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使用视觉功能和角膜健康状况仪器评估 Fuchs 内皮角膜营养不良患者的报告视觉障碍。

Patient-Reported Visual Disability in Fuchs' Endothelial Corneal Dystrophy Measured by the Visual Function and Corneal Health Status Instrument.

机构信息

Department of Ophthalmology, Mayo Clinic, Rochester, Minnesota; Eye Center Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Department of Ophthalmology, Mayo Clinic, Rochester, Minnesota.

出版信息

Ophthalmology. 2018 Dec;125(12):1854-1861. doi: 10.1016/j.ophtha.2018.06.018. Epub 2018 Aug 10.

Abstract

PURPOSE

Measuring patient-reported visual disability in Fuchs' endothelial corneal dystrophy (FECD) may be helpful in determining when to intervene and for understanding the outcomes of intervention. In this study, we aimed to validate a new patient-reported visual disability questionnaire, the Visual Function and Corneal Health Status (V-FUCHS) instrument, in FECD before and after endothelial keratoplasty (EK).

DESIGN

Cross-sectional study with instrument readministration at 6 weeks.

PARTICIPANTS

Patients with a range of severity of FECD, including after EK, and patients with healthy corneas.

METHODS

The V-FUCHS instrument was developed based on patient interviews, expert consultations, and pretesting. Psychometric methods of classic test theory were applied to estimate reliability and validity, including testing V-FUCHS against Catquest-9SF, a cataract-specific visual disability questionnaire. Ordered polytomous Rasch-based partial credit models and item response theory diagnostics were used to define the response patterns.

MAIN OUTCOME MEASURES

Reliability (primary) and validity (secondary).

RESULTS

The final instrument was completed by 65% of patients with a range of severity of FECD (n = 41), after undergoing EK for FECD (n = 70), and with healthy corneas (n = 28). Participants were phakic or pseudophakic. Exploratory factor analysis among FECD and patients who underwent EK showed 2 independent factors of visual disability: 7 items related to visual acuity and 8 items related to glare or diurnal variation. Retest reliability was substantial (intraclass correlation coefficient, ≥0.8, both factors). Among all patients, the visual acuity factor was correlated with Catquest-9SF scores (r = 0.65; P < 0.001; n = 96). The glare or diurnal variation factor increased with FECD severity (P < 0.001, n = 69) and was higher in FECD than healthy participants (P < 0.001). Diagnostics revealed that both factors were well calibrated and met Rasch model expectations.

CONCLUSIONS

The V-FUCHS instrument is valid and reliable for assessing visual disability in FECD. The instrument allows for standardized, comprehensive, and rapid assessment of disease-specific visual disability and may be useful in clinical practice and research as a patient-reported outcome measure.

摘要

目的

在 Fuchs 内皮角膜营养不良(FECD)中测量患者报告的视觉障碍可能有助于确定何时进行干预以及了解干预的结果。本研究旨在验证一种新的患者报告视觉障碍问卷,即视觉功能和角膜健康状况(V-FUCHS)量表,用于 FECD 患者内皮角膜移植(EK)前后。

设计

横断面研究,仪器在 6 周时重新评估。

参与者

患有不同严重程度的 FECD 的患者,包括 EK 后患者,以及健康角膜的患者。

方法

V-FUCHS 量表是根据患者访谈、专家咨询和预测试开发的。经典测试理论的心理测量方法用于估计可靠性和有效性,包括将 V-FUCHS 与专门用于白内障的视觉障碍问卷 Catquest-9SF 进行比较。有序多项罗吉特基于部分信用模型和项目反应理论诊断用于定义反应模式。

主要观察指标

可靠性(主要)和有效性(次要)。

结果

患有不同严重程度的 FECD(n=41)、接受 FECD EK(n=70)和健康角膜的患者(n=28)中有 65%完成了最终的仪器评估。参与者为有晶状体或无晶状体。FECD 患者和接受 EK 的患者的探索性因子分析显示,视觉障碍有 2 个独立因素:7 项与视力相关的项目和 8 项与眩光或昼夜变化相关的项目。重测信度很高(组内相关系数,≥0.8,两个因素)。在所有患者中,视力因素与 Catquest-9SF 评分相关(r=0.65;P<0.001;n=96)。眩光或昼夜变化因素随 FECD 严重程度增加(P<0.001,n=69),且在 FECD 患者中高于健康参与者(P<0.001)。诊断结果表明,这两个因素均经过良好校准,符合罗吉特模型的预期。

结论

V-FUCHS 量表可用于评估 FECD 患者的视觉障碍,具有可靠性和有效性。该仪器可用于标准化、全面、快速评估疾病特异性视觉障碍,可作为患者报告的结果测量指标在临床实践和研究中使用。

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