Abstract | STUDY OBJECTIVE: 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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Authors | Neera Sah, Vimala Ramesh, Bupesh Kaul, Patricia Dalby, Kenneth Shestak, Manuel C Vallejo |
Journal | Journal of clinical anesthesia
(J Clin Anesth)
Vol. 21
Issue 4
Pg. 249-52
(Jun 2009)
ISSN: 1873-4529 [Electronic] United States |
PMID | 19502023
(Publication Type: Journal Article, Randomized Controlled Trial)
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Chemical References |
- Antiemetics
- Cholinergic Antagonists
- Ondansetron
- Scopolamine
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Topics |
- Administration, Cutaneous
- Adult
- Ambulatory Surgical Procedures
(adverse effects)
- Antiemetics
(therapeutic use)
- Cholinergic Antagonists
(administration & dosage, therapeutic use)
- Double-Blind Method
- Drug Therapy, Combination
- Female
- Humans
- Male
- Middle Aged
- Ondansetron
(therapeutic use)
- Pain
(etiology)
- Postoperative Nausea and Vomiting
(prevention & control)
- Prospective Studies
- Scopolamine
(administration & dosage, therapeutic use)
- Surgery, Plastic
(adverse effects)
- Time Factors
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