Do classic psychedelics increase the risk of seizures? A scoping review
- PMID: 38917636
- DOI: 10.1016/j.euroneuro.2024.05.002
Do classic psychedelics increase the risk of seizures? A scoping review
Abstract
Seizures are a concerning adverse event frequently associated with the use of psychedelics, and hence, studies involving these substances tend to exclude patients with past history of epilepsy. This is especially relevant because epileptic seizures are markedly increased in the population suffering from mental disorders, and psychedelic assisted therapy is being researched as a promising treatment for several of them. To determine the extent of the current literature on the relationship between classic psychedelics and seizures, a scoping review was performed using the PRISMA-ScR (Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews). The search was conducted in PubMed, Web of Science, Google scholar, LILACS and Scielo, and both animal and human models were included. A total of 16 publications on humans, and 11 on animals, were found. The results are heterogeneous, but globally suggest that psychedelics may not increase the risk of seizures in healthy individuals or animals in the absence of other drugs. However, concomitant use of other substances or drugs, such as kambo or lithium, could increase the risk of seizures. Additionally, these conclusions are drawn from data lacking sufficient external validity, so they should be interpreted with caution. Future paths for research and a summary on possible neurobiological underpinnings that might clarify the relationship between classical psychedelics and seizures are also provided.
Keywords: Adverse events; Drug-related adverse reactions; Epilepsy; Hallucinogens; Psychedelics; Seizures.
Copyright © 2024 Elsevier B.V. and ECNP. All rights reserved.
Conflict of interest statement
Declaration of competing interest During the past three years, O.S.A has received travel awards (air tickets + hotel) for taking part in annual psychiatric meetings from Lundbeck and Janssen-Cilag. He also has acted as a speaker for Lundbeck, and as a consultant for MAPS Foundation. None of them are related to this publication. FJGL has received honararia and speaking fees from UCB Pharma, Angellini and Eisai, none of them related to the topic of the present manuscript. AF has received educational and travel support from Janssen-Cilag, Lundbeck and Rovi, and speaking fees from Abbott, unrelated to this study. The other authors report no conflicts of interest.
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