跨性别和非二元手术登记处:建立一个以患者为中心的生殖器性别确认手术登记处

IF 2 4区 医学 Q1 Social Sciences
Transgender Health Pub Date : 2024-10-09 eCollection Date: 2024-10-01 DOI:10.1089/trgh.2022.0111
Geolani W Dy, Gaines Blasdel, Daniel Dugi, Christi Butler, James M Hotaling, Jeremy B Myers, Isak Goodwin, Rachel Bluebond-Langner, Lee C Zhao, Cori A Agarwal
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引用次数: 0

摘要

目的:有关生殖器性别确认手术(GGAS)的长期临床和患者报告结果(PROs)的高质量数据还很缺乏,变性人和非二元性(TGNB)群体的声音历来没有被纳入研究发展中。这些因素限制了目前的研究在指导患者、临床医生、付款人和其他 GGAS 利益相关者进行决策时的效用。变性和非二元手术(TRANS)登记处的开发旨在满足 GGAS 利益相关者的需求,并解决传统 GGAS 研究的局限性:TRANS 注册表的开发分为几个开发阶段,从 2019 年 5 月开始至今。在这些阶段中,利益相关者始终参与其中,包括:确定关键临床结果和PROs,在电子健康记录(EHR)中创建和实施数据收集工具,以及开发集中式登记基础设施:TRANS 登记处是一个前瞻性观察登记处,登记对象为寻求阴道成形术和外阴成形术的患者。电子病历支持的基础设施允许患者和临床医生向 TRANS 登记处提供纵向结果数据。我们介绍了社区参与设计 TRANS 注册表的方法,包括经验教训、挑战和未来方向:TRANS 登记处是首个使用电子病历支持方法对寻求阴道整形术和外阴整形术的个人健康状况进行前瞻性跟踪的多中心倡议,TGNB 社区成员和临床医生作为合作伙伴参与了这一过程。这一过程可作为需要高质量纵向结果数据的其他新兴领域的登记发展模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transgender and Non-Binary Surgery Registry: Building a Patient-Focused Registry for Genital Gender Affirming Surgery.

Purpose: High quality data regarding long-term clinical and patient-reported outcomes (PROs) of genital gender-affirming surgery (GGAS) are lacking, and transgender and non-binary (TGNB) community voices have not historically been included in research development. These factors limit the utility of current research for guiding patients, clinicians, payers, and other GGAS stakeholders in decision-making. The Transgender and Non-Binary Surgery (TRANS) Registry has been developed to meet the needs of GGAS stakeholders and address limitations of traditional GGAS research.

Methods: Development of the TRANS Registry occurred over several developmental phases beginning in May 2019 to present. Stakeholder engagement was performed throughout these phases, including: determination of key clinical outcomes and PROs, creation and implementation of data collection tools within the electronic health record (EHR), and development of centralized registry infrastructure.

Results: The TRANS Registry is a prospective observational registry of individuals seeking vaginoplasty and vulvoplasty. The EHR-enabled infrastructure allows patients and clinicians to contribute longitudinal outcomes data to the TRANS Registry. We describe our community engaged approach to designing the TRANS Registry, including lessons learned, challenges, and future directions.

Conclusions: The TRANS Registry is the first multicenter initiative to prospectively track the health of individuals seeking vaginoplasty and vulvoplasty using EHR-enabled methods, engaging TGNB community members and clinicians as partners in the process. This process may be used as a model for registry development in other emerging fields where high-quality longitudinal outcomes data are needed.

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来源期刊
Transgender Health
Transgender Health Social Sciences-Gender Studies
CiteScore
4.30
自引率
10.00%
发文量
122
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