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Anxiety during ketamine infusions is associated with negative treatment responses in major depressive disorder.

Sabine Aust, Matti Gärtner, Laura Basso, Christian Otte, Katja Wingenfeld, Woo Ri Chae, Isabella Heuser-Collier, Francesca Regen, Nicoleta Carmen Cosma, Franziska Van Hall, Simone Grimm, Malek Bajbouj

European Neuropsychopharmacology April 2019 DOI: 10.1016/j.euroneuro.2019.02.005 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Observational cohort Peer reviewed
Sample size 31
Population Patients with treatment-resistant major depressive disorder (mean age 49.5 years, 16 women)
Intervention Ketamine
Dose 0.5 mg/kg over 40 min, three infusions per week
Duration Two consecutive weeks of infusions (six infusions total); assessments at baseline, 4 and 24 hours, and end of treatment
Measures Montgomery-Åsberg Depression Rating Scale (MADRS), 5-Dimensional Altered States of Consciousness Rating Scale (5D-ASC)
Topics Altered states of consciousness Anxiety Depression Ketamine Esketamine
Keywords Subjective experiences
Key findings Ketamine produced a response in 55% of patients (17 of 31) after six infusions, while 45% (14 of 31) did not respond. Anxiety-related experiences during the first infusion were higher in non-responders, and both early MADRS reduction and ketamine-induced anxiety predicted end-of-treatment response. The authors argue these subjective experiences may serve as a phenotypic response predictor.

Abstract

About 20 to 30 percent of patients with Major Depressive Disorder (MDD) do not respond to standard treatment and are considered treatment-resistant. The N-methyl-d-aspartate (NMDA) glutamate receptor antagonist ketamine has demonstrated rapid antidepressant effects in treatment-resistant MDD, but it is unknown whether its acute psychological effects are related to the later antidepressant effect. Therefore, we investigated the association between antidepressant responses to ketamine and the quality of ketamine-induced psychological experiences in MDD. A total of 31 patients (M = 49.5 ± 11.2 years, 16 women) were treated with three ketamine infusions per week (0.5 mg/ kg over 40 min) administered for two consecutive weeks. Depression severity was assessed using the Montgomery-Åsberg Depression Rating Scale (MADRS) at baseline, after four and 24 h and at end of treatment. The 5-Dimensional Altered States of Consciousness Rating Scale (5D-ASC) was applied four hours after the first infusion to assess the subjective quality of acute psychological effects. Patients with a ≥ 50% MADRS reduction from baseline to end of treatment were considered as responders. After six infusions, 17 of 31 patients (55%) showed a response to ketamine treatment, while 14 patients (45%) had no response. Anxiety-related experiences induced by ketamine were significantly higher in non-responders. Percentage MADRS reduction after four hours and individual levels of ketamine-induced anxiety were predictive of a response at end of treatment. The study demonstrated the considerable impact of ketamine-induced anxiety on the antidepressant efficacy of ketamine. It underpins the importance of considering patients' subjective experiences and underlines the possibility of a phenotypic response predictor.

Comparable studies

Other observational and cohort studies on ketamine for anxiety, most cited first.

Study Year Design Participants
Treating bipolar depression with esketamine: Safety and effectiveness data from a naturalistic multicentric study on esketamine in bipolar versus unipolar treatment‐resistant depression Patients with treatment-resistant bipolar depression (B-TRD) and unipolar... 2023 Observational cohort n = 70
The effectiveness of ketamine on anxiety, irritability, and agitation: Implications for treating mixed features in adults with major depressive or bipolar disorder Adults with treatment-resistant major depressive disorder or bipolar disorder 2020 Retrospective analysis n = 201
At-home, sublingual ketamine telehealth is a safe and effective treatment for moderate to severe anxiety and depression: Findings from a large, prospective, open-label effectiveness trial. Outpatients receiving at-home ketamine-assisted therapy 2022 Prospective study n = 1,247
Predicting outcome with Intranasal Esketamine treatment: A machine-learning, three-month study in Treatment-Resistant Depression (ESK-LEARNING) Treatment-resistant depression patients 2023 Retrospective, multicentric, real-world study n = 149
Esketamine in treatment-resistant depression patients comorbid with substance-use disorder: A viewpoint on its safety and effectiveness in a subsample of patients from the REAL-ESK study Patients with treatment-resistant depression and a substance use disorder 2023 Observational, retrospective, multicentre study n = 26

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