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昂丹司琼在全凭静脉麻醉下腹腔镜胆囊切除术中的预防性止吐效果。与氟哌利多、甲氧氯普胺和安慰剂的随机双盲对照研究。

Prophylactic anti-emetic efficacy of ondansetron in laparoscopic cholecystectomy under total intravenous anaesthesia. A randomised, double-blind comparison with droperidol, metoclopramide and placebo.

作者信息

Helmy S A

机构信息

Department of Anaesthesia, Faculty of Medicine, Cairo University, Egypt.

出版信息

Anaesthesia. 1999 Mar;54(3):266-71. doi: 10.1046/j.1365-2044.1999.00335.x.

Abstract

The prophylactic anti-emetic efficacy and safety of pre-operative intravenous ondansetron was evaluated in a randomised, double-blind, comparison with droperidol, metoclopramide and placebo in 160 ASA grade 1 and 2 patients undergoing laparoscopic cholecystectomy under total intravenous anaesthesia. The patients were randomly allocated to receive ondansetron (4 mg), droperidol (1.25 mg), metoclopramide (10 mg) or placebo given as a single intravenous dose immediately before induction of a standardised general anaesthetic. There were no significant differences between the four study groups with regard to the demographic and anaesthetic data, postoperative analgesia, postoperative sedation scores, duration of postoperative hospital stay and incidence of adverse events. The incidence of nausea and vomiting was significantly lower (p < 0.05) between 1 h and 4 h after surgery in the ondansetron group compared with the droperidol, metoclopramide and placebo groups. The incidence of nausea was similar in the four groups in the other study periods: 0-1 h and 4-24 h. The incidence of vomiting was lower in the ondansetron, droperidol and metoclopramide groups than in the placebo group between 1 and 4 h but was the same between 4 and 24 h. As a result of the lower incidence of nausea and vomiting between 1 h and 4 h in the ondansetron group, the overall incidence of nausea and vomiting was lower during the first 24 h after surgery in this group than in the other three groups.

摘要

在160例接受全静脉麻醉下行腹腔镜胆囊切除术的ASA 1级和2级患者中,进行了一项随机、双盲研究,比较术前静脉注射昂丹司琼与氟哌利多、甲氧氯普胺及安慰剂的预防呕吐疗效和安全性。患者被随机分配接受昂丹司琼(4mg)、氟哌利多(1.25mg)、甲氧氯普胺(10mg)或安慰剂,在诱导标准化全身麻醉前立即静脉单次给药。四个研究组在人口统计学和麻醉数据、术后镇痛、术后镇静评分、术后住院时间及不良事件发生率方面无显著差异。与氟哌利多、甲氧氯普胺及安慰剂组相比,昂丹司琼组术后1小时至4小时恶心呕吐发生率显著降低(p<0.05)。在其他研究时间段(0 - 1小时和4 - 24小时),四组恶心发生率相似。在1至4小时期间,昂丹司琼、氟哌利多和甲氧氯普胺组呕吐发生率低于安慰剂组,但在4至24小时期间相同。由于昂丹司琼组在1小时至4小时恶心呕吐发生率较低,该组术后24小时内恶心呕吐总发生率低于其他三组。

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