Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, New York.
Department of Health Evidence and Policy, Icahn School of Medicine at Mount Sinai, New York, New York.
JAMA Psychiatry. 2014 Jun;71(6):681-8. doi: 10.1001/jamapsychiatry.2014.62.
Few pharmacotherapies have demonstrated sufficient efficacy in the treatment of posttraumatic stress disorder (PTSD), a chronic and disabling condition.
To test the efficacy and safety of a single intravenous subanesthetic dose of ketamine for the treatment of PTSD and associated depressive symptoms in patients with chronic PTSD.
DESIGN, SETTING, AND PARTICIPANTS: Proof-of-concept, randomized, double-blind, crossover trial comparing ketamine with an active placebo control, midazolam, conducted at a single site (Icahn School of Medicine at Mount Sinai, New York, New York). Forty-one patients with chronic PTSD related to a range of trauma exposures were recruited via advertisements.
Intravenous infusion of ketamine hydrochloride (0.5 mg/kg) and midazolam (0.045 mg/kg).
The primary outcome measure was change in PTSD symptom severity, measured using the Impact of Event Scale-Revised. Secondary outcome measures included the Montgomery-Asberg Depression Rating Scale, the Clinical Global Impression-Severity and -Improvement scales, and adverse effect measures, including the Clinician-Administered Dissociative States Scale, the Brief Psychiatric Rating Scale, and the Young Mania Rating Scale.
Ketamine infusion was associated with significant and rapid reduction in PTSD symptom severity, compared with midazolam, when assessed 24 hours after infusion (mean difference in Impact of Event Scale-Revised score, 12.7 [95% CI, 2.5-22.8]; P = .02). Greater reduction of PTSD symptoms following treatment with ketamine was evident in both crossover and first-period analyses, and remained significant after adjusting for baseline and 24-hour depressive symptom severity. Ketamine was also associated with reduction in comorbid depressive symptoms and with improvement in overall clinical presentation. Ketamine was generally well tolerated without clinically significant persistent dissociative symptoms.
This study provides the first evidence for rapid reduction in symptom severity following ketamine infusion in patients with chronic PTSD. If replicated, these findings may lead to novel approaches to the pharmacologic treatment of patients with this disabling condition.
clinicaltrials.gov Identifier: NCT00749203.
很少有药物疗法在治疗创伤后应激障碍(PTSD)方面显示出足够的疗效,PTSD 是一种慢性且使人丧失能力的疾病。
测试单次静脉亚麻醉剂量氯胺酮治疗慢性 PTSD 患者 PTSD 及相关抑郁症状的疗效和安全性。
设计、地点和参与者:一项概念验证、随机、双盲、交叉试验,比较氯胺酮与活性对照药物咪达唑仑,在一个地点(纽约市西奈山伊坎医学院)进行。通过广告招募了 41 名患有慢性 PTSD 的患者,这些患者与各种创伤暴露有关。
静脉输注盐酸氯胺酮(0.5mg/kg)和咪达唑仑(0.045mg/kg)。
主要结局测量指标是 PTSD 症状严重程度的变化,使用修订后的事件影响量表(IES-R)进行测量。次要结局测量指标包括蒙哥马利-阿斯伯格抑郁评定量表、临床总体印象严重程度和改善量表以及不良影响测量指标,包括临床医生管理的分离状态量表、简明精神病评定量表和 Young 躁狂评定量表。
与咪达唑仑相比,氯胺酮输注与 PTSD 症状严重程度的显著快速降低相关,在输注后 24 小时评估时(IES-R 评分的平均差异,12.7[95%置信区间,2.5-22.8];P=0.02)。在交叉和第一期分析中,治疗后氯胺酮治疗的 PTSD 症状缓解更明显,并且在调整基线和 24 小时抑郁症状严重程度后仍然显著。氯胺酮还与共病抑郁症状的减轻以及整体临床表现的改善相关。氯胺酮通常耐受性良好,没有临床上显著的持续分离症状。
这项研究首次提供了在慢性 PTSD 患者中,氯胺酮输注后症状严重程度迅速减轻的证据。如果得到复制,这些发现可能会为治疗这种使人丧失能力的疾病的药物治疗带来新的方法。
clinicaltrials.gov 标识符:NCT00749203。