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Psychedelic Therapy: A Primer for Primary Care Clinicians-Ketamine.

Viviana D Evans, Alejandro Arenas, Kenneth Shinozuka, Burton J Tabaac, Bryce D Beutler, Kirsten Cherian, Chelsey Fasano, Owen S Muir

American journal of therapeutics DOI: 10.1097/MJT.0000000000001721 via PubMed

Summary

AI-generated from the abstract

Ketamine, originally a dissociative anesthetic, is now used for treatment-resistant depression, major depressive disorder with suicidal ideation, and PTSD. A single intravenous infusion shows antidepressant effects within hours, with a weighted effect size of d = 0.96 at 24 hours (N = 518). It reduces PTSD symptom severity (Clinician-Administered PTSD Scale scores: -11.88 points) and suicidal ideation in emergency settings (Scale for Suicidal Ideation scores: -4.96 points) compared to midazolam. However, effects may subside within weeks, requiring repeated administrations. Risks include temporary cognitive impairment, cardiovascular instability, liver toxicity with prolonged use, and ketamine cystitis. Ketamine also reduces postoperative pain and opioid consumption.

Study at a glance

Characteristics Review Peer reviewed
Intervention Ketamine
Dose 0.5 mg/kg
Keywords Mental health Depression treatment Ketamine therapy Psychiatric medicine Pain management
Citations 10
Key finding Ketamine produces rapid antidepressant, anti-suicidal, and anti-PTSD effects but requires repeated dosing due to short duration, and carries risks including cognitive impairment and bladder toxicity.

Abstract

Ketamine, an arylcyclohexylamine dissociative anesthetic agent, has evolved into a versatile therapeutic. It has a rapid-onset, well-understood cardiovascular effects and a favorable safety profile in clinical use. Its enantiomeric compound, esketamine, was approved by the Food and Drug Administration in 2019 for both treatment-resistant depression and major depressive disorder with suicidal ideation. Research indicates dose-dependent impacts on cognition, particularly affecting episodic and working memory following both acute administration and chronic use, albeit temporarily for the former and potentially persistent for the latter. Alongside acute risks to cardiovascular stability, ketamine use poses potential liver toxicity concerns, especially with prolonged or repeated exposure within short time frames. The drug's association with "ketamine cystitis," characterized by bladder inflammation, adds to its profile of physiological risks. Data demonstrate a single intravenous infusion of ketamine exhibits antidepressant effects within hours (weighted effect size averages of depression scores (N = 518) following a single 0.5 mg/kg infusion of ketamine is d = 0.96 at 24 hours). Ketamine is also effective at reducing posttraumatic stress disorder (PTSD) symptom severity following repeated infusions (Clinician-Administered PTSD Scale scores: -11.88 points compared with midazolam control). Ketamine also decreased suicidal ideation in emergency settings (Scale for Suicidal Ideation scores: -4.96 compared with midazolam control). Through its opioid-sparing effect, ketamine has revolutionized postoperative pain management by reducing analgesic consumption and enhancing recovery. Many studies indicate that ketamine's therapeutic effects may subside within weeks. Repeated administrations, given multiple times per week, are often required to sustain decreases in suicidality and depressive symptoms. Ketamine's comprehensive clinical profile, combined with its robust effects on depression, suicidal ideation, PTSD, chronic pain, and other psychiatric conditions, positions it as a substantial contender for transformative therapeutic application.

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