Psychedelic Therapy: A Primer for Primary Care Clinicians—Psilocybin

Author:

Tabaac Burton J.12,Shinozuka Kenneth34ORCID,Arenas Alejandro5,Beutler Bryce D.6,Cherian Kirsten7,Evans Viviana D.8,Fasano Chelsey9,Muir Owen S.1011

Affiliation:

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

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

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

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

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

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

7. Department of Psychiatry & Behavioral Sciences, Stanford University, Palo Alto, CA;

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

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

10. Fermata Health, Brooklyn, NY; and

11. Acacia Clinics, Sunnyvale, CA.

Abstract

Background: The primary psychoactive drug in magic mushrooms, psilocybin, induces profound alterations in consciousness through the 5-HT2A receptor. This review consolidates current research findings to elucidate the pharmacology, safety profile, and clinical applications of psilocybin. Areas of Uncertainty: Despite initial concerns that psilocybin could cause psychosis, contemporary research has demonstrated that psilocybin is generally safe. The most common adverse effects are nausea and headache, yet both tend to be transient. Serious adverse events can generally be avoided in controlled settings such as clinical trials. However, in the largest clinical trial to date, there were a total of 7 reported cases of suicidal ideation, up to 12 weeks after receiving a single 25 mg dose of psilocybin. That being said, all 7 cases did not respond to the treatment. Although selective serotonin reuptake inhibitors may blunt the hallucinogenic qualities of psilocybin, preliminary research suggests that they may enhance its antidepressant effects. Therapeutic Advances: In clinical trials, psilocybin has shown promise for treating major depressive disorder and treatment-resistant depression. Initial studies indicated that 42%–57% of patients underwent remission after psilocybin-assisted therapy, which suggests that psilocybin is more effective than existing antidepressant medications. Clinical data have also demonstrated that psilocybin can manage substance use disorders and end-of-life anxiety with clinical outcomes that are sustained for months and sometimes years after 1 or 2 doses. Limitations: However, larger Phase II trials with more than 100 depressed participants have shown a much smaller remission rate of 25%–29%, though these studies still observed that psilocybin causes a significant reduction in depressive symptoms. Conclusions: Aside from ketamine, psilocybin is the most clinically well-researched psychedelic drug, with trials that have enrolled hundreds of participants and multiple therapeutic applications. Phase III trials will determine whether psilocybin lives up to the promise that it showed in previous clinical trials.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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