Characterization of Oral Ketamine Use: A Retrospective Review.
Miranda Hetrick, Emily Casey, Jacob Radcliff, Tanya Uritsky
Journal of pain & palliative care pharmacotherapy March 1, 2025 DOI: 10.1080/15360288.2024.2401979 via PubMed
Summary
AI-generated from the abstractOral ketamine was administered safely for pain control in hospitalized patients, with a low incidence of safety events. The median starting dose was 1 mg/kg/day and the median maximum dose was 1.6 mg/kg/day. Median oral morphine equivalent doses decreased from the first to the last day of therapy. The study population included adults at a large academic hospital, many of whom may have had high opioid tolerance or opioid-induced hyperalgesia. The findings suggest oral ketamine is a safe analgesic option, though further research on efficacy and safety is needed.
Study at a glance
| Characteristics | Retrospective cohort study Peer reviewed |
|---|---|
| Population | Hospitalized patients aged 18 years or older receiving oral ketamine |
| Intervention | Oral ketamine |
| Dose | 1 mg/kg/day median starting dose, 1.6 mg/kg/day median maximum dose |
| Topics | Addiction Ketamine |
| Keywords | Oral ketamine Pain management Ketamine therapy Opioid alternatives |
| Citations | 2 |
| Key finding | Oral ketamine was administered safely for analgesia with a low incidence of safety events, and median oral morphine equivalent doses decreased during therapy. |
Abstract
Ketamine is an N-methyl D-aspartate (NMDA) receptor antagonist used to treat pain at subanesthetic doses. Ketamine is beneficial for pain control in patients who have a high tolerance to opioids and are experiencing opioid-induced hyperalgesia. This study characterizes oral ketamine use for analgesia at a large academic hospital and reports safety outcomes for hospitalized patients. This study was a retrospective electronic health record (EHR) review of patients ≥ 18 years or older receiving oral ketamine. The primary endpoint was median ketamine starting dose and maximum dose (mg/kg/day) during treatment duration. Secondary outcomes included oral Morphine Milligram Equivalents (MMEs), buprenorphine dose, minimum and maximum pain scores on the first and last day of therapy. Safety endpoints were reported. The median starting dose was 1 mg/kg/day, and the median maximum dose was 1.6 mg/kg/day. Median MMEs decreased from the first day to the last day of oral ketamine therapy. The study population experienced a low incidence of safety events overall. Oral ketamine was administered safely for analgesia, with patients receiving ketamine doses that were on the lower end of the established therapeutic range. Evaluation of the efficacy and safety of oral ketamine use for analgesia should be further studied.