Amiodarone Dosing for Atrial Fibrillation with RVR
For atrial fibrillation with rapid ventricular response, administer IV amiodarone as a 150 mg bolus over 10 minutes, followed by 1 mg/min infusion for 6 hours, then 0.5 mg/min for 18 hours, with a maximum of 2.1 grams in the first 24 hours. 1
Intravenous Loading Regimen
The standard IV loading approach delivers approximately 1000 mg over the first 24 hours: 2
- Initial bolus: 150 mg over 10 minutes 1
- First 6 hours: 1 mg/min continuous infusion (360 mg) 1, 2
- Next 18 hours: 0.5 mg/min continuous infusion (540 mg) 1, 2
- Breakthrough episodes: Additional 150 mg boluses over 10 minutes can be given for recurrent RVR or hemodynamic instability 2
The maintenance infusion rate of 0.5 mg/min (720 mg/24 hours) should continue after the first 24 hours, and can be cautiously maintained for 2-3 weeks. 2 In controlled trials, mean daily doses above 2100 mg were associated with increased hypotension risk. 2
Oral Loading Regimen (When IV Not Required)
If the patient is hemodynamically stable and oral therapy is appropriate: 1, 3
- Loading dose: 600-800 mg daily in divided doses 1, 3
- Duration: Continue until 10 grams total administered (typically 2-4 weeks) 1, 3
- Maintenance: 200 mg daily after loading complete 1, 3
A single oral loading dose of 25-30 mg/kg (approximately 1800-2100 mg for a 70 kg patient) has shown 64% conversion rate within 24 hours in recent-onset atrial fibrillation, though this approach is less commonly used in current practice. 4
Critical Administration Requirements
Amiodarone must be delivered through specific routes to prevent complications: 2
- Use a volumetric infusion pump (not drop counters, which can underdose by 30%) 2
- Administer through a central venous catheter whenever possible 2
- Concentrations >2 mg/mL cause high rates of peripheral vein phlebitis and should only be given via central line 2
- Use an in-line filter during administration 2
- Infusions >2 hours must use glass or polyolefin bottles with D5W (not evacuated glass containers) 2
Mandatory Monitoring During Loading
Continuous surveillance is essential to detect life-threatening complications: 1, 3, 5
- Continuous ECG monitoring for bradycardia, heart block, and QT prolongation 5
- Heart rate checks at weekly intervals minimum during loading phase 3
- Blood pressure monitoring (hypotension occurs in 16% of IV patients) 5
- Baseline and serial thyroid function tests (hypothyroidism risk in elderly) 3
- Liver transaminases at baseline and during loading 3
- If bradycardia or heart block develops, immediately discontinue or reduce infusion rate 5
Critical Drug Interactions Requiring Dose Adjustments
Before starting amiodarone, adjust these medications to prevent toxicity: 3, 5
- Digoxin: Reduce dose by 50% (levels predictably double) 3, 5
- Warfarin: Reduce dose and monitor INR at least weekly for first 6 weeks (peak interaction at 7 weeks) 3, 5
- Rate-controlling medications: Reduce or discontinue beta-blockers and calcium channel blockers as amiodarone takes effect to prevent excessive bradycardia 3
- Grapefruit juice: Must be completely avoided (inhibits metabolism) 3, 5
Absolute Contraindications
Do not administer amiodarone in these situations: 5
- Severe bradycardia or heart rate <60 bpm without pacemaker 5
- Second- or third-degree heart block without pacemaker 5
- Severe hepatic dysfunction 3
- Baseline QT prolongation with history of torsades de pointes 1
When to Choose IV vs. Oral Loading
IV amiodarone is indicated when: 1
- RVR does not respond to other pharmacological therapies 1
- Hemodynamic instability is present 1
- Rapid rate control is needed 6
Oral loading is appropriate when: 1, 3
- Patient is hemodynamically stable 1
- Gradual rate control is acceptable 3
- Long-term rhythm control is the primary goal 1
Expected Time to Effect
Amiodarone has delayed onset compared to other agents: 1, 6
- IV administration: Mean conversion time 171 minutes (approximately 3 hours) in recent-onset AF 6
- Oral loading: Inferior to Class IC drugs at 1-2 hours, but equivalent at 24 hours 1
- Full antiarrhythmic effect: May take days to weeks despite adequate serum levels 7
Common Pitfalls to Avoid
Loading infusions at concentrations and rates exceeding recommendations have resulted in hepatocellular necrosis, acute renal failure, and death. 2, 8 A case report documented acute multi-organ toxicity (hepatotoxicity, AKI, pulmonary distress) within 24 hours of standard IV dosing, which resolved rapidly after discontinuation. 8
Never use drop counter infusion sets - they reduce drop size and can underdose by 30%. 2
Do not initiate dofetilide out of hospital if considering alternative agents for cardioversion. 1