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干燥综合征相关生活质量量表(SRQoL)的开发与内容效度验证

The Development and Content Validation of the Sjögren's Related Quality of Life Instrument (SRQoL).

作者信息

Marvel Jessica, Gargon Elizabeth, Howse Chloe, Chohan Aishwarya, Mayhew Megan, Kenney Gayle, Stone Linda, Fisher Benjamin A, Steenackers Monia, Williamson Nicola, Perella Chiara, Goswami Pushpendra

机构信息

Novartis Services Inc., East Hanover, NJ, USA.

Patient-Centered Outcomes, Adelphi Values Ltd., Bollington, UK.

出版信息

Rheumatol Ther. 2024 Dec;11(6):1591-1609. doi: 10.1007/s40744-024-00718-6. Epub 2024 Oct 10.

Abstract

INTRODUCTION

Several clinical outcome assessment (COA) instruments assess Sjögren's disease (Sjögren's) symptoms, but do not provide comprehensive assessment of the health-related quality of life (HRQoL) impact of Sjögren's. This study aimed to develop a patient-reported outcome (PRO) instrument for the assessment of HRQoL, intended for use in clinical trials and clinical practice in the assessment of treatment benefit.

METHODS

Review of study sponsor proprietary data and qualitative interviews informed the development of a conceptual model, the Sjögren's Related Quality of Life (SRQoL) and patient global impression of severity (PGI-S) and change (PGI-C) items. Combined concept elicitation and cognitive debriefing interviews with patients with Sjögren's explored their HRQoL impact experience and content validity of the SRQoL and PGI items.

RESULTS

Twenty participants were interviewed about their Sjögren's experience. Following inductive analysis of interviews, concepts were categorized into eight domains: emotional well-being (e.g., worry and stress; n = 20/20; 100%), sleep (e.g., daytime sleepiness and waking up during the night; n = 20/20; 100%), activities of daily living (e.g., difficulty looking at screens and difficulty driving; n = 20/20; 100%), cognition (e.g., concentration difficulties and word finding difficulties; n = 19/20; 95.0%), physical functioning (e.g., difficulty walking and difficulty exercising; n = 19/20; 95.0%), social and family functioning (e.g., dependent on others and relationship difficulties; n = 17/20; 85.0%), work (n = 15/20; 75.0%), and sexual functioning (n = 12/20; 60.0%). SRQoL and PGI items, instructions, response options, and recall period were well understood and relevant to participants.

CONCLUSIONS

The SRQoL is a new PRO instrument to assess Sjögren's impact on HRQoL, developed in accordance with regulatory guidance. This study provides considerable insight into the patient experience of Sjögren's and evidence to support the content validity of the SRQoL. Future research should evaluate the psychometric properties of the SRQoL to support its use in clinical trials and clinical practice and further validate its use as an assessment of treatment benefit.

摘要

引言

多种临床结局评估(COA)工具可评估干燥综合征的症状,但未全面评估干燥综合征对健康相关生活质量(HRQoL)的影响。本研究旨在开发一种患者报告结局(PRO)工具,用于评估HRQoL,旨在用于临床试验和临床实践中评估治疗效果。

方法

回顾研究申办者的专有数据并进行定性访谈,为概念模型、干燥综合征相关生活质量(SRQoL)以及患者总体严重程度印象(PGI-S)和变化印象(PGI-C)项目的开发提供依据。对干燥综合征患者进行概念引出和认知反馈访谈相结合的方式,探讨他们的HRQoL影响体验以及SRQoL和PGI项目的内容效度。

结果

对20名参与者进行了关于他们干燥综合征经历的访谈。对访谈进行归纳分析后,概念被分为八个领域:情绪健康(如担忧和压力;n = 20/20;100%)、睡眠(如白天嗜睡和夜间醒来;n = 20/20;100%)、日常生活活动(如看屏幕困难和驾驶困难;n = 20/20;100%)、认知(如注意力不集中和找词困难;n = 19/20;95.0%)、身体功能(如行走困难和锻炼困难;n = 19/20;95.0%)、社会和家庭功能(如依赖他人和关系困难;n = 17/20;85.0%)、工作(n = 15/20;75.0%)和性功能(n = 12/20;60.0%)。SRQoL和PGI项目、说明、回答选项以及回忆期都易于理解且与参与者相关。

结论

SRQoL是一种新的PRO工具,用于评估干燥综合征对HRQoL的影响,是根据监管指南开发的。本研究为干燥综合征患者的体验提供了相当多的见解,并为支持SRQoL的内容效度提供了证据。未来的研究应评估SRQoL的心理测量特性,以支持其在临床试验和临床实践中的应用,并进一步验证其作为治疗效果评估工具的用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12fe/11557853/7f8ef5941857/40744_2024_718_Fig1_HTML.jpg

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