Substance P (neurokinin-1) antagonist prevents postoperative vomiting after abdominal hysterectomy procedures

被引:55
作者
Gesztesi, Z
Scuderi, PE
White, PF
Wright, W
Wender, RH
D'Angelo, R
Black, S
Dalby, PL
MacLean, D
机构
[1] Univ Texas, SW Med Ctr, Dept Anesthesiol & Pain Management, Dallas, TX 75235 USA
[2] Wake Forest Univ, Bowman Gray Sch Med, Winston Salem, NC USA
[3] Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA
[4] Univ Pittsburgh, Med Ctr, Pittsburgh, PA USA
关键词
drug interactions; emesis; ondansetron;
D O I
10.1097/00000542-200010000-00009
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: The safety and antiemetic efficacy of CP-122, 721, a novel neurokinin-1 antagonist, was evaluated when administered alone or in combination with ondansetron. Methods: Using a randomized, double-blind, placebo-controlled study design, CP-122,721 was initially compared with placebo and subsequently to ondansetron alone and in combination for prophylaxis against postoperative nausea and vomiting in 243 women undergoing abdominal hysterectomy. In the dose-ranging studies (n = 86), patients received either CP-122,721 100 mg Cvs. placebo) or 200 mg (vs. placebo) orally 60-90 min before induction of anesthesia. In the interaction study (n = 157), patients received CP-122,721 200 mg or placebo 60-30 min before Induction of anesthesia, and ondansetron 4 mg or saline 2 ml intravenously 15-30 min before the end of surgery. Patients assessed their level of nausea and pain on arrival In the postanesthesia care unit and at 0.5-, 1-, 1.5-, 2-, 4-, 8-, 12-, and 24-h intervals postoperatively. Emetic episodes, need for rescue antiemetic-antinausea medication, postoperative complications, and patient satisfaction were recorded. Results: In the initial dose-ranging study, only 10% of the patients experienced emesis within the first 8 h after surgery with CP-122,721 200 mg compared with 50% in the placebo group. CP-122,721 200 mg also decreased the need for rescue medication (25% vs. 48%. CP-122,721 100 mg was less effective than 200 mg in decreasing the incidence of repeated episodes of emesis. In the interaction study, 6% of the patients receiving CP-122,721 200 mg orally experienced emesis less than 2 h after surgery compared with 17% with ondansetron alone. With combined therapy, only 2% experienced emesis. In addition, the median times for 75% of patients to remain free from postoperative nausea and vomiting were 82, 75, and 362 min in the ondansetron, CP-122,721, and combination groups, respectively. Conclusions: Oral CP-122,721 200 mg decreased emetic episodes compared with ondansetron (4 mg intravenously) during the first 24 h after gynecologic surgery; however, there was no difference in patient satisfaction.
引用
收藏
页码:931 / 937
页数:7
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