Uniformed University of Health Sciences, Bethesda, Maryland.
Wholeness Center, Fort Collins.
Curr Opin Psychiatry. 2024 Jul 1;37(4):277-281. doi: 10.1097/YCO.0000000000000946. Epub 2024 May 7.
The pace of psychedelic treatments continues to increase. Regulation and coherent clinical guidance have not been established. A philosophical divide limits effective resolution of a practice delivery quandary: is this primarily a pharmacological or psychotherapeutic intervention?
Lykos (formerly MAPS) has submitted its new drug application (NDA) request to the FDA for 3-4-methylenedioxymethamphetamine (MDMA)-assisted psychotherapy for PTSD and is expecting a response by the summer of 2024. Australia endorsed psilocybin and MDMA for regulated use in 2023. Multiple phase II and III clinical trials are also being conducted in the United States and Europe to study the use of psilocybin. Currently, Colorado and Oregon have legalized psilocybin in different manners. In Colorado, plants containing psilocybin, ibogaine, dimethyltryptamine (DMT) and mescaline (other than peyote) are now legal to possess, share and cultivate. Guidelines for regulated treatment with psilocybin containing mushrooms are in process with service delivery to begin early in 2025. In Oregon, clients must complete a preparation session with a licensed facilitator before consuming psilocybin products at a licensed service center. A prescription is not required. It is expected that other states will follow suit with a ballot measure likely in Massachusetts this year. Additionally, in the United States, the DEA, state boards, pharmaceutical distributors, and professional liability carriers all share mounting concerns about the in-home use of compounded ketamine used as a psychedelic therapeutic via remote prescribing.
Psychedelic treatments are rapidly entering the mainstream of medical care delivery in the United States. Clinical guidelines are urgently needed to ensure well tolerated practice and coherent regulation. The delivery of this guidance is limited by a core philosophical disagreement. Resolution of this conflict will be needed to deliver coherent clinical guidelines. Current research and clinical experience provide a solid foundation for practical clinical guidance and the introduction of psychedelics into healthcare.
迷幻药物治疗的步伐持续加快,但尚未建立监管和连贯的临床指导。哲学上的分歧限制了实践困境的有效解决:这主要是一种药理学干预还是心理治疗干预?
Lykos(前身为 MAPS)已向 FDA 提交了用于 PTSD 的 3,4-亚甲二氧基甲基苯丙胺(MDMA)辅助心理治疗的新药申请(NDA),预计将于 2024 年夏季做出回应。澳大利亚于 2023 年批准了迷幻蘑菇和 MDMA 的监管使用。美国和欧洲也正在进行多项 2 期和 3 期临床试验,以研究使用迷幻蘑菇。目前,科罗拉多州和俄勒冈州以不同的方式将迷幻蘑菇合法化。在科罗拉多州,含有迷幻蘑菇、伊博加因、二甲色胺(DMT)和三甲氧苯乙胺(除了佩奥特碱)的植物现在可以合法拥有、分享和种植。含有迷幻蘑菇的受监管治疗指南正在制定中,预计将于 2025 年初开始提供服务。在俄勒冈州,客户在获得许可的服务中心使用含有迷幻蘑菇的产品之前,必须先与持牌治疗师完成准备课程。不需要处方。预计其他州也将效仿,今年马萨诸塞州可能会进行投票。此外,在美国,DEA、州委员会、药品分销商和专业责任承保人都对通过远程处方在家中使用复合氯胺酮作为迷幻治疗药物表示担忧。
迷幻药物治疗在美国迅速成为医疗保健提供的主流。迫切需要临床指南以确保耐受良好的实践和连贯的监管。提供这种指导的局限性在于核心哲学分歧。解决这一冲突将需要制定连贯的临床指南。当前的研究和临床经验为实用的临床指导和将迷幻药物引入医疗保健提供了坚实的基础。