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在英国背景下探索家族性乳腺癌决策辅助工具的需求:一项针对转介至癌症遗传学服务机构的患者的定性研究

Exploring the requirements for a decision aid on familial breast cancer in the UK context: a qualitative study with patients referred to a cancer genetics service.

作者信息

Iredale Rachel, Rapport Frances, Sivell Stephanie, Jones Wendy, Edwards Adrian, Gray Jonathon, Elwyn Glyn

机构信息

Institute of Medical Genetics, Cardiff University School of Medicine, Cardiff, UK.

出版信息

J Eval Clin Pract. 2008 Feb;14(1):110-5. doi: 10.1111/j.1365-2753.2007.00811.x.

DOI:10.1111/j.1365-2753.2007.00811.x
PMID:18211652
Abstract

RATIONALE

Patients concerned about a family history of breast cancer can face difficult decisions about screening, prophylactic surgery and genetic testing. Decision aids can facilitate patient decision making and currently include leaflets and computerized tools. These are largely aimed at the North American market. However, no decision aids concerning familial breast cancer exist in the UK.

METHODS

Focus groups were held with 39 women over 18 years of age referred to a cancer genetics clinic, and who had been given a risk assessment for developing breast cancer. Each focus group examined three existing North American decision aids (1 paper-based and 2 CD-ROMs) and explored what a decision aid in a UK context should look like and the information it should contain.

RESULTS

There was enthusiasm for the development of decision aids that suit the local context in terms of its health care policy, in paper-based and CD-ROM formats. This paper identifies areas of agreement and disagreement in terms of both content and presentation styles, and also reports some of the suggestions received about where, when and with whom decision aids should be used. Participants suggested that decision aids would be most effective when they allowed a user-selected range of formats.

CONCLUSION

There is still significant unmet demand for information and decision support in the context of publicly funded health care. The patient perspective provides a unique insight into issues of design, style and communication.

摘要

理论依据

担心有乳腺癌家族病史的患者在筛查、预防性手术和基因检测方面可能面临艰难抉择。决策辅助工具有助于患者做出决策,目前包括宣传册和计算机化工具。这些主要面向北美市场。然而,英国不存在有关家族性乳腺癌的决策辅助工具。

方法

对39名18岁以上转诊至癌症遗传学诊所且已接受乳腺癌发病风险评估的女性进行了焦点小组访谈。每个焦点小组研究了三种现有的北美决策辅助工具(1种纸质版和2种光盘版),并探讨了英国背景下的决策辅助工具应是什么样的以及应包含哪些信息。

结果

对于开发符合当地医疗保健政策背景的纸质版和光盘版决策辅助工具,大家充满热情。本文确定了在内容和呈现方式方面的共识和分歧领域,还报告了一些关于决策辅助工具应在何时、何地以及由谁使用的建议。参与者建议,当决策辅助工具允许用户选择多种格式时,其效果最佳。

结论

在公共资助的医疗保健背景下,对信息和决策支持仍有大量未得到满足的需求。患者的观点为设计、风格和沟通问题提供了独特的见解。

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