Gardiner Stuart K, Demirel Shaban
Devers Eye Institute, Legacy Research Institute, Portland, Oregon.
Devers Eye Institute, Legacy Research Institute, Portland, Oregon.
Am J Ophthalmol. 2017 Apr;176:148-156. doi: 10.1016/j.ajo.2017.01.013. Epub 2017 Jan 25.
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.
Comparison of prognostic indices.
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.
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).
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.
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。
预后指标的比较。
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。
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)。
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。