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本文引用的文献

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Structure versus Function in Glaucoma: The Debate That Doesn't Need to Be.青光眼的结构与功能:无需进行的争论
Ophthalmology. 2016 Jun;123(6):1170-2. doi: 10.1016/j.ophtha.2016.03.023.
2
Unsupervised Gaussian Mixture-Model With Expectation Maximization for Detecting Glaucomatous Progression in Standard Automated Perimetry Visual Fields.用于检测标准自动视野计视野中青光眼进展的基于期望最大化的无监督高斯混合模型
Transl Vis Sci Technol. 2016 May 3;5(3):2. doi: 10.1167/tvst.5.3.2. eCollection 2016 May.
3
Progression of primary open angle glaucoma in asymmetrically myopic eyes.原发性开角型青光眼在不对称性近视眼中的进展
Graefes Arch Clin Exp Ophthalmol. 2016 Jul;254(7):1331-7. doi: 10.1007/s00417-016-3332-z. Epub 2016 Apr 11.
4
Suitability of the Visual Field Index according to Glaucoma Severity.根据青光眼严重程度的视野指数适用性
J Curr Glaucoma Pract. 2015 Sep-Dec;9(3):65-8. doi: 10.5005/jp-journals-10008-1186. Epub 2016 Feb 2.
5
Changes in Retinal Nerve Fiber Layer Reflectance Intensity as a Predictor of Functional Progression in Glaucoma.视网膜神经纤维层反射强度变化作为青光眼功能进展的预测指标
Invest Ophthalmol Vis Sci. 2016 Mar;57(3):1221-7. doi: 10.1167/iovs.15-18788.
6
Structural and Functional Progression in the Early Manifest Glaucoma Trial.早期显性青光眼试验中的结构与功能进展
Ophthalmology. 2016 Jun;123(6):1173-80. doi: 10.1016/j.ophtha.2016.01.039. Epub 2016 Mar 2.
7
Rates of glaucomatous visual field change before and after transscleral cyclophotocoagulation: a retrospective case series.经巩膜睫状体光凝术前后青光眼性视野改变的发生率:一项回顾性病例系列研究
BMC Ophthalmol. 2015 Dec 14;15:179. doi: 10.1186/s12886-015-0166-0.
8
Progression of visual field in patients with primary open-angle glaucoma - ProgF study 1.原发性开角型青光眼患者视野进展 - ProgF研究1
Acta Ophthalmol. 2015 Dec;93(8):e615-20. doi: 10.1111/aos.12788. Epub 2015 Jun 12.
9
The Effect of Stimulus Size on the Reliable Stimulus Range of Perimetry.刺激大小对视野检查可靠刺激范围的影响。
Transl Vis Sci Technol. 2015 Mar 27;4(2):10. doi: 10.1167/tvst.4.2.10. eCollection 2015 Mar.
10
Prediction of Glaucomatous Visual Field Progression Using Baseline Clinical Data.使用基线临床数据预测青光眼性视野进展
J Glaucoma. 2016 Feb;25(2):228-35. doi: 10.1097/IJG.0000000000000146.

使用标准全视野指标检测青光眼的变化

Detecting Change Using Standard Global Perimetric Indices in Glaucoma.

作者信息

Gardiner Stuart K, Demirel Shaban

机构信息

Devers Eye Institute, Legacy Research Institute, Portland, Oregon.

Devers Eye Institute, Legacy Research Institute, Portland, Oregon.

出版信息

Am J Ophthalmol. 2017 Apr;176:148-156. doi: 10.1016/j.ajo.2017.01.013. Epub 2017 Jan 25.

DOI:10.1016/j.ajo.2017.01.013
PMID:28130041
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5376527/
Abstract

PURPOSE

Various global indices are available to summarize results from standard automated perimetry. This study asks which index can detect significant deterioration earliest, for a fixed specificity.

DESIGN

Comparison of prognostic indices.

METHODS

Two cohorts were tested. A test-retest cohort contained 5 reliable visual fields, within a short interval, from 45 eyes of 23 participants with glaucoma and/or likelihood of developing glaucoma. A separate longitudinal cohort contained 508 eyes from 330 participants, tested on average 13 times. Three global indices were extracted: mean deviation (MD), pattern standard deviation (PSD), and visual field index (VFI). For each index we defined a critical P value Crit, such that 5% of test-retest series showed significant deterioration with P < Crit, using artificial "test dates" in random order. Therefore these criteria have 95% specificity over series of 5 tests. The times to detect significant deterioration in the longitudinal cohort were compared using a survival analysis model.

RESULTS

The median time to detect significant deterioration with MD was 7.3 years (95% confidence interval [CI] 6.8-7.9 years). For VFI, the median was 8.5 years (95% CI 7.9-9.0 years); this comparison had P = .088. For PSD, the median was 10.5 years (95% CI 9.3-11.7 years), slower than MD with P < .001. Within the first 5 years of a series, MD detected significant deterioration in 138 eyes, vs 104 for VFI (P = .0013) and 107 for PSD (P = .029).

CONCLUSIONS

MD detected significant deterioration sooner than VFI or PSD. In particular, MD detected more eyes in the first 5 years of their follow-up, which were presumably undergoing more rapid progression.

摘要

目的

有多种总体指标可用于总结标准自动视野检查的结果。本研究旨在探讨在固定特异性的情况下,哪种指标能最早检测到显著恶化。

设计

预后指标的比较。

方法

测试了两个队列。一个重测队列包含23名青光眼患者和/或有患青光眼可能性的参与者的45只眼睛在短时间间隔内的5次可靠视野检查。另一个独立的纵向队列包含330名参与者的508只眼睛,平均测试了13次。提取了三个总体指标:平均偏差(MD)、模式标准差(PSD)和视野指数(VFI)。对于每个指标,我们定义了一个临界P值Crit,使得5%的重测系列在P < Crit时显示出显著恶化,使用随机顺序的人工“测试日期”。因此,这些标准在5次测试系列中的特异性为95%。使用生存分析模型比较纵向队列中检测到显著恶化的时间。

结果

MD检测到显著恶化的中位时间为7.3年(95%置信区间[CI] 6.8 - 7.9年)。对于VFI,中位时间为8.5年(95% CI 7.9 - 9.0年);此比较的P = 0.088。对于PSD,中位时间为10.5年(95% CI 9.3 - 11.7年),比MD慢,P < 0.001。在系列的前5年中,MD在138只眼中检测到显著恶化,而VFI为104只眼(P = 0.0013),PSD为107只眼(P = 0.029)。

结论

MD比VFI或PSD更早检测到显著恶化。特别是,MD在随访的前5年中检测到更多的眼睛,这些眼睛可能进展更快。