IV Amiodarone Infusion Protocol
Administer IV amiodarone as a 150 mg bolus over 10 minutes, followed by 1 mg/min for 6 hours (360 mg total), then 0.5 mg/min for the remaining 18 hours (540 mg total), delivering approximately 1,050 mg in the first 24 hours. 1, 2, 3
Standard Dosing Regimen
Initial Loading Phase
- Bolus dose: Dilute 150 mg amiodarone in 100 mL of D5W and infuse over 10 minutes through a volumetric pump (never use drop counters, which can underdose by up to 30%). 2, 3
- Maximum initial infusion rate: Do not exceed 30 mg/min during the loading phase. 3
Early Maintenance Phase (Hours 1-6)
- Infusion rate: 1 mg/min for 6 hours, delivering approximately 360 mg total during this period. 1, 2, 3
- This rate maintains therapeutic plasma levels during the acute phase when arrhythmia suppression is critical. 2
Late Maintenance Phase (Hours 7-24)
- Infusion rate: 0.5 mg/min for the remaining 18 hours, delivering approximately 540 mg. 1, 2, 3
- Total 24-hour dose: Approximately 1,050 mg (150 mg bolus + 360 mg + 540 mg). 2
Beyond 24 Hours
- Continued maintenance: 0.5 mg/min (720 mg per 24 hours) can be safely continued for 2-3 weeks regardless of age, renal function, or left ventricular function. 3
- Maximum cumulative dose: Do not exceed 2.2 g in any 24-hour period. 1, 2, 3
Breakthrough Arrhythmia Management
Supplemental Bolus Dosing
- For recurrent VF or hemodynamically unstable VT: Administer 150 mg supplemental boluses (diluted in 100 mL D5W over 10 minutes) as needed. 2, 3
- Maximum supplemental boluses: Up to 6-8 additional 150 mg boluses may be given within 24 hours for refractory arrhythmias. 2
- Timing: The first supplemental bolus may be repeated after 10-30 minutes if breakthrough arrhythmias persist. 4
Critical Administration Requirements
Vascular Access and Concentration Limits
- Preferred route: Use a central venous catheter whenever possible with a dedicated line. 2, 3
- Concentration limits for peripheral access: Do not exceed 2 mg/mL concentration for infusions longer than 1 hour unless using a central line (concentrations >2 mg/mL cause severe phlebitis in peripheral veins). 2, 3
- Central line requirement: Mandatory for concentrations >2 mg/mL. 2
Diluent and Equipment Specifications
- Required diluent: Use only 5% dextrose in water (D5W); normal saline or lactated Ringer's causes precipitation. 4, 3
- Container requirements: For infusions >2 hours, use glass or polyolefin bottles (not evacuated glass containers, which may cause precipitation). 3
- Infusion pump: Must use a volumetric infusion pump; drop counters underdose by up to 30%. 3
- In-line filter: Use during all administrations. 4, 3
Mandatory Monitoring Parameters
Cardiovascular Surveillance
- Continuous ECG monitoring: Required throughout infusion for heart rate, rhythm, PR interval, QRS duration, and QT interval. 2, 4
- Blood pressure: Monitor continuously; hypotension occurs in 16-26% of patients receiving IV amiodarone. 2, 4
- Bradycardia monitoring: Occurs in 4.9% of IV patients; if heart rate decreases by ≥10 bpm, reduce infusion rate immediately. 4
- AV block surveillance: Watch for second- or third-degree heart block, which represents an absolute contraindication to continued therapy without pacemaker support. 2, 4
Expected Timeline of Effect
- Onset of action: Antiarrhythmic effects typically appear 20-30 minutes after administration. 4
- Peak conversion time: Most conversions to sinus rhythm occur after 6-8 hours and usually require a cumulative dose of at least 1 g. 4, 5
- This delayed onset makes amiodarone less appropriate as a first-line agent for immediate rhythm control unless the patient is hemodynamically stable. 4
Absolute and Relative Contraindications
Absolute Contraindications
- High-degree AV block: Second- or third-degree AV block or sick sinus syndrome without a functioning pacemaker. 2, 4
- Post-heart transplant: Contraindicated in patients who have had a heart transplant. 2
Relative Contraindications (Use Only if Life-Threatening)
- Baseline bradycardia: Heart rate <60 bpm; use only if arrhythmia is immediately life-threatening and no alternatives exist. 4
- Hypotension: Systolic blood pressure <100 mmHg increases risk of further hemodynamic compromise. 4
- Severe LV dysfunction: Moderate or severe left ventricular dysfunction increases risk of hypotension and bradycardia. 4
- Hepatic dysfunction: Use with extreme caution; higher concentrations and faster rates than recommended have caused hepatocellular necrosis and acute renal failure leading to death. 2, 3
Critical Drug Interactions During Infusion
Immediate Dose Adjustments Required
- Digoxin: Reduce dose by 50% immediately when starting amiodarone; digoxin levels will double. 2, 4
- Warfarin: Reduce dose by 33-50% and check INR within 3-5 days (interaction peaks at 7 weeks). 2, 4
- Other rate-control agents: Concomitant beta-blockers, calcium channel blockers, or digoxin create additive bradycardia effects; consider dose reduction. 4
Drugs to Avoid
- QT-prolonging agents: Avoid concomitant use without expert consultation due to additive QT prolongation. 2
Common Pitfalls and How to Avoid Them
Dosing Errors
- Drop counter use: Never use drop counter infusion sets; they underdose by up to 30% due to altered surface properties of amiodarone solutions. 3
- Excessive loading rates: Infusions at rates much faster than recommended have resulted in hepatocellular necrosis, acute renal failure, and death. 3
Vascular Complications
- Peripheral phlebitis: Concentrations >2.5 mg/mL cause high incidence of peripheral vein phlebitis; limit peripheral infusions to ≤2 mg/mL. 3
- Inadequate line selection: Always attempt central access for prolonged infusions to prevent phlebitis and allow higher concentrations if needed. 2, 3
Hemodynamic Instability
- Hypotension management: If hypotension develops during bolus, slow or temporarily stop the infusion; most hypotension is related to the rapid bolus rather than the maintenance infusion. 1
- Unstable patients: If the patient becomes hemodynamically unstable at any time, proceed immediately with synchronized cardioversion rather than continuing pharmacologic therapy. 1, 4