Elder Charles R, Debar Lynn L, Ritenbaugh Cheryl, Rumptz Maureen H, Patterson Charlotte, Bonifay Allison, Cowan Penney, Lancaster Lindsay, Deyo Richard A
Physician Lead for Integrative Medicine at Kaiser Permanente Northwest and an Affiliate Investigator at the Center for Health Research in Portland, OR.
Senior Investigator at the Kaiser Permanente Center for Health Research in Portland, OR.
Perm J. 2017;21:16-101. doi: 10.7812/TPP/16-101.
Supporting day-to-day self-care activities has emerged as a best practice when caring for patients with chronic pain, yet providing this support may introduce challenges for both patients and primary care physicians. It is essential to develop tools that help patients identify the issues and outcomes that are most important to them and to communicate this information to primary care physicians at the point of care.
We describe our process to engage patients, primary care physicians, and other stakeholders in the context of a pilot randomized controlled trial of a patient-centered assessment process implemented in an everyday practice setting. We identify lessons on how to engage stakeholders and improve patient-centered care for those with chronic conditions within the primary care setting.
A qualitative analysis of project minutes, interviews, and focus groups was conducted to evaluate stakeholder experiences. Stakeholders included patients, caregivers, clinicians, medical office support staff, health plan administrators, an information technology consultant, and a patient advocate.
Our stakeholders included many patients with no prior experience with research. This approach enriched the applicability of feedback but necessitated extra time for stakeholder training and meeting preparation. Types of stakeholders varied over the course of the project, and more involvement of medical assistants and Information Technology staff was required than originally anticipated.
Meaningful engagement of patient and physician stakeholders must be solicited in a well-coordinated manner with broad health care system supports in place to ensure full execution of patient-centered processes.
在护理慢性疼痛患者时,支持日常自我护理活动已成为一种最佳实践,但提供这种支持可能会给患者和初级保健医生带来挑战。开发工具以帮助患者识别对他们最重要的问题和结果,并在护理点将这些信息传达给初级保健医生至关重要。
我们描述了在日常实践环境中实施的以患者为中心的评估过程的试点随机对照试验背景下,让患者、初级保健医生和其他利益相关者参与的过程。我们确定了关于如何在初级保健环境中让利益相关者参与并改善慢性病患者以患者为中心的护理的经验教训。
对项目会议记录、访谈和焦点小组进行定性分析,以评估利益相关者的经历。利益相关者包括患者、护理人员、临床医生、医疗办公室支持人员、健康计划管理人员、信息技术顾问和患者权益倡导者。
我们的利益相关者包括许多以前没有研究经验的患者。这种方法丰富了反馈的适用性,但需要额外的时间进行利益相关者培训和会议准备。在项目过程中,利益相关者的类型各不相同,并且需要比最初预期更多的医疗助理和信息技术人员的参与。
必须以协调良好的方式征求患者和医生利益相关者的有意义参与,并要有广泛的医疗保健系统支持,以确保以患者为中心的过程得到充分执行。