Department of Ophthalmology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Eye (Lond). 2009 Aug;23(8):1647-52. doi: 10.1038/eye.2008.348. Epub 2008 Nov 14.
To investigate whether frequency-doubling perimetry (FDT) and nerve fibre analyser (GDx) test results are able to predict glaucomatous visual field loss in glaucoma suspect patients.
A large cohort of glaucoma suspect patients (patients with ocular hypertension or a positive family history of glaucoma without visual field abnormalities at baseline) was followed prospectively for 4 years with SAP (HFA 30-2 SITA fast), FDT (C-20 full threshold), and GDx (version 2.010) in a clinical setting. After the follow-up period, baseline FDT and GDx test results of converters (glaucoma suspect patients who had converted to a reproducible abnormal SAP test result during follow-up) were compared to that of non-converters (suspects with normal SAP test results at the end of the follow-up) by calculating relative risks. Cutoff point for FDT was >1 depressed test point P<0.01 in the total deviation probability plot; cutoff point for GDx was the number >29.
Of 174 glaucoma suspect patients, 26 had developed reproducible glaucomatous visual field loss (conversion rate: 3.7% per year). Relative risk was 1.8 (95% confidence interval: 0.9-3.7; P=0.10) for FDT and 2.7 (95% confidence interval: 1.2-6.3; P=0.01) for GDx. Positive predictive value was 0.22 for both FDT and GDx; negative predictive value was 0.88 for FDT and 0.92 for GDx.
In a clinical setting, especially GDx may be helpful for identifying glaucoma suspect patients at risk of developing glaucomatous visual field loss as assessed by SAP.
探讨频域光相干断层扫描(FDT)和神经纤维分析(GDx)的检测结果能否预测青光眼患者的视野损失。
对大量青光眼疑似患者(高眼压或有阳性青光眼家族史但基线时无视野异常的患者)进行前瞻性随访,时间为 4 年,采用标准自动视野计(HFA 30-2 SITA 快速)、FDT(C-20 全阈值)和 GDx(2.010 版)进行临床检测。在随访结束后,计算相对风险,比较转换者(在随访期间转为重复性异常 SAP 检测结果的青光眼疑似患者)和未转换者(随访结束时 SAP 检测结果正常的疑似患者)的基线 FDT 和 GDx 检测结果。FDT 的截断值为全偏差概率图中>1 个的抑郁测试点(P<0.01);GDx 的截断值为>29。
174 例青光眼疑似患者中,26 例出现了可重复性的青光眼视野损失(转换率:每年 3.7%)。FDT 的相对风险为 1.8(95%置信区间:0.9-3.7;P=0.10),GDx 的相对风险为 2.7(95%置信区间:1.2-6.3;P=0.01)。FDT 和 GDx 的阳性预测值分别为 0.22 和 0.22;阴性预测值分别为 0.88 和 0.92。
在临床环境中,尤其是 GDx 可能有助于识别出 SAP 评估为有发展为青光眼视野损失风险的青光眼疑似患者。