What Is the Aim of PEDIATRIC “Gender-Affirming” Care?

IF 2.3 3区 哲学 Q1 ETHICS Hastings Center Report Pub Date : 2024-06-06 DOI:10.1002/hast.1583
Moti Gorin
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Abstract

The original “Dutch Protocol”—the treatment model comprised of puberty blockers, cross-sex hormones, and surgery—was intended to improve the mental and physical health of pediatric patients experiencing distress over their sexed bodies. Consequently, both researchers and clinicians have couched eligibility for treatment and measures of treatment efficacy in terms of the interventions’ effects on outcomes such as gender dysphoria, depression, anxiety, and suicide. However, recent systematic reviews have concluded that the scientific evidence supporting these interventions is uncertain, leading to significant international differences in what treatments are offered to youth. Against this backdrop, a different argumentative approach has emerged in support of gender-affirming care. This approach appeals not to reductions in patient morbidity or mortality but to patient autonomy, where medical intervention is pursued as a means to the satisfaction of a patient's “embodiment goals.” In this article, I raise objections to autonomy-based justifications for pediatric gender-affirming care, concluding that these arguments misunderstand the place of autonomy in clinical decision-making and, consequently, put patients at risk of medical harm.

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儿科 "性别确认 "护理的目的是什么?
最初的 "荷兰方案"--由青春期阻断剂、异性荷尔蒙和手术组成的治疗模式--旨在改善因性别身体而苦恼的儿科患者的身心健康。因此,研究人员和临床医生都以干预措施对性别焦虑症、抑郁症、焦虑症和自杀等结果的影响来衡量治疗资格和疗效。然而,最近的系统性综述得出结论,支持这些干预措施的科学证据并不确定,导致国际上在为青少年提供何种治疗方面存在显著差异。在此背景下,出现了一种不同的论证方法来支持性别确认护理。这种方法呼吁的不是降低病人的发病率或死亡率,而是病人的自主权,即医疗干预是满足病人 "体现目标 "的一种手段。在这篇文章中,我对基于自主权的儿科性别确认护理理由提出了反对意见,并得出结论认为,这些论点误解了自主权在临床决策中的地位,从而使患者面临医疗伤害的风险。
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来源期刊
Hastings Center Report
Hastings Center Report 医学-卫生保健
CiteScore
3.50
自引率
3.00%
发文量
99
审稿时长
6-12 weeks
期刊介绍: The Hastings Center Report explores ethical, legal, and social issues in medicine, health care, public health, and the life sciences. Six issues per year offer articles, essays, case studies of bioethical problems, columns on law and policy, caregivers’ stories, peer-reviewed scholarly articles, and book reviews. Authors come from an assortment of professions and academic disciplines and express a range of perspectives and political opinions. The Report’s readership includes physicians, nurses, scholars, administrators, social workers, health lawyers, and others.
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