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帕洛诺司琼、格拉司琼和昂丹司琼作为预防中耳手术患者术后恶心和呕吐的止吐药的比较。

Comparison of palanosetron, granisetron and ondansetron as anti-emetics for prevention of postoperative nausea and vomiting in patients undergoing middle ear surgery.

作者信息

Basu Anjana, Saha Debdas, Hembrom Bani P, Roy Amit, Naaz Anjum

机构信息

Department of Anaesthesiology, RG Kar Medical College, Kolkata.

出版信息

J Indian Med Assoc. 2011 May;109(5):327-9.

PMID:22187767
Abstract

The objective of the study was to compare the efficacy of palanosetron (0.25 mg), granisetron (3.0 mg) and ondansetron (8.0 mg) used as anti-emetics for the prevention of postoperative nausea/vomiting in patients undergoing middle ear surgery. The study was done among 75 adult patients (age group 30-45 years) of which 50 were males and rest (25) females, all of ASA I and ASA II. The patients were randomly allocated into 3 equal groups: Group I (n = 25) received injection palanosetron (0.25 mg) IV, group II (n = 25) received injection granisetron (3 mg) IV and group III (n = 25) received injection ondansetron (8.0 mg) IV at the end of the surgical procedure. A standard general anaesthesia technique was employed. Emetic episodes and safety assessments were performed during two periods of 0-6 hours in the postanaesthesia care unit and 6-24 hours in the ward after anaesthesia. The incidence of emesis-free patients during the 0-6 hours period was 100% for group I; 72% for group II and 56% for group III. During the 6-24 hours period incidence of emesis-free patients were 96% for group I; 56% for group II and 32% for group III. So to conclude, a single dose of palanosetron (0.25 mg) is a superior anti-emetic to granisetron (3.0 mg) or ondansetron (8.0 mg) in complete prevention of postoperative nausea and vomiting after middle ear surgery during the first 24 hours period.

摘要

本研究的目的是比较帕洛诺司琼(0.25毫克)、格拉司琼(3.0毫克)和昂丹司琼(8.0毫克)作为止吐药预防中耳手术患者术后恶心/呕吐的疗效。该研究在75名成年患者(年龄30 - 45岁)中进行,其中50名男性,其余25名女性,均为ASA I级和ASA II级。患者被随机分为3组,每组25人:第一组(n = 25)在手术结束时静脉注射帕洛诺司琼(0.25毫克);第二组(n = 25)静脉注射格拉司琼(3毫克);第三组(n = 25)静脉注射昂丹司琼(8.0毫克)。采用标准的全身麻醉技术。在麻醉后护理单元的0 - 6小时和麻醉后病房的6 - 24小时两个时间段进行呕吐发作情况和安全性评估。在0 - 6小时期间,第一组无呕吐患者的发生率为100%;第二组为72%,第三组为56%。在6 - 24小时期间,第一组无呕吐患者的发生率为96%;第二组为56%,第三组为32%。因此可以得出结论,在完全预防中耳手术后24小时内的术后恶心和呕吐方面,单剂量的帕洛诺司琼(0.25毫克)作为止吐药优于格拉司琼(3.0毫克)或昂丹司琼(8.0毫克)。

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