Faculty of Health Sciences, University of Southampton, Southampton, UK.
National Institute for Health Research (NIHR) Collaboration for Applied Health Research and Care (CLAHRC) Wessex, University of Southampton, Southampton, UK.
Support Care Cancer. 2019 Jan;27(1):297-309. doi: 10.1007/s00520-018-4307-x. Epub 2018 Jun 28.
To develop a decision support tool for young women with breast cancer considering genetic testing for BRCA1/2 mutations soon after cancer diagnosis.
A four-stage iterative development process was employed; stage 1, literature review exploring the availability and efficacy of empirically tested decision support tools; stage 2, in-depth interviews with 29 young women (< 50 years) recently diagnosed with breast cancer, exploring information requirements and experiences of genetic testing decision making; stage 3, three focus groups (N = 21) exploring preferences for information presentation and prioritisation of content; stage 4, think-aloud interviews to refine the prototype (N = 16).
Participants wanted information regarding the pros and cons of testing, the testing process and implications for their family, presented in a way that allowed them to choose the level of detail they required. They preferred the term 'altered gene', valued a medical word definition function and warnings before accessing sensitive information.
Participants valued the decision support tool, the accessibility of the information and its clinical endorsement. The decision support tool has considerable clinical utility as an adjunct to genetic counselling or for use in busy oncology clinics where formal genetic counselling may be unavailable.
为刚被诊断患有乳腺癌、考虑进行 BRCA1/2 基因突变基因检测的年轻女性开发一种决策支持工具。
采用四阶段迭代开发过程;第 1 阶段,文献综述,探讨现有经过实证检验的决策支持工具的有效性;第 2 阶段,对 29 名近期被诊断患有乳腺癌的年轻女性(<50 岁)进行深入访谈,探讨其对基因检测决策的信息需求和经验;第 3 阶段,进行了 3 次焦点小组讨论(N=21),探讨信息呈现偏好和内容优先级;第 4 阶段,进行出声思维访谈以完善原型(N=16)。
参与者希望获得关于检测利弊、检测过程以及对其家庭影响的信息,以允许他们选择所需的详细程度。他们更喜欢使用“改变的基因”一词,重视医学词汇定义功能和访问敏感信息前的警告。
参与者重视决策支持工具、信息的可及性及其临床认可。该决策支持工具具有重要的临床应用价值,可作为遗传咨询的辅助手段,或在繁忙的肿瘤学诊所中使用,在这些诊所中可能无法提供正式的遗传咨询。