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Randomized Controlled Trial Comparative Study Clinical Trial
Ondansetron, droperidol and their combination for the prevention of post-operative vomiting in children.
- A Klockgether-Radke, S Neumann, P Neumann, U Braun, and H Mühlendyck.
- Department of Anaesthesiology, Emergency Medicine and Intensive Care, Georg-August-University of Göttingen, Germany.
- Eur J Anaesthesiol. 1997 Jul 1;14(4):362-7.
AbstractIn this study the antiemetic effects of droperidol, ondansetron and their combination were evaluated in 160 ASA Grade I and II children undergoing surgery for strabismus, who were randomly assigned to one of four groups: Group D received droperidol 75 micrograms kg-1, group O ondansetron 0.1 mg kg-1, group D+O received both droperidol 75 micrograms kg-1 and ondansetron 0.1 mg kg-1, and group N NaCl as placebo. Emesis within the first 24 h occurred in 95.0% of the children with placebo medication, compared with 32.5% (D), 40.0% (O) and 45.0% (D+O) in the groups with antiemetic prophylaxis. The differences between group N and all other groups were significant (P < 0.001). However, there were no statistically significant differences between the groups D, O and D+O. It is concluded that droperidol (75 micrograms kg-1) and ondansetron (0.1 mg kg-1) both significantly reduce PONV in children undergoing surgery for strabismus. Neither ondansetron, nor the combination D+O were superior to droperidol alone.
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