Amiodarone Intravenous Infusion Preparation and Administration
Prepare amiodarone by administering an initial loading dose of 150 mg diluted in 100 mL D5W infused over 10 minutes, followed by a maintenance infusion of 1 mg/min for 6 hours (360 mg), then 0.5 mg/min for the remaining 18 hours (540 mg), with a maximum total dose of 2.2 g over 24 hours. 1, 2, 3
Standard Preparation Protocol
Loading Dose
- Mix 150 mg amiodarone in 100 mL of D5W 2, 3
- Infuse over 10 minutes using a volumetric infusion pump (never use drop counter sets, as they can underdose by up to 30%) 3
- For cardiac arrest with VF/pulseless VT unresponsive to defibrillation, use 300 mg IV/IO bolus, with a second 150 mg bolus if rhythm persists 2
Maintenance Infusion Preparation
- First 6 hours: 1 mg/min (total 360 mg over 6 hours) 1, 2, 3
- Next 18 hours: 0.5 mg/min (total 540 mg over 18 hours) 1, 2, 3
- Prepare concentrations of 1-6 mg/mL depending on access 3
Critical Administration Requirements
Vascular Access and Concentration Rules
- For concentrations >2 mg/mL, a central venous catheter is mandatory 2, 3
- For infusions >1 hour, do not exceed 2 mg/mL concentration unless using a central line to prevent severe peripheral vein phlebitis 2, 3
- Concentrations >3 mg/mL are associated with high incidence of peripheral vein phlebitis 3
Equipment and Container Requirements
- Use only glass or polyolefin bottles containing D5W for infusions exceeding 2 hours 3
- Do not use evacuated glass containers for admixing, as buffer incompatibility may cause precipitation 3
- Use an in-line filter during administration 3
- Must use a volumetric infusion pump (drop counters cause 30% underdosing) 3
- Administer through a dedicated central venous catheter whenever possible 3
Supplemental Dosing for Breakthrough Arrhythmias
- For breakthrough VF or hemodynamically unstable VT: administer 150 mg supplemental bolus mixed in 100 mL D5W over 10 minutes 3
- Maximum of 6-8 supplemental boluses in any 24-hour period 1
- Do not exceed initial infusion rate of 30 mg/min 3
- Total daily dose should not exceed 2.2 g over 24 hours (mean daily doses >2100 mg associated with increased hypotension risk) 2, 3
Monitoring Requirements During Infusion
Immediate Monitoring
- Continuous cardiac monitoring for hypotension (occurs in 16% of IV patients), bradycardia (4.9%), AV block, and QT prolongation 2, 4
- Blood pressure monitoring every 5-10 minutes during loading dose 4
- Watch for phlebitis at infusion site if using peripheral access 2
High-Risk Populations Requiring Extra Caution
- Patients with severe left ventricular dysfunction: significant hypotension risk during loading phase 5
- Hepatic dysfunction: use with extreme caution, as higher concentrations and faster rates than recommended have caused hepatocellular necrosis and acute renal failure leading to death 3
Absolute Contraindications
Do not administer amiodarone without a functioning pacemaker in patients with: 2
- Second- or third-degree AV block
- Sick sinus syndrome
- Severe sinus node dysfunction
Critical Drug Incompatibilities
Use separate IV lines for these medications (amiodarone forms precipitates with): 3
- The FDA label specifies multiple Y-site incompatibilities requiring dedicated IV access 3
Dose adjustments required for: 4
- Digoxin: reduce dose by 50% (levels will double) 4
- Warfarin: reduce dose by 33-50%, monitor INR at least weekly (interaction peaks at 7 weeks) 4
- Avoid concomitant QT-prolonging drugs without expert consultation 4
Duration of Therapy
- Maintenance infusion of 0.5 mg/min can continue for 2-3 weeks regardless of age, renal function, or left ventricular function 3
- Limited experience beyond 3 weeks of continuous IV therapy 3
- When transitioning to oral: use 400-600 mg daily in divided doses for 2-4 weeks, then 100-200 mg daily maintenance 4