Electrophysiology CINRE, hospital BORY
Atrial Fibrillation: Guidelines (2026) Compendium / 13.2 Pharmacological (intravenous) cardioversion of atrial fibrillation

Pharmacological (intravenous) cardioversion of atrial fibrillation


Pharmacological (intravenous) cardioversion is used for acute cardioversion of atrial fibrillation (AF).

Indications for pharmacological (intravenous) cardioversion of AF:

  • Symptomatic AF episode (patient is hemodynamically stable)
    • The patient has known paroxysmal or persistent AF.
  • First episode of AF
  • Planned cardioversion for persistent AF
    • However, electrical cardioversion is preferred because it is more effective.
Diagram of pharmacological cardioversion of atrial fibrillation using intravenous antiarrhythmic drugs, highlighting the need to exclude left atrial thrombus before restoration of sinus rhythm.

Before pharmacological (intravenous) cardioversion, left atrial thrombus must be excluded:

  • Anticoagulation (>4 weeks; not discontinued on the day of cardioversion), or
  • Transoesophageal echocardiography (not older than 24 hours).

If the patient has a first-ever AF episode lasting <24 hours, cardioversion may be considered without thrombus exclusion.

  • AF duration <24 hours based on symptoms cannot be confirmed with absolute certainty,
  • because the patient may have asymptomatic AF paroxysms.

Contraindications

  • Digoxin intoxication (arrhythmias due to increased automaticity may worsen after cardioversion)
  • Hypokalaemia (<3.2 mmol/l)
  • Atrial thrombus (most commonly in the left atrial appendage)
  • INR >4.5

Relative contraindications

  • Acute critical condition (sepsis, myocardial infarction, etc.) or risk state (alcohol, drugs, stress, etc.)

Antiarrhythmic drugs used for (intravenous) cardioversion of AF:

  • Propafenone (Class IC) – may trigger 1:1 conducted atrial flutter
  • Flecainide (Class IC) – may trigger 1:1 conducted atrial flutter
  • Amiodarone (Class III) – safe in structural heart disease
  • Vernakalant (Class III) – atrial-selective antiarrhythmic drug
  • Ibutilide (Class III) – may be used in pre-excited AF
  • Procainamide (Class IA) – may be used in pre-excited AF
Antiarrhythmic drugs for cardioversion of atrial fibrillation (intravenous)
Antiarrhythmic drug Class Time to conversion Success rate Typical patient
Propafenone IC < 6 h 43–89 % Patient without structural heart disease
Flecainide IC < 6 h 52–95 % Patient without structural heart disease
Amiodarone III 6–8 h 44–80 % Patient with structural heart disease /
HFrEF
Vernakalant III < 10 min 50–70 % Recent-onset AF (< 7 days)
Ibutilide III 30–90 min (AF)
< 60 min (atrial flutter)
30–50 % (AF)
60–75 % (atrial flutter)
AF or atrial flutter, including pre-excited AF
Procainamide IA < 30 min 50–75 % AF with pre-excitation
Diagram of the effect of class IC antiarrhythmic drugs without concomitant AV nodal blockade illustrating the risk of conversion of atrial fibrillation to unblocked atrial flutter with 1:1 conduction.

Class IC antiarrhythmic drugs and 1:1 conducted atrial flutter

  • Class IC antiarrhythmic drugs slow conduction in the atrial myocardium.
  • In AF, chaotic electrical activity may slow and organize into a regular re-entry circuit.
  • The result is atrial flutter (often with a lower atrial rate of ~200/min).
    • The AV node may conduct this “slower” flutter with 1:1 AV conduction.
    • This results in 1:1 conducted atrial flutter with a ventricular rate of ~200/min.
  • To prevent 1:1 conducted atrial flutter, Class IC antiarrhythmic drugs should be administered together with drugs that slow AV nodal conduction:
    • Beta-blockers
    • Verapamil
    • Diltiazem
  • The risk of 1:1 conducted atrial flutter with Class IC antiarrhythmic drugs is:
    • 2–6% – if no concomitant AV nodal–blocking therapy is administered.
Diagram illustrating combination therapy with class IC antiarrhythmic drugs and AV nodal blocking agents showing conversion of atrial fibrillation into atrial flutter with 3:1 atrioventricular conduction.
Prevention of 1:1 conducted atrial flutter before Class IC administration (propafenone, flecainide)
Drug Route Dose Timing before Class IC
Metoprolol oral 25 mg 30 min before Class IC administration
Metoprolol intravenous 5 mg administered over 1–2 minutes 20 min before Class IC administration
Verapamil oral 80 mg 30 min before Class IC administration
Verapamil intravenous 5 mg administered over 1–2 minutes 5 min before Class IC administration
Diltiazem oral 60 mg 30 min before Class IC administration
Diltiazem intravenous 15 mg administered over 1–2 minutes 5 min before Class IC administration

