Abstract

BackgroundKetamine has emerged as a rapid-acting antidepressant in treatment-resistant depression (TRD) increasingly used in non-research, clinical settings. Few studies, however, have examined neurocognitive effects of repeated racemic ketamine infusion treatments in patients with TRD. In an effort to identify potential effects after serial infusions, we conducted a retrospective chart review to identify statistically significant changes in cognition in patient undergoing serial intravenous infusions; concomitantly, we examined baseline cognition as potential predictor of anti-depressant potential.MethodsTwenty-two patients with TRD were examined after they finished the induction phase of 8–10 repeated intravenous ketamine infusions and completed the assessments of their depressive symptoms (measured by the 16-item Quick Inventory of Depressive Symptomatology-Self Report Scale: QIDS-SR16) and cognitive function (measured by the Montreal Cognitive Assessment: MoCA) before the first and the last ketamine treatments.ResultsRepeated ketamine infusions administered through an escalating dose protocol with 8–10 infusion sessions produced a 47.2% reduction response in depression; there was no evidence of impairment as reflected in MoCA testing. There was a moderate association between baseline cognition and antidepressant response with a Pearson correlation of 0.453.ConclusionIn this naturalistic sample of patients with TRD in our clinical service, repeated ketamine infusions significantly decreased depression symptoms without impairing cognitive performance. The baseline cognition may positively predict antidepressant responses of repeated ketamine treatment.

Highlights

  • Ketamine has emerged as a rapid-acting antidepressant in treatment-resistant depression (TRD) increasingly used in non-research, clinical settings

  • Depression symptom severity was evaluated with the 16-item Quick Inventory of Depressive Symptomatology-Self Report scale (QIDS-SR16) that is scored on a scale of 0 to 27, with 0 representing a complete absence of depressive symptoms and 27 representing the most severe symptoms [31]

  • Twenty-two patients completed their depressive symptoms measured by QIDS-SR16 and neurocognitive function measured by Montreal Cognitive Assessment (MoCA) before the first and last treatment

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Summary

Introduction

Ketamine has emerged as a rapid-acting antidepressant in treatment-resistant depression (TRD) increasingly used in non-research, clinical settings. Few studies have examined neurocognitive effects of repeated racemic ketamine infusion treatments in patients with TRD. An N-methyl-D-aspartate receptor antagonist, was demonstrated to have a rapid antidepressant action in a randomized double-blind trial for the first time in 2000 [4]. Since emerging studies have indicated rapid and robust antidepressant effects of ketamine in adults with TRD [5,6,7,8,9]. A single subanesthetic (0.5 mg/ kg) dose infusion of intravenous (IV) ketamine has rapidacting and robust antidepressant effects in at least 50% of patients, the effects dissipate by day 10 to day 14 [10,11,12,13,14]. The findings of this study suggest that patients may require multiple ketamine sessions to respond

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