McKenzie Emily, Matkin Lucy, Sousa Fialho Luz, Emelurumonye Ifeoma Nneka, Gintner Timea, Ilesanmi Christiana, Jagger Beth, Quinney Shannon, Anderson Elizabeth, Baandrup Lone, Bakhshy Amrit Kumar, Brabban Alison, Coombs Tim, Correll Christoph U, Cupitt Caroline, Keetharuth Anju Devianee, Lima Dania Nimbe, McCrone Paul, Moller Mary, Mulder Cornelis L, Roe David, Sara Grant, Shokraneh Farhad, Sin Jacqueline, Woodberry Kristen A, Addington Donald
Department of Psychiatry, University of Calgary, Calgary, Canada (McKenzie, Addington).
Department of Zoology, University of Oxford, Oxford, United Kingdom (Matkin).
Psychiatr Serv. 2022 Mar 1;73(3):249-258. doi: 10.1176/appi.ps.202000888. Epub 2021 Aug 9.
The objective of this project was to develop a set of patient-reported outcome measures for adolescents and adults who meet criteria for a psychotic disorder.
A research team and an international consensus working group, including service users, clinicians, and researchers, worked together in an iterative process by using a modified Delphi consensus technique that included videoconferencing calls, online surveys, and focus groups. The research team conducted systematic literature searches to identify outcomes, outcome measures, and risk adjustment factors. After identifying outcomes important to service users, the consensus working group selected outcome measures, risk adjustment factors, and the final set of outcome measures. International stakeholder groups consisting of >100 professionals and service users reviewed and commented on the final set.
The consensus working group identified four outcome domains: symptoms, recovery, functioning, and treatment. The domains encompassed 14 outcomes of importance to service users. The research team identified 131 measures from the literature. The consensus working group selected nine measures in an outcome set that takes approximately 35 minutes to complete.
A set of patient-reported outcome measures for use in routine clinical practice was identified. The set is free to service users, is available in at least two languages, and reflects outcomes important to users. Clinicians can use the set to improve clinical decision making, and administrators and researchers can use it to learn from comparing program outcomes.
本项目的目的是为符合精神障碍标准的青少年和成年人制定一套患者报告的结局指标。
一个研究团队和一个国际共识工作组,包括服务使用者、临床医生和研究人员,采用改进的德尔菲共识技术,通过视频会议、在线调查和焦点小组等方式,以迭代过程共同开展工作。研究团队进行了系统的文献检索,以确定结局、结局指标和风险调整因素。在确定对服务使用者重要的结局后,共识工作组选择了结局指标、风险调整因素以及最终的结局指标集。由100多名专业人员和服务使用者组成的国际利益相关者团体对最终结果进行了审查并发表了评论。
共识工作组确定了四个结局领域:症状、康复、功能和治疗。这些领域涵盖了对服务使用者重要的14个结局。研究团队从文献中确定了131项指标。共识工作组在一个结局指标集中选择了9项指标,完成该指标集大约需要35分钟。
确定了一套用于常规临床实践的患者报告结局指标。该指标集对服务使用者免费,至少有两种语言版本,并且反映了对使用者重要的结局。临床医生可以使用该指标集来改善临床决策,管理人员和研究人员可以使用它通过比较项目结局来进行学习。