Flecainide Use in Patients with Right Bundle Branch Block
Flecainide should not be initiated in patients with Right Bundle Branch Block (RBBB) due to the risk of complete heart block and potentially fatal conduction disturbances. 1
Contraindications Based on FDA Labeling
The FDA label for flecainide explicitly states that it is contraindicated in:
- Pre-existing second- or third-degree AV block
- Right bundle branch block when associated with a left hemiblock (bifascicular block), unless a pacemaker is present 1
While isolated RBBB is not specifically listed as an absolute contraindication, the drug significantly impacts cardiac conduction, making it potentially dangerous in patients with pre-existing conduction abnormalities.
Effects on Cardiac Conduction
Flecainide significantly affects cardiac conduction parameters:
- Increases PR interval by approximately 25% (average 0.04 seconds)
- Increases QRS duration by approximately 25% (average 0.02 seconds)
- Can cause new bundle branch blocks in approximately 4% of patients 1
In patients with existing RBBB, these effects can lead to:
- Progression to complete heart block
- Significant QRS prolongation beyond safe limits
- Potential for life-threatening arrhythmias
Risk Assessment
The risk of using flecainide in patients with RBBB stems from:
Conduction System Effects: Flecainide slows cardiac conduction throughout the heart, including the remaining functioning bundle branch 1
QRS Widening: Guidelines recommend that QRS widening should not exceed 150% of pretreatment QRS duration 2. In patients with RBBB who already have widened QRS, additional widening may reach dangerous levels.
Proarrhythmic Risk: Patients with conduction abnormalities are at higher risk for proarrhythmic effects of flecainide 2
Alternative Approaches
For patients with RBBB requiring antiarrhythmic therapy:
For Atrial Fibrillation:
For Supraventricular Tachycardias:
Monitoring Requirements
If flecainide must be used (which is generally not recommended in RBBB):
- Continuous cardiac monitoring during initiation
- Pacemaker backup should be available
- Regular ECG monitoring to assess PR interval, QRS duration, and QT interval 2
- Immediate discontinuation if QRS widens >25% from baseline 2
Conclusion
The presence of RBBB represents a significant risk factor for adverse outcomes with flecainide therapy. The potential for progression to complete heart block and life-threatening arrhythmias outweighs potential benefits in most clinical scenarios. Alternative antiarrhythmic strategies should be strongly considered for patients with RBBB requiring rhythm control.