Suppr超能文献

在迷幻药医学中建立最佳实践和黄金标准的必要性。

The need for establishing best practices and gold standards in psychedelic medicine.

作者信息

Feduccia Allison, Agin-Liebes Gabby, Price Collin M, Grinsell Nicole, Paradise Summer, Rabin David M

机构信息

Psychedelic Support, Santa Cruz, CA, USA.

Department of Psychiatry, Weill Institute for Neurosciences, Neuroscape, University of California, San Francisco, CA, USA.

出版信息

J Affect Disord. 2023 Jul 1;332:47-54. doi: 10.1016/j.jad.2023.03.083. Epub 2023 Mar 30.

Abstract

Psychedelic substances are under investigation in several drug development programs. Controlled clinical trials are providing evidence for safe and effective use of psychedelic therapies for treating mental health conditions. With the anticipated FDA approval of MDMA-assisted therapy for posttraumatic stress disorder in 2023 and psilocybin therapy for depression disorders soon after, now is the time for the medical community to become informed on best practices and to actively participate in developing standards of care for these new treatments. Given the emergence of numerous drug sponsors and other companies developing therapeutic modalities for combination with psychedelic medications, it is essential that the medical professional field is at the forefront of communicating unbiased information related to safety and effectiveness. Gold standards have long been a part of medicine and serve to distinguish treatments and assessments as the highest quality by which all others can be compared to. For a treatment to be established as a gold standard, several factors are considered including the quantity and quality of the supporting data, the rigor of trials, and the safety and efficacy compared to other treatments. In this article, we review the origins of psychedelic-assisted therapy (PAT), minimum requirements for safe use of psychedelics, criteria for gold standards in mental health, and the nuances regarding how to establish gold standards in psychedelic medicine and guide clinical decision making.

摘要

目前有多项药物研发项目正在对迷幻物质进行研究。对照临床试验正在为迷幻疗法安全有效地治疗精神健康疾病提供证据。随着预计美国食品药品监督管理局(FDA)将于2023年批准MDMA辅助疗法用于治疗创伤后应激障碍,以及不久后批准裸盖菇素疗法用于治疗抑郁症,现在是医学界了解最佳实践并积极参与制定这些新疗法护理标准的时候了。鉴于众多药物赞助商和其他公司纷纷涌现,致力于开发与迷幻药物联合使用的治疗方式,医疗专业领域必须站在传达有关安全性和有效性的公正信息的前沿。长期以来,金标准一直是医学的一部分,用于区分治疗方法和评估手段,将其视为可与所有其他方法进行比较的最高质量标准。一种治疗方法要被确立为金标准,需要考虑几个因素,包括支持数据的数量和质量、试验的严谨性以及与其他治疗方法相比的安全性和有效性。在本文中,我们回顾了迷幻辅助疗法(PAT)的起源、安全使用迷幻药物的最低要求、精神健康领域金标准的标准,以及在迷幻医学中如何确立金标准并指导临床决策的细微差别。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验