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格拉司琼可预防剖宫产脊髓麻醉期间的恶心和呕吐。

Granisetron prevents nausea and vomiting during spinal anaesthesia for caesarean section.

作者信息

Fujii Y, Tanaka H, Toyooka H

机构信息

Department of Anaesthesiology, Toride Kyodo General Hospital, Ibaraki, Japan.

出版信息

Acta Anaesthesiol Scand. 1998 Mar;42(3):312-5. doi: 10.1111/j.1399-6576.1998.tb04922.x.

Abstract

BACKGROUND

Nausea and vomiting during spinal anaesthesia for caesarean section are common and unpleasant complications. This study was undertaken to evaluate the efficacy of granisetron, a selective 5-hydroxytryptamine type 3 receptor antagonist, for prophylactic treatment of nausea and vomiting in parturients undergoing nonemergent caesarean section under spinal anaesthesia.

METHODS

In a randomized, double-blind, placebo-controlled trial, 100 patients, 21-38 years, received either placebo (saline) or granisetron at 3 different doses (20 micrograms.kg-1, 40 micrograms.kg-1 or 80 micrograms.kg-1) (n = 25 for each) intravenously immediately after clamping of the foetal umbilical cord. Nausea, vomiting and safety assessments were performed during spinal anaesthesia for caesarean section.

RESULTS

The treatment groups were similar with regard to maternal characteristics and operative management. The incidence of nausea and vomiting was 64%, 52%, 14% and 12% after administration of placebo and granisetron in a dose of 20 micrograms.kg-1, 40 micrograms.kg-1 and 80 micrograms.kg-1, respectively (P < 0.05; overall Fisher's exact probability test). No clinically important adverse effects were observed in any group.

CONCLUSION

Prophylactic use of granisetron in a minimum dose of 40 micrograms.kg-1 is effective for preventing nausea and vomiting during spinal anaesthesia for caesarean section.

摘要

背景

剖宫产脊髓麻醉期间的恶心和呕吐是常见且令人不适的并发症。本研究旨在评估选择性5-羟色胺3型受体拮抗剂格拉司琼对接受非急诊剖宫产脊髓麻醉的产妇恶心和呕吐的预防性治疗效果。

方法

在一项随机、双盲、安慰剂对照试验中,100例年龄在21至38岁的患者在胎儿脐带钳夹后立即静脉注射安慰剂(生理盐水)或3种不同剂量(20微克·千克-1、40微克·千克-1或80微克·千克-1)的格拉司琼(每组25例)。在剖宫产脊髓麻醉期间进行恶心、呕吐及安全性评估。

结果

治疗组在产妇特征和手术管理方面相似。安慰剂组以及20微克·千克-1、40微克·千克-1和80微克·千克-1剂量格拉司琼组恶心和呕吐的发生率分别为64%、52%、14%和12%(P<0.05;总体Fisher精确概率检验)。任何组均未观察到具有临床意义的不良反应。

结论

预防性使用最低剂量为40微克·千克-1的格拉司琼可有效预防剖宫产脊髓麻醉期间的恶心和呕吐。

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