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评估共同创作的面向患者的材料,以提高对基因检测结果的理解。

Evaluating co-created patient-facing materials to increase understanding of genetic test results.

机构信息

Boston College William F. Connell School of Nursing, Chestnut Hill, MA, USA.

Harvard Reproductive Endocrine Sciences Center and Reproductive Endocrine Unit, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.

出版信息

J Genet Couns. 2021 Apr;30(2):598-605. doi: 10.1002/jgc4.1348. Epub 2020 Oct 24.

Abstract

Patients often have difficulty understanding genetic test reports. Technical language and jargon can impede comprehension and limit patients using results to act on findings. One potential way to improve patient understanding of genetic test reports is to provide patient-facing materials. This study aimed to examine understandability and actionability of co-created patient-facing materials for genetic test results in a research context. We combined interprofessional perspectives and patient engagement to co-create patient-facing materials for patients undergoing research genetic testing for congenital hypogonadotropic hypogonadism (Kallmann syndrome). The iterative development process was guided by principles of health literacy and human-centered design (i.e., design thinking). Readability was assessed using eight validated algorithms. Patients and parents evaluated materials using a web-based survey. The gold standard Patient Education Materials Assessment Tool for print materials (PEMAT-P) was employed to measure understandability (content, style, use of numbers, organization, design, use of visual aids) and actionability. PEMAT-P scores >80% were considered high quality. Results were analyzed descriptively and correlations performed to identify relationships between education/health literacy and PEMAT-P ratings. A consensus score of eight algorithms indicated the materials were an 8 -9th grade reading level. Our findings are consistent with the U.S. Department of Health and Human Services 'average difficulty' classification (i.e., 7th-9th grade). In total, 61 patients/parents evaluated the materials. 'Visual Aids' received the lowest mean PEMAT-P rating (89%). All other parameters scored 90%-97%. PEMAT-P scores did not differ according to educational attainment (less than college vs. college or more, p = 0.28). Participants with adequate health literacy were more likely to approve of the 'organization' of information (p < 0.05). Respondents with low health literacy had more favorable views of 'visual aids' (p < 0.01). Involving patients in a co-creation process can produce high-quality patient-facing materials that are easier to understand.

摘要

患者通常难以理解基因检测报告。专业术语和行话会阻碍理解,并限制患者根据检测结果采取行动。提高患者对基因检测报告理解的一种潜在方法是提供面向患者的材料。本研究旨在研究在研究背景下,共同创建用于遗传检测结果的面向患者的材料对患者理解的可理解性和可操作性。我们结合了多专业的观点和患者的参与,为接受研究性遗传检测以诊断先天性低促性腺激素性性腺功能减退症(卡尔曼综合征)的患者共同创建了面向患者的材料。迭代开发过程以健康素养和以人为中心的设计(即设计思维)原则为指导。使用了八种经过验证的算法来评估可读性。患者和家长使用在线调查评估材料。使用经过验证的用于印刷材料的患者教育材料评估工具(PEMAT-P)的黄金标准来衡量可理解性(内容、风格、数字使用、组织、设计、使用视觉辅助)和可操作性。PEMAT-P 得分>80%被认为是高质量的。使用描述性统计方法进行分析,并进行相关性分析以确定教育/健康素养与 PEMAT-P 评分之间的关系。八种算法的共识评分表明材料处于 8-9 年级的阅读水平。我们的研究结果与美国卫生与公众服务部的“平均难度”分类一致(即 7-9 年级)。共有 61 名患者/家长评估了这些材料。“视觉辅助”获得的 PEMAT-P 评分最低(89%)。其他所有参数的评分为 90%-97%。根据教育程度,PEMAT-P 评分没有差异(少于大学与大学或以上,p=0.28)。具有足够健康素养的参与者更有可能认可信息的“组织”(p<0.05)。健康素养较低的受访者对“视觉辅助”的看法更为有利(p<0.01)。让患者参与共同创作过程可以产生更易于理解的高质量面向患者的材料。

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