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      Ketamine and esketamine in suicidal thoughts and behaviors: a systematic review

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          Abstract

          Background:

          More than 2% of the general population experience suicidal ideas each year and a large number of them will attempt suicide. Evidence-based therapeutic options to manage suicidal crisis are currently limited.

          Objectives:

          The aim of this study was to overview the findings on the use of ketamine and esketamine for the treatment of suicidal ideas and acts.

          Design:

          Systematic review.

          Data Sources and methods:

          PubMed, article references, and Clinicaltrials.gov up to June 30, 2022. Meta-analyses published within the last 2 years were also reviewed.

          Results:

          We identified 12 randomized controlled trials with reduction of suicidal ideation as the primary objective and 14 trials as secondary objectives. Intravenous racemic ketamine was superior to control drugs (placebo or midazolam) within the first 72 h, in spite of large placebo effects. Adverse events were minor and transient. In contrast, intranasal esketamine did not differ from placebo in large-scale studies. Limitations, clinical considerations, and opportunities for future research include the following points: large placebo effects when studying suicidal ideation reduction; small concerns about blinding quality due to dissociative effects; no studies on the risk/prevention of suicidal acts and mortality; lack of studies beyond affective disorders; no studies in adolescents and older people; lack of knowledge of long-term side effects, notably liability for abuse; no robust predictive markers; limited understanding of the mechanisms of ketamine on suicidal ideas; need for improved assessment of suicidal ideation in clinical trials; need for studies in outpatient settings, emergency room, and liaison consultation; need for research on ketamine administration; limited knowledge on the positive and negative effects of concomitant treatments.

          Conclusion:

          Overall, there is compelling evidence for a favorable short-term benefit-risk balance with intravenous racemic ketamine but not intranasal esketamine. The place of ketamine will have to be defined within a multimodal care strategy for suicidal patients. Caution remains necessary for clinical use, and pharmacovigilance will be essential.

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          Most cited references97

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          Pain and emotion interactions in subregions of the cingulate gyrus.

          Brent Vogt (2005)
          Acute pain and emotion are processed in two forebrain networks, and the cingulate cortex is involved in both. Although Brodmann's cingulate gyrus had two divisions and was not based on any functional criteria, functional imaging studies still use this model. However, recent cytoarchitectural studies of the cingulate gyrus support a four-region model, with subregions, that is based on connections and qualitatively unique functions. Although the activity evoked by pain and emotion has been widely reported, some view them as emergent products of the brain rather than of small aggregates of neurons. Here, we assess pain and emotion in each cingulate subregion, and assess whether pain is co-localized with negative affect. Amazingly, these activation patterns do not simply overlap.
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            A randomized trial of an N-methyl-D-aspartate antagonist in treatment-resistant major depression.

            Existing therapies for major depression have a lag of onset of action of several weeks, resulting in considerable morbidity. Exploring pharmacological strategies that have rapid onset of antidepressant effects within a few days and that are sustained would have an enormous impact on patient care. Converging lines of evidence suggest the role of the glutamatergic system in the pathophysiology and treatment of mood disorders. To determine whether a rapid antidepressant effect can be achieved with an antagonist at the N-methyl-D-aspartate receptor in subjects with major depression. A randomized, placebo-controlled, double-blind crossover study from November 2004 to September 2005. Mood Disorders Research Unit at the National Institute of Mental Health. Patients Eighteen subjects with DSM-IV major depression (treatment resistant). After a 2-week drug-free period, subjects were given an intravenous infusion of either ketamine hydrochloride (0.5 mg/kg) or placebo on 2 test days, a week apart. Subjects were rated at baseline and at 40, 80, 110, and 230 minutes and 1, 2, 3, and 7 days postinfusion. Main Outcome Measure Changes in scores on the primary efficacy measure, the 21-item Hamilton Depression Rating Scale. Subjects receiving ketamine showed significant improvement in depression compared with subjects receiving placebo within 110 minutes after injection, which remained significant throughout the following week. The effect size for the drug difference was very large (d = 1.46 [95% confidence interval, 0.91-2.01]) after 24 hours and moderate to large (d = 0.68 [95% confidence interval, 0.13-1.23]) after 1 week. Of the 17 subjects treated with ketamine, 71% met response and 29% met remission criteria the day following ketamine infusion. Thirty-five percent of subjects maintained response for at least 1 week. Robust and rapid antidepressant effects resulted from a single intravenous dose of an N-methyl-D-aspartate antagonist; onset occurred within 2 hours postinfusion and continued to remain significant for 1 week.
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              Antidepressant effects of ketamine in depressed patients.

