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Meta-Analysis
. 2020 Dec;50(16):2655-2666.
doi: 10.1017/S003329172000389X. Epub 2020 Nov 4.

Post-acute psychological effects of classical serotonergic psychedelics: a systematic review and meta-analysis

Affiliations
Meta-Analysis

Post-acute psychological effects of classical serotonergic psychedelics: a systematic review and meta-analysis

Simon B Goldberg et al. Psychol Med. 2020 Dec.

Abstract

Background: Scientific interest in the therapeutic effects of classical psychedelics has increased in the past two decades. The psychological effects of these substances outside the period of acute intoxication have not been fully characterized. This study aimed to: (1) quantify the effects of psilocybin, ayahuasca, and lysergic acid diethylamide (LSD) on psychological outcomes in the post-acute period; (2) test moderators of these effects; and (3) evaluate adverse effects and risk of bias.

Methods: We conducted a systematic review and meta-analysis of experimental studies (single-group pre-post or randomized controlled trials) that involved administration of psilocybin, ayahuasca, or LSD to clinical or non-clinical samples and assessed psychological outcomes ⩾24 h post-administration. Effects were summarized by study design, timepoint, and outcome domain.

Results: A total of 34 studies (24 unique samples, n = 549, mean longest follow-up = 55.34 weeks) were included. Classical psychedelics showed significant within-group pre-post and between-group placebo-controlled effects on a range of outcomes including targeted symptoms within psychiatric samples, negative and positive affect-related measures, social outcomes, and existential/spiritual outcomes, with large between-group effect in these domains (Hedges' gs = 0.84 to 1.08). Moderator tests suggest some effects may be larger in clinical samples. Evidence of effects on big five personality traits and mindfulness was weak. There was no evidence of post-acute adverse effects.

Conclusions: High risk of bias in several domains, heterogeneity across studies, and indications of publication bias for some models highlight the need for careful, large-scale, placebo-controlled randomized trials.

Keywords: Anxiety; LSD; ayahuasca; depression; meta-analysis; psilocybin; psychedelics; psychological effects.

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Conflict of interest statement

Conflicts of Interest

In the prior 12 months, Charles L. Raison has served as a consultant for Usona Institute, Alkermes and Shire. All other authors declare that there is no conflict of interest.

Figures

Figure 1.
Figure 1.
PRISMA flow diagram
Figure 2.
Figure 2.
Cochrane risk of bias assessment. Random sequence = random sequence generation; Allocat Concealment = allocation concealment; Blinding Person/Partic = blinding of personnel and participants; Blind Outcome = blinding of outcome assessment; Attrition bias = incomplete outcome data.
Figure 3.
Figure 3.
Forest plots displaying effects of classical psychedelics across psychological outcome domains. Each point represents an effect size estimates (Hedges’ g units) and a corresponding 95% confidence interval. Targeted sx = targeted symptoms within psychiatric samples; Depression = depression outcomes restricted to samples with depression; Neg = negative; Pos = positive; Exist/spirit = Existential / spiritual; ES = effect size in Hedges’ g units; FU = follow-up; NA = not available.

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