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

Joost J Breeksema, Bouwe W Kuin, Jeanine Kamphuis, Wim van den Brink, Eric Vermetten, Robert A Schoevers
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引用次数: 25

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.

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5 -羟色胺类致幻剂和MDMA临床治疗的不良事件:一项混合方法的系统综述。
导读:小规模的临床研究表明,迷幻药在治疗几种精神障碍方面有很好的效果。在迷幻药成为注册药物之前,了解所有不良事件(ae)以做出平衡的治疗决定是很重要的。目的:系统回顾临床研究中5 -羟色胺类致幻剂和3,4-甲基二氧基甲基苯丙胺(MDMA)给药期间和之后的不良反应。方法:我们系统地检索PubMed、PsycINFO、Embase和ClinicalTrials.gov,检索自2000年以来描述定量和定性研究结果的致幻剂临床试验。结果:我们纳入了44篇文章(34篇定量+ 10篇定性),描述了598例独特患者使用MDMA和5 -羟色胺能致幻剂(裸盖菇素、麦角酸二乙胺和死藤水)的治疗方法。在许多研究中,ae没有被系统地评估。尽管存在这些限制,但治疗总体上似乎耐受性良好。恶心、头痛和焦虑是诊断和化合物中常见的急性不良反应。晚期ae包括头痛(裸盖菇素、MDMA)、疲劳、情绪低落和焦虑(MDMA)。服用MDMA期间发生1例严重AE(室性早搏增加,需短暂住院治疗);没有其他不良事件需要医疗干预。定性研究表明,心理上具有挑战性的经历也可能对治疗有益。除死藤水外,大部分患者在进入研究前都有过服用迷幻药的经历。结论:由于研究设计(缺乏对ae的系统评估)和样本选择,在致幻剂治疗的背景下,ae的定义不明确,并且可能在文献中被低估。急性挑战经历可能具有治疗意义,但要更好地了解迷幻药治疗背景下的ae,需要系统和详细的报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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