IV Amiodarone Administration for Atrial Fibrillation
For acute atrial fibrillation, administer IV amiodarone as a 150 mg bolus over 10 minutes, followed by 1 mg/min for 6 hours (360 mg), then 0.5 mg/min for 18 hours (540 mg), with a maximum total dose of 2.2 g over 24 hours. 1, 2, 3
Loading Dose Protocol
- Initial bolus: 150 mg IV over 10 minutes for acute rate control or cardioversion 1, 2, 3
- Early maintenance infusion: 1 mg/min for 6 hours (delivers 360 mg) 1, 2, 3
- Late maintenance infusion: 0.5 mg/min for 18 hours (delivers 540 mg) 1, 2, 3
- Maximum 24-hour dose: 2.2 g total 1, 2, 3
Alternative rapid loading regimens have been studied but are less standardized:
- 5–7 mg/kg over 30–60 minutes followed by continuous infusion has shown 55–95% conversion rates 1, 4
- Most conversions occur after 6–8 hours of therapy, not immediately 2, 3, 4
Mandatory Monitoring Requirements
Continuous cardiac monitoring is required throughout the infusion because hypotension occurs in approximately 16% of patients, with additional risks of bradycardia and AV block 2, 3
- Blood pressure monitoring every 15–30 minutes initially, with readiness to reduce infusion rate or add vasopressors 2
- Daily 12-lead ECG to assess QT interval and detect new heart block; hold therapy if QT >500 ms 2
- Heart rate checks every 4–6 hours initially, then at least once daily 2
- Continuous telemetry for ≥24 hours after IV discontinuation 2
Expected Efficacy
- Conversion to sinus rhythm typically occurs after 6–8 hours of therapy, not within the first 1–2 hours 1, 2, 4
- Conversion rates: 34–69% with bolus-only regimens and 55–95% with bolus plus continuous infusion 2, 4
- Predictors of successful conversion include shorter AF duration, smaller left atrial size, and higher amiodarone dose 1, 4
- Amiodarone is not superior to Class IC drugs (flecainide, propafenone) for rapid conversion but is safer in structural heart disease 1, 4
Patient-Specific Indications
Amiodarone is the preferred antiarrhythmic in patients with heart failure or reduced ejection fraction because Class IC agents are contraindicated in structural heart disease 2, 3, 4
- Class IIa recommendation for rate control in Wolff-Parkinson-White syndrome with accessory pathways when conversion or ablation is not immediately feasible 1, 3
- Safe in renal impairment because amiodarone undergoes hepatic metabolism, not renal excretion; no dose adjustment needed 2, 3
- Relatively contraindicated in significant pulmonary disease; if no alternative exists, use the lowest effective dose for the shortest duration 2, 3
Critical Drug Interactions During IV Therapy
Reduce digoxin dose by 50% immediately when amiodarone is started because amiodarone roughly doubles digoxin levels 2
- Reduce warfarin dose by 30–50% and obtain INR check 3–5 days after initiation; amiodarone markedly increases INR 2
- Reduce or discontinue beta-blockers and calcium-channel blockers as amiodarone's rate-control effect develops to avoid excessive bradycardia 2
- Avoid coadministration with other QT-prolonging medications without expert consultation 5, 3
Transition to Oral Therapy
Begin oral loading while the IV infusion continues at 0.5 mg/min, using a duration-based conversion strategy that accounts for tissue drug already accumulated 2, 5
- If IV therapy <1 week: start oral 800–1600 mg daily 2, 5
- If IV therapy 1–3 weeks: start oral 600–800 mg daily 2, 5
- If IV therapy >3 weeks: start oral 400 mg daily 2, 5
- Continue IV infusion at 0.5 mg/min for 24 hours after the first oral dose, then discontinue 2
- Continue oral loading until cumulative 10 g dose is achieved, then switch to maintenance 200–400 mg daily 2, 5
Common Pitfalls to Avoid
- Do not expect immediate conversion: amiodarone's full antiarrhythmic effect requires days to weeks despite therapeutic serum levels due to its extremely long half-life (26–107 days) 2, 5
- Do not use peripheral IV for prolonged infusions: administer through central venous catheter to avoid phlebitis 6
- Do not combine with other rate-controlling agents initially: amiodarone provides rate control on its own and combination increases bradycardia risk 1, 2
- Do not use in WPW with AF alongside beta-blockers, digoxin, adenosine, or calcium-channel blockers: these can precipitate ventricular fibrillation 3