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Propofol: effective dose and induction characteristics in unpremedicated children
R S Hannallah1, S B Baker, W Casey
1Department of Anesthesiology, Children's National Medical Center, Washington, D.C. 20010.
Insights
Propofol is an effective anesthetic induction agent for children aged 3-12 years. Recommended doses range from 2.5-3.0 mg/kg for smooth transitions to maintenance anesthesia.
Area of Science:
- Anesthesiology
- Pediatric Anesthesia
- Pharmacology
Background:
- Propofol is a widely used intravenous anesthetic agent.
- Its efficacy and safety in pediatric populations require thorough investigation.
- Understanding optimal dosing and effects is crucial for pediatric anesthesia.
Purpose of the Study:
- To evaluate the induction dose, characteristics, and effects of propofol in children.
- To determine the effective dose (ED50 and ED95) for successful induction.
- To assess cardiovascular and respiratory effects during propofol induction.
Main Methods:
- A study involving 90 unpremedicated children aged 3-12 years.
- Propofol was administered intravenously at doses of 1-3 mg/kg over 10-30 seconds.
- Successful induction criteria included loss of eyelash reflex and mask acceptance.
Main Results:
- The effective dose for loss of eyelash reflex was 1.3 mg/kg (ED50) and 2.0 mg/kg (ED95).
- Successful induction with mask acceptance required 1.5 mg/kg (ED50) and 2.3 mg/kg (ED95).
- Adverse events included pain on injection (6.6%), involuntary movement (12.7%), apnea (21%), and hypotension (48% with halothane).
Conclusions:
- Propofol is an effective agent for anesthetic induction in children.
- A recommended dose of 2.5-3.0 mg/kg ensures smooth induction for maintenance anesthesia.
- Intravenous administration via antecubital veins is associated with low incidence of injection pain.
Abstract:
The induction dose, induction characteristics, and cardiovascular and respiratory effects of propofol were studied in 90 unpremedicated children 3-12 yr old. Propofol in a dose of 1-3 mg.kg-1 was injected in an antecubital vein over 10-30 s. Successful induction was defined by loss of eyelash reflex occurring within 50 s of the conclusion of propofol injection and followed by subsequent acceptance of face mask without excessive movement. The effective dose of propofol resulting in loss of eyelash reflex in 50% (ED50) and 95% (ED95) of children were 1.3 (1.1-1.4) and 2.0 (1.7-2.6) mg.kg-1 (95% confidence interval). The corresponding ED50 and ED95 for a successful induction that included acceptance of face mask were 1.5 (1.3-1.7) and 2.3 (2.1-3.0), respectively. There was a 6.6% incidence of mild to moderate pain on injection and a 12.7% incidence of involuntary movement. Apnea (cessation of breathing greater than 20 s) was seen in 21% of patients. Blood pressure decreased by more than 20% of baseline value in 48% of patients who received halothane (1-3%) after the bolus injection of propofol. It is concluded that propofol is an effective induction agent in children. A dose of 2.5-3.0 mg.kg-1 is recommended to ensure a smooth transition to an inhalational maintenance technique. The use of antecubital veins is associated with a low incidence of pain on injection.
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