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Published on: February 6, 2019
Evaluation of propofol for repeated prolonged deep sedation in children undergoing proton radiation therapy
1Department of Anaesthesia, University Children's Hospital, Steinwiesstrasse 75, CH 8032 Zurich, Switzerland.
Insights
Fixed-dose propofol infusion is safe and effective for deep sedation in children undergoing proton radiation therapy (PRT). This method ensures adequate anesthesia without needing dose adjustments during repeated, prolonged procedures.
Area of Science:
- Pediatric Anesthesiology
- Radiation Oncology
- Pharmacology
Background:
- Proton radiation therapy (PRT) requires deep sedation in pediatric patients.
- Repeated and prolonged sedation can pose safety and sufficiency challenges.
Purpose of the Study:
- To evaluate the safety and sufficiency of a fixed dose rate propofol infusion.
- To assess its use for repeated prolonged deep sedation in children undergoing PRT.
Main Methods:
- Monitored anesthesia data in children receiving propofol sedation for PRT.
- Administered midazolam followed by propofol boluses for induction.
- Maintained sedation with a fixed propofol infusion rate of 10 mg kg(-1) h(-1).
Main Results:
- Eighteen children (1.4–4.2 yr) underwent 497 PRT procedures.
- Average propofol induction dose was 3.7 mg kg(-1).
- No changes to the fixed propofol infusion rate were needed due to patient condition.
Conclusions:
- Fixed rate propofol infusion is safe and adequate for repeated prolonged deep sedation in pediatric PRT.
- This sedation strategy proved effective for all young patients.
Background:
The aim of this study is to evaluate the safety and sufficiency of a fixed dose rate propofol infusion for repeated prolonged deep sedation in children for proton radiation therapy (PRT).
Methods:
With ERB approval, we recorded anaesthesia monitoring data in children undergoing repeated prolonged propofol sedation for PRT. Sedation was introduced with a single bolus of i.v. midazolam 0.1 mg kg(-1) followed by repeated small boluses of propofol until sufficient depth of sedation was obtained. Sedation was maintained with fixed dose rate propofol infusion of 10 mg kg(-1) h(-1) in all patients up to the end of the radiation procedure. Patient characteristics, number and duration of sedation, propofol induction dose, necessity to alter propofol infusion rate, and heart rate, mean arterial pressure, respiratory rate were noted at the end of the radiation procedure before cessation of the propofol infusion. Data are mean (sd) or range (median) as appropriate.
Results:
Eighteen children aged from 1.4 to 4.2 yr (2.6 yr) had 27.6 (sd 2.0) (497 in total) radiation procedures within 44.1 (4.0) days lasting 55.7 (8.8) min. Propofol bolus dose for induction, monitoring, and positioning was 3.7 (1.0) mg kg(-1). Propofol bolus requirements were quite stable over the successive weeks of treatment and variability was larger between individuals than over time. In none of the children did propofol infusion rate need to be changed from the pre-set 10 mg kg(-1) h(-1) flow rate because of haemodynamic state, respiratory conditions or inadequate anaesthesia.
Conclusions:
Repeated prolonged deep sedation over several weeks in very young children using a fixed rate propofol infusion was safe and adequate for all patients.
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