⚡ Propafenone hydrochloride is a Class Ic antiarrhythmic used for the suppression of supraventricular and ventricular tachyarrhythmias.
It slows cardiac conduction, particularly through the His–Purkinje system and accessory pathways.
💡 Key safety tip: if the QRS interval widens by >20% from baseline, the dose should be reduced or stopped until ECG normalises.
📘 About
- Always check the BNF entry for latest indications, cautions, and monitoring requirements.
- Pharmacologically similar to flecainide but somewhat less potent.
- Possesses mild β-blocking and calcium-channel-blocking activity, which can contribute to bradycardia or bronchospasm in susceptible patients.
- Used under specialist supervision for rhythm control of atrial fibrillation, paroxysmal supraventricular tachycardia (PSVT), and certain ventricular arrhythmias.
⚙️ Mode of Action
- Blocks fast sodium channels in phase 0 of the cardiac action potential → slows conduction velocity and prolongs QRS complex.
- Suppresses re-entry pathways, including those in Wolff–Parkinson–White (WPW) and other accessory tracts.
- Weak non-selective β-blocking activity → caution in asthma/COPD or heart failure.
- Negative inotropic effect may worsen LV dysfunction.
💊 Indications & Doses
- Ventricular arrhythmias: 150 mg three times daily, increased if necessary to a maximum of 300 mg three times daily.
- Supraventricular arrhythmias (including AF/PSVT): specialist-initiated, similar oral dosing range; ECG and plasma level monitoring required during titration.
- Available as immediate-release and modified-release tablets — not interchangeable mg-for-mg.
⚗️ Monitoring
- Baseline and periodic ECGs: check QRS, PR, and QT intervals.
- Stop or reduce dose if QRS widens > 20% or if PR > 200 ms.
- Monitor electrolytes (especially K⁺ and Mg²⁺) and renal/hepatic function.
🔄 Interactions
- See BNF for full details.
- ⚠️ Additive conduction slowing with other antiarrhythmics (e.g. amiodarone, β-blockers, verapamil).
- Inhibits CYP2D6 → may raise levels of metoprolol, desipramine, or certain SSRIs.
- Plasma levels increased by CYP2D6 inhibitors (e.g. fluoxetine, paroxetine, quinidine).
⚠️ Cautions
- Initiate under specialist supervision with ECG monitoring.
- Use with caution in structural heart disease, ischaemic cardiomyopathy, or LV dysfunction due to pro-arrhythmic risk.
- May exacerbate bradycardia or hypotension.
- Caution in hepatic impairment (hepatic metabolism → active metabolites).
🚫 Contraindications
- Severe obstructive pulmonary disease (β-blocking effect).
- Heart block (2°/3°) without pacemaker support.
- Brugada syndrome or history of pro-arrhythmia with Class I agents.
- Cardiogenic shock (unless arrhythmia-induced).
- Severe bradycardia, uncontrolled heart failure.
💥 Adverse Effects
- Cardiac: conduction block, bradycardia, new or worsened arrhythmia, heart failure exacerbation.
- Neurological: dizziness, blurred vision, tremor.
- GI: nausea, metallic taste, constipation.
- Hepatic: transient enzyme elevation or cholestatic jaundice.
- Rare: agranulocytosis, lupus-like reactions.
🧠 Teaching Note
Propafenone is a Class Ic sodium-channel blocker with additional β-blocking effects.
It highlights why all Class I agents must be used with care — they can convert a stable rhythm disturbance into a lethal one, particularly in structural heart disease (CAST trial).
Always titrate slowly, monitor the ECG, and reassess if QRS widens or symptoms worsen.
📚 References
- BNF: Propafenone
- Resuscitation Council UK — Arrhythmia Management (2023)
- Katzung BG. Basic & Clinical Pharmacology (15th ed.)
- ACC/AHA/HRS Guidelines for the Management of Atrial Fibrillation (2023)