Molecular and Integrative Biology, Institute of Systems, University of Liverpool, Liverpool, United Kingdom; Walton Centre NHS Foundation Trust, Liverpool, United Kingdom.
Northern Care Alliance NHS Trust, Salford, United Kingdom.
Mult Scler Relat Disord. 2023 Dec;80:105115. doi: 10.1016/j.msard.2023.105115. Epub 2023 Oct 30.
Visual dysfunction is common in people with Multiple Sclerosis (pwMS), associated with a variety of visual symptoms. Capturing the patient experience of these complex patterns of visual pathology is challenging. A valid and reliable patient reported measure, capable of detecting clinically significant change, would have considerable research and clinical benefits. We examined the properties of the MS Vision Questionnaire (MSVQ-7) in a large MS population.
Data were collected from participants in the UK-wide Trajectories of Outcome in Neurological Conditions-MS (TONiC-MS) study: MS subtype and Expanded Disability Status Scale (EDSS) band from the clinical team, as well as serial packs including the MSVQ-7 and questionnaires on depression, anxiety and stigma. A calibration sample of 1000 pwMS contributing several years of follow-up were split into training and validation samples for a Confirmatory Factor Analysis and Rasch analysis. The Minimal Detectable Change (MDC) was computed as well as the Minimal Clinically Important Change (MIC), by an anchor-based method, for different MS subtypes.
The MSVQ-7 is unidimensional and can be fit to the Rasch model with a solution discarding 3% of variance. Providing all 7 items are answered, the total can be converted to an interval-level metric for calculation of change scores and other parametric analyses. The % of missing values did not exceed 1.7%. Among 5478 pwMS, 80% reported visual problems. MSVQ-7 scores were categorised as mild for 36.1%, moderate for 33.6% and severe for 10.3%, and varied by MS subtype. In the follow-up sample of 2227 pwMS, 42.5% changed MSVQ-7 category between baseline and first follow-up (mean 22.6 months). The MIC exceeded the MDC so clinically significant change exceeds measurement error. While MDC was identical for relapsing and progressive MS, MIC varied by MS subtype, with smaller MIC in relapsing MS. Over one-quarter of the follow-up sample reported a clinically significant change in MSVQ-7: 12.2% improved and 13.5% deteriorated. For pwMS recruited within 2 years of diagnosis, 17.3% reported significant change on follow-up, all improving. MSVQ-7 scores showed strong associations with anxiety, depression and stigma (effect sizes>0.8). Duration, EDSS band and MS subtype all had effect sizes 0.2-0.49. A multinomial logistic regression exploring vision disturbance and depression, adjusted for age, gender, MS subtype, duration and disability, showed vision is the strongest significant predictor of depression. Each unit increase in interval MSVQ-7 increases risk by 10% of 'possible' and by 17% of 'probable' depression.
The MSVQ-7 is a brief self-report measure of visual problems for pwMS. It can easily be converted to interval-level measurement for change scores or power calculations and has good precision and discrimination. Visual problems were reported by 80% of pwMS and changed over time, evidencing the need for regular monitoring. MIC varied by MS subtype, indicating that perception of impact changes over the disease course. Visual dysfunction significantly affects depression risk and perceived stigma, highlighting the importance of routine assessment of visual problems in comprehensive care. The MSVQ-7 has strong psychometric properties for adoption as a measure for vision in clinical and research settings.
多发性硬化症(pwMS)患者常见视觉功能障碍,伴有多种视觉症状。捕捉这些复杂的视觉病理模式的患者体验具有挑战性。一种有效的、可靠的患者报告的测量方法,能够检测到临床显著的变化,将具有相当大的研究和临床益处。我们在一个大型 MS 人群中研究了 MS 视觉问卷(MSVQ-7)的特性。
数据来自英国范围内的神经疾病轨迹研究(TONiC-MS):临床团队提供 MS 亚型和扩展残疾状况量表(EDSS)等级,以及包括 MSVQ-7 和抑郁、焦虑和耻辱感问卷在内的系列问卷。1000 名 pwMS 的校准样本为后续研究提供了几年的随访数据,这些样本被分为训练样本和验证样本,用于验证性因素分析和 RASCH 分析。通过锚定方法计算了最小可检测变化(MDC)和最小临床重要变化(MIC),适用于不同的 MS 亚型。
MSVQ-7 是一个单维度的,可以通过 RASCH 模型拟合,解决方案丢弃了 3%的方差。如果所有 7 个项目都回答,总分数可以转换为区间水平的度量,用于计算变化分数和其他参数分析。缺失值的百分比不超过 1.7%。在 5478 名 pwMS 中,80%报告有视觉问题。MSVQ-7 评分分为轻度(36.1%)、中度(33.6%)和重度(10.3%),因 MS 亚型而异。在 2227 名 pwMS 的随访样本中,42.5%的人在基线和第一次随访之间改变了 MSVQ-7 类别(平均随访时间为 22.6 个月)。MIC 超过 MDC,因此临床显著变化超过测量误差。虽然 MDC 在复发型和进展型 MS 中是相同的,但 MIC 因 MS 亚型而异,复发型 MS 的 MIC 较小。超过四分之一的随访样本报告了 MSVQ-7 的临床显著变化:12.2%的人改善,13.5%的人恶化。对于在诊断后 2 年内招募的 pwMS,17.3%的人在随访时报告有显著变化,所有改善。MSVQ-7 评分与焦虑、抑郁和耻辱感(效应大小>0.8)有很强的相关性。病程、EDSS 等级和 MS 亚型的效应大小为 0.2-0.49。探索视力障碍和抑郁的多元逻辑回归,调整了年龄、性别、MS 亚型、病程和残疾,显示视力是抑郁的最强显著预测因素。MSVQ-7 的间隔评分每增加一个单位,“可能”的抑郁风险增加 10%,“可能”的抑郁风险增加 17%。
MSVQ-7 是一种用于 pwMS 视觉问题的简短自我报告测量方法。它可以很容易地转换为区间水平的测量,用于变化分数或功效计算,具有良好的精度和区分度。80%的 pwMS 报告有视觉问题,并且随着时间的推移而变化,这证明了需要定期监测。MIC 因 MS 亚型而异,表明在疾病过程中对影响的感知会发生变化。视觉功能障碍显著影响抑郁风险和感知耻辱感,突出了在综合护理中常规评估视觉问题的重要性。MSVQ-7 具有很强的心理测量学特性,可作为临床和研究环境中视觉的测量方法。