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让患者权益倡导者及其他利益相关者参与设计癌症护理中以患者为中心的沟通衡量标准。

Engaging Patient Advocates and Other Stakeholders to Design Measures of Patient-Centered Communication in Cancer Care.

作者信息

Treiman Katherine, McCormack Lauren, Olmsted Murrey, Roach Nancy, Reeve Bryce B, Martens Christa E, Moultrie Rebecca R, Sanoff Hanna

机构信息

RTI International, 3040 E. Cornwallis Road, PO Box 12194, Research Triangle Park, NC, 27709-2194, USA.

RTI International, 6110 Executive Blvd, Rockville, MD, 20852, USA.

出版信息

Patient. 2017 Feb;10(1):93-103. doi: 10.1007/s40271-016-0188-6.

Abstract

BACKGROUND

Patient-centered communication (PCC) is an essential component of patient-centered care and contributes to patient satisfaction, health-related quality of life, and other important patient outcomes.

OBJECTIVE

The aim of this study was to develop and test survey questions to assess patients' experiences with PCC in cancer care.

METHODS

We used a conceptual model developed by the National Cancer Institute as our framework. The survey questions align with the six core functions of PCC defined in the model: Exchanging Information, Managing Uncertainty, Enabling Patient Self-Management, Fostering Healing Relationships, Making Decisions, and Responding to Emotions. The study focused on colorectal cancer patients. We conducted two rounds of cognitive interviewing to evaluate patients' ability to understand and provide valid answers to the PCC questions. Interviews were conducted in Maryland and North Carolina in 2014. We involved a patient advocacy group, Fight Colorectal Cancer, and a multidisciplinary panel of stakeholders throughout the measurement development process to ensure that the survey questions capture aspects of PCC that are important to patients and meet the needs of potential end users, including researchers, healthcare organizations, and health professionals.

RESULTS

Patient and other stakeholder input informed revisions of draft survey questions, including changes to survey instructions, frame of reference for questions, response scales, and language.

CONCLUSION

This study demonstrated the feasibility and value of engaging patients and other stakeholders in a measurement development study. The Patient-Centered Outcomes Research Institute (PCORI) conceptual model of patient-centered outcomes research provides a useful guide for patient engagement in research. Research funders should call for meaningful roles for patients and other stakeholders in health research, including in the development of patient-centered outcomes.

摘要

背景

以患者为中心的沟通(PCC)是以患者为中心的医疗的重要组成部分,有助于提高患者满意度、与健康相关的生活质量以及其他重要的患者结局。

目的

本研究的目的是开发并测试调查问题,以评估癌症护理中患者的PCC体验。

方法

我们使用美国国立癌症研究所开发的概念模型作为框架。调查问题与该模型中定义的PCC的六个核心功能一致:信息交流、管理不确定性、促进患者自我管理、建立治疗性医患关系、做出决策以及应对情绪。该研究聚焦于结直肠癌患者。我们进行了两轮认知访谈,以评估患者理解PCC问题并提供有效答案的能力。访谈于2014年在马里兰州和北卡罗来纳州进行。在整个测量开发过程中,我们邀请了一个患者倡导组织“抗击结直肠癌”以及一个多学科利益相关者小组,以确保调查问题涵盖对患者重要的PCC方面,并满足潜在最终用户(包括研究人员、医疗保健机构和卫生专业人员)的需求。

结果

患者和其他利益相关者的意见为调查问题草案的修订提供了依据,包括对调查说明、问题的参照框架、回答量表和语言的修改。

结论

本研究证明了让患者和其他利益相关者参与测量开发研究的可行性和价值。以患者为中心的结局研究的患者为中心结局研究所(PCORI)概念模型为患者参与研究提供了有用的指导。研究资助者应要求患者和其他利益相关者在健康研究中发挥有意义的作用,包括在以患者为中心的结局的开发中。

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