• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

开发乳腺癌选择决策支持工具:用于帮助年轻乳腺癌女性决定是否进行 BRCA1/2 基因突变遗传检测。

Development of Breast Cancer Choices: a decision support tool for young women with breast cancer deciding whether to have genetic testing for BRCA1/2 mutations.

机构信息

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.

出版信息

Support Care Cancer. 2019 Jan;27(1):297-309. doi: 10.1007/s00520-018-4307-x. Epub 2018 Jun 28.

DOI:10.1007/s00520-018-4307-x
PMID:29955974
Abstract

PURPOSE

To develop a decision support tool for young women with breast cancer considering genetic testing for BRCA1/2 mutations soon after cancer diagnosis.

METHODS

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).

RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

方法

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)。

结果

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。

结论

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。

相似文献

1
Development of Breast Cancer Choices: a decision support tool for young women with breast cancer deciding whether to have genetic testing for BRCA1/2 mutations.开发乳腺癌选择决策支持工具:用于帮助年轻乳腺癌女性决定是否进行 BRCA1/2 基因突变遗传检测。
Support Care Cancer. 2019 Jan;27(1):297-309. doi: 10.1007/s00520-018-4307-x. Epub 2018 Jun 28.
2
Systematic review of the empirical investigation of resources to support decision-making regarding BRCA1 and BRCA2 genetic testing in women with breast cancer.支持乳腺癌女性进行 BRCA1 和 BRCA2 基因检测决策的资源的实证研究系统评价。
Patient Educ Couns. 2018 May;101(5):779-788. doi: 10.1016/j.pec.2017.11.016. Epub 2017 Nov 26.
3
Development and pilot testing of a decision aid for men considering genetic testing for breast and/or ovarian cancer-related mutations (BRCA1/2).针对考虑进行乳腺癌和/或卵巢癌相关突变(BRCA1/2)基因检测的男性开发并进行预试验的决策辅助工具。
Genet Test. 2008 Dec;12(4):523-32. doi: 10.1089/gte.2008.0035.
4
Effect of a computer-based decision aid on knowledge, perceptions, and intentions about genetic testing for breast cancer susceptibility: a randomized controlled trial.基于计算机的决策辅助工具对乳腺癌易感性基因检测的知识、认知及意愿的影响:一项随机对照试验。
JAMA. 2004 Jul 28;292(4):442-52. doi: 10.1001/jama.292.4.442.
5
Decision-making on preimplantation genetic diagnosis and prenatal diagnosis: a challenge for couples with hereditary breast and ovarian cancer.胚胎植入前基因诊断和产前诊断的决策:对遗传性乳腺癌和卵巢癌夫妇的一项挑战。
Hum Reprod. 2014 May;29(5):1103-12. doi: 10.1093/humrep/deu034. Epub 2014 Mar 6.
6
Involvement and Influence of Healthcare Providers, Family Members, and Other Mutation Carriers in the Cancer Risk Management Decision-Making Process of BRCA1 and BRCA2 Mutation Carriers.医疗保健提供者、家庭成员及其他突变携带者在BRCA1和BRCA2突变携带者癌症风险管理决策过程中的参与及影响
J Genet Couns. 2018 Sep;27(5):1291-1301. doi: 10.1007/s10897-018-0254-4. Epub 2018 Mar 29.
7
A qualitative study on decision-making about BRCA1/2 testing in Italian women.一项关于意大利女性进行 BRCA1/2 检测决策的定性研究。
Eur J Cancer Care (Engl). 2019 Sep;28(5):e13083. doi: 10.1111/ecc.13083. Epub 2019 May 5.
8
Revisiting breast cancer patients who previously tested negative for BRCA mutations using a 12-gene panel.重新访视那些先前使用12基因检测 panel检测BRCA突变呈阴性的乳腺癌患者。
Breast Cancer Res Treat. 2017 Jan;161(1):135-142. doi: 10.1007/s10549-016-4038-y. Epub 2016 Oct 31.
9
BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes.BRCAPRO验证、BRCA1/BRCA2基因检测的敏感性以及其他乳腺癌易感基因的患病率。
J Clin Oncol. 2002 Jun 1;20(11):2701-12. doi: 10.1200/JCO.2002.05.121.
10
Genetic counseling and management of newly diagnosed breast cancer patients at genetic risk for BRCA germline mutations.对新诊断出有BRCA种系突变遗传风险的乳腺癌患者进行遗传咨询与管理。
Breast J. 2006 May-Jun;12(3):280-1; author reply 282-4. doi: 10.1111/j.1075-122X.2006.00260.x.

