Department of Psychiatry, Depression and Anxiety Center for Discovery and Treatment, Icahn School of Medicine at Mount Sinai, New York (Feder, Costi, Rutter, A.B. Collins, Jha, Horn, Kautz, Corniquel, K.A. Collins, Bevilacqua, Murrough, Charney); Department of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York (Govindarajulu); Nathan Kline Institute for Psychiatric Research, Orangeburg, N.Y. (K.A. Collins); Department of Anesthesiology, Perioperative and Pain Medicine, Icahn School of Medicine at Mount Sinai, New York (Glasgow, Brallier); Department of Psychiatry, Yale University School of Medicine, New Haven, Conn. (Pietrzak); Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York (Murrough, Charney); and Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, New York (Charney).
Drs. Murrough and Charney share senior authorship.
Am J Psychiatry. 2021 Feb 1;178(2):193-202. doi: 10.1176/appi.ajp.2020.20050596. Epub 2021 Jan 5.
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.
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.
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.
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.
创伤后应激障碍(PTSD)是一种慢性且使人丧失能力的障碍,现有药物治疗的疗效有限。作者之前进行的一项单剂量静脉注射氯胺酮治疗 PTSD 患者的概念验证随机对照试验显示,在注射后 24 小时内 PTSD 症状显著且快速减轻。本研究是第一项测试重复静脉注射氯胺酮治疗慢性 PTSD 的疗效和安全性的随机对照试验。
慢性 PTSD 患者(N=30)随机(1:1)分配接受 6 次氯胺酮(0.5mg/kg)或咪达唑仑(0.045mg/kg)(有活性的安慰剂对照)输注,连续 2 周。在第一次输注后 24 小时和每周就诊时进行临床医生评定和自我报告评估。主要结局测量指标是使用 DSM-5 临床医生管理 PTSD 量表(CAPS-5)评估从基线到 2 周(所有输注完成后)时 PTSD 症状严重程度的变化。次要结局测量指标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)和副作用测量指标。
与咪达唑仑组相比,氯胺酮组从基线到第 2 周时 CAPS-5 和 MADRS 总分的改善明显更大。在第 2 周时,氯胺酮组的 CAPS-5 总分比咪达唑仑组低 11.88 分(SE=3.96)(d=1.13,95%CI=0.36,1.91)。氯胺酮组有 67%的参与者为治疗应答者,而咪达唑仑组仅有 20%。在氯胺酮应答者中,从 2 周疗程输注结束后,中位数无应答时间为 27.5 天。氯胺酮输注总体耐受良好,无严重不良事件。
这项随机对照试验提供了重复氯胺酮输注在降低慢性 PTSD 患者症状严重程度方面的有效性的首个证据。需要进一步的研究来了解氯胺酮作为慢性 PTSD 治疗方法的全部潜力。