Indications:
- Ventricular fibrillation or pulseless ventricular tachycardia that does not respond to initial defibrillation attempts
- Sustained ventricular tachycardia with a pulse
Contraindications:
Trauma patients
Co-administration with procainamide
Precautions:
- Do not shake (prevents foaming)
- Draw-up with large gauge needle (at least 18g)
- Protect from light
- Avoid contact with plastic
- Administer at IV/IO port closest to the patient
- Use with caution in renal failure patients
Side Effects:
- Bradycardia
- Hypotension
Adult Dose:
Standing order:
Ventricular fibrillation (VF); Pulseless ventricular tachycardia (pulseless VTach);
- First Dose: 300 mg
- Second Dose: 150 mg
Sustained, unstable ventricular tachycardia with a pulse (unstable VTach);
- First Dose: 300 mg
- Second Dose: 150 mg
BIOTEL AUTHORIZATION REQUIRED:
Stable or unstable, sustained ventricular tachycardia (VT) WITH pulse
- 150 mg - over 10 minutes (Dilute 300 mg in 250 mL NS and infuse at 12.5 mL/min for 10 minutes, then discontinue infusion. BioTel may recommend alternate infusion instructions.)
Pediatric Dose:
Standing order:
Ventricular fibrillation (VF)/Pulseless ventricular tachycardia (pulseless VTach):
- First Dose: 5 mg/kg, flush with 10 mL Normal Saline
- Second Dose: 5 mg/kg, flush with 10 mL Normal Saline
BIOTEL AUTHORIZATION REQUIRED:
Sustained, unstable ventricular tachycardia with a pulse (unstable VTach);
- 5 mg/kg in 100 mL NS slow infusion over 30 minutes
- Synchronized cardioversion is preferred in most cases.
Route: IV or IO
Drug Action:
- Alters movement of sodium, potassium and calcium through normal channels:
- Increases the refractory period of all cardiac tissues
- Slows repolarization
- Decreases cardiac automaticity
- Blocks alpha and beta adrenergic receptors
Class: Antiarrhythmic
Onset: Within minutes
Duration: Variable