一个回顾性的多机构评估乳房放射学和病理报告的可读性和一个新的病人工具(MedEd)利用美国识字标准。

IF 3.1 2区 医学 Q2 ONCOLOGY
Samantha Greenseid, Gande Li, Olivia Mihulka, Arianna Vazquez, Alex Verosky, Salvador Rodriguez Franco, Samhita Bheemireddy, Madeline G Higgins, Sarah Leslie, Sarah Tevis, Kristin Rojas
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引用次数: 0

摘要

背景:健康素养是癌症生存期间患者参与和预后的关键因素。根据《21世纪治愈法案》(21st Century Cures Act),患者现在可以立即获得放射学和病理报告,但这些文件通常超过美国医学协会(American Medical Association)推荐的六年级阅读水平。虽然先前的研究已经检查了一般的乳腺癌材料,但个性化临床报告的可读性仍未得到探索。方法:在这项多机构回顾性研究中,我们分析了来自科罗拉多大学和迈阿密大学的120份去识别的乳房放射学和病理学报告,包括六种报告类型。使用6个已验证的指标评估可读性。此外,还评估了98个meed定义和96个meed指导的在线患者教育材料(OPEMs)。MedEd是一个Chrome插件,旨在突出关键的乳房健康术语,并提供医生策划的定义与审查教育内容的链接。结果:在所有机构中,大多数临床报告超过高中阅读水平,外科病理报告是最不容易获得的。MedEd定义和OPEMs显示出更好的可读性,但仍然超过了推荐的六年级水平。结论:乳腺癌相关的报道和教育材料对许多幸存者来说仍然难以理解。改进面向患者的工具的设计——可能通过人工智能集成和患者共同开发——可以增强可及性、赋权和共同决策。对癌症幸存者的启示:这项研究强调了乳房放射学和病理学报告的可读性与许多癌症幸存者的文化水平之间的关键差距。由于患者可以通过电子门户直接访问这些文件,医学语言的复杂性可能导致困惑、焦虑和脱离护理。幸存者在治疗后的监测中可能特别脆弱,因为了解后续成像和病理对共同决策至关重要。像medi这样的工具——尽管很有希望——必须继续发展以满足国家扫盲标准。简化医疗报告,整合以患者为中心的人工智能支持的教育工具,可以增强幸存者的理解力,培养自主性,并最终提高他们在整个生存过程中的信心和成果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A retrospective multi-institutional assessment of breast radiology and pathology report readability and a novel patient tool (MedEd) utilizing American literacy standards.

Background: Health literacy is a critical factor in patient engagement and outcomes during cancer survivorship. With the 21st Century Cures Act, patients now receive immediate access to radiology and pathology reports, yet these documents often exceed the 6th-grade reading level recommended by the American Medical Association. While prior studies have examined general breast cancer materials, the readability of individualized clinical reports remains unexplored.

Methods: In this multi-institutional retrospective study, 120 de-identified breast radiology and pathology reports from the University of Colorado and the University of Miami were analyzed across six report types. Readability was assessed using six validated indices. Additionally, 98 MedEd definitions and 96 MedEd-directed online patient education materials (OPEMs) were evaluated. MedEd is a Chrome plug-in designed to highlight key breast health terms and provide physician-curated definitions with links to vetted educational content.

Results: Across institutions, most clinical reports exceeded a high school reading level, with surgical pathology reports being the least accessible. MedEd definitions and OPEMs demonstrated better readability but still surpassed the recommended 6th-grade level.

Conclusions: Breast cancer-related reports and educational materials remain difficult for many survivors to comprehend. Improved design of patient-facing tools-potentially through AI integration and patient co-development-may enhance accessibility, empowerment, and shared decision-making.

Implications for cancer survivors: This study underscores a critical gap between the readability of breast radiology and pathology reports and the literacy levels of many cancer survivors. As patients gain immediate access to these documents through electronic portals, the complexity of medical language can lead to confusion, anxiety, and disengagement from care. Survivors may be particularly vulnerable during post-treatment surveillance when understanding follow-up imaging and pathology is vital for shared decision-making. Tools like MedEd-while promising-must continue to evolve to meet national literacy standards. Simplifying medical reports and integrating patient-centered, Al-supported education tools can enhance survivors' comprehension, foster autonomy, and ultimately improve their confidence and outcomes throughout survivorship.

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来源期刊
CiteScore
7.00
自引率
10.80%
发文量
149
审稿时长
>12 weeks
期刊介绍: Cancer survivorship is a worldwide concern. The aim of this multidisciplinary journal is to provide a global forum for new knowledge related to cancer survivorship. The journal publishes peer-reviewed papers relevant to improving the understanding, prevention, and management of the multiple areas related to cancer survivorship that can affect quality of care, access to care, longevity, and quality of life. It is a forum for research on humans (both laboratory and clinical), clinical studies, systematic and meta-analytic literature reviews, policy studies, and in rare situations case studies as long as they provide a new observation that should be followed up on to improve outcomes related to cancer survivors. Published articles represent a broad range of fields including oncology, primary care, physical medicine and rehabilitation, many other medical and nursing specialties, nursing, health services research, physical and occupational therapy, public health, behavioral medicine, psychology, social work, evidence-based policy, health economics, biobehavioral mechanisms, and qualitative analyses. The journal focuses exclusively on adult cancer survivors, young adult cancer survivors, and childhood cancer survivors who are young adults. Submissions must target those diagnosed with and treated for cancer.
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