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Short-Term Propofol Infusion and Associated Effects on Serum Lactate in Pediatric Patients
Sean Indra1, Haitham Haddad, Mary Ann OʼRiordan
1From the *Children's Hospital of Michigan, Detroit, MI; and †Rainbow Babies and Children's Hospital, University Hospitals, Case Medical Center, Cleveland, OH.
Insights
Short-duration propofol sedation in children did not increase serum lactate levels, indicating no significant metabolic stress. This suggests outpatient propofol use is safe for pediatric procedural sedation.
Area of Science:
- Pediatric Anesthesiology
- Clinical Pharmacology
- Metabolic Medicine
Background:
- Propofol infusion syndrome (PIS) is a rare but serious complication associated with high-dose, long-duration propofol infusions.
- The metabolic stress response, indicated by serum lactate levels, is a key marker for PIS.
- The safety of short-duration propofol sedation in pediatric outpatient settings regarding metabolic stress remains understudied.
Purpose of the Study:
- To investigate the relationship between short-duration propofol procedural sedation and adverse metabolic stress in children.
- To assess changes in serum lactate levels as a marker of metabolic stress following outpatient propofol administration in pediatric patients.
Main Methods:
- A prospective, longitudinal study involving 50 pediatric patients (ages 2-18 years) undergoing outpatient procedural sedation.
- Patients received propofol via bolus or bolus and continuous infusion.
- Serum lactate levels were measured pre- and post-procedure.
Main Results:
- The average procedure length was 40.3 minutes with a mean propofol dose of 8.2 mg/kg.
- A significant decrease in serum lactate was observed post-procedure (average change of -0.3 mmol/L, P < 0.001).
- No significant association was found between propofol dosage or procedure length and postprocedure lactate values.
Conclusions:
- Short-duration propofol procedural sedation in children is not associated with an increase in serum lactate.
- This suggests that the risks of propofol infusion syndrome may be significantly lower with short-duration, outpatient use compared to long-duration/high-dose infusions.
- Propofol appears to be a safe option for procedural sedation in pediatric outpatient settings without inducing significant metabolic stress.
Objectives:
This study aimed to determine if short-duration procedural sedation in children with propofol is related to an adverse metabolic stress response measured by serum lactate. Propofol infusion syndrome is associated with high-dose and long-duration infusion. It has not been studied with short-duration, outpatient propofol administration.
Methods:
This was a prospective, longitudinal study that included 50 patients between the ages of 2 and 18 years who were undergoing outpatient procedural sedation with propofol at a pediatric sedation unit. Patients received bolus or bolus and continuous infusion doses of propofol. Serum lactate values were obtained before and after the patients' sedated procedures.
Results:
The average length of procedure was 40.3 minutes, and the mean dose of propofol per patient was 8.2 mg/kg. The highest measured lactate value was 1.8 mmol/L. The average (SD) preprocedure and postprocedure lactate values were 1.0 (0.3) and 0.7 (0.2) mmol/L, respectively, resulting in an overall significant decrease in lactate of -0.3 (0.3) mmol/L (P < 0.001). There was a significant (P = 0.01) positive relationship between age and postprocedure lactate value, when controlling for the length of the procedure in a multivariable regression. No significant association was found between propofol dosage and length of the procedure with lactate values.
Conclusion:
In this study, we did not find a significant increase in metabolic stress, measured by serum lactate. Using propofol for short-duration procedural sedation may not carry similar risks for propofol infusion syndrome to those for long-duration/high-dose infusion therapy.
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