Table 4. Summary of findings from quasi-experimental studies.
Authors | Design | n | Palliative care diagnosis | Intervention (dose, route, duration) | Control | Main outcomes | Secondary outcomes | Depression measures | Results (depression) | Side effects |
---|---|---|---|---|---|---|---|---|---|---|
Falk58 | Observational, retrospective chart review | 16 (eight intervention, eight control) | Inpatient/palliative care unit; cancer (various) | Single dose of 0.25 mg/kg IV S-ketamine | Standard care (does not require ketamine for pain) | Anxiety | Depression | STADI score before and 1-4 days after treatment | No significant effect of S-ketamine on depression, compared with control (F1,14 = 0.31, p = 0.59) and baseline (F1,14 = 1.80, p = 0.20) | No serious side effects, changes in restlessness/anxiety or persistent psychotomimetic effects |
Irwin16 | Open label trial | 14 (intervention) | Hospice; multiple (cancer and non-cancer) | Daily oral doses of 0.5 mg/kg ketamine for 28 days | None | Depression | Anxiety | HADS score at baseline and days 3, 7, 14, 21, and 28 | HADS-D scores on days 14 (mean = 3.5, 95%CI 1.09-5.90, p = 0.01), 21 (mean = 4.1, 95%CI 2.0-6.2, p = 0.002), and 28 (mean = 4, 95%CI 2.3-5.9, p = 0.001) were significantly lower than the baseline scores | No vital sign changes or serious side effects Mild side effects (diarrhea, trouble sleeping, and trouble sitting) were observed in 12.5% of the patients |
HADS = Hospital Anxiety and Depression Rating Scale; IV = intravenous; STADI = State Trait Anxiety Depression Inventory.