Acute Adverse Effects of Amiodarone and Procainamide
The most common acute adverse effects of amiodarone include hypotension, bradycardia, QT prolongation, and gastrointestinal symptoms, while procainamide primarily causes hypotension, which occurs more frequently (19%) than with amiodarone (6%). 1
Amiodarone Acute Adverse Effects
Cardiovascular Effects
- Hypotension is one of the most important treatment-emergent adverse effects during IV amiodarone administration 2
- Bradycardia and heart block occur in 1-3% of patients receiving amiodarone 3
- QT prolongation is common, though torsades de pointes is rare (less than 2%) 2
- Proarrhythmia, including worsening of existing arrhythmias or precipitation of new arrhythmias, can occur 2
Pulmonary Effects
- Early-onset pulmonary toxicity can develop within days to weeks of starting IV amiodarone 2
- Acute respiratory distress syndrome (ARDS) occurs in approximately 2% of patients during clinical studies involving 48 hours of therapy 2
- Manifestations include pulmonary infiltrates, bronchospasm, wheezing, fever, dyspnea, cough, hemoptysis, and hypoxia 2, 4
- Post-operative patients are at higher risk for developing amiodarone pulmonary toxicity 4
Gastrointestinal Effects
- Nausea, anorexia, and constipation are common gastrointestinal side effects 3, 5
- These symptoms are often dose-related and usually improve when the dosage is reduced 3, 5
Hepatic Effects
- Liver function test abnormalities are common during amiodarone therapy 2
- Acute, centrolobular confluent hepatocellular necrosis leading to hepatic coma, acute renal failure, and death has been associated with high-dose, rapid infusion of amiodarone 2
Injection Site Reactions
- Pain, erythema, edema, pigment changes, venous thrombosis, phlebitis, thrombophlebitis, cellulitis, necrosis, and skin sloughing can occur at the injection site 2
Procainamide Acute Adverse Effects
Cardiovascular Effects
- Hypotension is the most significant acute adverse effect, occurring in 19% of patients receiving procainamide compared to 6% with amiodarone 1
- Hypotension can be severe enough to require cessation of infusion or immediate cardioversion 1
Comparative Safety Profile
- In a randomized comparison of IV procainamide vs. IV amiodarone for treatment of tolerated wide QRS tachycardia, major cardiac adverse events occurred in 9% of procainamide patients versus 41% of amiodarone patients 6
- Despite this safety difference, both medications show similar modest efficacy in terminating ventricular tachycardia (30% for procainamide vs. 25% for amiodarone) 1
Monitoring and Management
Amiodarone Monitoring
- Close surveillance of heart rate is essential, especially during the first week of treatment 3
- Monitor for QTc prolongation during infusion 2
- Assess for signs of respiratory distress including dyspnea, cough, or hypoxia 4
- Monitor liver function tests and watch for signs of hepatic injury 2
Procainamide Monitoring
- Close blood pressure monitoring during administration is critical due to the high risk of hypotension 1
Clinical Pitfalls and Caveats
- Combining amiodarone with other QT-prolonging medications (fluoroquinolones, macrolide antibiotics, azoles) increases the risk of torsades de pointes 2
- The rate of administration for amiodarone should be carefully controlled to minimize the risk of hypotension and hepatic injury 2
- Patients with pre-existing lung disease may be at higher risk for amiodarone pulmonary toxicity 4, 7
- Amiodarone-induced pulmonary toxicity can be easily missed as it may mimic other conditions such as pneumonia or heart failure 4
- Both medications have relatively low efficacy for acute termination of ventricular tachycardia, with success rates of only 25-30% 1