Cella David, Yount Susan, Rothrock Nan, Gershon Richard, Cook Karon, Reeve Bryce, Ader Deborah, Fries James F, Bruce Bonnie, Rose Mattias
Evanston Northwestern Healthcare, Evanston, Illinois 60201, USA.
Med Care. 2007 May;45(5 Suppl 1):S3-S11. doi: 10.1097/01.mlr.0000258615.42478.55.
The National Institutes of Health (NIH) Patient-Reported Outcomes Measurement Information System (PROMIS) Roadmap initiative (www.nihpromis.org) is a 5-year cooperative group program of research designed to develop, validate, and standardize item banks to measure patient-reported outcomes (PROs) relevant across common medical conditions. In this article, we will summarize the organization and scientific activity of the PROMIS network during its first 2 years.
The network consists of 6 primary research sites (PRSs), a statistical coordinating center (SCC), and NIH research scientists. Governed by a steering committee, the network is organized into functional subcommittees and working groups. In the first year, we created an item library and activated 3 interacting protocols: Domain Mapping, Archival Data Analysis, and Qualitative Item Review (QIR). In the second year, we developed and initiated testing of item banks covering 5 broad domains of self-reported health.
The domain mapping process is built on the World Health Organization (WHO) framework of physical, mental, and social health. From this framework, pain, fatigue, emotional distress, physical functioning, social role participation, and global health perceptions were selected for the first wave of testing. Item response theory (IRT)-based analysis of 11 large datasets supplemented and informed item-level qualitative review of nearly 7000 items from available PRO measures in the item library. Items were selected for rewriting or creation with further detailed review before the first round of testing in the general population and target patient populations.
The NIH PROMIS network derived a consensus-based framework for self-reported health, systematically reviewed available instruments and datasets that address the initial PROMIS domains. Qualitative item research led to the first wave of network testing which began in the second year.
美国国立卫生研究院(NIH)患者报告结局测量信息系统(PROMIS)路线图计划(www.nihpromis.org)是一项为期5年的合作组研究项目,旨在开发、验证和标准化题库,以测量常见医疗状况下相关的患者报告结局(PROs)。在本文中,我们将总结PROMIS网络头两年的组织情况和科学活动。
该网络由6个主要研究站点(PRSs)、一个统计协调中心(SCC)和NIH研究科学家组成。在指导委员会的管理下,网络被组织成功能性子委员会和工作组。第一年,我们创建了一个项目库并启动了3个相互作用的方案:领域映射、档案数据分析和定性项目审查(QIR)。第二年,我们开发并启动了涵盖自我报告健康5个广泛领域的题库测试。
领域映射过程建立在世界卫生组织(WHO)的身体、心理和社会健康框架之上。从这个框架中,疼痛、疲劳、情绪困扰、身体功能、社会角色参与和整体健康认知被选作首轮测试对象。基于项目反应理论(IRT)对11个大型数据集的分析补充并为项目库中近7000个来自现有PRO测量指标的项目提供了项目层面的定性审查信息。在对普通人群和目标患者群体进行首轮测试之前,经过进一步详细审查后选择项目进行重写或创建。
NIH PROMIS网络得出了一个基于共识的自我报告健康框架,系统地审查了涉及PROMIS初始领域的现有工具和数据集。定性项目研究促成了第二年开始的首轮网络测试。