首页> 外文期刊>Value in health: the journal of the International Society for Pharmacoeconomics and Outcomes Research >Development and Validation of the FSIQ-RMS: A New Patient-Reported Questionnaire to Assess Symptoms and Impacts of Fatigue in Relapsing Multiple Sclerosis
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Development and Validation of the FSIQ-RMS: A New Patient-Reported Questionnaire to Assess Symptoms and Impacts of Fatigue in Relapsing Multiple Sclerosis

机译:FSIQ-RMS的开发和验证:新患者报告的问卷调查问卷,以评估疲劳在复发多发性硬化时的疲劳症状和影响

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Objectives: A new patient-reported outcome (PRO) instrument to measure fatigue symptoms and impacts in relapsing multiple sclerosis (RMS) was developed in a qualitative stage, followed by psychometric validation and migration from paper to an electronic format. Methods: Adult patients with relapsing-remitting multiple sclerosis (RRMS) were interviewed to elicit fatigue-related symptoms and impacts. A draft questionnaire was debriefed in cognitive interviews with further RRMS patients, and revised. Content confirmation interviews were conducted with patients with progressiverelapsing multiple sclerosis (PRMS) and relapsing secondaryprogressive multiple sclerosis (RSPMS). Psychometric analyses used data from adult patients with different RMS subtypes and matched non-RMS controls in a multicenter, observational study. After item reduction, the final instrument was migrated to a smartphone (eDiary) and usability was confirmed in interviews with additional adult RMS patients. Results: The qualitative stage included 37 RRMS, 5 PRMS, and 5 RSPMS patients. Saturation of concepts was reached during concept elicitation. Cognitive interviews confirmed that participants understood the instructions, items, and response options of the instrument-named FSIQ-RMS-as intended. Psychometric validation included 164 RMS and 74 control patients. Internal consistency and test-retest reliability were demonstrated. The symptoms domain discriminated along the RMS symptom-severity continuum and between patients and controls. Patients were able to attribute fatiguerelated symptoms to RMS. Usability and conceptual equivalence of the eDiary were confirmed (n = 10 participants). Conclusions: With 7 symptom items and 13 impact items (in 3 impacts subdomains: physical, cognitive and emotional, and coping) after item reduction, the FSIQ-RMS is a comprehensive, valid, and reliable measure of fatigue-related symptoms and impacts in RMS patients.
机译:目的:在定性阶段开发了一种新的患者报告的结果(Pro)仪器,用于测量疲劳症状和复发多发性硬化症(RMS)的影响,然后进行精神验证和纸张迁移到电子格式。方法:采访了复发延迟多发性硬化症(RRMS)的成年患者,以引发疲劳有关的症状和影响。调查问卷草案在认知访谈中汇报了更多RRMS患者,并修订。内容确认访谈与患者进行多发性硬化症(PRMS)并复发次生前进的多发性硬化(RSPM)。心理测量分析来自成年患者的不同RMS亚型和多中心,观测研究中的非RMS对照的使用数据。减少物品后,最终仪器被迁移到智能手机(EDIAR),并且可用性在与其他成人RMS患者的访谈中确认。结果:定性阶段包括37次RRM,5例,5例RSPMS患者。在概念引出期间达到了概念的饱和度。认知访谈确认参与者了解仪器的指令,项目和响应选项 - 根据预期的方式命名为FSIQ-RMS。心理学验证包括164亿卢比和74名控制患者。内部一致性和测试 - 重保持可靠性都已证明。症状结构域沿着危害症状严重程度和患者和对照组歧视。患者能够将疲劳性症状归因于RMS。确认了EDARY的可用性和概念等值(n = 10名参与者)。结论:7个症状项目和13项(3个影响亚域名:物理,认知和情绪和应对)在减少项目后,FSIQ-rms是疲劳相关症状的全面,有效,可靠的衡量标准和影响rms患者。

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