Co-creating a suite of patient decision aids for parents of an infant or young child with differences of sex development: A methods roadmap.

Frontiers in urology Pub Date : 2023-01-01 Epub Date: 2023-01-04 DOI:10.3389/fruro.2022.1020152
Sophie Lightfoot, Meg Carley, William Brinkman, Melissa D Gardner, Larry D Gruppen, Noi Liang, Kendra Pinkelman, Phyllis W Speiser, Kristina I Suorsa-Johnson, Brian VanderBrink, Jessica Wisniewski, David E Sandberg, Dawn Stacey
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Abstract

Introduction: Parents and guardians of infants and young children with differences of sex development (DSD) often face numerous health and social decisions about their child's condition. While proxy health decisions can be stressful in any circumstance, they are further exacerbated in this clinical context by significant variations in clinical presentation, parental lack of knowledge about DSD, irreversibility of some options (e.g., gonadectomy), a paucity of research available about long-term outcomes, and anticipated decisional regret. This study aimed to engage clinicians, parents, and an adult living with DSD to collaboratively develop a suite of patient decision aids (PDAs) to respond to the decisional needs of parents and guardians of infants and young children diagnosed with DSD.

Methods: We used a systematic co-development process guided by the Ottawa Decision Support Framework and the International Patient Decision Aids Standards (IPDAS). The five steps were: literature selection, establish the team, decisional needs assessment, create the PDAs, and alpha testing.

Results: We developed four PDAs to support parents/guardians of infants or young children diagnosed with DSD about four priority decisions identified through our decisional needs assessment: genetic testing, gender of rearing, genital surgery and gonadal surgery. All four PDAs include information for parents about DSD, the options, reasons to choose or avoid each option, and opportunities for parents/guardians to rate the importance of features of each option to clarify their values for these features. Qualitative feedback was positive from clinicians, parents and an adult living with DSD.

Conclusions: These PDAs are clinical tools designed to support parents/guardians and to promote making an informed and shared DSD-related decision. While these tools are specific to DSD, they contain themes and elements translatable to other pediatric populations.

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为性别发育不同的婴儿或幼儿的父母共同创建一套患者决策辅助:方法路线图
引言有性别发展差异(DSD)的婴儿和幼儿的父母和监护人经常面临关于其孩子状况的许多健康和社会决定。虽然在任何情况下,代理健康决策都可能带来压力,但在这种临床背景下,临床表现的显著差异、父母对DSD缺乏了解、某些选择的不可逆性(如性腺切除术)、缺乏关于长期结果的研究以及预期的决策后悔会进一步加剧这种压力。本研究旨在让临床医生、父母和患有DSD的成年人共同设计一套患者决策辅助工具(PDA),以满足诊断为DSD的婴幼儿的父母和监护人的决策需求。方法在渥太华决策支持框架和国际艾滋病患者决策标准(IPDAS)的指导下,我们使用了一个系统的联合设计过程。五个步骤是:文献选择、建立团队、决策需求评估、创建PDA和阿尔法测试。结果我们的健康专业人员、父母、患有DSD的成年人和PDA专家团队共同设计了四个PDA,以支持诊断为DSD的婴儿或幼儿的父母/监护人。这些PDA解决了通过我们的决策需求评估确定的四个优先决策:基因检测、养育性别、生殖器手术和性腺手术。所有四个PDA都包括家长关于DSD的信息、选项、选择或避免每个选项的原因,以及家长/监护人评估每个选项功能重要性的机会,以澄清他们对这些功能的价值。当阿尔法在一个中心与跨专业DSD专业团队进行测试时,我们团队的定性反馈是积极的。结论这些PDA是临床工具,旨在支持父母/监护人参与做出知情的DSD决策;接下来的步骤是确定父母的决策结果。虽然这些工具是DSD特有的,但它们的共同设计过程可以转移到其他儿科人群的PDA的共同设计中。
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