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布托啡诺复合托烷司琼预防妇科腔镜术后不良反应的临床研究▲
Clinical analysis of butorphanol combined with tropisetron for preventing postoperative adverse reactions after laparoscopic gynecological surgery

微创医学 201505期 页码:589-592

作者机构:广西灵山县人民医院麻醉科,灵山县535400

基金信息:▲基金项目:广西医药卫生科研课题(编号:桂卫Z 2012487);作者简介:刘晓慧(1972~),女,学士,副主任医师,研究方向:临床麻醉。

DOI:DOI:10.11864/j.issn.1673.2015.05.08

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目的探讨布托啡诺复合托烷司琼预防妇科腹腔镜术后不良反应的效果及应用价值。方法采用随机双盲法将240例行腹腔镜手术患者分为3组,每组80例,全麻诱导后Ⅰ组静脉注射生理盐水2 mL,Ⅱ组注射盐酸托烷司琼5 mg,Ⅲ组注射酒石酸布托啡诺1 mg+盐酸托烷司琼5 mg,对比三组患者术后RSS、VAS、RS评分情况,记录其拔管时间、清醒时间、拔管期躁动、术后寒战、恶心呕吐等不良反应发生率。结果Ⅲ组呼吸恢复时间、睁眼时间、拔管时间明显短于Ⅱ组和Ⅰ组(P<0.05);Ⅲ组患者术后2 h、4 h、6 h、12 h不同时段RSS、VAS评分明显优于Ⅱ组和Ⅰ组(P<0.05);Ⅲ组患者术后PONV、寒战、拔管期躁动等不良反应发生率明显低于Ⅱ组和Ⅰ组(P<0.05),且程度较轻。结论布托啡诺复合托烷司琼能缩短术后患者清醒时间、拔管时间,降低术后PONV、寒战、拔管期躁动等不良反应发生率和严重程度,值得推广应用。
ObjectiveTo evaluate the effect of butorphanol combined with tropisetron for preventing postoperative adverse reactions after laparoscopic gynecological surgery. Methods240 cases undergoing laparoscopic gynecological surgery were randomly divided into three groups, 80 cases in each group. After induction of general anesthesia, group 1 as control group was given 2 ml of normal saline intravenously, group II was given 5 mg of tropisetron hydrochloride intravenously, group III was given 1mg of butorphanol tartrate 1mg plus 5mg of tropisetron hydrochloride. The RSS, VAS, RS scores, the time to extubation, the time to resuscitation, as well as the adverse reactions were recorded, including extubation-induced agitation, postoperative chills, nausea, vomiting and so on. ResultsThe time to respiratory recovery, resuscitation and extubation in group III were significantly shorter than those of group Ⅱ and group Ⅰ (P<0.05). In group Ⅲ, the RSS, VAS scores of 2h, 4h, 6h, 12h after operation were significantly better than those in group Ⅱ and group Ⅰ (P<0.05). In group Ⅲ, the rates of postoperative nausea and vomiting (PONV), chills and extubation-induced agitation were significantly lower than those of group Ⅰ and Ⅱ (P<0.05). ConclusionButorphanol combined with tropisetron may shorten the time to extubation and resuscitation, reduce the rates of extubation-induced agitation, PONV, and post-operative chills, worthy of clinical pomotion.
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