Propofol Versus Sevoflurane Anesthesia for Acute Postoperative Pain Management in Pediatric Adenotonsillectomy: A

Zhi-Peng Zhong1, Yu Gao1, Cheng Fan1

  • 1Department of Anesthesiology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.

Paediatric Anaesthesia
|September 8, 2025
PubMed

Insights

Propofol and sevoflurane anesthesia show similar effectiveness for managing acute pain after pediatric adenotonsillectomy. Postoperative pain intensity and incidence were comparable between the two anesthetic agents within the first 24 hours.

Area of Science:

  • Anesthesiology and Pain Management
  • Pediatric Surgery
  • Clinical Trials

Background:

  • Post-adenotonsillectomy pain in children is common, severe, and often poorly managed.
  • The comparative efficacy of propofol versus sevoflurane for acute pain control following this procedure is not well-established.

Purpose of the Study:

  • To evaluate the postoperative analgesic effectiveness of propofol compared to sevoflurane anesthesia in pediatric patients undergoing adenotonsillectomy.
  • To determine if there are significant differences in acute pain management between the two anesthetic agents.

Main Methods:

  • A single-blind, randomized controlled trial involving 144 children aged 2-7 years.
  • Patients were randomized to receive either propofol or sevoflurane anesthesia.
  • Primary outcome: proportion of patients with acute pain (FLACC scale > 3) within 24 hours; Secondary outcomes: pain scores (PPPM, NRS) and adverse events.

Main Results:

  • No significant difference in the incidence of acute pain (FLACC > 3) within 24 hours between propofol and sevoflurane groups (42.3% vs. 47.9%).
  • The propofol group showed slightly higher pain scores on postoperative days 2-3, but these differences were below clinically important thresholds.

Conclusions:

  • Propofol and sevoflurane anesthesia provide comparable clinical efficacy for managing acute postoperative pain in children after adenotonsillectomy.
  • Neither anesthetic agent demonstrated superior pain control within the first 24 hours or over a two-week follow-up period.
Abstract

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