Olanzapine for the Prevention of Postdischarge Nausea and Vomiting after Ambulatory Surgery: A Randomized Controlled Trial

被引:17
|
作者
Hyman, Jaime B. [1 ]
Park, Chang [1 ]
Lin, Hung-Mo [2 ]
Cole, Beatriz [1 ]
Rosen, Leigh [3 ]
Fenske, Suzanne S. [6 ]
Barr Grzesh, Rachel L. [3 ]
Blank, Stephanie V. [4 ]
Polsky, Sylvie B. [7 ]
Hartnett, Matthew [1 ]
Taub, Peter J. [5 ]
Palvia, Vijay [3 ]
DeMaria, Samuel [1 ]
Ascher-Walsh, Charles [3 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Anesthesiol Perioperat & Pain Med, One Gustave L Levy Pl,Box 1010, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Dept Populat Hlth Sci & Policy, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Dept Obstet Gynecol & Reprod Sci, Div Gynecol, New York, NY 10029 USA
[4] Icahn Sch Med Mt Sinai, Blavatnik Family Womens Hlth Res Inst, Dept Obstet & Gynecol, Div Gynecol Oncol, New York, NY 10029 USA
[5] Icahn Sch Med Mt Sinai, Dept Surg, Div Plast & Reconstruct Surg, New York, NY 10029 USA
[6] Suzanne Fenske MD PC, Brookville, NY USA
[7] Brigham & Womens Hosp, Dept Anesthesiol Perioperat & Pain Med, 75 Francis St, Boston, MA 02115 USA
关键词
CHEMOTHERAPY-INDUCED NAUSEA; LOW-DOSE HALOPERIDOL; POSTOPERATIVE NAUSEA; DOUBLE-BLIND; TRANSDERMAL SCOPOLAMINE; HIGH-RISK; PHASE-II; ONDANSETRON; EFFICACY; DROPERIDOL;
D O I
10.1097/ALN.0000000000003286
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: Postdischarge nausea and vomiting after ambulatory surgery is a common problem that is not adequately addressed in current practice. This prospective, randomized, double-blind, parallel-group, placebo-controlled study was designed to test the hypothesis that oral olanzapine is superior to placebo at preventing postdischarge nausea and vomiting. Methods: In a single-center, double-blind, randomized, placebo-controlled trial, the authors compared a single preoperative dose of olanzapine 10mg to placebo, in adult female patients 50 years old or less, undergoing ambulatory gynecologic or plastic surgery with general anesthesia. All patients received standard antiemetic prophylaxis with dexamethasone and ondansetron. The primary composite outcome was nausea and/or vomiting in the 24h after discharge. Secondary outcomes included severe nausea, vomiting, and side effects. Results: A total of 140 patients were randomized and evaluable. The primary outcome occurred in 26 of 69 patients (38%) in the placebo group and in 10 of 71 patients (14%) in the olanzapine group (relative risk, 0.37; 95% CI, 0.20 to 0.72; P = 0.003). Severe nausea occurred in 14 patients (20%) in the placebo group and 4 patients (6%) in the olanzapine group (relative risk, 0.28; 95% CI, 0.10 to 0.80). Vomiting occurred in eight patients (12%) in the placebo group and two patients (3%) in the olanzapine group (relative risk, 0.24; 95% CI, 0.05 to 1.10). The median score for sedation (scale 0 to 10, with 10 being highest) in the 24h after discharge was 4 (interquartile range, 2 to 7) in the placebo group and 6 (interquartile range, 3 to 8) in the olanzapine group (P = 0.023). Conclusions: When combined with ondansetron and dexamethasone, the addition of olanzapine relative to placebo decreased the risk of nausea and/or vomiting in the 24 hafter discharge from ambulatory surgery by about 60% with a slight increase in reported sedation.
引用
收藏
页码:1419 / 1428
页数:10
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