Propofol Dosage and Administration for General Anesthesia
For general anesthesia induction and maintenance, propofol should be administered at 1-2.5 mg/kg IV for induction (titrated to effect) followed by maintenance infusion of 50-200 mcg/kg/min, with dosage adjustments based on patient factors including age, comorbidities, and ASA status. 1
Induction Dosing
Adult Patients
- Standard healthy adults (ASA I-II, <55 years): 2-2.5 mg/kg IV titrated at approximately 40 mg every 10 seconds until onset of anesthesia 1
- Elderly, debilitated, or ASA III-IV patients: Reduced dosage of 1-1.5 mg/kg IV (approximately 20 mg every 10 seconds) 1
- Neurosurgical patients: Slower induction using 20 mg boluses every 10 seconds (typically 1-2 mg/kg total) 1
- Cardiac patients: 0.5-1.5 mg/kg administered slowly at approximately 20 mg every 10 seconds 1
Pediatric Patients
- Children 3-16 years (ASA I-II): 2.5-3.5 mg/kg IV 1
- ASA III-IV pediatric patients: Lower dosage recommended 1
Maintenance Dosing
Adult Patients
- Continuous infusion: 100-200 mcg/kg/min initially (first 10-15 minutes), then decreased by 30-50% during first half-hour 1
- Optimal maintenance rate: 50-100 mcg/kg/min to optimize recovery times 1
- Intermittent bolus method: 25-50 mg increments in response to clinical signs 1
Pediatric Patients
- Initial infusion rate: 200-300 mcg/kg/min immediately following induction 1
- After first half-hour: 125-150 mcg/kg/min typically needed 1
- Note: Younger pediatric patients may require higher maintenance rates than older children 1
Cardiac Anesthesia
- Primary agent: ≥100 mcg/kg/min with supplemental opioid analgesia 1
- With primary opioid: ≥50 mcg/kg/min to ensure amnesia 1
- Avoid: Rapid bolus induction in cardiac patients 1
Special Considerations
Pharmacokinetic Profile
- Onset of action: 30-45 seconds (one arm-brain circulation) 2
- Duration of effect: 4-8 minutes 2
- Metabolism: Rapid liver metabolism by conjugation to glucuronide and sulfate 2
- Elimination: Water-soluble compounds excreted by kidney 2
Patient-Specific Factors
- Factors altering pharmacokinetics: Weight, sex, age, and concomitant diseases 2
- Co-administered medications: Opioids, benzodiazepines, and other CNS depressants potentiate propofol's sedative effects 2, 1
- Contraindications: Allergies to egg, soy, or sulfites (present in propofol formulation) 2, 3
Monitoring Requirements
- Continuous monitoring of oxygen saturation, blood pressure, and cardiac activity 3
- Supplemental oxygen administration as needed 3
- Dedicated provider for patient monitoring during propofol sedation 3
Potential Adverse Effects
- Cardiovascular: Decreased cardiac output, systemic vascular resistance, and arterial pressure 2
- Respiratory: Respiratory depression responsive to dose reduction or interruption 2
- Pain on injection: Reported in up to 30% of patients 2, 3
- Apnea requiring assisted ventilation: Approximately 1 per 500-1000 procedures 3
Practical Administration Tips
- Avoid rapid bolus administration, especially in elderly, debilitated, or ASA III-IV patients 1
- For pediatric patients, minimize injection pain by using lidocaine pretreatment or administering via larger veins 1
- Titrate downward in absence of light anesthesia signs to avoid unnecessarily high rates 1
- For procedures longer than 30 minutes, consider reducing infusion rates by 30-50% after the first half-hour to prevent accumulation 3, 1
By following these dosing guidelines and considering patient-specific factors, propofol can provide effective induction and maintenance of general anesthesia with rapid, predictable emergence and minimal postoperative complications.