首页> 外文期刊>Western Journal of Emergency Medicine >Low-dose Ketamine Does Not Improve Migraine in the Emergency Department: A Randomized Placebo-controlled Trial
【24h】

Low-dose Ketamine Does Not Improve Migraine in the Emergency Department: A Randomized Placebo-controlled Trial

机译:低剂量氯胺酮不能改善急诊室的偏头痛:随机安慰剂对照试验

获取原文
获取外文期刊封面目录资料

摘要

Introduction: Patients frequently present to the emergency department (ED) with migraine headaches. Although low-dose ketamine demonstrates analgesic efficacy for acute pain complaints in the ED, headaches have historically been excluded from these trials. This study evaluates the efficacy and safety of low-dose ketamine for treatment of acute migraine in the ED.Methods: This randomized, double-blinded, placebo-controlled trial evaluated adults 18 to 65 years of age with acute migraine at a single academic ED. Subjects were randomized to receive 0.2 milligrams per kilogram of intravenous (IV) ketamine or an equivalent volume of normal saline. Numeric Rating Scale (NRS-11) pain scores, categorical pain scores, functional disability scores, side effects, and adverse events were assessed at baseline (T0) and 30 minutes post-treatment (T30). The primary outcome was between-group difference in NRS score reduction at 30 minutes. Results: We enrolled 34 subjects (ketamine=16, placebo=18). Demographics were similar between treatment groups. There was no statistically significant difference in NRS score reductions between ketamine and placebo-treated groups after 30 minutes. Median NRS score reductions at 30 minutes were 1.0 (interquartile range [IQR] 0 to 2.25) for the ketamine group and 2.0 (IQR 0 to 3.75) for the placebo group. Between-group median difference at 30 minutes was -1.0 (IQR -2 to 1, p=0.5035). No significant differences between treatment groups occurred in categorical pain scores, functional disability scores, rescue medication request rate, and treatment satisfaction. Side Effect Rating Scale for Dissociative Anesthetics scores in the ketamine group were significantly greater for generalized discomfort at 30 minutes (p=0.008) and fatigue at 60 minutes (p=0.0216). No serious adverse events occurred in this study. Conclusion: We found that 0.2mg/kg IV ketamine did not produce a greater reduction in NRS score compared to placebo for treatment of acute migraine in the ED. Generalized discomfort at 30 minutes was significantly greater in the ketamine group. Overall, ketamine was well tolerated by migraine-suffering subjects. To optimize low-dose ketamine as an acute migraine treatment, future studies should investigate more effective dosing and routes of administration.
机译:简介:偏头痛患者经常到急诊科就诊。尽管小剂量的氯胺酮在急诊室表现出对急性疼痛症状的镇痛作用,但历史上从这些试验中排除了头痛。这项研究评估了低剂量氯胺酮在急诊室治疗急性偏头痛的有效性和安全性。方法:这项随机,双盲,安慰剂对照试验评估了18到65岁的成人在一次学术急诊中患有急性偏头痛的情况。 。将受试者随机接受每公斤静脉内(IV)氯胺酮0.2毫克或等量的生理盐水。在基线(T0)和治疗后30分钟(T30)评估数字评分量表(NRS-11)的疼痛评分,分类疼痛评分,功能障碍评分,副作用和不良事件。主要结局是30分钟时NRS评分降低的组间差异。结果:我们招募了34名受试者(氯胺酮= 16,安慰剂= 18)。治疗组之间的人口统计学相似。 30分钟后,氯胺酮和安慰剂治疗组之间的NRS得分降低无统计学意义的差异。氯胺酮组在30分钟时的NRS得分中位数降低为1.0(四分位间距[IQR] 0至2.25),而安慰剂组为2.0(IQR 0至3.75)。 30分钟时组间中位数差异为-1.0(IQR -2至1,p = 0.5035)。治疗组之间在类别疼痛评分,功能障碍评分,急救药物需求率和治疗满意度方面无显着差异。氯胺酮组在30分钟时的全身不适(p = 0.008)和60分钟时的疲劳(p = 0.0216)时,氯胺酮组的麻醉药副作用评分等级显着更高。在这项研究中没有发生严重的不良事件。结论:我们发现,与安慰剂相比,0.2mg / kg静脉内氯胺酮与ED相比不会产生更大的NRS评分降低。氯胺酮组30分钟时的全身不适明显更大。总体而言,偏头痛患者对氯胺酮的耐受性良好。为了优化低剂量氯胺酮作为急性偏头痛的治疗方法,未来的研究应研究更有效的剂量和给药途径。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
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