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Propofol for tracheal intubation in children anesthetized with sevoflurane: a dose-response study
Jerrold Lerman1, Timothy T Houle, Benjamin T Matthews
1Department of Anesthesia, Women and Children's Hospital of Buffalo, SUNY @ Buffalo and University of Rochester, Rochester, NY, USA. jerrold.lerman@gmail.com
Insights
In children, 3 mg/kg intravenous propofol during sevoflurane anesthesia improves tracheal intubation conditions. However, this dose significantly increases the incidence and duration of apnea compared to lower doses.
Area of Science:
- Anesthesiology
- Pediatric Anesthesia
- Pharmacology
Background:
- Tracheal intubation is a critical procedure in pediatric anesthesia.
- Intravenous propofol is commonly used to facilitate intubation during sevoflurane induction.
- Optimal propofol dosage for intubating conditions and respiratory effects in children requires further study.
Purpose of the Study:
- To evaluate the dose-response relationship of intravenous propofol for tracheal intubation.
- To assess the incidence and duration of apnea following propofol administration in pediatric patients.
- To compare intubating conditions and respiratory side effects across different propofol doses.
Main Methods:
- A randomized, dose-response study involving 60 healthy children.
- Children received sevoflurane/nitrous oxide anesthesia with varying doses of intravenous propofol (0, 0.5, 1, 2, or 3 mg/kg).
- Intubating conditions were assessed using a standardized scale; apnea, heart rate, and blood pressure were recorded.
Main Results:
- The 3 mg/kg propofol dose resulted in significantly better laryngoscopy and intubation conditions compared to 0 and 0.5 mg/kg doses.
- Apnea incidence was highest (8/10) with 3 mg/kg propofol, significantly greater than with 0 mg/kg (3/14) and 0.5 mg/kg (3/12).
- Apnea duration and the risk of apnea increased dose-dependently with propofol, while heart rate and blood pressure decreased over time.
Conclusions:
- Intravenous propofol at 3 mg/kg significantly improves tracheal intubating conditions in pediatric patients under sevoflurane/nitrous oxide anesthesia.
- This higher propofol dose is associated with a notable increase in the incidence and duration of apnea.
- Clinicians should carefully weigh the benefits of improved intubating conditions against the increased risk of prolonged apnea when using 3 mg/kg propofol.
Background:
Tracheal intubation during sevoflurane induction is frequently facilitated with i.v. propofol. We designed a dose-response study to evaluate the intubating conditions, and the incidence and duration of apnea after i.v. propofol in children.
Methods/Materials:
Sixty healthy children were randomly assigned to 0, 0.5, 1, 2 or 3 mg x kg(-1) i.v. propofol during sevoflurane/nitrous oxide anesthesia. Tracheal intubation was performed approximately 30 s after propofol by an anesthesiologist who was blind to the treatment. The anesthesiologist assessed the responses to laryngoscopy and intubation using a standardized scale. Incidence and duration of apnea after propofol as well as heart rate, and systolic blood pressure before and after laryngoscopy were recorded. Data were analyzed using one-way and repeated measures ANOVA, the Jonckheere-Terpstra test, and logistic regression, with P < 0.05 accepted.
Results:
The laryngoscopy score after 3 mg x kg(-1) propofol was less than that after 0 mg x kg(-1) (P < 0.01) and 0.5 mg x kg(-1) (P < 0.05). Incidence of apnea after propofol 3 mg x kg(-1), 8/10, was greater than after 0 mg x kg(-1), 3/14 (P < 0.011) and 0.5 mg x kg(-1), 3/12 (P < 0.03). Duration of apnea after 3 mg x kg(-1) was greater than after 0 and 0.5 mg x kg(-1) (P < 0.01). The risk of apnea increased 1.83 fold for each 1 mg x kg(-1) dose increase in propofol (P < 0.01). Mean heart rate and systolic pressure decreased with the main effect, time.
Conclusion:
During sevoflurane/nitrous oxide anesthesia, propofol 3 mg x kg(-1) provides superior intubating conditions with an increased incidence of and prolonged apnea compared with 0 and 0.5 mg x kg(-1).
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