Evaluating Measurement Properties of Patient-Reported Outcome Measures in Glaucoma

IF 2.8 Q1 OPHTHALMOLOGY Ophthalmology. Glaucoma Pub Date : 2023-09-01 DOI:10.1016/j.ogla.2023.04.007
Anastasiya Vinokurtseva MD , Matthew P. Quinn MD, PhD , Mandy Wai BSc , Victoria Leung BMSc , Monali Malvankar-Mehta PhD , Cindy M.L. Hutnik MD, PhD
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Abstract

Topic

The purpose of the current study was to systematically identify and evaluate existing patient-reported outcome measures (PROMs) for clinical glaucoma practice.

Clinical Relevance

Understanding and incorporating patient preferences into decision-making is now recognized as critical for optimal resource allocation, especially in technologically advancing areas, such as minimally invasive surgeries. Patient-reported outcome measures are instruments designed to evaluate the health outcomes that are most important to patients. Despite their recognized importance, especially in the era of patient-centered care, their routine use in clinical settings remains low.

Methods

A systematic literature search was conducted in 6 databases (EMBASE, MEDLINE, PsycINFO, Scopus, BIOSIS, and Web of Science) from the date of inception. Studies were included in the qualitative review if they reported measurement properties of PROMs in adult patients with glaucoma. COnsensus-based Standards for the selection of health Measurement INstruments guidelines were used to assess the included PROMs. The study protocol is registered with PROSPERO (registration number: CRD42020176064).

Results

The literature search yielded 2661 records. After deduplication, 1259 studies entered level 1 screening, and based on title and abstract review, 164 records proceeded to full-text screening. In 48 included studies, 70 instrument reports discuss 43 distinct instruments in 3 major categories: glaucoma-specific, vision-specific, and general health-related quality of life. Most used measures were glaucoma-specific (Glaucoma Quality of Life [GQL] and Glaucoma Symptom Scale [GSS]) and vision-specific (National Eye Institute Visual Function Questionnaire [NEI VFQ-25]). All 3 have sufficient validity (especially construct), with GQL and GSS having sufficient internal consistency, cross-cultural validity, and reliability, with reports suggesting high methodological quality.

Conclusion

The GQL, GSS, and NEI VFQ-25 are the 3 most used questionnaires in a research setting, having considerable validation in a patient population with glaucoma. Limited reports on interpretability, responsiveness, and feasibility in all 43 identified instruments make identifying a single optimal questionnaire for clinical use challenging and highlight the need for further studies.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

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评估青光眼患者报告结果测量的测量特性
主题当前研究的目的是系统地识别和评估临床青光眼实践中现有的患者报告结果测量(PROM)。临床相关性了解患者偏好并将其纳入决策现在被认为是优化资源分配的关键,尤其是在技术进步的领域,如微创手术。患者报告的结果测量是旨在评估对患者最重要的健康结果的工具。尽管它们具有公认的重要性,尤其是在以患者为中心的护理时代,但它们在临床环境中的常规使用率仍然很低。方法从创建之日起,在EMBASE、MEDLINE、PsycINFO、Scopus、BIOSIS和Web of Science 6个数据库中进行系统的文献检索。如果研究报告了成年青光眼患者PROM的测量特性,则将其纳入定性审查。基于康森索斯的健康测量仪器选择标准指南用于评估纳入的PROM。研究方案已在PROSPERO注册(注册号:CRD42020176064)。结果文献检索得到2661条记录。重复数据消除后,1259项研究进入1级筛选,根据标题和摘要审查,164项记录进入全文筛选。在48项纳入的研究中,70份仪器报告讨论了3大类43种不同的仪器:青光眼特异性、视力特异性和一般健康相关生活质量。最常用的测量方法是青光眼特异性(青光眼生活质量[GQL]和青光眼症状量表[GSS])和视力特异性(国家眼科研究所视觉功能问卷[NEI VFQ-25])。所有3项都具有足够的有效性(尤其是结构),GQL和GSS具有足够的内部一致性、跨文化有效性和可靠性,报告表明方法论质量很高。结论GQL、GSS和NEI VFQ-25是研究环境中使用最多的三种问卷,在青光眼患者群体中具有相当大的验证性。关于所有43种已确定仪器的可解释性、响应性和可行性的有限报告,使得确定一份用于临床的最佳问卷具有挑战性,并强调了进一步研究的必要性。财务披露专有或商业披露可在本文末尾的脚注和披露中找到。
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来源期刊
Ophthalmology. Glaucoma
Ophthalmology. Glaucoma OPHTHALMOLOGY-
CiteScore
4.80
自引率
6.90%
发文量
140
审稿时长
46 days
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