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静脉注射昂丹司琼治疗儿童术后已发生的呕吐。S3A - 381研究组。

Intravenous ondansetron in established postoperative emesis in children. S3A-381 Study Group.

作者信息

Khalil S, Rodarte A, Weldon B C, Weinstein M, Grunwald Z, Ginsberg B, Kaye R, Otto A, Wheeler M, Lawhorn C D, Prillaman B A, Creed M

机构信息

Department of Anesthesiology, University of Texas Houston Health Science Center 77030, USA.

出版信息

Anesthesiology. 1996 Aug;85(2):270-6. doi: 10.1097/00000542-199608000-00007.

Abstract

BACKGROUND

In pediatric postsurgical patients, postoperative vomiting is a common occurrence that can delay recovery and result in unplanned hospital admissions after outpatient surgery. This randomized, double-blind, placebo-controlled, multicenter study evaluated the efficacy and safety of ondansetron in the control of established postoperative emesis in outpatients aged 2-12 yr.

METHODS

Screened for the study were 2,720 ASA physical status 1-3 children undergoing outpatient surgery during general anesthesia, which included nitrous oxide. Children experiencing two emetic episodes within 2 h of discontinuation of nitrous oxide were given intravenous ondansetron (n = 192; 0.1 mg/kg for children weighing < or = 40 kg; 4 mg for children weighing > 40 kg) or placebo (n = 183).

RESULTS

The proportion of children with no emetic episodes and no use of rescue medication was significantly greater (P < 0.001) in the ondansetron group compared with placebo for both 2- and 24-h periods after study drug administration (78% of the ondansetron group and 34% of the placebo group for 2 h; 53% of the ondansetron group and 17% of the placebo group for 24 h). Among patients with at least one emetic episode or with rescue medication use, the median time to onset of emesis or rescue was 127 min in the ondansetron group compared with 58 min in the placebo group (P < 0.001). The median time from study drug administration until discharge was significantly shorter (P < 0.01) in the ondansetron group (153 min, range 44-593 min) compared with the placebo group (173 min, range 82-622 min). The incidence of potentially drug-related adverse events was similar in the ondansetron (3% of patients) and the placebo (4% of patients) groups.

CONCLUSION

A single dose of ondansetron (0.1 mg/kg up to 4 mg) is effective and well tolerated in the prevention of further episodes of postoperative emesis in children after outpatient surgery. Administration of ondansetron also may result in a shorter time to discharge.

摘要

背景

在儿科术后患者中,术后呕吐很常见,可能会延迟康复,并导致门诊手术后计划外的住院治疗。这项随机、双盲、安慰剂对照、多中心研究评估了昂丹司琼对2至12岁门诊患者术后既定呕吐的控制效果和安全性。

方法

筛选了2720例在全身麻醉(包括氧化亚氮)下接受门诊手术的美国麻醉医师协会(ASA)身体状况为1至3级的儿童。在停用氧化亚氮后2小时内出现两次呕吐发作的儿童,静脉注射昂丹司琼(n = 192;体重≤40 kg的儿童为0.1 mg/kg;体重>40 kg的儿童为4 mg)或安慰剂(n = 183)。

结果

在给药后2小时和24小时,昂丹司琼组无呕吐发作且未使用急救药物的儿童比例均显著高于安慰剂组(P < 0.001)(昂丹司琼组2小时为78%,安慰剂组为34%;昂丹司琼组24小时为53%,安慰剂组为17%)。在至少有一次呕吐发作或使用急救药物的患者中,昂丹司琼组呕吐或急救发作的中位时间为127分钟,而安慰剂组为58分钟(P < 0.001)。与安慰剂组(173分钟,范围82至622分钟)相比,昂丹司琼组从给药到出院的中位时间显著缩短(P < 0.01)(153分钟,范围44至593分钟)。昂丹司琼组(3%的患者)和安慰剂组(4%的患者)潜在药物相关不良事件的发生率相似。

结论

单剂量昂丹司琼(0.1 mg/kg,最大4 mg)在预防儿童门诊手术后进一步的术后呕吐发作方面有效且耐受性良好。使用昂丹司琼还可能缩短出院时间。

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