Adverse events in clinical treatments with serotonergic psychedelics and MDMA: A mixed-methods systematic review

Introduction: Small-scale clinical studies with psychedelic drugs have shown promising results for the treatment of several mental disorders. Before psychedelics become registered medicines, it is important to know the full range of adverse events (AEs) for making balanced treatment decisions. Objec...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of Psychopharmacology 2022-10, Vol.36 (10), p.1100-1117
Hauptverfasser: Breeksema, Joost J, Kuin, Bouwe W, Kamphuis, Jeanine, van den Brink, Wim, Vermetten, Eric, Schoevers, Robert A
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1117
container_issue 10
container_start_page 1100
container_title Journal of Psychopharmacology
container_volume 36
creator Breeksema, Joost J
Kuin, Bouwe W
Kamphuis, Jeanine
van den Brink, Wim
Vermetten, Eric
Schoevers, Robert A
description Introduction: Small-scale clinical studies with psychedelic drugs have shown promising results for the treatment of several mental disorders. Before psychedelics become registered medicines, it is important to know the full range of adverse events (AEs) for making balanced treatment decisions. Objective: To systematically review the presence of AEs during and after administration of serotonergic psychedelics and 3,4-methyenedioxymethamphetamine (MDMA) in clinical studies. Methods: We systematically searched PubMed, PsycINFO, Embase, and ClinicalTrials.gov for clinical trials with psychedelics since 2000 describing the results of quantitative and qualitative studies. Results: We included 44 articles (34 quantitative + 10 qualitative), describing treatments with MDMA and serotonergic psychedelics (psilocybin, lysergic acid diethylamide, and ayahuasca) in 598 unique patients. In many studies, AEs were not systematically assessed. Despite this limitation, treatments seemed to be overall well tolerated. Nausea, headaches, and anxiety were commonly reported acute AEs across diagnoses and compounds. Late AEs included headaches (psilocybin, MDMA), fatigue, low mood, and anxiety (MDMA). One serious AE occurred during MDMA administration (increase in premature ventricular contractions requiring brief hospitalization); no other AEs required medical intervention. Qualitative studies suggested that psychologically challenging experiences may also be therapeutically beneficial. Except for ayahuasca, a large proportion of patients had prior experience with psychedelic drugs before entering studies. Conclusions: AEs are poorly defined in the context of psychedelic treatments and are probably underreported in the literature due to study design (lack of systematic assessment of AEs) and sample selection. Acute challenging experiences may be therapeutically meaningful, but a better understanding of AEs in the context of psychedelic treatments requires systematic and detailed reporting.
doi_str_mv 10.1177/02698811221116926
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9548934</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_02698811221116926</sage_id><sourcerecordid>2707602546</sourcerecordid><originalsourceid>FETCH-LOGICAL-c443t-7e88cea7131462c5f4cbaa2e2fef5b1125b6d47a30c6d75a737bd74e6ac060c73</originalsourceid><addsrcrecordid>eNp1kcFuEzEQhi1URNPCA_RmiUsvW2yv195wQIpKWyq14gJny2vPJq5218HjpOTt65AKVBAnSzPf98u_hpAzzi441_oDE2retpwLwTlXc6FekRmXildatM0Rme331R44JieID4xxJVXzhhzXihW_lTOyXvgtJAQKW5gy0jBRN4QpODvQnMDm8df4MeQVRUgxxwnSMji6xp1bgYchOKR28vT-8_3iI13QMfwEX42QV9EjxR1mGG0uRoJtgMe35HVvB4R3z-8p-X599e3yS3X39eb2cnFXOSnrXGloWwdW87oUEq7ppeusFSB66JuuVG465aW2NXPK68bqWndeS1DWMcWcrk_Jp0PuetON4F2pkexg1imMNu1MtMG83ExhZZZxa-aNbOe1LAHnzwEp_tgAZjMGdDAMdoK4QSM004qJRqqCvv8LfYibNJV6hRJCac4ULxQ_UC5FxAT9789wZvb3NP_cszgXBwftEv6k_l94AlukoHg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2722671061</pqid></control><display><type>article</type><title>Adverse events in clinical treatments with serotonergic psychedelics and MDMA: A mixed-methods systematic review</title><source>SAGE Publications</source><creator>Breeksema, Joost J ; Kuin, Bouwe W ; Kamphuis, Jeanine ; van den Brink, Wim ; Vermetten, Eric ; Schoevers, Robert A</creator><creatorcontrib>Breeksema, Joost J ; Kuin, Bouwe W ; Kamphuis, Jeanine ; van den Brink, Wim ; Vermetten, Eric ; Schoevers, Robert A</creatorcontrib><description>Introduction: Small-scale clinical studies with psychedelic drugs have shown promising results for the treatment of several mental disorders. Before psychedelics become registered medicines, it is important to know the full range of adverse events (AEs) for making balanced treatment decisions. Objective: To systematically review the presence of AEs during and after administration of serotonergic psychedelics and 3,4-methyenedioxymethamphetamine (MDMA) in clinical studies. Methods: We systematically searched PubMed, PsycINFO, Embase, and ClinicalTrials.gov for clinical trials with psychedelics since 2000 describing the results of quantitative and qualitative studies. Results: We included 44 articles (34 quantitative + 10 qualitative), describing treatments with MDMA and serotonergic psychedelics (psilocybin, lysergic acid diethylamide, and ayahuasca) in 598 unique patients. In many studies, AEs were not systematically assessed. Despite this limitation, treatments seemed to be overall well tolerated. Nausea, headaches, and anxiety were commonly reported acute AEs across diagnoses and compounds. Late AEs included headaches (psilocybin, MDMA), fatigue, low mood, and anxiety (MDMA). One serious AE occurred during MDMA administration (increase in premature ventricular contractions requiring brief hospitalization); no other AEs required medical intervention. Qualitative studies suggested that psychologically challenging experiences may also be therapeutically beneficial. Except for ayahuasca, a large proportion of patients had prior experience with psychedelic drugs before entering studies. Conclusions: AEs are poorly defined in the context of psychedelic treatments and are probably underreported in the literature due to study design (lack of systematic assessment of AEs) and sample selection. Acute challenging experiences may be therapeutically meaningful, but a better understanding of AEs in the context of psychedelic treatments requires systematic and detailed reporting.</description><identifier>ISSN: 0269-8811</identifier><identifier>EISSN: 1461-7285</identifier><identifier>DOI: 10.1177/02698811221116926</identifier><identifier>PMID: 36017784</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Adverse events ; Anxiety ; Clinical trials ; Drug abuse ; Ecstasy ; Headache ; Lysergide ; MDMA ; Mental disorders ; Mixed methods research ; Nausea ; Patients ; Psilocybin ; Psychedelic drugs ; Review ; Systematic review ; Ventricle</subject><ispartof>Journal of Psychopharmacology, 2022-10, Vol.36 (10), p.1100-1117</ispartof><rights>The Author(s) 2022</rights><rights>The Author(s) 2022 2022 British Association for Psychopharmacology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-7e88cea7131462c5f4cbaa2e2fef5b1125b6d47a30c6d75a737bd74e6ac060c73</citedby><cites>FETCH-LOGICAL-c443t-7e88cea7131462c5f4cbaa2e2fef5b1125b6d47a30c6d75a737bd74e6ac060c73</cites><orcidid>0000-0002-8787-4610 ; 0000-0003-0579-4404</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/02698811221116926$$EPDF$$P50$$Gsage$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/02698811221116926$$EHTML$$P50$$Gsage$$Hfree_for_read</linktohtml><link.rule.ids>230,313,314,776,780,788,881,21798,27899,27901,27902,43597,43598</link.rule.ids></links><search><creatorcontrib>Breeksema, Joost J</creatorcontrib><creatorcontrib>Kuin, Bouwe W</creatorcontrib><creatorcontrib>Kamphuis, Jeanine</creatorcontrib><creatorcontrib>van den Brink, Wim</creatorcontrib><creatorcontrib>Vermetten, Eric</creatorcontrib><creatorcontrib>Schoevers, Robert A</creatorcontrib><title>Adverse events in clinical treatments with serotonergic psychedelics and MDMA: A mixed-methods systematic review</title><title>Journal of Psychopharmacology</title><addtitle>J Psychopharmacol</addtitle><description>Introduction: Small-scale clinical studies with psychedelic drugs have shown promising results for the treatment of several mental disorders. Before psychedelics become registered medicines, it is important to know the full range of adverse events (AEs) for making balanced treatment decisions. Objective: To systematically review the presence of AEs during and after administration of serotonergic psychedelics and 3,4-methyenedioxymethamphetamine (MDMA) in clinical studies. Methods: We systematically searched PubMed, PsycINFO, Embase, and ClinicalTrials.gov for clinical trials with psychedelics since 2000 describing the results of quantitative and qualitative studies. Results: We included 44 articles (34 quantitative + 10 qualitative), describing treatments with MDMA and serotonergic psychedelics (psilocybin, lysergic acid diethylamide, and ayahuasca) in 598 unique patients. In many studies, AEs were not systematically assessed. Despite this limitation, treatments seemed to be overall well tolerated. Nausea, headaches, and anxiety were commonly reported acute AEs across diagnoses and compounds. Late AEs included headaches (psilocybin, MDMA), fatigue, low mood, and anxiety (MDMA). One serious AE occurred during MDMA administration (increase in premature ventricular contractions requiring brief hospitalization); no other AEs required medical intervention. Qualitative studies suggested that psychologically challenging experiences may also be therapeutically beneficial. Except for ayahuasca, a large proportion of patients had prior experience with psychedelic drugs before entering studies. Conclusions: AEs are poorly defined in the context of psychedelic treatments and are probably underreported in the literature due to study design (lack of systematic assessment of AEs) and sample selection. Acute challenging experiences may be therapeutically meaningful, but a better understanding of AEs in the context of psychedelic treatments requires systematic and detailed reporting.</description><subject>Adverse events</subject><subject>Anxiety</subject><subject>Clinical trials</subject><subject>Drug abuse</subject><subject>Ecstasy</subject><subject>Headache</subject><subject>Lysergide</subject><subject>MDMA</subject><subject>Mental disorders</subject><subject>Mixed methods research</subject><subject>Nausea</subject><subject>Patients</subject><subject>Psilocybin</subject><subject>Psychedelic drugs</subject><subject>Review</subject><subject>Systematic review</subject><subject>Ventricle</subject><issn>0269-8811</issn><issn>1461-7285</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><recordid>eNp1kcFuEzEQhi1URNPCA_RmiUsvW2yv195wQIpKWyq14gJny2vPJq5218HjpOTt65AKVBAnSzPf98u_hpAzzi441_oDE2retpwLwTlXc6FekRmXildatM0Rme331R44JieID4xxJVXzhhzXihW_lTOyXvgtJAQKW5gy0jBRN4QpODvQnMDm8df4MeQVRUgxxwnSMji6xp1bgYchOKR28vT-8_3iI13QMfwEX42QV9EjxR1mGG0uRoJtgMe35HVvB4R3z-8p-X599e3yS3X39eb2cnFXOSnrXGloWwdW87oUEq7ppeusFSB66JuuVG465aW2NXPK68bqWndeS1DWMcWcrk_Jp0PuetON4F2pkexg1imMNu1MtMG83ExhZZZxa-aNbOe1LAHnzwEp_tgAZjMGdDAMdoK4QSM004qJRqqCvv8LfYibNJV6hRJCac4ULxQ_UC5FxAT9789wZvb3NP_cszgXBwftEv6k_l94AlukoHg</recordid><startdate>20221001</startdate><enddate>20221001</enddate><creator>Breeksema, Joost J</creator><creator>Kuin, Bouwe W</creator><creator>Kamphuis, Jeanine</creator><creator>van den Brink, Wim</creator><creator>Vermetten, Eric</creator><creator>Schoevers, Robert A</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>AFRWT</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8787-4610</orcidid><orcidid>https://orcid.org/0000-0003-0579-4404</orcidid></search><sort><creationdate>20221001</creationdate><title>Adverse events in clinical treatments with serotonergic psychedelics and MDMA: A mixed-methods systematic review</title><author>Breeksema, Joost J ; Kuin, Bouwe W ; Kamphuis, Jeanine ; van den Brink, Wim ; Vermetten, Eric ; Schoevers, Robert A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-7e88cea7131462c5f4cbaa2e2fef5b1125b6d47a30c6d75a737bd74e6ac060c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adverse events</topic><topic>Anxiety</topic><topic>Clinical trials</topic><topic>Drug abuse</topic><topic>Ecstasy</topic><topic>Headache</topic><topic>Lysergide</topic><topic>MDMA</topic><topic>Mental disorders</topic><topic>Mixed methods research</topic><topic>Nausea</topic><topic>Patients</topic><topic>Psilocybin</topic><topic>Psychedelic drugs</topic><topic>Review</topic><topic>Systematic review</topic><topic>Ventricle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Breeksema, Joost J</creatorcontrib><creatorcontrib>Kuin, Bouwe W</creatorcontrib><creatorcontrib>Kamphuis, Jeanine</creatorcontrib><creatorcontrib>van den Brink, Wim</creatorcontrib><creatorcontrib>Vermetten, Eric</creatorcontrib><creatorcontrib>Schoevers, Robert