Amiodarone for AFib RVR with Hypotension
Intravenous amiodarone is indicated for AFib with rapid ventricular response and hypotension, and it should be administered as both a loading dose followed by a continuous maintenance infusion, not as a one-time push alone. 1, 2
Dosing Protocol for AFib RVR with Hypotension
Initial Loading Dose
- Administer 150 mg IV over 10 minutes as the initial loading dose, mixed in 100 mL of D5W 2
- This loading dose specifically addresses the acute rate control needed in hemodynamically compromised patients 1
Mandatory Maintenance Infusion
- Follow immediately with 1 mg/min infusion for 6 hours, then reduce to 0.5 mg/min thereafter 2
- The total recommended dose is approximately 1000 mg over the first 24 hours 2
- Continuing the infusion is essential - the loading dose alone provides insufficient sustained therapeutic effect 2
Breakthrough Episodes
- For recurrent VF or hemodynamically unstable VT during treatment, administer supplemental 150 mg boluses (in 100 mL D5W over 10 minutes) 2
- The maintenance infusion rate may be increased to achieve effective arrhythmia suppression 2
Guideline Support for Amiodarone in This Context
Class I Recommendation (Strongest Evidence)
- IV amiodarone is recommended to control heart rate acutely in patients with heart failure, which commonly coexists with hypotension in AFib RVR 1
- This is a Class I, Level of Evidence B recommendation from the AHA/ACC/HRS guidelines 1
Class IIa Recommendation
- IV amiodarone can be useful to control heart rate when other measures are unsuccessful or contraindicated 1
- This is particularly relevant when hypotension precludes use of beta-blockers or calcium channel blockers 1
Critical Safety Considerations
Hypotension Management
- Hypotension is the most common adverse reaction (occurring in 16% of patients), typically appearing in the first several hours and related to infusion rate rather than dose 2
- Slow the infusion rate initially if hypotension worsens; add vasopressor drugs, positive inotropic agents, or volume expansion as needed 2
- Monitor the infusion rate closely and do not exceed recommended rates 2
Administration Requirements
- Use a volumetric infusion pump - drop counter sets can result in up to 30% underdosing 2
- Administer through a central venous catheter whenever possible, especially for concentrations >2 mg/mL 2
- Use an in-line filter during administration 2
Bradycardia Risk
- Drug-related bradycardia occurs in approximately 5% of patients 2
- Have temporary pacing capability readily available, particularly in patients with pre-existing conduction abnormalities 2
- Slow or discontinue infusion if significant bradycardia develops 2
Common Pitfalls to Avoid
Never Give as Single Push Without Infusion
- The one-time bolus alone is inadequate - amiodarone's mechanism requires sustained plasma levels for rate control 2
- The loading dose initiates therapy but the maintenance infusion sustains the therapeutic effect 2
Contraindications in Specific Populations
- Avoid standard AV nodal blockers (beta-blockers, calcium channel blockers) in hypotensive patients - they are contraindicated with decompensated heart failure 1
- This makes amiodarone the preferred agent when hypotension suggests cardiac decompensation 1
Monitoring Requirements
- Monitor QTc interval during infusion - prolongation to ≥500 ms increases torsades de pointes risk (though this occurs in <2% of patients) 2
- Monitor liver enzymes, though baseline elevations are not a contraindication to treatment 2
Clinical Context and Evidence Quality
The 2014 AHA/ACC/HRS guidelines provide the strongest evidence base for this approach 1. Research studies demonstrate that IV amiodarone loading doses of 5-7.5 mg/kg followed by continuous infusion achieve conversion to sinus rhythm in approximately 50-80% of patients with recent-onset AFib 3, 4. The combination of loading plus maintenance infusion has been validated in critically ill patients with impaired left ventricular function and hypotension requiring vasopressor support 5.
The maintenance infusion can be continued for 2-3 weeks if needed, with the rate adjusted based on arrhythmia suppression 2. Mean daily doses above 2100 mg in the first 24 hours are associated with increased hypotension risk 2.