...
首页> 外文期刊>International journal of clinical pharmacology and therapeutics >Application of low-dose etomidate combined with oxycodone and midazolam in endoscopic injection sclerotherapy
【24h】

Application of low-dose etomidate combined with oxycodone and midazolam in endoscopic injection sclerotherapy

机译:低剂量依托咪酯联合羟考酮和咪达唑仑在内镜下注射硬化治疗中的应用

获取原文
获取原文并翻译 | 示例

摘要

Objective: To evaluate the ad-verse effects and particularly the anesthetic effect of low-dose etomidate combined with oxycodone and midazolam in endoscopic injection sclerotherapy. Materials and meth-ods: We herein report a prospective, double-blind, randomized controlled trial. It includ-ed patients with liver cirrhosis (age, 18 - 65 years; BMI, 18 - 25 kg/m2) who were treated with endoscopic injection sclerotherapy, and the patients were randomly assigned to the propofol group or the etomidate group. The incidence of respiratory depression was the primary outcome measure. The occurrence of various adverse effects and endoscopist satisfaction score were the secondary out-come measures. Results: In this study, we enrolled a total of 96 patients. The incidence of respiratory depression in the propofol group was 19, while that in the etomi-date group was only 4 (9/47 vs. 2/49; p = 0.026). Regarding the secondary outcome measures, the incidence of hypoxia in the propofol group was 15, while that in the etomidate group was only 2 (7/47 vs. 1/49; p = 0.029). Injection-site pain occurred in 0 and 23 of the patients in the etomidate group and propofol group, respectively (p < 0.001). Endoscopist satisfaction scores were classified as "poor", "fair", "good", and "very good". The scores were 17 higher (46/49 vs. 36/47; p = 0.026) for the "very good" lev-el and 15 lower (3/49 vs. 10/47; p = 0.038) for the "good" level in the etomidate group than in the propofol group. Conclusion: Low -dose etomidate combined with oxycodone and midazolam for endoscopic injection sclerotherapy could reduce the incidence of hypoxia without increasing the incidence of complications.
机译:目的:评价低剂量依托咪酯联合羟考酮和咪达唑仑在内镜下注射硬化治疗中的不良反应,特别是麻醉效果。材料和甲基:我们在此报告一项前瞻性、双盲、随机对照试验。它包括肝硬化患者(年龄,18 - 65 岁;BMI,18 - 25 kg/m2),接受内窥镜下注射硬化疗法治疗,患者随机分配至丙泊酚组或依托咪酯组。呼吸抑制的发生率是主要结局指标。各种不良反应的发生和内镜医师满意度评分是次要的出结果指标。结果:在这项研究中,我们共招募了 96 名患者。丙泊酚组呼吸抑制的发生率为19%,而依托伊组仅为4%(9/47 vs. 2/49;p = 0.026)。关于次要结局指标,丙泊酚组的缺氧发生率为15%,而依托咪酯组的缺氧发生率仅为2%(7/47 vs. 1/49;p = 0.029)。依托咪酯组和丙泊酚组分别有0%和23%的患者出现注射部位疼痛(p < 0.001)。内窥镜医师满意度得分分为“差”、“一般”、“好”和“非常好”。与丙泊酚组相比,“非常好”lev-el组的得分高出17%(46/49 vs. 36/47;p = 0.026),“良好”水平的得分比丙泊酚组低15%(3/49 vs. 10/47;p = 0.038)。结论:低剂量依托咪酯联合羟考酮、咪达唑仑进行内镜下注射硬化治疗,可降低缺氧发生率,且不增加并发症发生率。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号