1. Ketamine augmentation for major depressive disorder and suicidal ideation: Preliminary experience in an inpatient psychiatry setting
- Author
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Beverley A. Orser, Sue Belo, Saulo Castel, Mark Sinyor, Carlos A. Zarate, Marissa Williams, Anthony J. Levitt, Margaret Vincent, Ayal Schaffer, Linda Mah, and Dr. Brenda Smith Bipolar Fund (Toronto Canada)
- Subjects
Adult ,Male ,Suicide Prevention ,Canada ,medicine.medical_specialty ,ketamine ,medicine.medical_treatment ,Poison control ,Drug Administration Schedule ,Article ,Suicidal Ideation ,law.invention ,inpatients ,Young Adult ,03 medical and health sciences ,0302 clinical medicine ,Electroconvulsive therapy ,Double-Blind Method ,Randomized controlled trial ,Rating scale ,law ,Internal medicine ,medicine ,Clinical endpoint ,Humans ,Ketamine ,Infusions, Intravenous ,Suicidal ideation ,suicide ,Psychiatric Status Rating Scales ,Depressive Disorder, Major ,major depressive disorder ,business.industry ,Middle Aged ,medicine.disease ,030227 psychiatry ,Psychiatry and Mental health ,Clinical Psychology ,midazolam ,Major depressive disorder ,Female ,medicine.symptom ,business ,Excitatory Amino Acid Antagonists ,030217 neurology & neurosurgery ,medicine.drug - Abstract
Background Ketamine is known to rapidly reduce depressive symptoms and suicidal ideation (SI) in patients with major depressive disorder (MDD), but evidence is limited for its acceptability and effectiveness in “real-world” settings. This case series examines serial ketamine infusions in reducing SI and depression scores in adults with MDD admitted to a tertiary care hospital. Methods Five inpatients with MDD and SI admitted to hospital in Toronto, Canada received six infusions of 0.5 mg/kg intravenous (IV) ketamine (n = 5) over approximately 12 days, in addition to treatment-as-usual. Suicide and depression rating scores (Scale for Suicidal Ideation, SSI; Montgomery-Asberg Depression Rating Scale, MADRS) were obtained at baseline, on treatment days, on days 14 and 42 (primary endpoint). Results All patients experienced benefit with ketamine. SSI scores diminished by 84% from 14.0 ± 4.5 at baseline to 2.2 ± 2.5 at study endpoint. MADRS scores diminished by 47% from 42.2 ± 5.3 at baseline to 22.4 ± 8.0. Two patients withdrew from the study, one to initiate electroconvulsive therapy and one due to an adverse event (dissociative effects) during the ketamine infusion. Limitations The major limitation of this study is the small sample size. Discussion These preliminary pilot data are promising with a greater than two-fold reduction in SI following ketamine infusions. They demonstrate that six serial ketamine infusions may be safe and feasible. These findings support the need for large scale randomized controlled trials to confirm the efficacy of serial ketamine for treatment of SI in “real-world” settings.
- Published
- 2018
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