| Name: |
PROCAINAMIDE HCI (PronestylR) |
| Classification: |
antiarrhythmic
- useful in supraventricular and ventricular tachycardias
- may be useful when lidocaine is ineffective
- undergoes hepatic metabolism to active metabolite, N-acetyl-procainamide (NAPA)
|
| Dose: |
- Bolus:
- 100mg IV direct q5 minutes to a maximum of 1 g then maintenance infusion 2 - 6mg/min
or
- 17mg/kg IV direct as loading dose followed by maintenance infusion 2.8mg/kg/hr
- dose must be reduced in renal failure to maintenance infusion 1.4mg/kg/hr
|
| Administration: |
- IV Direct:
- administration rate should not exceed 25-50 mg/min
- IV Infusion:
- yellow discoloration is acceptable; dark amber solutions should be discarded
|
| Adverse Effects: |
- Cardiac:
- arrhythmias: ventricular tachycardia or fibrillation, Torsades de Pointes (associated with high levels of procainamide and/or NAPA; secondary to prolonged QT interval)
- heart block
- prolongation of PR, QRS, QT intervals (up to 50%)
- bradycardia, asystole
- decreased BP, decreased CO
- Immunologic:
- lupus erythematosus like syndrome
- fever
- neutropenia, agranulocytosis, thrombocytopenia
- Others:
|
| Contraindications: |
- myasthenia gravis
- in complete heart block or type II second degree heart block unless functional pacemaker in place (can suppress a ventricular escape rhythm)
- following electrical conversion
|
| Drug Interactions: |
- procainamide + amiodarone = increased plasma procainamide concentration
- procainamide + cimetidine = increased plasma procainamide concentration
- procainamide + lidocaine = increased CNS toxicity
- procainamide + neuromuscular blockers = increased neuromuscular blockade
|
| Monitoring Therapy: |
- ECG (PR, QRS, QT widening by 50%)
- BP
- cardiac index
- CBC, platelets
- procainamide serum level: therapeutic: 17-68 uM/L (pre-dose)
- procainamide + NAPA serum level: therapeutic: 43-128 uM/L (pre-dose)
|
| CCTC Protocol: |
- May be administered by IV infusion by an RN.
- May be titrated by an approved nurse in the CCTC.
|