创伤性氯胺酮能减轻创伤后应激障碍的症状吗?

Spartan medical research journal Pub Date : 2020-10-30
Jack Brodeur, Ryley Mancine, Alyse Ley, Jed Magen
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摘要

简介急性应激障碍(ASD)和创伤后应激障碍(PTSD)是一种慢性疾病,可影响严重创伤后的患者。由于这些患者通常会首先到急诊科就诊,因此急诊科医生必须随时了解氯胺酮或其他麻醉剂的最新使用情况,这些麻醉剂可能会阻碍病情发展或减轻可能会损害正常功能的症状。本临床综述旨在回顾有关使用创伤周氯胺酮如何降低自闭症和创伤后应激障碍发病率的文献。2019年,作者完成了MEDLINE检索,共检索到25篇文章,第一作者和第二作者对这些文章进行了初步评估。本稿件讨论了符合纳入标准的四篇文章:尽管早先有两个研究小组发现,创伤周围使用氯胺酮会导致创伤后应激障碍症状(如再经历、分离、回避和过度虑惊)的增加,但后来的两项研究表明,氯胺酮对创伤后应激障碍的发展没有影响。此外,2012年的一个研究小组认为,使用异丙酚可减轻创伤后6个月的创伤后应激障碍症状。另一个2017年的研究小组发现,手术次数与创伤后应激障碍的发展直接相关:根据迄今为止的文献,创伤周围氯胺酮似乎不会影响ASD和随后的创伤后应激障碍的预防或发展。需要进行更多的研究,以明确氯胺酮在治疗急性创伤反应时的精神药理作用。根据后面两项研究的结果,未来的研究应考虑异丙酚是否会导致创伤后应激障碍的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Does Peritraumatic Ketamine Reduce Symptoms of Post-Traumatic Stress Disorder?

Introduction: Acute stress disorder (ASD) and post-traumatic stress disorder (PTSD) are chronic diseases which can affect patients following a severe trauma. As these patients typically first present to the emergency department, it is critical for emergency physicians to remain updated on the use of ketamine or other anesthetic agents which may impede development or reduce symptoms which may impair normal functioning. The purpose of this clinical review was is to review the literature regarding how the use of peritraumatic ketamine could decrease the incidence of ASD and PTSD. In 2019, the authors completed a MEDLINE search was performed yielding 25 articles which were initially evaluated by the first and second authors. Four articles which met inclusion criteria are discussed in this manuscript.

Summary of evidence: Although two earlier research groups have found that peritraumatic ketamine administration contributed to increased symptoms of PTSD (e g., reexperiencing, dissociation, avoidance, and hyperarousal), two later studies have indicated that ketamine had no effect on PTSD development. Additionally, one 2012 study group has suggested propofol use may alleviate PTSD symptoms at six months post-trauma. Another 2017 study team found that the number of surgical procedures was directly correlated with increased PTSD development.

Conclusions: Based on the literature to date, peritraumatic ketamine does not appear to influence the prevention nor development of ASD and subsequent PTSD. More research is needed to clarify the psychopharmacologic effects of ketamine when used in the management of reactions to acute trauma experiences. Based on the results of the two later works, future research is indicated considering whether propofol may contribute to PTSD development.

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