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迷幻辅助治疗中的知情同意

Informed Consent in Psychedelic-Assisted Therapy.

作者信息

Bradberry Mazdak M, Appelbaum Paul S, Gukasyan Natalie

机构信息

Department of Psychiatry, New York State Psychiatric Institute, Columbia University, New York, NY, USA.

出版信息

Curr Top Behav Neurosci. 2024 Dec 31. doi: 10.1007/7854_2024_559.

Abstract

Humans have long used classical serotonergic psychedelics, such as psilocybin, for a variety of purposes. Entactogens, such as methylenedioxymethamphetamine (MDMA), emerged during the twentieth century and have likewise seen use in a broad range of settings. Interest has arisen in the use of classical psychedelics and entactogens, together termed "psychedelics," for therapeutic purposes in Western clinical settings. Care in these settings is governed by standards for the communication and assumption of risk in the process of informed consent. Rigorous informed consent standards in psychedelic medicine are not only essential for quality care but also critical to the mitigation of risk, particularly in research settings and for vulnerable individuals. This chapter describes practical elements of informed consent in psychedelic therapy, with a focus on effective communication of the risks and potential benefits of classical psychedelic and entactogen treatments as they are currently understood.

摘要

长期以来,人类一直将经典的血清素能致幻剂,如裸盖菇素,用于各种目的。致幻剂,如亚甲二氧基甲基苯丙胺(摇头丸),在20世纪出现,同样在广泛的场景中被使用。在西方临床环境中,人们对将经典致幻剂和致幻剂(统称为“致幻剂”)用于治疗目的产生了兴趣。这些环境中的护理受知情同意过程中风险沟通和承担标准的约束。迷幻药医学中严格的知情同意标准不仅对高质量护理至关重要,而且对降低风险也至关重要,特别是在研究环境中以及对弱势群体而言。本章描述了迷幻疗法中知情同意的实际要素,重点是有效传达目前所理解的经典迷幻剂和致幻剂治疗的风险和潜在益处。

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