A taxonomy of regulatory and policy matters relevant to psychedelic-assisted therapy in Australia

Samuel P Hatfield, Nicollette LR Thornton, Kayla Greenstien, Nick Glozier
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Abstract

Objectives:The Australian government recently rescheduled psilocybin and 3,4-methylenedioxymethamphetamine for limited clinical uses. This change has raised various regulatory concerns and challenges for the field of psychedelic-assisted therapy. To provide clarity, we aimed to comprehensively catalogue the matters relating to psychedelic-assisted therapy that are or could be regulated.Methods:We conducted a desktop review of the literature and current regulatory sources, semi-structured interviews with professionals who had expertise in fields relating to psychedelic-assisted therapy and a framework analysis to generate a taxonomy of relevant regulatory matters. In relation to each matter, we further identified what type of regulation (if any) currently applies to that matter, any uncertainty as to how the matter should be addressed in clinical practice in the context of current regulation and whether there are conflicting views as to how the matter could or should be further regulated.Results:The taxonomy is structured into six main regulatory domains, three of which have a substantial proportion of matters with uncertainty or conflicting views: Service Establishment, Practitioner, and Treatment Delivery. Key examples of such matters include the location of services and facilities required, which professionals are eligible to become psychedelic therapists, and with what qualifications and experience. Matters in the remaining three domains, Patient Evaluation, Drug Supply and Service Oversight, appear by comparison relatively settled, with regulation either well-established or thought unnecessary.Conclusions:The taxonomy provides a roadmap for health services establishing and implementing a psychedelic-assisted therapy program, or for government and other policymakers when determining areas that may require further regulation.
澳大利亚与迷幻药辅助疗法有关的监管和政策事项分类法
目的:澳大利亚政府最近将迷幻药和 3,4-亚甲二氧基甲基苯丙胺重新列入限制临床使用的目录。这一变化给迷幻药辅助治疗领域带来了各种监管问题和挑战。方法:我们对文献和当前监管来源进行了桌面审查,对在迷幻辅助疗法相关领域拥有专业知识的专业人士进行了半结构化访谈,并进行了框架分析,从而对相关监管事项进行了分类。对于每个事项,我们进一步确定了目前适用于该事项的监管类型(如果有的话)、在当前监管背景下临床实践中应如何处理该事项的不确定性,以及对于该事项可以或应该如何进一步监管是否存在相互冲突的观点:服务机构、从业人员和治疗提供。这些事项的主要例子包括服务地点和所需设施、哪些专业人员有资格成为迷幻治疗师、具备哪些资格和经验。结论:分类法为医疗服务机构建立和实施迷幻辅助治疗项目提供了路线图,也为政府和其他政策制定者确定可能需要进一步监管的领域提供了参考。
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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