Amiodarone IV Bolus Dosing for Life-Threatening Arrhythmias
For life-threatening ventricular arrhythmias in hemodynamically stable adults, administer 150 mg IV over 10 minutes, followed by 1 mg/min for 6 hours, then 0.5 mg/min for the remaining 18 hours (maximum 2.2 g over 24 hours). 1, 2
Cardiac Arrest Protocol (VF/Pulseless VT)
If the patient is in cardiac arrest with ventricular fibrillation or pulseless ventricular tachycardia unresponsive to defibrillation and epinephrine, give 300 mg IV/IO bolus over 10 minutes, with a second 150 mg bolus if the rhythm persists. 1
Standard Loading Protocol for Hemodynamically Stable Patients
- Initial bolus: 150 mg IV diluted in 100 mL D5W over 10 minutes 1, 2
- First maintenance infusion: 1 mg/min for 6 hours (360 mg total) 1, 2
- Second maintenance infusion: 0.5 mg/min for remaining 18 hours (540 mg total) 1, 2
- Total first 24-hour dose: Approximately 1,050 mg 1, 2
Breakthrough Arrhythmias
- For breakthrough episodes of VF or hemodynamically unstable VT during the infusion, administer supplemental 150 mg boluses (mixed in 100 mL D5W) over 10 minutes 1, 2
- Do not exceed an initial infusion rate of 30 mg/min 2
- Mean daily doses above 2,100 mg are associated with increased risk of hypotension 2
Critical Administration Requirements
Use a central venous catheter for concentrations >2 mg/mL, as peripheral vein phlebitis occurs frequently at higher concentrations. 1, 2
- For infusions >1 hour, do not exceed 2 mg/mL concentration unless using a central line 1, 2
- Always use a volumetric infusion pump (not drop counters, which can underdose by up to 30%) 2
- Use an in-line filter during administration 2
- Administer in glass or polyolefin bottles containing D5W for infusions exceeding 2 hours 2
Absolute Contraindications
Do not administer amiodarone without a functioning pacemaker in patients with second- or third-degree AV block, sick sinus syndrome, or severe sinus node dysfunction. 1, 3
Monitoring Requirements During Infusion
- Continuous ECG monitoring for heart rate, AV conduction abnormalities, and QT prolongation is mandatory 3
- Blood pressure monitoring during infusion to detect hypotension (occurs in 16% of IV patients) 1, 2
- Monitor for bradycardia (occurs in 4.9% of IV patients) and heart block 1, 3
- If bradycardia or heart block develops, discontinue or reduce infusion rate immediately 3
Dose-Related Adverse Effects
- Hypotension is the most common adverse event (26% in clinical trials), with no clear dose-response relationship 4
- Bradycardia requiring intervention occurs in approximately 5% of patients 1
- Phlebitis at infusion site is concentration-dependent (use central line for concentrations >2 mg/mL) 1, 2
Special Considerations for Pre-Existing Bradycardia
If the patient has baseline bradycardia (e.g., heart rate 57 bpm), amiodarone is relatively contraindicated unless the clinical situation is immediately life-threatening and no safer alternatives exist. 3
- Drug-related bradycardia occurs in 4.9% regardless of dose 3
- If proceeding with life-threatening arrhythmia, monitor continuously and reduce infusion rate if heart rate decreases by ≥10 bpm 3
- Consider alternative agents (beta-blockers, calcium channel blockers) if the arrhythmia is not immediately life-threatening 3
Critical Drug Interactions During IV Infusion
- Digoxin: Reduce dose by 50% when starting amiodarone, as levels will double 1
- Warfarin: Reduce dose by 33-50% and monitor INR at least weekly (interaction peaks at 7 weeks) 1, 3
- QT-prolonging drugs: Avoid concomitant use without expert consultation 1
- Concomitant AV nodal blocking agents (beta-blockers, calcium channel blockers) create additive bradycardia risk 3
Efficacy Data
- Dose-response efficacy is demonstrated in refractory ventricular arrhythmias, with higher doses (500-1,000 mg/24h) showing significantly longer time to first arrhythmic event compared to lower doses (125 mg/24h) 1, 4
- The event rate decreases with increasing doses: 0.07,0.04, and 0.02 events per hour for 125,500, and 1,000 mg dose groups respectively 4
- Antiarrhythmic effect onset occurs rapidly, typically in less than 30 minutes 5