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类风湿关节炎患者在药物干预结局措施中优先考虑的项目制定和表面效度。

Item Development and Face Validity of the Rheumatoid Arthritis Patient Priorities in Pharmacological Interventions Outcome Measures.

机构信息

Department of Anthropology, Durham University, Durham, DH1 3LE, UK.

Academic Rheumatology Unit, Bristol Royal Infirmary, University of Bristol, Bristol, BS2 8HW, UK.

出版信息

Patient. 2016 Apr;9(2):103-15. doi: 10.1007/s40271-015-0130-3.

Abstract

BACKGROUND

The assessment of rheumatoid arthritis (RA) is dominated by core sets and indices that have been developed by RA professionals. Previous research developed a set of eight priority treatment outcomes generated by patients to complement the professionally developed core sets for RA.

OBJECTIVE

This study aimed to facilitate quantitative measurement of these outcomes.

METHODS

Two consultation meetings with patient research partners diagnosed with RA (n = 18) were held to identify face validity in existing instruments (Phase 1) at the Bristol Royal Infirmary. Where validated measures did not exist, new numerical rating scales (NRS) were constructed and discussed at two focus groups with patients diagnosed with RA (n = 8) at the Bristol Royal Infirmary and the Royal National Hospital for Rheumatic Diseases (Phase 2). Feedback on the stem question, time frame, anchors and layout was recorded and transcribed verbatim.

RESULTS

Of the eight priorities, existing NRS for pain, activities of daily living and fatigue were voted as acceptable (Phase 1), but new NRS were required for five priorities. The partners strongly recommended that the three separate domains of severity, effect and ability to cope in each measurement area be assessed, as in the existing validated fatigue NRS. Focus group participants (Phase 2) made significant contributions to the phrasing of questions, for example how to ensure 'mobility' could be uniformly understood and how changes in valued activities be judged appropriately.

CONCLUSION

Through extensive patient feedback, 24 NRS were constructed based on priorities identified by patients and encompassing domains where existing questionnaires contain many more items and do not address three important concepts endorsed by patients: severity, effect and coping. The Rheumatoid Arthritis Patient Priorities in Pharmacological Interventions patient-reported outcome measures are now ready for the evaluation of comprehension, construct validity and sensitivity through an observational study.

摘要

背景

类风湿关节炎(RA)的评估主要由 RA 专业人员开发的核心集和指标主导。先前的研究开发了一组由患者生成的八个优先治疗结果,以补充 RA 的专业开发的核心集。

目的

本研究旨在促进这些结果的定量测量。

方法

在布里斯托尔皇家医院举行了两次与患有 RA 的患者研究伙伴的咨询会议(n=18),以确定现有的仪器是否具有表面有效性(第 1 阶段)。在不存在验证性测量的情况下,在布里斯托尔皇家医院和皇家国家风湿病医院(第 2 阶段)的两个与患有 RA 的患者进行的焦点小组中,构建和讨论了新的数字评定量表(NRS)。记录并逐字转录对起始问题、时间框架、锚点和布局的反馈。

结果

在八项重点中,现有的疼痛、日常生活活动和疲劳 NRS 被投票认为是可以接受的(第 1 阶段),但需要为五项重点制定新的 NRS。合作伙伴强烈建议在每个测量区域评估严重程度、影响和应对能力这三个单独的领域,就像现有的验证性疲劳 NRS 一样。焦点小组参与者(第 2 阶段)对问题的措辞做出了重大贡献,例如如何确保“移动性”可以被统一理解,以及如何适当判断有价值的活动的变化。

结论

通过广泛的患者反馈,根据患者确定的重点,构建了 24 个 NRS,涵盖了现有问卷包含更多项目且未解决患者认可的三个重要概念的领域:严重程度、影响和应对。类风湿关节炎患者在药物干预中的优先事项患者报告的结果测量现在已经准备好通过观察性研究评估理解、结构有效性和敏感性。

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