In pre-excited AF, antiarrhythmic drugs that prolong the effective refractory period (ERP) of the accessory pathway are recommended:

  • Procainamide (Class IA)
  • Ibutilide (Class III)
  • Electrical cardioversion (in case of hemodynamic instability) – vital indication.

In pre-excited AF, antiarrhythmic drugs that slow AV nodal conduction are contraindicated.

  • If AV nodal conduction is slowed, AF impulses may preferentially conduct to the ventricles via the accessory pathway,
  • with a risk of ventricular fibrillation and sudden cardiac death.
Diagram of preexcited atrial fibrillation illustrating the contraindication of AV nodal blocking drugs due to the risk of degeneration into ventricular fibrillation via conduction over an accessory pathway.
Contraindicated antiarrhythmic drugs – pre-excited atrial fibrillation
Drug Class Reason contraindicated
Verapamil, diltiazem IV (Ca2+ channel blockers) Slow only the AV node → increase conduction via the accessory pathway
Beta-blockers II Slow the AV node → risk of rapid 1:1 conduction over the accessory pathway
Digoxin Inotropic agent, AV nodal blocker Increases parasympathetic tone → AV nodal slowing, preferential accessory pathway conduction
Adenosine AV nodal blocker Blocks the AV node → allows rapid impulse conduction via the accessory pathway
Amiodarone (intravenous) III Unpredictable effect on the accessory pathway, risk of accelerated conduction

Maintenance of sinus rhythm (SR) after cardioversion, despite antiarrhythmic therapy, is individual.

  • SR persists in 50–90% of patients (first 3 months).
  • Elimination of AF risk factors and triggers is essential (sometimes difficult: stress, sleep deprivation).

Atropine dosing for bradycardia after AF cardioversion:

  • Dose: 0.5–1 mg intravenous bolus
  • Interval: every 3–5 minutes
  • Maximum dose: 3 mg
Pharmacological (intravenous) cardioversion of atrial fibrillation Class
Left atrial thrombus is considered excluded if all of the following criteria are met:
  • Non-valvular newly diagnosed AF lasting < 24 hours (based on symptoms)
  • CHA₂DS₂-VA score 0–1
  • No history of TIA or stroke
  • EF > 50 %
I
Flecainide or propafenone (intravenous) are recommended for pharmacological cardioversion of atrial fibrillation in patients without structural heart disease. I
Before administration of Class IC antiarrhythmic drugs (flecainide, propafenone), AV nodal–blocking agents (beta-blocker, verapamil, diltiazem) should be administered to prevent 1:1 conducted atrial flutter. IIa
Vernakalant (intravenous) is recommended for pharmacological cardioversion of atrial fibrillation in patients with EF >40%, without myocardial infarction within the last 30 days and without severe aortic stenosis. I
Amiodarone (intravenous) is recommended for pharmacological cardioversion of atrial fibrillation in patients with structural heart disease. I
Pharmacological cardioversion is not recommended in patients (without a pacemaker) who have:
  • sick sinus syndrome,
  • second- or third-degree AV block,
  • QTc interval > 500 ms.
III
In pre-excited AF, the following are contraindicated:
  • Adenosine
  • Verapamil
  • Diltiazem
  • Beta-blockers
  • Digoxin
  • Amiodarone
III


Guideline algorithm for acute cardioversion in newly diagnosed atrial fibrillation without pre-excitation with antiarrhythmic selection based on left ventricular ejection fraction.


Guideline algorithm for acute cardioversion in newly diagnosed pre-excited atrial fibrillation with contraindication to AV nodal blockers and antiarrhythmic selection based on ejection fraction.

These guidelines are unofficial and do not represent formal guidelines issued by any professional cardiology society. They are intended for educational and informational purposes only.

Peter Blahut, MD

Peter Blahut, MD (Twitter(X), LinkedIn, PubMed)