Repeated intravenous ketamine therapy in a patient with treatment-resistant major depression
Michael Liebrenz, Rudolf Stohler, Alain Borgeat
The World Journal of Biological Psychiatry May 12, 2008 DOI: 10.1080/15622970701420481 via OpenAlex
Summary
AI-generated from the abstractIn a 55-year-old man with treatment-resistant major depression and co-occurring alcohol and benzodiazepine dependence, a single intravenous infusion of ketamine (0.5 mg/kg) produced a pronounced improvement in depression symptoms, peaking two days later (Hamilton Depression Rating Scale down 56.6%, Beck Depression Inventory down 65.4%). Positive effects began fading by day 7 and returned to baseline by day 35. A second infusion six weeks later was less effective, reducing symptoms by 43% and 35% respectively, with effects lasting only 7 days. Repeated ketamine administration can be beneficial, but the diminished response to the second dose suggests that optimal dosing and scheduling require further investigation.
Study at a glance
| Characteristics | Single-case trial Open-label Peer reviewed |
|---|---|
| Sample size | 1 |
| Population | 55-year-old male patient with treatment-resistant major depression and co-occurring alcohol and benzodiazepine dependence |
| Intervention | Ketamine |
| Dose | 0.5 mg/kg |
| Duration | 6 weeks |
| Citations | 73 |
| Key finding | A single ketamine infusion produced substantial but temporary improvement in depression symptoms, while a second infusion was less effective and shorter-lasting. |
Abstract
BACKGROUND: The intravenous administration of ketamine, an N-methyl-D-aspartate receptor antagonist, results in a great improvement of depression symptoms, but it is not clear for how long. This single-case trial was conducted to explore the duration of improvement and the effects of a second administration on the clinical outcome. METHODS: In an open label trial, a 55-year-old male patient with treatment-resistant major depression and a co-occurring alcohol and benzodiazepine dependence received two intravenous infusions of 0.5 mg/kg ketamine over the course of 6 weeks. Depression severity was assessed by means of a weekly clinical interview, the 21-item Hamilton Depression Rating Scale (HDRS), and the 21-item Beck Depression Inventory (BDI). RESULTS: The first ketamine infusion lead to a pronounced improvement of symptoms, peaking on the second day post infusion (HDRS -56.6%, BDI -65.4%). Positive effects started fading by day 7, reaching baseline by day 35. The second infusion was less efficacious: HDRS and BDI were reduced by 43 and 35%, respectively, and returned to baseline by day 7. CONCLUSION: In this patient with a co-occurring substance use disorder, repeated administrations of ketamine produced positive results. Since the second application has been less efficacious, doses and schedule of administrations need to be further investigated.