A randomized, double-blind comparison of the NK1 antagonist, aprepitant, versus ondansetron for the prevention of postoperative nausea and vomiting

被引:115
|
作者
Gan, Tong J. [1 ]
Apfel, Christian C.
Kovac, Anthony
Philip, Beverly K.
Singla, Neil
Minkowitz, Harold
Habib, Ashraf S.
Knighton, Jennifer
Carides, Alexandra D.
Zhang, Hong
Horgan, Kevin J.
Evans, Judith K.
Lawson, Francasca C.
机构
[1] Duke Univ, Med Ctr, Dept Anesthesiol, Durham, NC 27710 USA
[2] Univ Calif San Francisco, Dept Anesthesiol & Perioperat Care, Mt Zion Med Ctr, San Francisco, CA 94143 USA
[3] Univ Kansas, Med Ctr, Kansas City, KS 66103 USA
[4] Brigham & Womens Hosp, Dept Anesthesiol Perioperat & Pain Med, Boston, MA 02115 USA
[5] Huntington Mem Hosp, Clin Management Serv Inc, Pasadena, CA USA
[6] Mem Hermann Mem City Hosp, Houston, TX USA
[7] Merck Res Labs, Blue Bell, PA USA
来源
ANESTHESIA AND ANALGESIA | 2007年 / 104卷 / 05期
关键词
D O I
10.1213/01.ane.0000263277.35140.a3
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
BACKGROUND: Antiemetics currently in use are not totally effective. Neurokinin-1 receptor antagonists are a new class of antiemetic that have shown promise for chemotherapy-induced nausea and vomiting. This is the first study evaluating the efficacy and tolerability of the neurokinin-1 receptor antagonist, aprepitant, for the prevention of postoperative nausea and vomiting. METHODS: In this multicenter, double-blind trial, we randomly assigned 805 patients receiving general anesthesia for open abdominal surgery to a preoperative dose of aprepitant 40 mg orally, aprepitant 125 mg orally, or ondansetron 4 mg IV. Vomiting, nausea, and use of rescue therapy were assessed over 48 h after surgery. Treatments were compared using logistic regression. RESULTS: Incidence rates for the primary end point (complete response [no vomiting and no use of rescue] over 0-24 h after surgery, tested for superiority of aprepitant) were not different across groups (45% with aprepitant 40 mg, 43% with aprepitant 125 mg, and 42% with ondansetron). The incidence of no vomiting (0-24 h) was higher with aprepitant 40 mg (90%) and aprepitant 125 mg (95%) versus ondansetron (74%) (P < 0.001 for both comparisons), although between-treatment use of rescue and nausea control was not different. Both aprepitant doses also had higher incidences of no vomiting over 0-48 h (P < 0.001). No statistically significant differences were seen among the side effect profiles of the treatments. CONCLUSIONS: Aprepitant was superior to ondansetron for prevention of vomiting in the first 24 and 48 h, but no significant differences were observed between aprepitant and ondansetron for nausea control, use of rescue, or complete response.
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收藏
页码:1082 / 1089
页数:8
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