What is the recommended dose and administration protocol for Amiodarone (anti-arrhythmic medication) given via intravenous (IV) push to a critically ill patient, likely experiencing a life-threatening arrhythmia such as ventricular tachycardia or fibrillation, with consideration of potential hypotension, past medical history, and impaired renal function?

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Amiodarone IV Push Administration

Amiodarone should NOT be given as a true "IV push" in the traditional sense—it must be administered as a controlled infusion over at least 10 minutes, even in cardiac arrest situations, to minimize life-threatening hypotension and hepatorenal toxicity. 1

Cardiac Arrest Protocol (VF/Pulseless VT)

For patients in ventricular fibrillation or pulseless ventricular tachycardia unresponsive to CPR and defibrillation:

  • First dose: 300 mg IV/IO as a rapid bolus (administered over approximately 1-2 minutes during active resuscitation) 2
  • Second dose: 150 mg IV/IO if VF/pulseless VT persists after the first dose 2
  • This bolus dosing should only occur after multiple defibrillation attempts and epinephrine administration 2

Hemodynamically Stable Ventricular Arrhythmias

For stable ventricular tachycardia or breakthrough VF/VT episodes:

  • Loading dose: 150 mg mixed in 100 mL D5W infused over 10 minutes 3, 1
  • Do NOT exceed 30 mg/min infusion rate to prevent hepatocellular necrosis and acute renal failure 1
  • This can be repeated if breakthrough arrhythmias occur 1

Standard 24-hour protocol following initial loading:

  • 1 mg/min (360 mg) for first 6 hours 3, 1
  • Then 0.5 mg/min (540 mg) for next 18 hours 3, 1
  • Total first 24 hours: approximately 1000 mg 2, 1

Critical Administration Requirements

Equipment and access:

  • Must use volumetric infusion pump—drop counter sets can underdose by up to 30% 1
  • Administer through central venous catheter whenever possible 3, 1
  • Use in-line filter during administration 3, 1

Concentration limits:

  • For infusions >1 hour: do NOT exceed 2 mg/mL concentration unless using central line 1
  • Concentrations >3 mg/mL cause high incidence of peripheral vein phlebitis 1
  • Infusions >2 hours must use glass or polyolefin bottles with D5W 1

Contraindications and High-Risk Situations

Absolute contraindications:

  • Second- or third-degree AV block without pacemaker 3, 2
  • Sick sinus syndrome without pacemaker 2

Extreme caution required (relative contraindication):

  • Heart rate <60 bpm without pacemaker—only use if immediately life-threatening and no alternatives exist 3
  • Severe sinus node dysfunction 2

Bradycardia considerations:

  • Drug-related bradycardia occurs in 4.9% of IV amiodarone patients 3
  • If heart rate decreases by 10 bpm during infusion, reduce rate immediately 3

Monitoring Requirements

Continuous monitoring mandatory:

  • ECG for heart rate, AV conduction abnormalities, QT prolongation 3
  • Blood pressure—hypotension occurs in 16-26% of patients 3, 2, 4
  • Watch for second- or third-degree heart block (absolute contraindication to continued therapy) 3

Special Considerations for Critically Ill Patients

Hypotension management:

  • Occurs in approximately 26% of patients receiving IV amiodarone 2, 4
  • Minimize risk by infusing 150 mg doses over full 10 minutes 1
  • Hypotension may require vasopressor support 5

Renal impairment:

  • Maintenance infusion up to 0.5 mg/min can be continued for 2-3 weeks regardless of renal function 1
  • Rapid infusions at higher concentrations than recommended have caused acute renal failure and death 1

Drug interactions requiring immediate dose adjustments:

  • Reduce digoxin by 50% immediately—amiodarone doubles digoxin levels 3, 6
  • Reduce warfarin by 30-50% and check INR within 3-5 days 6
  • Concomitant beta-blockers, calcium channel blockers increase bradycardia risk 3

Common Pitfalls to Avoid

  • Never administer faster than 10 minutes for non-arrest situations—this causes severe hypotension and organ toxicity 1
  • Never use concentrations >2 mg/mL peripherally for >1 hour—causes phlebitis 1
  • Never use evacuated glass containers for mixing—causes precipitation 1
  • Do not exceed 2100 mg in first 24 hours—associated with increased hypotension risk 1

References

Guideline

Amiodarone Dosing and Administration Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Administering IV Amiodarone with Bradycardia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Amiodarone Oral to Intravenous Equivalency

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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