Echegaray Mariana V F, Mello Rodrigo P, Magnavita Guilherme M, Leal Gustavo C, Correia-Melo Fernanda S, Jesus-Nunes Ana Paula, Vieira Flávia, Bandeira Igor D, Caliman-Fontes Ana Teresa, Telles Manuela, Guerreiro-Costa Lívia N F, Marback Roberta Ferrari, Souza-Marques Breno, Lins-Silva Daniel H, Santos-Lima Cassio, Cardoso Taiane de Azevedo, Kapczinski Flávio, Lacerda Acioly L T, Quarantini Lucas C
Laboratório de Neuropsicofarmacologia, Serviço de Psiquiatria do Hospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, Brazil.
Laboratório de Neuropsicofarmacologia, Serviço de Psiquiatria do Hospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, Brazil. Programa de Pós-graduação em Medicina e Saúde, Faculdade de Medicina da Bahia, Universidade Federal da Bahia, Salvador, Brazil.
Trends Psychiatry Psychother. 2023 Sep 17. doi: 10.47626/2237-6089-2022-0593.
Ketamine and esketamine have both shown significant antidepressant effects in treatment-resistant depression (TRD), and conflicting evidence suggests that induced dissociation by these drugs can be a clinical predictor of esketamine/ketamine's efficacy.
This study is a secondary analysis from a bi-center, randomized, controlled trial. Participants were randomly assigned 1:1 to receive an IV infusion of esketamine (.25 mg/kg) or racemic ketamine (.50 mg/kg) over 40 minutes. Dissociative symptoms were assessed using the Clinician-Administered Dissociative State Scale (CADSS) 40 minutes following the beginning of the infusion. The variation in depression scores was measured with the Montgomery-Asberg Depression Rating Scale (MADRS), which was administered before the intervention as a baseline measure and 24 hrs, 72 hrs, and 7 days following infusion.
Sixty-one patients were included in the analysis. Examining CADSS scores of 15 or below, for every 1-point increment in the CADSS score, there was a mean change of -0.5 (SD = 0.25; p-value 0.04) of predicted MADRS score from baseline to 24 hrs. The results for 72 hrs and 7 days following infusion were not significant. Limitations: This study was not designed to assess the relationship between ketamine or esketamine-induced dissociation and antidepressant effects as the main outcome, therefore confounding variables for this relationship were not controlled.
We suggest a positive relationship between dissociation intensity, measured by CADSS, and antidepressant effect 24 hours after ketamine and esketamine infusion for a CADSS score of up to 15 points.
氯胺酮和艾司氯胺酮在难治性抑郁症(TRD)中均显示出显著的抗抑郁作用,且相互矛盾的证据表明,这些药物诱导的解离状态可能是艾司氯胺酮/氯胺酮疗效的临床预测指标。
本研究是一项来自双中心、随机、对照试验的二次分析。参与者按1:1随机分配,在40分钟内接受静脉输注艾司氯胺酮(0.25mg/kg)或消旋氯胺酮(0.5mg/kg)。输注开始40分钟后,使用临床医生评定的解离状态量表(CADSS)评估解离症状。抑郁评分的变化用蒙哥马利-阿斯伯格抑郁评定量表(MADRS)测量,在干预前作为基线测量,在输注后24小时、72小时和7天进行测量。
61名患者纳入分析。检查CADSS评分在15分及以下的情况,CADSS评分每增加1分,从基线到24小时预测的MADRS评分平均变化为-0.5(标准差=0.25;p值0.04)。输注后72小时和7天的结果不显著。局限性:本研究并非旨在评估氯胺酮或艾司氯胺酮诱导的解离与作为主要结果的抗抑郁作用之间的关系,因此未控制该关系的混杂变量。
我们认为,对于CADSS评分高达15分的情况,以CADSS测量的解离强度与氯胺酮和艾司氯胺酮输注后24小时的抗抑郁作用之间存在正相关。