引用本文的文献

1
Optimizing risk-reducing surgery and aspirin decision aids for Lynch syndrome carriers using the person-based approach: A think-aloud interview study.采用基于个体的方法优化林奇综合征携带者的降低风险手术和阿司匹林决策辅助工具:一项出声思考访谈研究。
J Genet Couns. 2025 Aug;34(4):e70089. doi: 10.1002/jgc4.70089.
2
The development and evaluation of educational resources for young women with neurofibromatosis type 1 undergoing breast cancer surveillance.针对接受乳腺癌监测的1型神经纤维瘤病年轻女性的教育资源开发与评估。
Womens Health (Lond). 2025 Jan-Dec;21:17455057251337118. doi: 10.1177/17455057251337118. Epub 2025 Jun 29.
3

本文引用的文献

1
Systematic review of the empirical investigation of resources to support decision-making regarding BRCA1 and BRCA2 genetic testing in women with breast cancer.支持乳腺癌女性进行 BRCA1 和 BRCA2 基因检测决策的资源的实证研究系统评价。
Patient Educ Couns. 2018 May;101(5):779-788. doi: 10.1016/j.pec.2017.11.016. Epub 2017 Nov 26.
2
Gaps in Incorporating Germline Genetic Testing Into Treatment Decision-Making for Early-Stage Breast Cancer.将生殖系基因检测纳入早期乳腺癌治疗决策过程中的差距。
J Clin Oncol. 2017 Jul 10;35(20):2232-2239. doi: 10.1200/JCO.2016.71.6480. Epub 2017 Apr 12.
3
Information requirements of young women with breast cancer treated with mastectomy or breast conserving surgery: A systematic review.
Validation of a guidelines-based digital tool to assess the need for germline cancer genetic testing.
用于评估遗传性癌症基因检测需求的基于指南的数字工具的验证
Hered Cancer Clin Pract. 2024 Nov 8;22(1):24. doi: 10.1186/s13053-024-00298-0.
4
Patient decision support resources inform decisions about cancer susceptibility genetic testing and risk management: a systematic review of patient impact and experience.患者决策支持资源为癌症易感性基因检测和风险管理决策提供信息:对患者影响和体验的系统评价
Front Health Serv. 2023 May 31;3:1092816. doi: 10.3389/frhs.2023.1092816. eCollection 2023.
5
Development and early-stage evaluation of a patient portal to enhance familial communication about hereditary cancer susceptibility testing: A patient-driven approach.开发并初步评估一个患者门户,以加强遗传性癌症易感性检测的家族间沟通:一种以患者为导向的方法。
Health Expect. 2023 Apr;26(2):774-784. doi: 10.1111/hex.13702. Epub 2023 Jan 20.
6
Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery.遗传咨询师:一项混合方法随机对照试验的方案,旨在评估一个用于遗传服务提供的数字平台。
BMJ Open. 2022 Apr 29;12(4):e060899. doi: 10.1136/bmjopen-2022-060899.
7
Systematic Development of Patient Decision Aids: An Update from the IPDAS Collaboration.系统开发患者决策辅助工具:来自 IPDAS 合作组织的最新更新。
Med Decis Making. 2021 Oct;41(7):736-754. doi: 10.1177/0272989X211014163. Epub 2021 Jun 19.
8
Developing a web-based patient decision aid for gastrostomy in motor neuron disease: a study protocol.为运动神经元病患者开发一种基于网络的胃造口术决策辅助工具:研究方案。
BMJ Open. 2019 Dec 18;9(12):e032364. doi: 10.1136/bmjopen-2019-032364.
接受乳房切除术或保乳手术治疗的年轻乳腺癌女性的信息需求:一项系统综述。
Breast. 2016 Feb;25:1-13. doi: 10.1016/j.breast.2015.11.001. Epub 2015 Nov 30.
4
Poly (ADP-ribose) polymerase inhibitors: recent advances and future development.聚(ADP - 核糖)聚合酶抑制剂:最新进展与未来发展
J Clin Oncol. 2015 Apr 20;33(12):1397-406. doi: 10.1200/JCO.2014.58.8848. Epub 2015 Mar 16.
5
Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer.在一个未因乳腺癌家族史而进行选择的大型三阴性乳腺癌队列中,17个乳腺癌易感基因的遗传性突变情况。
J Clin Oncol. 2015 Feb 1;33(4):304-11. doi: 10.1200/JCO.2014.57.1414. Epub 2014 Dec 1.
6
From observation to intervention: development of a psychoeducational intervention to increase uptake of BRCA genetic counseling among high-risk breast cancer survivors.从观察到干预:开发一种心理教育干预措施以提高高危乳腺癌幸存者对BRCA基因咨询的接受度。
J Cancer Educ. 2014 Dec;29(4):709-19. doi: 10.1007/s13187-014-0643-9.
7
A systematic development process for patient decision aids.患者决策辅助工具的系统开发流程。
BMC Med Inform Decis Mak. 2013;13 Suppl 2(Suppl 2):S2. doi: 10.1186/1472-6947-13-S2-S2. Epub 2013 Nov 29.
8
Addressing health literacy in patient decision aids.解决患者决策辅助工具中的健康素养问题。
BMC Med Inform Decis Mak. 2013;13 Suppl 2(Suppl 2):S10. doi: 10.1186/1472-6947-13-S2-S10. Epub 2013 Nov 29.
9
More breast cancer patients prefer BRCA-mutation testing without prior face-to-face genetic counseling.更多乳腺癌患者希望在未经面对面遗传咨询的情况下进行 BRCA 基因突变检测。
Fam Cancer. 2014 Jun;13(2):143-51. doi: 10.1007/s10689-013-9686-z.
10
Using the framework method for the analysis of qualitative data in multi-disciplinary health research.运用多学科健康研究中定性数据分析的框架方法。
BMC Med Res Methodol. 2013 Sep 18;13:117. doi: 10.1186/1471-2288-13-117.