Propofol Induction Dose
For healthy adults under 55 years (ASA I-II), the induction dose is 2-2.5 mg/kg administered as incremental boluses of approximately 40 mg every 10 seconds until loss of consciousness occurs. 1
Standard Induction Dosing by Patient Population
Healthy Adults (ASA I-II, <55 years)
- Dose: 2-2.5 mg/kg administered as approximately 40 mg every 10 seconds, titrated to clinical response 1
- This applies to unpremedicated patients or those premedicated with oral benzodiazepines or intramuscular opioids 1
- The corresponding effect site concentration at loss of verbal response is approximately 2.34 μg/mL 2
Elderly, Debilitated, or ASA III-IV Patients
- Dose: 1-1.5 mg/kg administered as approximately 20 mg every 10 seconds 1
- Critical pitfall: Rapid bolus administration must be avoided in this population, as it significantly increases the risk of hypotension, apnea, airway obstruction, and oxygen desaturation 1
- The reduced clearance and higher blood concentrations in these patients necessitate the lower dosing 1
Pediatric Patients (3-16 years, ASA I-II)
- Dose: 2.5-3.5 mg/kg for unpremedicated or lightly premedicated children 1
- Younger pediatric patients within this age range require higher induction doses than older pediatric patients 1
- Lower dosages are recommended for ASA III-IV pediatric patients 1
- Pain on injection is a significant concern; consider pretreating small veins with lidocaine or using antecubital or larger veins 1
Neurosurgical Patients
- Dose: 1-2 mg/kg using slower boluses of 20 mg every 10 seconds 1
- Slower induction with careful titration to clinical responses results in reduced dosage requirements 1
Cardiac Anesthesia Patients
- Dose reduction required due to propofol's effects on preload (decreased ventricular filling) and afterload (decreased arterial resistance) 1
- The American Society of Anesthesiologists emphasizes careful titration in this population 1
Critical Administration Principles
Timing Between Doses
- Allow 3-5 minutes between dose adjustments to assess clinical effects and avoid excessive drug accumulation 1
- The onset of action is 30-45 seconds (equivalent to arm-brain circulation time) 3
Impact of Premedication
- Opioid and benzodiazepine premedication significantly reduces propofol requirements 1
- Morphine premedication (0.15 mg/kg) with nitrous oxide has been shown to decrease necessary propofol maintenance infusion rates compared to non-narcotic premedication 1
- When propofol is combined with small doses of opioids and benzodiazepines, subhypnotic doses of propofol can achieve adequate anesthesia while reducing hemodynamic instability 3
Common Pitfalls and Safety Considerations
Cardiovascular Depression
- Hypotension is the most common complication, occurring in a dose-dependent manner due to decreased cardiac output, systemic vascular resistance, and arterial pressure 3, 4
- Have vasopressors (ephedrine or metaraminol) immediately available 5
- Consider elevation of lower extremities when additional fluid therapy is contraindicated 5
Respiratory Depression
- Dose-dependent respiratory depression occurs, with potential for apnea, particularly with rapid bolus administration 3
- Continuous monitoring of heart rate, blood pressure, and pulse oximetry is mandatory 3
Contraindications
- Avoid in patients with egg, soy, or sulfite allergies, as propofol contains 10% soybean oil and 1.2% purified egg phosphatide 3
- Propofol is NOT contraindicated in sulfonamide allergy 3