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Psychiatric risks for worsened mental health after psychedelic use.

Alessia Marrocu, Hannes Kettner, Brandon Weiss, Richard J. Zeifman, David Erritzøe, Robin Carhart-Harris

Journal of Psychopharmacology March 4, 2024 DOI: 10.1177/02698811241232548 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Observational prospective study Peer reviewed
Sample size 807
Population Naturalistic, observational prospective studies participants
Intervention psychedelic use
Duration 4-week follow-up
Topics Psychedelic-assisted therapy
Keywords Psychedelic treatment Therapeutic psychedelics Therapeutic promise Beneficial psychedelic use Mental health screening Psychiatric screening Psychological assessment Safer Effective screening Risk assessment Safety assessment Harm reduction Minimizing negative experiences Responsible application Mental health predispositions Psychiatric risks Predisposition to psychosis Bipolar disorder Specific psychiatric vulnerabilities
Citations 51
Key findings A prior diagnosis of a personality disorder was associated with a greater than four-fold elevated risk of adverse psychological responses to psychedelics.

Abstract

Background: Resurgent psychedelic research has largely supported the safety and efficacy of psychedelic therapy for the treatment of various psychiatric disorders. As psychedelic use and therapy increase in prevalence, so does the importance of understanding associated risks. Cases of prolonged negative psychological responses to psychedelic therapy seem to be rare; however, studies are limited by biases and small sample sizes. The current analytical approach was motivated by the question of whether rare but significant adverse effects have been under-sampled in psychedelic research studies.

Methods: A “bottom margin analysis” approach was taken to focus on negative responders to psychedelic use in a pool of naturalistic, observational prospective studies ( N = 807). We define “negative response” by a clinically meaningful decline in a generic index of mental health, that is, one standard error from the mean decrease in psychological well-being 4 weeks post-psychedelic use (vs pre-use baseline). We then assessed whether a history of diagnosed mental illness can predict negative responses.

Results: We find that 16% of the cohort falls into the “negative responder” subset. Parsing the sample by self-reported history of psychiatric diagnoses, results revealed a disproportionate prevalence of negative responses among those reporting a prior personality disorder diagnosis (31%). One multivariate regression model indicated a greater than four-fold elevated risk of adverse psychological responses to psychedelics in the personality disorder subsample ( b = 1.425, p < 0.05).

Conclusion: We infer that the presence of a personality disorder may represent an elevated risk for psychedelic use and hypothesize that the importance of psychological support and good therapeutic alliance may be increased in this population.

Comparable studies

Other observational and cohort studies on psychedelic-assisted therapy, most cited first.

Study Year Design Participants
Ketamine Assisted Psychotherapy (KAP): Patient Demographics, Clinical Data and Outcomes in Three Large Practices Administering Ketamine with Psychotherapy Patients in a private practice setting 2019 Observational study n = 235
MDMA-Assisted Psychotherapy Using Low Doses in a Small Sample of Women with Chronic Posttraumatic Stress Disorder Women with chronic PTSD secondary to sexual assault 2008 Observational cohort n = 6
The Peak Experience Variable in DPT-Assisted Psychotherapy with Cancer Patients Cancer patients 1977 Observational study n = 128
Acute subjective effects in LSD- and MDMA-assisted psychotherapy Patients with psychiatric disorders (posttraumatic stress disorder and major... 2020 Observational study n = 18
Antidepressant effects of a psychedelic experience in a large prospective naturalistic sample. Individuals with depressive symptoms planning a psychedelic experience in naturalistic... 2022 Observational cohort n = 302

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