Amiodarone Infusion Protocol
Administer amiodarone as 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/24 hours), using a central venous catheter for concentrations >2 mg/mL. 1, 2, 3
Standard Infusion Protocol for Life-Threatening Ventricular Arrhythmias
Loading Phase
- Initial bolus: 150 mg IV diluted in 100 mL D5W infused over 10 minutes 2, 3
- First maintenance infusion: 1 mg/min for 6 hours (360 mg total) 1, 2, 3
- Second maintenance infusion: 0.5 mg/min for remaining 18 hours (540 mg total) 1, 2, 3
- Total 24-hour dose: Approximately 1,050 mg (do not exceed 2,100 mg/24 hours due to increased hypotension risk) 3
Cardiac Arrest Protocol (VF/Pulseless VT)
- First dose: 300 mg IV/IO bolus over 10 minutes if unresponsive to defibrillation and epinephrine 2
- Second dose: 150 mg IV/IO if rhythm persists 2
Breakthrough Arrhythmias
- Supplemental dosing: 150 mg IV in 100 mL D5W over 10 minutes for breakthrough VF or hemodynamically unstable VT 3
Critical Preparation and Administration Requirements
Concentration and Vascular Access
- Concentrations >2 mg/mL require mandatory central venous catheter to prevent severe peripheral vein phlebitis (occurs in 16% of patients) 2, 3
- For infusions >1 hour, do not exceed 2 mg/mL concentration unless using central line 2, 3
- Concentrations >3 mg/mL are associated with high incidence of peripheral vein phlebitis 3
Equipment and Compatibility
- Must use volumetric infusion pump (drop counter sets can underdose by up to 30% due to altered surface properties) 3
- Use in-line filter during administration 3
- Administer in glass or polyolefin bottles containing D5W for infusions >2 hours 3
- Do not use evacuated glass containers (may cause precipitation) 3
- No light protection needed during administration 3
Absolute Contraindications
Do not administer amiodarone without a functioning pacemaker in patients with: 2
Additional contraindications:
Special Populations and Dose Modifications
Hepatic Dysfunction
- Use with extreme caution in patients with liver disease 2
- Higher concentrations and faster infusion rates than recommended have resulted in hepatocellular necrosis and acute renal failure leading to death 3
- Amiodarone-induced hepatitis can occur, particularly with chronic use 4
Renal Dysfunction
- No specific dose adjustment required for IV amiodarone (primarily hepatically metabolized) 3
- However, renal phospholipidosis causing progressive kidney dysfunction has been reported, though rare 5
Thyroid Disease History
- Amiodarone contains iodine and causes thyroid dysfunction in 10% of patients 4
- Type 2 amiodarone-induced thyrotoxicosis can occur (elevated free T4, suppressed TSH) 6
- Monitor thyroid function closely but do not withhold in acute life-threatening arrhythmias 6, 4
Monitoring During Infusion
Cardiovascular Monitoring
- Hypotension occurs in 16% of IV patients - monitor blood pressure continuously 2
- Bradycardia occurs in 4.9% of IV patients 2
- Monitor for AV block, heart block, and QT prolongation 2
- Symptomatic bradycardia requiring pacemaker support occurs in approximately 6% 7
Infusion Site Monitoring
- Inspect peripheral IV sites frequently for phlebitis 2, 3
- Switch to central access if phlebitis develops 3
Critical Drug Interactions Requiring Immediate Action
Digoxin
Warfarin
QT-Prolonging Drugs
- Avoid concomitant use without expert consultation 2
Duration of Therapy
- Maintenance infusion of 0.5 mg/min can be continued for 2-3 weeks regardless of age, renal function, or left ventricular function 3
- Limited experience exists for IV amiodarone >3 weeks 3
- Infusions should be discontinued after 6-24 hours and need for further arrhythmia management reassessed 1
Common Pitfalls to Avoid
- Never use drop counter infusion sets - they underdose by up to 30% 3
- Never exceed 30 mg/min initial infusion rate 3
- Never infuse concentrations >2 mg/mL peripherally for >1 hour 3
- Do not administer in patients with high-grade AV block without pacemaker backup 2
- Recognize that higher doses (>2,100 mg/24h) significantly increase hypotension risk 3