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比较0.01mg/kg和0.005mg/kg氟哌利多作为门诊腹腔镜手术术前用药预防恶心和呕吐的效果。

Comparison of droperidol 0.01 mg/kg and 0.005 mg/kg as a premedication in the prevention of nausea and vomiting in the outpatient for laparoscopy.

作者信息

Tripple G E, Holland M S, Hassanein K

出版信息

AANA J. 1989 Oct;57(5):413-6.

PMID:2532444
Abstract

Patients undergoing outpatient laparoscopy and general anesthesia have a high incidence of postoperative nausea and vomiting. It is essential that anesthesia techniques accommodate the special needs of these outpatients. Droperidol is an effective antiemetic but larger doses above 1-1.25 mg may cause unwanted side effects which may prolong recovery and discharge. The current trend is to decrease the dose of droperidol to prevent side effects while still retaining the antiemetic properties. This experimental study compares droperidol 0.010 mg/kg and 0.005 mg/kg as a premedication for the prevention of nausea and vomiting in 32 female outpatients undergoing laparoscopy and general anesthesia. The patients were randomized into two groups. Group I received droperidol 0.010 mg/kg and Group II received 0.005 mg/kg as a preoperative antiemetic in double-blind fashion. Both groups received the same anesthetic for induction and maintenance of anesthesia. The patients were observed in the postanesthesia room for the incidence of nausea and vomiting. They were transported to the outpatient department and were also observed for nausea and vomiting. The t-test was used to show that there were no significant differences between groups in population characteristics. Chi-square analysis was used to determine statistical significance in the incidence of nausea or vomiting between the two groups. Analysis showed there was no statistically significant difference in the incidence of nausea or vomiting in the postanesthesia room or the outpatient department, although there was a significant clinical difference between the groups especially in the incidence of nausea in the outpatient department.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

接受门诊腹腔镜检查及全身麻醉的患者术后恶心呕吐发生率很高。麻醉技术必须适应这些门诊患者的特殊需求。氟哌利多是一种有效的止吐药,但剂量超过1 - 1.25毫克可能会引起不良副作用,这可能会延长恢复和出院时间。目前的趋势是降低氟哌利多剂量以预防副作用,同时仍保留其止吐特性。本实验研究比较了0.010毫克/千克和0.005毫克/千克氟哌利多作为术前用药对32例接受腹腔镜检查及全身麻醉的女性门诊患者预防恶心呕吐的效果。患者被随机分为两组。第一组接受0.010毫克/千克氟哌利多,第二组接受0.005毫克/千克氟哌利多作为术前止吐药,采用双盲方式。两组在诱导和维持麻醉时使用相同的麻醉剂。在麻醉后恢复室观察患者恶心呕吐的发生率。将他们转运至门诊并观察恶心呕吐情况。采用t检验显示两组在人口统计学特征上无显著差异。采用卡方分析确定两组恶心或呕吐发生率的统计学显著性。分析表明,在麻醉后恢复室或门诊,恶心或呕吐发生率无统计学显著差异,尽管两组之间存在显著的临床差异,尤其是在门诊恶心发生率方面。(摘要截选至250字)

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