以患者为中心的核心影响集的基础:从过去和现有方法的关键学习。

IF 3.4 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Patient-Patient Centered Outcomes Research Pub Date : 2023-07-01 DOI:10.1007/s40271-023-00630-1
Eleanor M Perfetto, T Rosie Love, Elisabeth M Oehrlein, Silke C Schoch, Suz Schrandt
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引用次数: 0

摘要

尽管越来越多的人致力于以患者为中心,但在始终如一地确定患者报告的疾病和/或治疗对他们最重要的影响方面,特别是在无数潜在的下游用途方面,仍然存在挑战。以患者为中心的核心影响集(PC-CIS),即患者认为最重要的特定疾病影响列表,被提议作为一种解决方案。但是,PC-CIS是一个新概念,目前在患者倡导团体的试点阶段。我们进行了环境扫描,以探索PC-CIS概念与过去/现有工作的重叠[例如,核心结果集(COS)],并告知进一步开发和运营的总体可行性。在专家咨询委员会的指导和建议下,我们进行了文献和相关网站的检索。为了与PC-CIS定义保持一致,审查了已确定的资源,并收集了关键的见解。我们确定了51种现有资源和5个关键见解:(1)现有的工作不符合PC-CIS的定义,因为我们已经明确了以患者为中心;(2)现有的cos开发工作是PC-CIS基础资源的宝贵来源;(3)现有的健康结局分类可以通过以患者为优先的影响来增强,以创建一个全面的影响分类。(4)目前的方法可能会在不经意间将患者的优先事项排除在核心列表/集合之外,需要进行修改以保护患者的声音;(5)需要明确和透明地说明患者如何参与个人过去/现有的努力。PC-CIS在概念上与过去/现有的努力不同,它明确强调耐心领导和耐心驱动。但是,PC-CIS开发可以利用过去/现有相关工作中的许多资源。
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A Foundation for Patient-Centered Core Impact Sets: Key Learnings from Past and Existing Approaches.

Despite growing commitment to patient centricity, challenges persist in consistently identifying the impacts of disease and/or treatment that patients report as most important to them, especially across myriad potential downstream uses. Patient-centered core impact sets (PC-CIS), disease-specific lists of impacts that patients report as most important, are proposed as a solution. But, PC-CIS is a new concept, currently in the pilot stage with patient advocacy groups. We conducted an environmental scan to explore PC-CIS conceptual overlap with past/existing efforts [e.g., core outcome sets (COS)] and to inform general feasibility for further development and operationalization. With guidance and advice from an expert advisory committee, we conducted a search of the literature and relevant websites. Identified resources were reviewed for alignment with the PC-CIS definition, and key insights were gleaned. We identified 51 existing resources and five key insights: (1) no existing efforts identified meet the definition of PC-CIS as we have specified it in terms of patient centricity, (2) existing COS-development efforts are a valuable source of foundational resources for PC-CIS, (3) existing health-outcome taxonomies can be augmented with patient-prioritized impacts to create a comprehensive impact taxonomy, (4) current approaches/methods can inadvertently exclude patient priorities from core lists/sets and will need to be modified to protect the patient voice, and (5) there is need for clarity and transparency on how patients were engaged in individual past/existing efforts. PC-CIS is conceptually unique from past/existing efforts in its explicit emphasis on patient leadership and being patient driven. However, PC-CIS development can leverage many resources from the past/existing related work.

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来源期刊
Patient-Patient Centered Outcomes Research
Patient-Patient Centered Outcomes Research HEALTH CARE SCIENCES & SERVICES-
CiteScore
6.60
自引率
8.30%
发文量
44
审稿时长
>12 weeks
期刊介绍: The Patient provides a venue for scientifically rigorous, timely, and relevant research to promote the development, evaluation and implementation of therapies, technologies, and innovations that will enhance the patient experience. It is an international forum for research that advances and/or applies qualitative or quantitative methods to promote the generation, synthesis, or interpretation of evidence. The journal has specific interest in receiving original research, reviews and commentaries related to qualitative and mixed methods research, stated-preference methods, patient reported outcomes, and shared decision making. Advances in regulatory science, patient-focused drug development, patient-centered benefit-risk and health technology assessment will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in The Patient may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances. All manuscripts are subject to peer review by international experts.
期刊最新文献
Reporting of Patient and Public Involvement in Technology Appraisal and Assessment Reports: A Rapid Scoping Review. 15th Meeting of the International Academy of Health Preference Research. Patients' Preferences for Sphingosine-1-Phosphate Receptor Modulators in Multiple Sclerosis Based on Clinical Management Considerations: A Choice Experiment. The Role of Patient-Reported Outcomes to Measure Treatment Satisfaction in Drug Development. Young People's Barriers and Facilitators of Engagement with Web-Based Mental Health Interventions for Anxiety and Depression: A Qualitative Study.
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