胺与埃托米达酸对快速序列输入管道对最大序列器官衰竭评估得分的影响:一项随机临床试验
Sarah K S Knack1, Matthew E Prekker2, Johanna C Moore1
1Department of Emergency Medicine, Hennepin County Medical Center, Minneapolis, Minnesota.
The Journal of emergency medicine
|September 23, 2023
概括
胺和埃托米达,通常用于急症监护中的快速序列输管 (RSI),在器官衰竭得分或低血压方面没有显著差异. 这项随机试验为重症患者的诱导剂选择提供了关键的见解.
科学领域:
- 关键护理医学 关键护理医学
- 紧急医疗 紧急医疗
- 药理学 药理学是指药理学的学科.
背景情况:
- 快速序列输管 (RSI) 诱导剂,埃托米达和胺,与重症患者的低血压有关.
- 诱导剂的选择可能会影响患者的治疗结果.
研究的目的:
- 为了比较胺与埃托米达的作用,作为RSI的单次诱导剂量.
- 为了评估对最大顺序性器官衰竭评估 (SOFA) 评分和低血压的发生率的影响.
主要方法:
- 一个单中心,随机,并行组试验,涉及急诊部的危急病患成年患者.
- 患者接受了基胺或埃托米达特用于RSI,根据知情同意的例外.
- 主要结局是住院后3天内最大的SOFA分数.
主要成果:
- 在基他胺 (中位数6.5) 和埃托米达 (中位数7) 组之间的最大SOFA得分没有显著差异 (p=0.79).
- 输管后低血压的发生率相似:基他胺为28%,埃托米达为26%.
- 三十天死亡率在统计学上没有差异 (11%的胺基因与21%的埃托米达).
结论:
- 胺和埃托米达在经历RSI的重症患者的最大SOFA得分和低血压发病率方面表现出可比的疗效.
- 在这组患者中,没有任何一种药物在预防低血压或改善器官衰竭得分方面表现出明显的优势.
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