International study to develop a patient-reported outcome measure to evaluate outcomes of gender-affirming care - the GENDER-Q.

IF 2.4 Q2 HEALTH CARE SCIENCES & SERVICES Journal of Patient-Reported Outcomes Pub Date : 2024-11-19 DOI:10.1186/s41687-024-00785-x
Manraj N Kaur, Shane D Morrison, Shelby L Kennedy, Tim C van de Grift, Astrid Højgaard, Amalie Lind Jacobsen, Natasha Johnson, Margriet G Mullender, Lotte Poulsen, Thomas Satterwhite, Richard Santucci, John Semple, Charlene Rae, Kinusan Savard, Jens Ahm Sørensen, Danny Young-Afat, Andrea L Pusic, Anne F Klassen
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Abstract

Background: To meaningfully understand outcomes of gender-affirming care, patient-reported outcome measures (PROMs) that are grounded in what matters to individuals seeking care are urgently needed. The objective of this study was to develop a comprehensive PROM to assess outcomes of gender-affirming care in clinical practice, research, and quality initiatives (the GENDER-Q).

Methods: Internationally established guidelines for PROM development were used to create a field test version of the GENDER-Q. In-depth interviews were conducted from December 2018 to March 2020 with youth and adults aged 16 years and older who were seeking or had received gender-affirming care at outpatient clinics providing gender-affirming care located within tertiary care centers or communities in Canada, Denmark, the Netherlands or the US. Data were analyzed and used to develop a conceptual framework and an item pool, which was used to develop preliminary scales. Between February 2021 to November 2021, iterative feedback was sought from clinicians and patient participants on the scales and used to refine or develop new scales. The revised scales were pilot-tested using a crowd-sourcing platform between February 2022 and April 2022.

Results: Data from interviews with 84 participants (aged 34 ± 14 years) resulted in a conceptual framework of the GENDER-Q with 13 domains measuring health-related quality of life, sexual, urination, gender practices, voice, hair, face and neck, body, breasts, genital feminization, chest, genital masculinization, and experience of care. Preliminary versions of 44 scales were developed covering most concepts in the conceptual framework. Iterative feedback was obtained from clinician experts (4 to 37 experts per scale; response rate, 67%) and 7-14 patient participants (depending on scale). All scales were refined, and 15 new scales were developed, resulting in 55 scales in the field test version of the GENDER-Q. In total, 601 transgender and gender diverse (TGD) people (aged 25 ± 6 years) participated in the pilot field test and the data were used to make changes to the field test survey.

Conclusion: The GENDER-Q was developed using extensive input from TGD individuals and clinician experts and represents the most comprehensive set of independently functioning scales that are available to date. An international field test of the GENDER-Q was completed in 2024 and the GENDER-Q is available for use in patient care, clinical research and quality improvement efforts.

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开展国际研究,制定患者报告的结果测量方法,以评估性别确认护理的结果 - GENDER-Q。
背景:为了有意义地了解性别平权护理的结果,迫切需要以寻求护理的个人所关心的问题为基础的患者报告结果测量(PROMs)。本研究的目的是开发一种全面的 PROM,用于评估临床实践、研究和质量计划中性别肯定护理的结果(GENDER-Q):方法:采用国际公认的 PROM 开发指南来创建 GENDER-Q 的实地测试版本。从 2018 年 12 月到 2020 年 3 月,我们对正在加拿大、丹麦、荷兰或美国的三级医疗中心或社区内提供性别平权护理的门诊诊所寻求或接受过性别平权护理的 16 岁及以上青年和成人进行了深入访谈。我们对数据进行了分析,并利用这些数据制定了一个概念框架和一个项目库,然后利用该框架和项目库制定了初步量表。2021 年 2 月至 2021 年 11 月期间,临床医生和患者参与者对量表进行了反复反馈,并用于完善或开发新的量表。2022 年 2 月至 2022 年 4 月期间,利用众包平台对修订后的量表进行了试点测试:对 84 名参与者(年龄为 34 ± 14 岁)的访谈数据形成了 GENDER-Q 的概念框架,包括 13 个领域,分别测量与健康相关的生活质量、性、排尿、性别行为、声音、头发、面部和颈部、身体、乳房、生殖器女性化、胸部、生殖器男性化和护理体验。初步制定的 44 个量表涵盖了概念框架中的大多数概念。临床专家(每个量表有 4 至 37 名专家;回复率为 67%)和 7 至 14 名患者参与者(视量表而定)提供了迭代反馈。对所有量表进行了改进,并开发了 15 个新量表,最终形成了 55 个量表的 GENDER-Q 实地测试版本。共有 601 名变性者和性别多元化者(年龄为 25 ± 6 岁)参加了现场测试,并根据测试数据对现场测试调查进行了修改:GENDER-Q 是在广泛听取变性者和临床专家意见的基础上开发出来的,是迄今为止最全面的独立功能量表。GENDER-Q 的国际实地测试已于 2024 年完成,GENDER-Q 可用于患者护理、临床研究和质量改进工作。
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来源期刊
Journal of Patient-Reported Outcomes
Journal of Patient-Reported Outcomes Health Professions-Health Information Management
CiteScore
3.80
自引率
7.40%
发文量
120
审稿时长
20 weeks
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