Psychedelic Therapy: A Primer for Primary Care Clinicians—Ketamine

Author:

Evans Viviana D.1,Arenas Alejandro2,Shinozuka Kenneth34ORCID,Tabaac Burton J.56,Beutler Bryce D.7,Cherian Kirsten8,Fasano Chelsey9,Muir Owen S.1011

Affiliation:

1. Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY;

2. Department of Anesthesiology, University of Washington School of Medicine, Seattle, WA;

3. Centre for Eudaimonia and Human Flourishing, University of Oxford, Oxford, United Kingdom;

4. Department of Psychiatry, University of Oxford, Oxford, United Kingdom;

5. University of Nevada, Reno School of Medicine, Reno, NV;

6. Department of Neurology, Carson Tahoe Health, Carson City, NV;

7. University of Southern California, Keck School of Medicine, Los Angeles, CA;

8. Department of Psychiatry and Behavioral Sciences, Stanford University, Palo Alto, CA;

9. Teachers College, Columbia University, New York, NY;

10. Fermata Health, Brooklyn, NY; and

11. Acacia Clinics, Sunnyvale, CA.

Abstract

Background: 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. Areas of Uncertainty: 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. Therapeutic Advances: 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. Limitations: 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. Conclusions: 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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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