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首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >Preoperative pregabalin does not reduce propofol ED50: A randomized controlled trial
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Preoperative pregabalin does not reduce propofol ED50: A randomized controlled trial

机译:术前普瑞巴林不会降低丙泊酚ED50:一项随机对照试验

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摘要

Background: In many studies, gabapentinoids, such as pregabalin, have been shown to reduce preoperative anxiety. This anxiolysis is often accompanied by sedation, one of the most frequent side effects of pregabalin. We hypothesized that pregabalin taken preoperatively could reduce propofol requirements for induction of general anesthesia. Methods: A randomized double-blind placebo-controlled trial was conducted after approval by the local ethics committee. Fifty women aged 18-40 yr, American Anesthesiologists Society physical status I and II, and scheduled to undergo elective laparoscopic gynecologic procedures were enrolled after written consent. Treatment group patients were given pregabalin 150 mg po one hour before surgery while patients in the control group received a placebo. The primary outcome was the propofol dose required to achieve a targeted anesthetic depth in 50% of the population, i.e., effective dose (ED)50. The ED50 was estimated using Dixon's up-And-down methodology. The targeted anesthetic depth was defined based on predetermined entropy monitoring values (State Entropy [SE] 50 and Response Entropy [RE]-SE 10). As a secondary outcome, we tested if pregabalin reduced pre-induction anxiety levels which were measured on a 0-100 scale. Results: The propofol ED50 was not statistically different between the pregabalin group (mean 1.33 mg·kg-1; 95% confidence interval [CI] 1.23 to 1.43) vs the placebo group (mean 1.37 mg·kg-1; 95% CI 1.28 to 1.46); P = 0.19. Also, pre-induction anxiety level was not different between groups (median 31; interquartile range [IQR] [10-52] vs median 42; IQR [4-71], respectively; P = 0.41). Conclusions: Preoperative pregabalin does not reduce propofol requirements in a population of healthy young women undergoing laparoscopic gynecologic procedures. This study failed to show a pre-induction anxiolytic effect of pregabalin in such a population. This trial was registered at www.clinicaltrials.gov (NCT01158859).
机译:背景:在许多研究中,加巴喷丁类药物(如普瑞巴林)已显示可减轻术前焦虑。这种抗焦虑通常伴随镇静作用,这是普瑞巴林最常见的副作用之一。我们假设术前服用普瑞巴林可以降低异丙酚诱导全身麻醉的需要。方法:经当地伦理委员会批准后,进行了一项随机双盲安慰剂对照试验。书面同意后,入选了美国麻醉医师协会I级和II级身体状况,并计划接受选择性腹腔镜妇科手术的50名18-40岁妇女。治疗组患者在手术前一小时口服普瑞巴林150 mg,对照组则接受安慰剂。主要结局是在50%的人群中达到目标麻醉深度所需的异丙酚剂量,即有效剂量(ED)50。 ED50是使用Dixon的上下方法估算的。根据预定的熵监测值(状态熵[SE] <50和响应熵[RE] -SE <10)定义目标麻醉深度。作为次要结果,我们测试了普瑞巴林是否降低了诱导前的焦虑水平(以0-100的评分衡量)。结果:普瑞巴林组(平均1.33 mg·kg-1; 95%置信区间[CI] 1.23至1.43)与安慰剂组(平均1.37 mg·kg-1; 95%CI 1.28)之间的丙泊酚ED50差异无统计学意义至1.46); P = 0.19。此外,各组的诱导前焦虑水平无差异(中位数31;四分位间距[IQR] [10-52]与中位数42; IQR [4-71]; P = 0.41)。结论:术前普瑞巴林不能降低接受腹腔镜妇科手术的健康年轻女性的丙泊酚需求。该研究未能显示普瑞巴林在此类人群中的诱导前抗焦虑作用。该试验已在www.clinicaltrials.gov(NCT01158859)上注册。

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