Starks Helene, Shaw Jennifer L, Hiratsuka Vanessa, Dillard Denise A, Robinson Renee
Department of Bioethics and Humanities, University of Washington, Box 357120, Seattle, WA, 98195-7120, USA,
Qual Life Res. 2015 May;24(5):1097-105. doi: 10.1007/s11136-014-0810-9. Epub 2014 Sep 23.
Southcentral Foundation, an Alaska Native tribal health organization, has had a depression screening program in primary care since 2001. Program monitoring identified gaps in antidepressant refills and patients' follow-up with behavioral health services. With extensive stakeholder participation, we developed an electronic, patient-centered, depression-management decision support tool (DM-DST). Quality of life and other outcomes are being assessed in a separate study; this case study reports on the multi-year stakeholder engagement process.
Data sources included interviews with patients and providers from integrated primary care teams, notes from research meetings, steering committee meetings, and consultations with tribal health system leadership, human subjects review committees, providers, and software designers, and a pilot test of the DS-DMT with patients and providers. We analyzed these sources using qualitative methods to assess the impact of stakeholder input on project processes and outcomes.
One comprehensive, iPad-based tool was originally planned to facilitate discussions about depression management. Stakeholder input emphasized the role of family and cultural context of depression and management and improving the usability of the DM-DST. Stakeholder direction led us to split the DM-DST into: (1) a brief iPad-based tool to facilitate conversations between patients and providers during clinic visits; and (2) a complementary Web site that provides detailed information and allows patients flexibility and time to learn more about depression and share information and preferences with family and friends.
Stakeholder input across the project substantially modified the DM-DST to ensure cultural applicability to patients and providers and facilitate integration into clinics.
自2001年以来,阿拉斯加原住民部落健康组织中南部基金会在初级保健中开展了抑郁症筛查项目。项目监测发现抗抑郁药续方以及患者接受行为健康服务的后续跟进方面存在差距。在众多利益相关者的广泛参与下,我们开发了一种以患者为中心的电子抑郁症管理决策支持工具(DM-DST)。生活质量和其他结果正在另一项研究中进行评估;本案例研究报告了多年来利益相关者的参与过程。
数据来源包括对综合初级保健团队的患者和提供者的访谈、研究会议记录、指导委员会会议记录,以及与部落卫生系统领导、人体研究审查委员会、提供者和软件设计师的磋商,还有对患者和提供者进行的DM-DMT试点测试。我们使用定性方法分析这些来源,以评估利益相关者的投入对项目过程和结果的影响。
最初计划开发一种基于iPad的综合工具,以促进关于抑郁症管理的讨论。利益相关者的投入强调了抑郁症及其管理的家庭和文化背景的作用,以及提高DM-DST的可用性。利益相关者的指导使我们将DM-DST分为:(1)一种基于iPad的简短工具,以促进患者和提供者在门诊就诊期间的对话;(2)一个配套网站,提供详细信息,并让患者有灵活性和时间更多地了解抑郁症,并与家人和朋友分享信息及偏好。
整个项目中利益相关者的投入对DM-DST进行了大幅修改,以确保其在文化上适用于患者和提供者,并便于融入诊所。