              A growing body of preclinical research suggests that brain glutamate systems may be involved in the pathophysiology of major depression and the mechanism of action of antidepressants. This is the first placebo-controlled, double-blinded trial to assess the treatment effects of a single dose of an N-methyl-D-aspartate (NMDA) receptor antagonist in patients with depression. Seven subjects with major depression completed 2 test days that involved intravenous treatment with ketamine hydrochloride (.5 mg/kg) or saline solutions under randomized, double-blind conditions. Subjects with depression evidenced significant improvement in depressive symptoms within 72 hours after ketamine but not placebo infusion (i.e., mean 25-item Hamilton Depression Rating Scale scores decreased by 14 +/- SD 10 points vs. 0 +/- 12 points, respectively during active and sham treatment). These results suggest a potential role for NMDA receptor-modulating drugs in the treatment of depression.
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                Author and article information

                Contributors
                Role: ConceptualizationRole: Writing - original draftRole: Writing - review & editing
                Role: ConceptualizationRole: Writing - original draftRole: Writing - review & editing
                Role: ConceptualizationRole: Writing - original draftRole: Writing - review & editing
                Role: ConceptualizationRole: Writing - review & editing
                Role: ConceptualizationRole: Writing - original draftRole: Writing - review & editing
                Role: ConceptualizationRole: Writing - review & editing
                Role: ConceptualizationRole: Writing - review & editing
                Role: ConceptualizationRole: Writing - original draftRole: Writing - review & editing
                Journal
                Ther Adv Psychopharmacol
                Ther Adv Psychopharmacol
                TPP
                sptpp
                Therapeutic Advances in Psychopharmacology
                SAGE Publications (Sage UK: London, England )
                2045-1253
                2045-1261
                7 February 2023
                2023
                : 13
                : 20451253231151327
                Affiliations
                [1-20451253231151327]Service de Psychiatrie, CHU Bicêtre, APHP, 78 Rue du Général Leclerc, 94270 Le Kremlin-Bicêtre, France
                [2-20451253231151327]Faculty of Medicine, University Paris-Saclay, Le Kremlin-Bicêtre, France
                [3-20451253231151327]MOODS Team, Inserm 1018, Centre de Recherche en Epidémiologie et Santé des Populations (CESP), Le Kremlin-Bicêtre, France
                [4-20451253231151327]Department of Psychiatry, CHU Nîmes, Univ Montpellier, Nîmes, France
                [5-20451253231151327]Department of Psychiatry & McGill Group for Suicide Studies, McGill University, Montréal, QC, Canada
                [6-20451253231151327]Faculty of Medicine, University Paris-Saclay, Le Kremlin-Bicêtre, France
                [7-20451253231151327]Department of Psychiatry, CHU Bicêtre, APHP, Le Kremlin-Bicêtre, France
                [8-20451253231151327]MOODS Team, Inserm 1018, Centre de Recherche en Epidémiologie et Santé des Populations (CESP), Le Kremlin-Bicêtre, France
                [9-20451253231151327]Faculty of Pharmacy, University Paris-Saclay, Orsay, France
                [10-20451253231151327]MOODS Team, Inserm 1018, Centre de Recherche en Epidémiologie et Santé des Populations (CESP), Le Kremlin-Bicêtre, France
                [11-20451253231151327]Faculty of Medicine, University Paris-Saclay, Le Kremlin-Bicêtre, France
                [12-20451253231151327]Department of Psychiatry, CHU Bicêtre, APHP, Le Kremlin-Bicêtre, France
                [13-20451253231151327]MOODS Team, Inserm 1018, Centre de Recherche en Epidémiologie et Santé des Populations (CESP), Le Kremlin-Bicêtre, France
                [14-20451253231151327]Faculty of Pharmacy, University Paris-Saclay, Orsay, France
                [15-20451253231151327]MOODS Team, Inserm 1018, Centre de Recherche en Epidémiologie et Santé des Populations (CESP), Le Kremlin-Bicêtre, France
                [16-20451253231151327]Department of Psychiatry and Psychotherapy, Jena University Hospital, Jena, Germany
                [17-20451253231151327]Clinical Affective Neuroimaging Laboratory (CANLAB), Magdeburg, Germany
                [18-20451253231151327]Center for Behavioral Brain Sciences, Magdeburg, Germany
                [19-20451253231151327]Department of Psychiatry and Psychotherapy, University Tübingen, Tübingen, Germany
                [20-20451253231151327]German Center for Mental Health (DZPG), site Jena Magdeburg Halle, Germany
                [21-20451253231151327]Center for Intervention and Research on adaptive and maladaptive Brain Circuits underlying Mental Health (C-I-R-C), site Jena Magdeburg Halle, Germany
                [22-20451253231151327]Department of Psychiatry, CHU Nîmes, Univ Montpellier, Nîmes, France
                [23-20451253231151327]Department of Psychiatry and Psychotherapy, Jena University Hospital, Jena, Germany
                [24-20451253231151327]Network for Suicide Prevention in Thuringia (NeST), Jena, Germany
                [25-20451253231151327]Center for Intervention and Research on adaptive and maladaptive Brain Circuits underlying Mental Health (C-I-R-C), site Jena Magdeburg Halle, Germany
                Author notes
                Author information
                https://orcid.org/0000-0001-5809-4503
                Article
                10.1177_20451253231151327
                10.1177/20451253231151327
                9912570
                36776623
                4bc6f918-41d0-4d46-aefd-071f42153d61
                © The Author(s), 2023

                This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License ( https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page ( https://us.sagepub.com/en-us/nam/open-access-at-sage).

                History
                : 1 August 2022
                : 1 January 2023
                Categories
                Systematic Review
                Custom metadata
                January-December 2023
                ts1

                efficacy,esketamine,drugs,intervention,ketamine,randomized controlled trial,rct,review,suicidal ideation,suicide attempt

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