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开发MyCancerGene数字健康门户网站以提高患者对遗传性癌症基因检测结果的理解:开发、用户及可用性测试研究

Developing the MyCancerGene Digital Health Portal to Improve Patients' Understanding of Germline Cancer Genetic Test Results: Development, User, and Usability Testing Study.

作者信息

Trieu Phillip, Fetzer Dominique, McLeod Briana, Schweickert Kathryn, Gutstein Lauren, Egleston Brian, Domchek Susan, Fleisher Linda, Wagner Lynne, Wen Kuang-Yi, Cacioppo Cara, Ebrahimzadeh Jessica E, Falcone Dana, Langer Claire, Wood Elisabeth, Karpink Kelsey, Posen Shelby, Selmani Enida, Bradbury Angela R

机构信息

Division of Hematology-Oncology, Abramson Cancer Center, The University of Pennsylvania, Philadelphia, PA, United States.

Fox Chase Cancer Center, Temple University, Philadelphia, PA, United States.

出版信息

JMIR Form Res. 2025 May 14;9:e56282. doi: 10.2196/56282.

DOI:10.2196/56282
PMID:40366732
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12120370/
Abstract

BACKGROUND

The use of multigene panels has significantly increased the likelihood that genetic testing will leave patients with uncertainties regarding test interpretation, implications, and recommendations, which will change over time. Effective longitudinal care models are needed to provide patients with updated information and to obtain patient and family history updates.

OBJECTIVE

To bridge this gap, we aimed to develop a patient- and genetic provider-informed digital genetic health portal (GHP), MyCancerGene, to improve longitudinal patient understanding of and responses to genetic testing.

METHODS

We used a 5-step process to develop MyCancerGene. To better understand their interest in and willingness to use a digital GHP, we surveyed 307 patients who completed genetic testing (step 1). We completed qualitative interviews with 10 patients and a focus group with 17 genetic providers to inform the content and function of MyCancerGene (step 2). Next, we developed initial intervention content (step 3) and completed user testing of intervention content with 25 providers and 28 patients (step 4). After developing the prototype intervention, we completed usability testing with 8 patients for their feedback on the final content, functions, and ease of use (step 5).

RESULTS

In surveys conducted in step 1, 90% of patients with positive results reported interest in a digital GHP, and over 75% of participants with variants of uncertain significance or uninformative negative results reported similar interest. The most frequently reported advantages among patients were increasing accessibility, convenience, and efficiency (103/224, 46%); keeping genetic information organized (54/224, 24.1%); and increasing or maintaining patient understanding of the information (38/224, 17%). In qualitative interviews (step 2), both patients and genetic providers endorsed the benefit of the tool for updating personal and family history and for providers to share new risk information, test interpretation, or other medical changes. Patient and provider input informed eight key components of the tool: (1) Landing Page, (2) Summary of Care page, (3) My Genetic Test Results page, (4) My Family History page, (5) Provide an Update page, (6) Review an Update page, (7) Resources page, and (8) the Screenings Tracker. They also recommended key functions, including the ability to download and print materials and the inclusion of reminders and engagement functions. Potential challenges identified by patients included privacy and security concerns (67/206, 32.5%) and the potential for electronic information to generate distress (20/206, 9.7%). While patients were comfortable with updates (ie, even variant reclassification upgrades or clinically significant results), 44% (11/25) of genetic providers were uncomfortable sharing variant reclassification upgrades through MyCancerGene.

CONCLUSIONS

MyCancerGene, a patient-centered digital GHP, was developed with extensive patient and genetic provider feedback and designed to enhance longitudinal patient understanding of and affective and behavioral responses to genetic testing, particularly in the era of evolving evidence and risk information.

摘要

背景

多基因检测板的使用显著增加了基因检测让患者在检测解读、意义及建议方面仍存在不确定性的可能性,且这些情况会随时间变化。需要有效的长期护理模式为患者提供最新信息,并获取患者及其家族史的最新情况。

目的

为弥合这一差距,我们旨在开发一个由患者和基因检测提供者提供信息的数字基因健康门户(GHP)——MyCancerGene,以提高患者长期对基因检测的理解及反应。

方法

我们采用五步流程来开发MyCancerGene。为更好地了解患者对数字GHP的兴趣及使用意愿,我们对307名完成基因检测的患者进行了调查(第一步)。我们对10名患者进行了定性访谈,并与17名基因检测提供者进行了焦点小组讨论,以确定MyCancerGene的内容和功能(第二步)。接下来,我们制定了初步干预内容(第三步),并与25名提供者和28名患者一起完成了干预内容的用户测试(第四步)。在开发出原型干预措施后,我们对8名患者进行了可用性测试,以获取他们对最终内容、功能及易用性的反馈(第五步)。

结果

在第一步进行的调查中,90%检测结果为阳性的患者表示对数字GHP感兴趣,超过75%意义不明确的变异或无信息价值的阴性结果参与者也表示出类似兴趣。患者中最常提到的优点是提高了可及性、便利性和效率(103/224,46%);使基因信息更有条理(54/224,24.1%);以及增加或维持患者对信息的理解(38/224,17%)。在定性访谈(第二步)中,患者和基因检测提供者都认可该工具在更新个人和家族史以及提供者分享新的风险信息、检测解读或其他医疗变化方面的益处。患者和提供者的意见为该工具的八个关键组成部分提供了依据:(1)着陆页,(2)护理总结页面,(3)我的基因检测结果页面,(4)我的家族史页面,(5)提供更新页面,(6)查看更新页面,(7)资源页面,以及(8)筛查追踪器。他们还推荐了关键功能,包括下载和打印材料的能力以及加入提醒和互动功能。患者指出的潜在挑战包括隐私和安全问题(67/206,32.5%)以及电子信息可能引发困扰(20/206,9.7%)。虽然患者对更新感到放心(即即使是变异重新分类升级或具有临床意义的结果),但44%(11/25)的基因检测提供者对通过MyCancerGene分享变异重新分类升级感到不安。

结论

MyCancerGene是一个以患者为中心的数字GHP,在患者和基因检测提供者的广泛反馈基础上开发而成,旨在增强患者长期对基因检测的理解以及情感和行为反应,特别是在证据和风险信息不断变化的时代。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f22a/12120370/7f03346526f8/formative_v9i1e56282_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f22a/12120370/1672e897722b/formative_v9i1e56282_fig1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f22a/12120370/ffa172afe74d/formative_v9i1e56282_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f22a/12120370/2d09fa6ab70c/formative_v9i1e56282_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f22a/12120370/175592685f61/formative_v9i1e56282_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f22a/12120370/7f03346526f8/formative_v9i1e56282_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f22a/12120370/1672e897722b/formative_v9i1e56282_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f22a/12120370/04badc6f6c93/formative_v9i1e56282_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f22a/12120370/ffa172afe74d/formative_v9i1e56282_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f22a/12120370/2d09fa6ab70c/formative_v9i1e56282_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f22a/12120370/175592685f61/formative_v9i1e56282_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f22a/12120370/7f03346526f8/formative_v9i1e56282_fig6.jpg

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