Transdermal scopolamine patch in addition to ondansetron for postoperative nausea and vomiting prophylaxis in patients undergoing ambulatory cosmetic surgery
- PMID: 19502023
- DOI: 10.1016/j.jclinane.2008.08.017
Transdermal scopolamine patch in addition to ondansetron for postoperative nausea and vomiting prophylaxis in patients undergoing ambulatory cosmetic surgery
Abstract
Study objective: To determine the efficacy of transdermal scopolamine in addition to ondansetron in decreasing the incidence of postoperative nausea and vomiting (PONV).
Design: Randomized controlled trial.
Setting: Academic hospital.
Patients: 126 ASA physical status I and II patients undergoing outpatient plastic surgery with three or more risk factors for PONV.
Interventions: Patients were randomly assigned to one of two groups to receive (Group 1) a transdermal scopolamine (TDS) patch or (Group 2), a placebo patch two hours before surgery.
Measurements: Occurrence of vomiting, severity of nausea using a visual analog scale (VAS), rescue medication, pain intensity and pain medications, and side effects were recorded every hour until discharge from hospital, then every 4 hours thereafter for a total of 24 hours.
Main results: A statistically significant reduction in postoperative nausea between 8 and 24 hours in patients receiving TDS was noted.
Conclusions: Transdermal scopolamine in addition to ondansetron benefits patients at high risk for PONV undergoing outpatient plastic surgery for up to 20 hours after surgery.
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