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Flávio Kapczinski

4 papers in the library · 20 citations · publishing 2023-2025

Papers

Does the intensity of dissociation predict antidepressant effects 24 hours after infusion of racemic ketamine or esketamine in treatment-resistant depression? A secondary analysis from a randomized controlled trial

Trends in Psychiatry and Psychotherapy May 27, 2025 Mariana V. F. Echegaray, Rodrigo P. Mello, Guilherme M. Magnavita et al. 11 citations

Among people with treatment-resistant depression, the intensity of dissociation caused by a single infusion of ketamine or esketamine is linked to greater antidepressant effect one day later, but only when dissociative symptoms are mild to moderate. For every one-point increase on a dissociation scale up to 15 points, depression scores improved by an average of 0.5 points after 24 hours. This relationship was not observed at 72 hours or 7 days after infusion. The study was not originally designed to test this relationship, so confounding factors were not controlled, and the finding should be considered suggestive rather than definitive.

Arketamine: a scoping review of its use in humans.

European archives of psychiatry and clinical neuroscience December 16, 2024 Gustavo C Leal, Isabel Lima-Araújo, David G Roiter et al. 7 citations

Arketamine, an enantiomer of ketamine, has been less studied than esketamine or racemic ketamine, but recent preclinical work suggests it may have prolonged antidepressant effects and a better safety profile. This scoping review of 20 studies involving 410 subjects found arketamine was primarily investigated for pain management and depression. Early evidence indicates it may reduce pain, though most studies were small and in non-clinical settings. In psychiatry, trials show potential antidepressant effects, but results are inconsistent and some studies unpublished. A consistent finding is arketamine's favorable safety profile, with fewer dissociative and psychotomimetic effects than esketamine or racemic ketamine. Larger, well-designed studies are needed to determine its therapeutic potential.

Subcutaneous ketamine reduces suicide risk and improves functioning in depression: A proof-of-concept study.

Psychiatry research July 1, 2024 Ana Paula Anzolin, Daniel Prates Baldez, Bruno Braga Montezano et al. 2 citations

Subcutaneous ketamine substantially reduced suicidal thoughts and depressive symptoms in patients with severe depression. In a naturalistic study at a Brazilian hospital, 26 patients with a current depressive episode received adjustable ketamine doses starting at 0.5 mg/kg. After about eight sessions, most patients achieved remission of suicidal ideation, as measured by the Columbia Suicide Severity Rating Scale. Higher ketamine doses were associated with greater improvements in depression, suicidal ideation, and overall functioning. Improvements were sustained over six months of follow-up in 18 patients. Side effects were minor and short-lived. The findings suggest subcutaneous ketamine is a promising, well-tolerated, and potentially cost-effective treatment for severe depression with suicidal tendencies, warranting further controlled trials.

Arketamine for bipolar depression: Open-label, dose-escalation, pilot study.

Journal of psychiatric research August 1, 2023 Igor D Bandeira, Gustavo C Leal, Fernanda S Correia-Melo et al.

In a pilot trial of six people with bipolar I or II disorder who had been depressed for at least four weeks, two intravenous infusions of arketamine (0.5 mg/kg followed one week later by 1 mg/kg) rapidly reduced depression severity. Depression scores on the Montgomery-Åsberg Depression Rating Scale fell from a baseline mean of 36.66 to 27.83 one day after the first infusion and from 32.0 to 17.66 one day after the second infusion. The drug was well tolerated with almost no dissociation and no manic symptoms. The findings suggest arketamine has rapid-acting antidepressant properties for bipolar depression, consistent with earlier animal research on major depression.