通过主动学习定量对比敏感度功能测试评估后玻璃体脱落的视觉功能受损情况

IF 0.5 Q4 OPHTHALMOLOGY
Journal of VitreoRetinal Diseases Pub Date : 2024-07-30 eCollection Date: 2024-09-01 DOI:10.1177/24741264241259245
Peyman Razavi, Filippos Vingopoulos, Mauricio Garcia, Francesco Romano, Hanna Choi, Xinyi Ding, Itika Garg, Grace Baldwin, Rebecca Zeng, Matthew Finn, Augustine Bannerman, Hannah Wescott, Leo A Kim, Deeba Husain, Demetrios Vavvas, John B Miller
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引用次数: 0

摘要

简介利用主动学习定量对比敏感度功能测试,研究玻璃体后脱离(PVD)患者是否存在视觉功能障碍。方法: 在这项横断面研究中,对玻璃体后脱离患者的对比敏感度进行了测试:在这项横断面研究中,使用自适应感官技术平台上的定量对比敏感度功能算法测量了患有 PVD 和未患有 PVD 的眼睛的对比敏感度。结果包括对比敏感度函数对数曲线下的面积、对比敏锐度以及每度 1 到 18 个周期(cpd)的对比敏感度阈值。此外,还测量了斯奈伦视力(VA)。在控制年龄和晶状体状态的前提下,进行了混合效应多元线性回归分析,以评估是否存在 PVD 与视觉功能之间的关联。结果:研究对象包括 205 名参与者的 232 只健康眼睛,其中 69 名患者的 80 只眼睛患有 PVD。视力和 PVD 之间没有明显联系。然而,PVD 与 1.5 cpd(β,-0.058;P = .003)和 3 cpd(β,-0.067;P = .004)对比敏感度阈值的降低有明显关系。较低(1 cpd)或较高(6、12、18 cpd)空间频率下的对比敏感度阈值与 PVD 的存在无明显相关性。即使在有症状的 PVD 眼睛亚组中,视力也没有明显下降,而定量对比敏感度功能结果显示在低空间频率(1.5 cpd 和 3 cpd)下存在视觉功能障碍。结论是通过定量对比敏感度功能测试测量的对比敏感度显示,患有 PVD 的眼睛存在视觉功能缺陷,而仅通过 VA 测试可能会漏掉这些缺陷。将该测试纳入视网膜临床可能会对患有 PVD 的眼睛进行更全面的功能评估,作为临床决策的辅助结果指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impaired Visual Function in Posterior Vitreous Detachment Assessed With the Active-Learning Quantitative Contrast Sensitivity Function Test.

Introduction: To investigate whether there is visual function impairment in patients with posterior vitreous detachment (PVD) using the active-learning quantitative contrast sensitivity function test. Methods: In this cross-sectional study, contrast sensitivity was measured in eyes with PVD and eyes without PVD using the quantitative contrast sensitivity function algorithm on the Adaptive Sensory Technology platform. Outcomes included the area under the log contrast sensitivity function curve, contrast acuity, and contrast sensitivity thresholds at 1 to 18 cycles per degree (cpd). Snellen visual acuity (VA) was also measured. Mixed-effects multiple linear regression analyses were performed to evaluate the association between the presence of PVD and visual function, controlling for age and lens status. Results: The cohort comprised 232 healthy eyes of 205 participants; of these, 80 eyes of 69 patients had PVD. There was no significant association between VA and PVD presence. However, PVD was significantly associated with decreased contrast sensitivity thresholds at 1.5 cpd (β, -0.058; P = .003) and 3 cpd (β, -0.067; P = .004). Contrast sensitivity thresholds at lower (1 cpd) or higher (6, 12, 18 cpd) spatial frequencies did not significantly correlate with PVD presence. Even in the subgroup of symptomatic PVD eyes, VA was not significantly decreased, while quantitative contrast sensitivity function outcomes showed visual function deficits at low spatial frequencies (1.5 cpd and 3 cpd). Conclusions: Contrast sensitivity measured with the quantitative contrast sensitivity function test showed visual function deficits in eyes with PVD that would have been missed with VA testing alone. Incorporating this test in the retina clinic might offer a more comprehensive functional assessment of eyes with PVD, serving as an adjunct outcome metric in clinical decision-making.

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