up to 118% in some patients 2
  • Approximately one-third of patients may develop new first-degree AV heart block (PR interval ≥ 0.2 seconds) 2
  • QRS complex duration typically increases about 25% (0.02 seconds) and up to 150% in some patients 2

Specific Bradyarrhythmias Associated with Flecainide

  • Clinically significant conduction changes observed with flecainide include:
    • Sinus node dysfunction such as sinus pause, sinus arrest, and symptomatic bradycardia (1.2% of patients) 2
    • Second-degree AV block (0.5% of patients) 2
    • Third-degree AV block (0.4% of patients) 2
  • Flecainide can also suppress ventricular escape rhythms, potentially worsening bradycardia 2

Risk Factors for Flecainide-Induced Bradycardia

  • Pre-existing sinus node dysfunction or sick sinus syndrome significantly increases risk 1, 2
  • Underlying AV conduction disturbances increase susceptibility to bradyarrhythmias 1, 2
  • Concomitant use of other medications that affect cardiac conduction (beta-blockers, calcium channel blockers) 1
  • Electrolyte disturbances, particularly hypokalemia or hyperkalemia, may enhance bradycardic effects 2
  • Higher flecainide doses correlate with increased risk of bradyarrhythmias 3

Clinical Implications and Management

  • Flecainide should be used with extreme caution in patients with sick sinus syndrome as it may cause sinus bradycardia, sinus pause, or sinus arrest 2
  • Patients with permanent pacemakers require careful monitoring as flecainide increases endocardial pacing thresholds 2
  • ECG monitoring is essential when initiating flecainide, with particular attention to PR and QRS intervals 4
  • If second- or third-degree AV block or right bundle branch block with left hemiblock occurs, flecainide therapy should be discontinued unless a temporary or implanted ventricular pacemaker is in place 2
  • Attempt to manage patients on the lowest effective dose to minimize conduction abnormalities 2

Special Considerations

  • Bradyarrhythmias may be more pronounced immediately after conversion from atrial fibrillation to sinus rhythm 5
  • In overdose situations, severe bradycardia and various degrees of AV block can occur and may be life-threatening 6, 7
  • Patients with structural heart disease are at higher risk for bradyarrhythmias and other adverse effects 1, 2
  • Flecainide is contraindicated in patients with sinus node dysfunction unless a pacemaker is present 1, 2

Monitoring Recommendations

  • Baseline ECG should be obtained prior to initiating flecainide 4
  • Regular ECG monitoring during treatment is recommended, with particular attention to PR and QRS intervals 4
  • When feasible, monitor plasma flecainide levels, attempting to keep trough levels below 0.7 to 1.0 mcg/mL 2
  • Electrolyte levels should be monitored and maintained within normal ranges 2

In conclusion, bradycardia is a well-documented adverse effect of flecainide that requires careful patient selection, appropriate monitoring, and dose adjustment to minimize risk.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Flecainide Dosing and Administration

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.

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