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Propofol and halothane versus sevoflurane in paediatric day-case surgery: induction and recovery characteristics
J K Moore1, E W Moore, R A Elliott
1Wirral Hospital Trust, Cheshire CH49 5PE, UK.
Insights
Sevoflurane anaesthesia in children led to more adverse events, including nausea, vomiting, and delirium, compared to propofol induction and halothane maintenance. Recovery was faster with sevoflurane, but it is not ideal for paediatric day surgery.
Area of Science:
- Anesthesiology
- Pediatric Anesthesia
- Pharmacology
Background:
- Paediatric day surgery requires careful anaesthetic management.
- Comparing anaesthetic agents is crucial for optimizing patient outcomes.
- Propofol and sevoflurane are commonly used in paediatric anaesthesia.
Purpose of the Study:
- To compare induction and recovery characteristics of propofol/halothane versus sevoflurane anaesthesia in children.
- To evaluate adverse events and recovery profiles in paediatric day surgery patients.
Main Methods:
- A randomized study of 322 children undergoing day surgery.
- Group 1: Intravenous propofol induction, halothane/nitrous oxide maintenance.
- Group 2: Sevoflurane/nitrous oxide anaesthesia alone. Data collected on induction/recovery times, adverse events, and discharge readiness.
Main Results:
- Sevoflurane induction was slower (5 min vs 3.1 min).
- Recovery was faster with sevoflurane (23.2 min vs 26.4 min).
- Sevoflurane group had higher incidence of excitatory movement, delirium, nausea, and vomiting.
Conclusions:
- Sevoflurane as a sole agent for paediatric day surgery is associated with increased adverse events.
- Propofol induction with halothane maintenance may offer a better safety profile.
- Further research into optimal anaesthetic strategies for paediatric day surgery is warranted.
Background:
The aim of this study was to compare the induction and recovery characteristics associated with propofol induction and halothane maintenance with sevoflurane anaesthesia in paediatric day surgery.
Methods:
In total, 322 children were assigned randomly to i.v. propofol induction and halothane/nitrous oxide maintenance or sevoflurane/nitrous oxide alone. The patients' age, sex, and type of surgery were recorded, as were the times required for anaesthetic induction, maintenance, recovery and time to discharge home. Postoperative nausea and vomiting, and the incidence of adverse events during induction and recovery were also noted.
Results:
No significant differences were detected in age, sex, type of surgery performed or intraoperative opioid administration. Excitatory movement was more common during induction with sevoflurane. The mean time required for induction with propofol was 3.1 min compared with 5 min in the sevoflurane group (P<0.001). The recovery time was shorter in the sevoflurane group compared with propofol/halothane (23.2 vs 26.4 min, P<0.002). The incidence of delirium in recovery was greater in the sevoflurane group (P<0.001). There was no difference between groups in the time spent on the postoperative ward before discharge home. On the postoperative ward the incidence of both nausea and vomiting was significantly higher in the sevoflurane group (P=0.034). Five children were admitted to hospital overnight, none for anaesthetic reasons.
Conclusions:
The increased incidence of adverse events during induction, postoperative nausea and vomiting and postoperative delirium in the sevoflurane group suggests that sevoflurane is not ideal as a sole agent for paediatric day case anaesthesia.
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