Randomized controlled trial on preemptive analgesia for acute postoperative pain management in children

In-Kyung Song1, Yong-Hee Park2, Ji-Hyun Lee1

  • 1Department of Anesthesiology and Pain medicine, Seoul National University Hospital, Seoul, Korea.

Paediatric Anaesthesia
|February 19, 2016
PubMed

Insights

Preemptive analgesia did not significantly improve postoperative pain control in pediatric patients undergoing corrective osteotomy. While emergence agitation was lower initially, overall pain management and analgesic needs were similar between groups.

Area of Science:

  • Anesthesiology
  • Pediatric Surgery
  • Pain Management

Background:

  • Preemptive analgesia aims to prevent central sensitization and manage acute postoperative pain.
  • Its effectiveness compared to conventional pain management remains debated.
  • This study investigates intravenous preemptive analgesia in pediatric patients.

Purpose of the Study:

  • To evaluate the efficacy of preemptive analgesia for acute postoperative pain control in pediatric patients undergoing corrective osteotomy.
  • To compare pain scores, emergence agitation, and analgesic requirements between preemptive and conventional analgesia groups.

Main Methods:

  • A prospective randomized controlled trial involving 51 children aged 3-7 years.
  • Patients received either preemptive (IV-PCA with fentanyl before incision) or conventional (IV-PCA with fentanyl after incision) analgesia.
  • Pain scores, emergence agitation, and analgesic consumption were recorded.

Main Results:

  • No significant difference in pain scores at 1 hour postoperatively.
  • Lower emergence agitation scores on PACU admission in the preemptive group (P=0.002).
  • No differences in overall IV-PCA use, pain scores, or complications between groups.

Conclusions:

  • Preemptive analgesia with IV-PCA fentanyl did not offer significant advantages for postoperative pain management after corrective osteotomy in children.
  • The findings suggest current conventional regimens may be sufficient for this patient population.
Abstract

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