Past Is Prologue: Ethical Issues in Pediatric Psychedelics Research and Treatment.

IF 0.8 4区 医学 Q2 HISTORY & PHILOSOPHY OF SCIENCE
Gail A Edelsohn, Dominic Sisti
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引用次数: 0

Abstract

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.

过去是序幕:儿童致幻剂研究和治疗中的伦理问题
摘要:最近的迷幻药临床试验旨在治疗成人的一系列精神疾病。MDMA和裸盖菇素联合心理治疗已分别被美国食品药品监督管理局指定为创伤后应激障碍(PTSD)和难治性抑郁症(TRD)的“突破性疗法”。考虑到对患有许多相同疾病的未成年人的潜在益处,将实验扩大到未成年人的呼声是不可避免的。本文考察了1959年至1974年对儿童进行的迷幻研究,强调了方法论和伦理上的缺陷。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,包括认识到迷幻药体验是一种难以言喻的体验,这使得父母、监护人和其他人的知情代理同意尤其具有挑战性。迷幻经历与新的好处和风险有关,例如显著的性格变化、基本价值观的转变,以及可能再次接触创伤记忆。这些影响可能会改变未成年人的人格发展过程。对未成年人进行合乎道德的迷幻药研究的建议包括严格遵守资格标准,包括全面的家庭和个人精神病、药物使用和创伤史。应该制定一个适合年龄的同意程序,其中包括与使用治疗触摸相关的考虑因素。此外,数据安全监测委员会、患者和家庭倡导者的监督,加上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。
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来源期刊
Perspectives in Biology and Medicine
Perspectives in Biology and Medicine 医学-科学史与科学哲学
CiteScore
1.40
自引率
20.00%
发文量
42
审稿时长
>12 weeks
期刊介绍: Perspectives in Biology and Medicine, an interdisciplinary scholarly journal whose readers include biologists, physicians, students, and scholars, publishes essays that place important biological or medical subjects in broader scientific, social, or humanistic contexts. These essays span a wide range of subjects, from biomedical topics such as neurobiology, genetics, and evolution, to topics in ethics, history, philosophy, and medical education and practice. The editors encourage an informal style that has literary merit and that preserves the warmth, excitement, and color of the biological and medical sciences.
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