Perspect Biol Med. 2023;66(1):129-144. doi: 10.1353/pbm.2023.0007.
Recent clinical trials of psychedelic drugs aim to treat a range of psychiatric conditions in adults. MDMA and psilocybin administered with psychotherapy have received FDA designation as "breakthrough therapies" for post-traumatic stress disorder (PTSD) and treatment-resistant depression (TRD) respectively. Given the potential benefit for minors burdened with many of the same disorders, calls to expand experimentation to minors are inevitable. This essay examines psychedelic research conducted on children from 1959 to 1974, highlighting methodological and ethical flaws. It provides ethics and policy recommendations for psychedelics research involving children and adolescents, including recognizing that the psychedelic experience is an ineffable one that makes informed proxy consent for parents, guardians, and others especially challenging. Psychedelic experiences are associated with novel benefits and risks, such as significant personality changes, shifts in fundamental values, and possible re-exposure to traumatic memories. These effects may alter the process of personality development in minors. Recommendations for ethically sound psychedelics research in minors include strict adherence to eligibility criteria, including a comprehensive family and individual psychiatric, substance use, and trauma history. An age-appropriate assent process that includes considerations related to the use of therapeutic touch should be developed. In addition, oversight by data safety monitoring boards and patient and family advocates, coupled with the adoption of pharmacoequity best practices, will help to ensure safety and fairness of psychedelics research in children.
最近的迷幻药物临床试验旨在治疗成年人的一系列精神疾病。与心理疗法一起使用的 MDMA 和裸盖菇素分别被 FDA 指定为创伤后应激障碍 (PTSD) 和治疗抵抗性抑郁症 (TRD) 的“突破性疗法”。鉴于许多未成年人也患有这些疾病,呼吁将实验扩大到未成年人是不可避免的。本文考察了 1959 年至 1974 年对儿童进行的迷幻药研究,强调了其中的方法学和伦理缺陷。它为涉及儿童和青少年的迷幻药研究提供了伦理和政策建议,包括认识到迷幻体验是一种难以言喻的体验,使得父母、监护人或其他人为其提供知情代理同意特别具有挑战性。迷幻体验与新的益处和风险相关,例如人格的重大变化、基本价值观的转变,以及可能重新暴露于创伤性记忆。这些影响可能会改变未成年人的人格发展过程。对未成年人进行合理迷幻药研究的建议包括严格遵守包括全面的家庭和个人精神病学、物质使用和创伤史在内的资格标准。应制定适合年龄的同意程序,其中包括与治疗性触摸使用相关的考虑因素。此外,数据安全监测委员会、患者和家庭倡导者的监督,以及采用药物公平最佳实践,将有助于确保儿童迷幻药研究的安全性和公平性。