重复使用氯胺酮治疗慢性创伤后应激障碍的随机对照试验。

Focus (American Psychiatric Publishing) Pub Date : 2023-07-01 Epub Date: 2023-06-28 DOI:10.1176/appi.focus.23021014
Adriana Feder, Sara Costi, Sarah B Rutter, Abigail B Collins, Usha Govindarajulu, Manish K Jha, Sarah R Horn, Marin Kautz, Morgan Corniquel, Katherine A Collins, Laura Bevilacqua, Andrew M Glasgow, Jess Brallier, Robert H Pietrzak, James W Murrough, Dennis S Charney
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引用次数: 0

摘要

目的:创伤后应激障碍(PTSD)是一种慢性致残性疾病:创伤后应激障碍(PTSD)是一种慢性致残性疾病,现有的药物疗法对其疗效有限。作者之前对创伤后应激障碍患者进行了单剂量氯胺酮静脉注射的概念验证随机对照试验,结果显示,氯胺酮静脉注射后 24 小时,创伤后应激障碍症状就会明显、快速减轻。本研究是第一项随机对照试验,旨在测试重复静脉注射氯胺酮治疗慢性创伤后应激障碍的有效性和安全性:方法:慢性创伤后应激障碍患者(30 人)被随机分配(1:1),在连续两周内接受六次氯胺酮(0.5 毫克/千克)或咪达唑仑(0.045 毫克/千克)(精神活性安慰剂对照)输注。在首次输注后 24 小时和每周回访时进行临床医生评分和自我报告评估。主要结果指标是创伤后应激障碍症状严重程度的变化,采用 DSM-5 临床医师管理创伤后应激障碍量表 (CAPS-5) 进行评估,从基线到 2 周(完成所有输液后)的变化情况。次要结果测量包括事件影响量表-修订版、蒙哥马利-阿斯伯格抑郁评定量表(MADRS)和副作用测量:从基线到第2周,氯胺酮组的CAPS-5和MADRS总分的改善幅度明显高于咪达唑仑组。第2周时,氯胺酮组的CAPS-5总分平均值比咪达唑仑组低11.88分(SE=3.96)(d=1.13,95% CI=0.36,1.91)。氯胺酮组有67%的参与者对治疗有反应,而咪达唑仑组只有20%。在氯胺酮应答者中,输注 2 周疗程后失去应答的中位时间为 27.5 天。氯胺酮输注总体上耐受性良好,未出现严重不良反应:这项随机对照试验首次证明了重复输注氯胺酮对减轻慢性创伤后应激障碍患者症状严重程度的疗效。为充分了解氯胺酮治疗慢性创伤后应激障碍的潜力,有必要开展进一步的研究。版权所有 © 2021。
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A Randomized Controlled Trial of Repeated Ketamine Administration for Chronic Posttraumatic Stress Disorder.

Objective: Posttraumatic stress disorder (PTSD) is a chronic and disabling disorder, for which available pharmacotherapies have limited efficacy. The authors' previous proof-of-concept randomized controlled trial of single-dose intravenous ketamine infusion in individuals with PTSD showed significant and rapid PTSD symptom reduction 24 hours postinfusion. The present study is the first randomized controlled trial to test the efficacy and safety of repeated intravenous ketamine infusions for the treatment of chronic PTSD.

Methods: Individuals with chronic PTSD (N=30) were randomly assigned (1:1) to receive six infusions of ketamine (0.5 mg/kg) or midazolam (0.045 mg/kg) (psychoactive placebo control) over 2 consecutive weeks. Clinician-rated and self-report assessments were administered 24 hours after the first infusion and at weekly visits. The primary outcome measure was change in PTSD symptom severity, as assessed with the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5), from baseline to 2 weeks (after completion of all infusions). Secondary outcome measures included the Impact of Event Scale-Revised, the Montgomery-Åsberg Depression Rating Scale (MADRS), and side effect measures.

Results: The ketamine group showed a significantly greater improvement in CAPS-5 and MADRS total scores than the midazolam group from baseline to week 2. At week 2, the mean CAPS-5 total score was 11.88 points (SE=3.96) lower in the ketamine group than in the midazolam group (d=1.13, 95% CI=0.36, 1.91). Sixty-seven percent of participants in the ketamine group were treatment responders, compared with 20% in the midazolam group. Among ketamine responders, the median time to loss of response was 27.5 days following the 2-week course of infusions. Ketamine infusions were well tolerated overall, without serious adverse events.

Conclusions: This randomized controlled trial provides the first evidence of efficacy of repeated ketamine infusions in reducing symptom severity in individuals with chronic PTSD. Further studies are warranted to understand ketamine's full potential as a treatment for chronic PTSD.Reprinted from Am J Psychiatry 2021; 178:193-202, with permission from American Psychiatric Association Publishing. Copyright © 2021.

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