Jules Stein Eye Institute, University of California at Los Angeles School of Medicine, Los Angeles, California 90025, USA.
Invest Ophthalmol Vis Sci. 2011 Jul 1;52(7):4765-73. doi: 10.1167/iovs.10-6414.
This study was conducted to measure the rate of visual field (VF) decay in glaucoma, to separate faster and slower components of decay, and to predict the rate of VF decay.
Patients who had primary glaucoma and 6 or more years of follow-up were included. Thresholds at each VF location were regressed with linear, quadratic, and exponential models. The best model was used to parse the VF into slower and faster rate components. Two independent cohorts (glaucoma [n = 87] and cataract [n = 38]) were used to determine the technique's ability to distinguish areas of glaucomatous VF changes from those caused by cataract. VF forecasts, derived from the first half of follow-up, were compared with actual VF thresholds at the end of follow-up.
The mean (±SD) years of follow-up and number of VFs for the main cohort (389 eyes of 309 patients) were 8.2 (±1.1) years and 15.7 (±3.0), respectively. The proportions of best fits were linear 2%, quadratic 1%, and exponential 97%. Proportions of eyes with exponential rates of decay ≥10% for the entire visual field (VF), faster components, and slower components were 20%, 56%, and 4%, respectively. The difference in decay rates between the faster and slower components was greater in the independent glaucoma cohort (19% ± 10%) than in the cataract cohort (5% ± 5%; P < 0.001). Test location forecasts significantly correlated with measured values (r(2) = 0.67; P < 0.001).
This method isolates faster and slower components of VF decay in glaucoma, can identify patients who are fast progressors, and can predict patterns of future VF loss with appropriate confidence intervals. (ClinicalTrials.gov number, NCT00000148.).
本研究旨在测量青光眼视野(VF)的衰退率,分离衰退的较快和较慢成分,并预测 VF 衰退的速率。
纳入患有原发性青光眼且随访时间超过 6 年的患者。使用线性、二次和指数模型对每个 VF 位置的阈值进行回归。使用最佳模型将 VF 分割为较慢和较快的速率成分。使用两个独立的队列(青光眼[87 例]和白内障[38 例])来确定该技术区分青光眼 VF 变化区域与白内障引起的 VF 变化区域的能力。从随访前半部分得出的 VF 预测值与随访结束时的实际 VF 阈值进行比较。
主要队列(309 例患者的 389 只眼)的平均(±SD)随访时间和 VF 数量分别为 8.2(±1.1)年和 15.7(±3.0)。最佳拟合比例分别为线性 2%、二次 1%和指数 97%。整个 VF、较快成分和较慢成分中,以指数方式衰减的比例分别为 20%、56%和 4%,其衰减率大于 10%。在独立的青光眼队列中,较快和较慢成分之间的衰减率差异(19%±10%)大于白内障队列(5%±5%;P<0.001)。测试位置预测值与实测值显著相关(r²=0.67;P<0.001)。
该方法可以分离青光眼 VF 衰退的较快和较慢成分,能够识别出快速进展的患者,并可以在适当的置信区间内预测未来 VF 损失的模式。(临床试验.gov 编号,NCT00000148。)