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帕洛诺司琼预防术后恶心和呕吐的疗效:一项随机、双盲、安慰剂对照试验。

Efficacy of palonosetron for the prevention of postoperative nausea and vomiting: a randomized, double-blinded, placebo-controlled trial.

作者信息

Chun H R, Jeon I S, Park S Y, Lee S J, Kang S H, Kim S I

机构信息

Department of Anesthesiology and Pain Medicine, Soonchunhyang University Hospital Seoul, 657, Hannam-dong, Yongsan-gu, Seoul, Republic of Korea.

出版信息

Br J Anaesth. 2014 Mar;112(3):485-90. doi: 10.1093/bja/aet340. Epub 2013 Oct 22.

DOI:10.1093/bja/aet340
PMID:24154700
Abstract

BACKGROUND

The aim of this study was to evaluate the efficacy of palonosetron, the latest 5-HT3 receptor antagonist, for the prevention of postoperative nausea and vomiting (PONV) during the first 72 h after operation.

METHODS

In this randomized, double-blinded, placebo-controlled study, 204 healthy inpatients who were undergoing elective surgery with general anaesthesia were enrolled. Patients were divided into two groups: the palonosetron group (palonosetron 0.075 mg i.v.; n=102) and the placebo group (normal saline i.v.; n=102). The treatments were given after the induction of anaesthesia. The incidence of nausea, vomiting, severity of nausea, and the use of rescue anti-emetics during the first 72 h after surgery were evaluated.

RESULTS

The incidence of PONV was lower in the palonosetron group compared with the placebo group during the 0-24 h (33% vs 47%) and 0-72 h period (33% vs 52%) (P<0.05), but not during the 24-72 h postoperative period (6% vs 11%). The incidence of nausea was also significantly lower in the palonosetron group than in the placebo group during the 0-24 and 0-72 h period (P<0.05), but not during the 24-72 h postoperative period. However, there were no significant differences in the incidence of vomiting, and the use of rescue anti-emetics between the groups.

CONCLUSIONS

Palonosetron 0.075 mg i.v. effectively reduced the incidence of PONV during the first 72 h after operation, with most of the reduction occurring in the first 24 h.

摘要

背景

本研究旨在评估最新的5-羟色胺3(5-HT3)受体拮抗剂帕洛诺司琼预防术后72小时内恶心和呕吐(PONV)的疗效。

方法

在这项随机、双盲、安慰剂对照研究中,纳入了204例接受全身麻醉择期手术的健康住院患者。患者分为两组:帕洛诺司琼组(静脉注射帕洛诺司琼0.075mg;n = 102)和安慰剂组(静脉注射生理盐水;n = 102)。麻醉诱导后给予治疗。评估术后72小时内恶心、呕吐的发生率、恶心的严重程度以及补救性止吐药的使用情况。

结果

帕洛诺司琼组在术后0 - 24小时(33% 对 47%)和0 - 72小时(33% 对 52%)期间的PONV发生率低于安慰剂组(P<0.05),但在术后24 - 72小时期间无差异(6% 对 11%)。帕洛诺司琼组在术后0 - 24小时和0 - 72小时期间的恶心发生率也显著低于安慰剂组(P<0.05),但在术后24 - 72小时期间无差异。然而,两组之间呕吐发生率和补救性止吐药的使用情况无显著差异。

结论

静脉注射0.075mg帕洛诺司琼可有效降低术后72小时内PONV的发生率,大部分降低发生在术后24小时内。

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