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Postoperative emesis following otoplasty in children
D Paxton1, R H Taylor, T M Gallagher
1Department of Anaesthesia, Royal Belfast Hospital for Sick Children, Northern Ireland.
Anaesthesia
|December 1, 1995
Summary
Ondansetron significantly reduced vomiting and allowed earlier oral intake in children undergoing otoplasty compared to droperidol or placebo. This antiemetic offers a better post-operative recovery for pediatric surgical patients.
Area of Science:
- Anesthesiology
- Pediatric Surgery
- Pharmacology
Background:
- Postoperative nausea and vomiting (PONV) are common complications in pediatric surgery.
- Effective antiemetic strategies are crucial for improving patient recovery and comfort.
- Otoplasty is a common pediatric surgical procedure where PONV can impact recovery.
Purpose of the Study:
- To compare the efficacy of ondansetron, droperidol, and placebo in preventing PONV in children undergoing otoplasty.
- To evaluate the impact of these agents on the time to oral fluid and food ingestion post-surgery.
Main Methods:
- A randomized controlled trial involving 60 unpremedicated children aged 3-14 years scheduled for otoplasty.
- Patients were assigned to receive ondansetron (0.1 mg/kg), droperidol (75 mcg/kg), or placebo at anesthesia induction.
- Standard general anesthesia with thiopental, atracurium, and halothane was administered, avoiding intraoperative opioids.
Main Results:
- Ondansetron significantly reduced vomiting incidence (15%) compared to droperidol (40%) and placebo (60%) (p < 0.01).
- Children receiving ondansetron tolerated oral fluids and solids earlier (p < 0.001).
- No significant difference in vomiting or oral intake time was observed between droperidol and placebo groups.
Conclusions:
- Ondansetron is an effective antiemetic for pediatric otoplasty, improving recovery by reducing nausea and vomiting.
- Ondansetron facilitates earlier resumption of oral feeding compared to droperidol or placebo.
- While a transient nodal rhythm was noted with ondansetron, it was not clinically significant, and no other adverse events were reported.