Measurement of paracentral stereopsis using a new method with the binocular open perimeter imovifa® in normal adults.

IF 2.1 3区 医学 Q2 OPHTHALMOLOGY
Japanese Journal of Ophthalmology Pub Date : 2024-07-01 Epub Date: 2024-05-18 DOI:10.1007/s10384-024-01066-2
Akemi Wakayama, Chota Matsumoto, Keisuke Utamura, Ryo Narita, Shunji Kusaka
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引用次数: 0

Abstract

Purpose: No method to quantitatively evaluate stereopsis within the 15º visual field has been clinically established. We developed a program to measure paracentral stereopsis and evaluated its feasibility in visually normal participants.

Study design: Experimental investigation METHODS: Ten visually normal volunteers with stereopsis of 60 arcseconds or better were included. The Stereo Eccentricity Analysis (SEA) program for stereopsis measurement across the visual field was integrated into the binocular visual field analyzer imovifa®. Subjects with established binocular stereopsis detected a stereoscopic circular target presented with crossed disparity on random dots at the fovea, 3°, 5°, 10°, and 15° on the 45°, 135°, 225°, and 315° meridians. The subjects performed two tasks for measurement in the periphery: a detection task by pressing the response button when the circular target was perceived and a localization task by tilting a joystick to indicate in which quadrant the circular target was perceived. The duration of the target presentation was 500 ms.

Results: The stereo thresholds at 0º and 3° did not significantly differ. The thresholds at 10º and 15º were significantly higher than at 0° (P < 0.01). While no inter-individual threshold difference was observed at the fovea, the difference was large at 15°. The stereo thresholds for the detection and localization tasks also did not differ significantly.

Conclusion: With the SEA program, paracentral stereopsis can be measured and the stereo threshold increases with eccentricity. The SEA program appears to be a feasible clinical method to evaluate paracentral stereopsis.

Abstract Image

使用一种新方法,利用双目开放式周边imovifa®测量正常成年人的旁中心立体视。
目的:目前临床上还没有一种方法可以定量评估 15º 视野内的立体视。我们开发了一种测量旁中心立体视的程序,并对其在视力正常者中的可行性进行了评估:研究设计:实验调查 方法:纳入 10 名视力正常、立体视达到或优于 60 弧秒的志愿者。用于测量整个视野立体视的立体偏心分析(SEA)程序被集成到双眼视野分析仪 imovifa® 中。已建立双眼立体视的受试者检测在眼窝、45°、135°、225°和 315°经线上的 3°、5°、10°和 15°随机点上呈现的交叉色差立体圆形目标。受试者在外围进行了两项测量任务:一项是检测任务,受试者在感知到圆形目标时按下反应按钮;另一项是定位任务,受试者通过倾斜操纵杆来指示感知到圆形目标的象限。目标呈现的持续时间为 500 毫秒:结果:0º 和 3º 时的立体阈值没有显著差异。10º 和 15º 的阈值明显高于 0°(P < 0.01)。虽然在眼窝处没有观察到个体间的阈值差异,但在 15°处差异很大。检测和定位任务的立体阈值也没有明显差异:结论:使用 SEA 程序可以测量旁中心立体视,立体视阈值随偏心率的增加而增加。SEA程序似乎是评估中心点旁立体视的一种可行的临床方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.80
自引率
8.30%
发文量
65
审稿时长
6-12 weeks
期刊介绍: The Japanese Journal of Ophthalmology (JJO) was inaugurated in 1957 as a quarterly journal published in English by the Ophthalmology Department of the University of Tokyo, with the aim of disseminating the achievements of Japanese ophthalmologists worldwide. JJO remains the only Japanese ophthalmology journal published in English. In 1997, the Japanese Ophthalmological Society assumed the responsibility for publishing the Japanese Journal of Ophthalmology as its official English-language publication. Currently the journal is published bimonthly and accepts papers from authors worldwide. JJO has become an international interdisciplinary forum for the publication of basic science and clinical research papers.
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