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格拉司琼、氟哌利多和胃复安用于治疗接受妇科手术的女性术后已出现的恶心和呕吐。

Granisetron, droperidol, and metoclopramide for the treatment of established postoperative nausea and vomiting in women undergoing gynecologic surgery.

作者信息

Fujii Y, Tanaka H, Somekawa Y

机构信息

Department of Anesthesiology, University of Tsukuba Institute of Clinical Medicine, Ibaraki, Japan.

出版信息

Am J Obstet Gynecol. 2000 Jan;182(1 Pt 1):13-6. doi: 10.1016/s0002-9378(00)70484-4.

Abstract

OBJECTIVE

The aim of this study was to evaluate granisetron, droperidol, and metoclopramide for efficacy and safety in the treatment of established postoperative nausea and vomiting after major gynecologic surgery.

STUDY DESIGN

One hundred twenty postoperative female patients were monitored for the first 3 hours after anesthesia in the postanesthesia care unit and for the next 24 hours after anesthesia in the ward. Patients who had postoperative nausea and vomiting within the first 3 hours after anesthesia received intravenously, in a randomized double-blind manner, 40 microg/kg granisetron, 20 microg/kg droperidol, or 0.2 mg/kg metoclopramide. Patients were then observed for 24 hours after drug administration.

RESULTS

Complete control of established postoperative nausea and vomiting, defined as no emesis and no need for another rescue antiemetic medication, was more frequent among the patients who had received granisetron (88%) than among those who had received droperidol (55%) or metoclopramide (50%) (P <.05). The severity of nausea was less in patients who had received granisetron than in those who had received droperidol or metoclopramide (P <.05). No clinically adverse events were observed in any of the groups.

CONCLUSION

Granisetron is more effective than droperidol or metoclopramide for the treatment of established postoperative nausea and vomiting during the first 3 hours after anesthesia in patients undergoing major gynecologic operations.

摘要

目的

本研究旨在评估格拉司琼、氟哌利多和甲氧氯普胺治疗妇科大手术后已发生的术后恶心呕吐的疗效和安全性。

研究设计

120名术后女性患者在麻醉后护理单元麻醉后最初3小时以及随后在病房麻醉后接下来24小时接受监测。在麻醉后最初3小时内发生术后恶心呕吐的患者,以随机双盲方式静脉注射40微克/千克格拉司琼、20微克/千克氟哌利多或0.2毫克/千克甲氧氯普胺。给药后对患者观察24小时。

结果

已发生的术后恶心呕吐得到完全控制(定义为无呕吐且无需另用抢救性止吐药物)的情况在接受格拉司琼的患者中(88%)比接受氟哌利多(55%)或甲氧氯普胺(50%)的患者中更常见(P<.05)。接受格拉司琼的患者恶心严重程度低于接受氟哌利多或甲氧氯普胺者(P<.05)。所有组均未观察到临床不良事件。

结论

对于接受妇科大手术的患者,在麻醉后最初3小时内,格拉司琼治疗已发生的术后恶心呕吐比氟哌利多或甲氧氯普胺更有效。

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