Association of low-dose ketamine with hallucinations in critically ill patients: a target trial emulation.
Ary Serpa Neto, Marcus Young, Jian Wen Chan, Natasha E Holmes, Kartik Kishore, Dinesh Pandey, Hossein Jahanabadi, Andrew Casamento, Rinaldo Bellomo
Intensive care medicine May 5, 2025 DOI: 10.1007/s00134-025-07926-w (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Retrospective cohort study with target trial emulation Peer reviewed |
|---|---|
| Sample size | 7,514 |
| Population | Critically ill patients in the intensive care unit |
| Intervention | low-dose ketamine |
| Dose | 0.11 (0.08-0.15) mg/kg/h |
| Duration | 30-day follow-up from ICU admission |
| Topics | Ketamine Esketamine |
| Keywords | Delirium Hallucination Ketamine side effects Intensive care medicine Pain management Psychiatric symptoms Analgesia and sedation |
| Citations | 9 |
| Key findings | Low-dose ketamine was associated with a significantly higher risk of hallucinations within 30 days of ICU admission (OR, 6.46 [95% CI 5.17-8.07]). |
Abstract
Ketamine use is a potentially modifiable risk factor for hallucinations. We aimed to use target trial emulation to investigate the association between low-dose ketamine and development of hallucinations in critically ill patients in the intensive care unit (ICU). Retrospective study using data from a university affiliated ICU in Melbourne, Australia. Application of marginal structural models and parametric g-formulas to assess the impact of low-dose ketamine on the development of hallucinations. We studied 7514 patients from June 2016 to April 2021. Of these, 625 patients (8%) received low-dose ketamine, beginning at a median of 0 (0-1) days from ICU admission and at a mean daily dose of 0.11 (0.08-0.15) mg/kg/h. Low-dose ketamine treated patients had a higher rate of hallucinations within 30 days of ICU admission (26% vs. 7%; p < 0.001) and the first episode of hallucination occurred earlier than in unexposed patient (2 [1-3] vs. 3 [1-7] days from ICU admission; p < 0.001). After adjustment for baseline and time-dependent confounders, low-dose ketamine was associated with a higher risk of hallucinations within 30 days (OR, 6.46 [95% CI 5.17-8.07]; p < 0.001). These findings were confirmed with parametric g-formulas. In ICU patients, low-dose ketamine was strongly associated with an increased risk of hallucinations. However, these findings should be interpreted with caution due to the observational nature of the study and the risk of residual confounding.
Comparable studies
Other non-randomized and open-label trials on ketamine, most cited first.