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比较 10-2 和 24-2 视野检查在青光眼早期中心异常眼中检测进展性中心视觉丧失的效果。

Comparing 10-2 and 24-2 Visual Fields for Detecting Progressive Central Visual Loss in Glaucoma Eyes with Early Central Abnormalities.

机构信息

Hamilton Glaucoma Center, Department of Ophthalmology, University of California, San Diego, La Jolla, California.

Ophthalmology, Department of Surgery, The University of Melbourne, Melbourne, Australia.

出版信息

Ophthalmol Glaucoma. 2019 Mar-Apr;2(2):95-102. doi: 10.1016/j.ogla.2019.01.003. Epub 2019 Jan 14.

Abstract

PURPOSE

To compare the ability of 10-2 visual field tests and central 12 locations of the 24-2 tests (C24-2) to detect central visual field progression in glaucoma eyes with early central visual field abnormalities.

DESIGN

Observational cohort study.

PARTICIPANTS

Three-hundred eyes of 180 participants with glaucoma or ocular hypertension.

METHODS

Participants with both 10-2 and 24-2 tests performed on ≥3 visits over ≥1-year period were included to estimate the longitudinal variability of 10-2 and C24-2 visual field mean deviation (MD). The variability estimates were then used to reconstruct real-world visual field results by computer simulations, in a scenario where eyes had a baseline 10-2 and C24-2 MD was -2 dB and exhibited various rates of change (-0.25, -0.50, -0.75 and -1.00 dB/year), and the time to detect these changes were evaluated using trend-based analyses.

MAIN OUTCOME MEASURES

Time required to detect progression.

RESULTS

Overall, the time to detect central visual field progression was reduced by 7-9% using the 10-2 compared to C24-2 MD values, equivalent to a total reduction of 0.1-0.3 dB lost. For example, 90% of eyes with a central 10-2 or C24-2 MD loss of -0.50 dB/year would be detected after 5.0 and 5.5 years of semi-annual testing respectively, or after 3.4 and 3.7 years respectively for eyes with a -1.00 dB/year loss.

CONCLUSIONS

Trend-based analyses using 10-2 MD resulted in a mild reduction (7-9%) in the time to detect central visual field progression compared to C24-2 MD in glaucoma eyes with early central visual field abnormalities. Further studies are needed to determine whether other progression analyses can better exploit the increased sampling of 10-2 tests. These findings provide evidence-based guidance on the potential value-add of 10-2 testing in the clinical management of glaucoma patients.

摘要

目的

比较 10-2 视野测试和中央 12 个位置的 24-2 测试(C24-2)在检测早期中央视野异常的青光眼眼中中央视野进展的能力。

设计

观察性队列研究。

参与者

180 名参与者的 300 只眼睛患有青光眼或高眼压症。

方法

纳入了在≥1 年期间进行了≥3 次 10-2 和 24-2 测试的参与者,以估计 10-2 和 C24-2 视野平均偏差(MD)的纵向变异性。然后,使用计算机模拟重建真实世界的视野结果,假设眼睛的基线 10-2 和 C24-2 MD 为-2 dB,并显示出各种变化率(-0.25、-0.50、-0.75 和-1.00 dB/年),并使用基于趋势的分析评估检测这些变化的时间。

主要观察指标

检测进展所需的时间。

结果

总体而言,与 C24-2 MD 值相比,使用 10-2 视野 MD 值可将中央视野进展的检测时间缩短 7-9%,相当于总共减少 0.1-0.3 dB 的损失。例如,90%的中央 10-2 或 C24-2 MD 每年损失 0.50 dB/年的眼睛,分别在 5.0 和 5.5 年的半年度测试后和每年损失 1.00 dB/年的眼睛分别在 3.4 和 3.7 年后会被检测到。

结论

使用 10-2 MD 进行基于趋势的分析与使用 C24-2 MD 相比,在患有早期中央视野异常的青光眼眼中,检测中央视野进展的时间略有缩短(7-9%)。需要进一步的研究来确定其他进展分析是否可以更好地利用 10-2 测试的增加采样。这些发现为 10-2 测试在青光眼患者临床管理中的潜在增值提供了循证指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac07/6860370/1964ff46f310/nihms-1518640-f0001.jpg

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