A single infusion of ketamine relieved bipolar depression within 40 minutes in patients with treatment-resistant bipolar disorder, according to a randomized, placebo-controlled, double-blind crossover study involving 18 patients.
The effect lasted at least 3 days, wrote Dr. Nancy Diazgranados and her colleagues from the National Institute of Mental Health. Patients in the study were an average of 48 years old, had suffered from bipolar I or bipolar II depression for an average of 28 years, and had failed an average of seven antidepressant treatments before the ketamine study. Fifty-five percent of the participants had failed to respond to electroconvulsive therapy.
Two-thirds of participants were on psychiatric disability, and all but one were unemployed (Arch. Gen. Psychiatry 2010;67:793-802).
Patients were randomly assigned to receive an infusion of 0.5 mg/kg of ketamine or placebo. Two weeks later, the patients who had been given ketamine were given placebo and vice versa. Of the 17 patients who completed the ketamine phase of the study, 12 (71%) responded to ketamine.
In contrast, of the 16 patients who completed the placebo phase of the study, only 1 (6%) responded to placebo.
Investigators assessed the patients at baseline using several rating scales, including the Montgomery-Åsberg Depression Rating Scale, the Hamilton Scale for Depression, and the Beck Depression Inventory. Patients showed statistically significant improvements in depression with ketamine, compared with placebo on all three scales beginning at 40 minutes after infusion and continuing for at least 3 days. Mean scores on the rating scales did not differ from placebo on days 7, 10, and 14.
Within 40 minutes, 9 of 16 patients receiving ketamine (56%) responded and an additional 2 (13%) experienced complete remission of their depression. One day after the infusion, 44% of the patients had responded and 31% had remitted.
None of the patients experienced serious adverse events during the study. Among the adverse events associated with ketamine and experienced by at least 10% of the patients were disassociation; feeling strange, weird, or bizarre; dry mouth; tachycardia; and increased blood pressure.
Ketamine has been used in human and veterinary medicine since 1962, most commonly for inducing and maintaining general anesthesia, sedation in intensive care, analgesia, and treatment of bronchospasm. In the late 1990s, it increasingly became known as a drug of abuse and a date-rape drug. A previous study showed that a single infusion of ketamine improved suicidal ideation within 40 minutes (“Single Ketamine Injection Reduces Suicidal Ideation,” November 2009, p. 13).
When used for general anesthesia, the initial dose of intravenous ketamine is typically 1.5-4.5 mg/kg, substantially higher than the level used in this study. Ketamine is thought to act as a noncompetitive inhibitor of the N-methyl-D-aspartate (NMDA) receptor, which is part of the glutaminergic neurotransmitter system. Several lines of evidence have implicated the glutaminergic system in bipolar disorder.