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首页> 外文期刊>European journal of anaesthesiology >Incidence of akathisia after postoperative nausea and vomiting prophylaxis with droperidol and ondansetron in outpatient surgery A multicentre controlled randomised trial
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Incidence of akathisia after postoperative nausea and vomiting prophylaxis with droperidol and ondansetron in outpatient surgery A multicentre controlled randomised trial

机译:术后恶心和呕吐预防后的akathisia发病率和滴羟乙酸和ondansetron在门诊手术中的多元控制随机试验

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摘要

BACKGROUND Akathisia, a distressing movement disorder induced by butyrophenones, has been described with low doses of droperidol used for postoperative nausea and vomiting (PONV) prophylaxis, but the incidence remains unclear. OBJECTIVES To determine the incidence of akathisia after PONV prophylaxis with two doses of droperidol in comparison with ondansetron, in patients undergoing ambulatory surgery. We hypothesised that the incidence of akathisia is higher with droperidol than that with ondansetron. DESIGN Randomised controlled double blind trial. SETTING Two University Hospital Centres and two private Clinics from January to September 2014. PATIENTS Patients (n=297) undergoing general anaesthesia for ambulatory surgery were randomly allocated to receive PONV prophylaxis with droperidol (0.625 or 1.25 mg) or ondansetron 4 mg; patients of the three groups also received 4 mg of dexamethasone. Exclusion criteria were contraindication to droperidol and ondansetron, use of psychotropic medications or benzodiazepines or history of psychotic illness. INTERVENTIONS Participants received droperidol (0.625 or 1.25 mg) or ondansetron 4 mg during general anaesthesia. After discharge from the postanaesthesia care unit presence and severity of akathisia were assessed using the Barnes Akathisia Rating Scale at 4 h postoperatively. MAIN OUTCOME MEASURES Score of the Global Clinical Assessment of Akathisia of Barnes Akathisia Rating Scale. RESULTS The number of akathisia observed was 1/118 (0.8%) in the ondansetron group, 1/84 (1.2%) in droperidol 0.625 mg group, and 3/87 (3.4%) in droperidol 1.25 mg group. The akathisia rate difference among the three groups was not significant (P = 0.52). We could not demonstrate significant differences in the incidence of akathisia between the two doses of droperidol. The only case of marked akathisia treated with benzodiazepines was observed after droperidol 1.25 mg. CONCLUSION The use of droperidol or ondansetron for PONV prophylaxis is associated to a low incidence of akathisia (0.8 to 3.4%) after general anaesthesia for ambulatory surgery. TRIAL REGISTRATION Clinicaltrials.gov: NCT01942343.
机译:背景技术Akathisia是由乳烯酮引起的令人痛苦的运动障碍,已经用低剂量的滴注醇用于术后恶心和呕吐(PONV)预防,但发病率仍不清楚。患有两剂滴管术后的PONV预防后,与ondansetron相比,目的是在接受动态手术的患者中确定痘痘预防后的痘苗预防。我们假设akathisia的发病率比与ondansetron的滴鼻醇更高。设计随机受控双盲试验。从2014年1月至9月举办两所大学医院中心和两所私人诊所。随机分配了经历过全身麻醉的患者(n = 297),以接受滴水醇(0.625或1.25mg)或ondansetron 4mg的PONV预防;三组患者也接受了4毫克地塞米松。排除标准是对蜕膜和ondansetron的禁忌症,使用精神药物或苯二氮卓或精神病疾病的历史。干预措施参与者在全身麻醉期间获得滴注醇(0.625或1.25mg)或ondansetron 4毫克。在术后4小时的4小时内使用Barnes akathisia评级规模评估akathisia的病例和严重程度后。主要观察结果评分Barnes Akathisia评级规模的Akathisia全球临床评估。结果观察到的Akathisia的数量为甲硅酮组1/118(0.8%),在蜕膜0.625mg组中的1/84(1.2%),滴落醇1.25mg组3/87(3.4%)。三组的akathisia率差异不显着(p = 0.52)。我们无法展示两种剂量滴水醇之间akathisia的发生率显着差异。在蜕膜1.25mg后观察到用苯并二氮杂噻嗪治疗的标记Akathisia的唯一情况。结论Droperidol或Ondansetron用于PONV预防,与动态手术一般麻醉后的akathisia(0.8〜3.4%)的低发生率有关。试验登记ClinicalTrials.gov:NCT01942343。

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    Strasbourg Univ Hosp Hautepierre CCOM Dept Anaesthesiol &

    Intens Care Strasbourg France;

    Clin Rhena Dept Anaesthesiol Strasbourg France;

    Strasbourg Univ Hosp Hautepierre CCOM Dept Anaesthesiol &

    Intens Care Strasbourg France;

    Strasbourg Univ Hosp Hautepierre CCOM Dept Anaesthesiol &

    Intens Care Strasbourg France;

    Clin Rhena Dept Anaesthesiol Strasbourg France;

    Univ Texas Southwestern Med Sch Dept Anaesthesiol &

    Pain Management Dallas TX USA;

    Strasbourg Univ Hosp Publ Hlth Serv GMRC Strasbourg France;

    Strasbourg Univ Hosp Hautepierre CCOM Dept Anaesthesiol &

    Intens Care Strasbourg France;

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  • 正文语种 eng
  • 中图分类 麻醉学;
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