A</creatorcontrib><collection>SAGE Open Access Journals</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Psychopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Breeksema, Joost J</au><au>Kuin, Bouwe W</au><au>Kamphuis, Jeanine</au><au>van den Brink, Wim</au><au>Vermetten, Eric</au><au>Schoevers, Robert A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adverse events in clinical treatments with serotonergic psychedelics and MDMA: A mixed-methods systematic review</atitle><jtitle>Journal of Psychopharmacology</jtitle><addtitle>J Psychopharmacol</addtitle><date>2022-10-01</date><risdate>2022</risdate><volume>36</volume><issue>10</issue><spage>1100</spage><epage>1117</epage><pages>1100-1117</pages><issn>0269-8811</issn><eissn>1461-7285</eissn><abstract>Introduction: Small-scale clinical studies with psychedelic drugs have shown promising results for the treatment of several mental disorders. Before psychedelics become registered medicines, it is important to know the full range of adverse events (AEs) for making balanced treatment decisions. Objective: To systematically review the presence of AEs during and after administration of serotonergic psychedelics and 3,4-methyenedioxymethamphetamine (MDMA) in clinical studies. Methods: We systematically searched PubMed, PsycINFO, Embase, and ClinicalTrials.gov for clinical trials with psychedelics since 2000 describing the results of quantitative and qualitative studies. Results: We included 44 articles (34 quantitative + 10 qualitative), describing treatments with MDMA and serotonergic psychedelics (psilocybin, lysergic acid diethylamide, and ayahuasca) in 598 unique patients. In many studies, AEs were not systematically assessed. Despite this limitation, treatments seemed to be overall well tolerated. Nausea, headaches, and anxiety were commonly reported acute AEs across diagnoses and compounds. Late AEs included headaches (psilocybin, MDMA), fatigue, low mood, and anxiety (MDMA). One serious AE occurred during MDMA administration (increase in premature ventricular contractions requiring brief hospitalization); no other AEs required medical intervention. Qualitative studies suggested that psychologically challenging experiences may also be therapeutically beneficial. Except for ayahuasca, a large proportion of patients had prior experience with psychedelic drugs before entering studies. Conclusions: AEs are poorly defined in the context of psychedelic treatments and are probably underreported in the literature due to study design (lack of systematic assessment of AEs) and sample selection. Acute challenging experiences may be therapeutically meaningful, but a better understanding of AEs in the context of psychedelic treatments requires systematic and detailed reporting.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>36017784</pmid><doi>10.1177/02698811221116926</doi><tpages>18</tpages><orcidid>https://orcid.org/0000-0002-8787-4610</orcidid><orcidid>https://orcid.org/0000-0003-0579-4404</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0269-8811
ispartof Journal of Psychopharmacology, 2022-10, Vol.36 (10), p.1100-1117
issn 0269-8811
1461-7285
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9548934
source SAGE Publications
subjects Adverse events
Anxiety
Clinical trials
Drug abuse
Ecstasy
Headache
Lysergide
MDMA
Mental disorders
Mixed methods research
Nausea
Patients
Psilocybin
Psychedelic drugs
Review
Systematic review
Ventricle
title Adverse events in clinical treatments with serotonergic psychedelics and MDMA: A mixed-methods systematic review
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T19%3A18%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Adverse%20events%20in%20clinical%20treatments%20with%20serotonergic%20psychedelics%20and%20MDMA:%20A%20mixed-methods%20systematic%20review&rft.jtitle=Journal%20of%20Psychopharmacology&rft.au=Breeksema,%20Joost%20J&rft.date=2022-10-01&rft.volume=36&rft.issue=10&rft.spage=1100&rft.epage=1117&rft.pages=1100-1117&rft.issn=0269-8811&rft.eissn=1461-7285&rft_id=info:doi/10.1177/02698811221116926&rft_dat=%3Cproquest_pubme%3E2707602546%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2722671061&rft_id=info:pmid/36017784&rft_sage_id=10.1177_02698811221116926&rfr_iscdi=true