Ophthalmology Department, Universidade Federal de Goiás, Goiânia, GO, Brazil.
VER-Excellence in Ophthalmology, Goiânia, GO, Brazil.
Arq Bras Oftalmol. 2021 Mar-Apr;84(2):113-120. doi: 10.5935/0004-2749.20210016.
To compare the use of visual field and/or optical coherence tomography (OCT) combined with color retinography by non-glaucoma specialists for differentiating glaucoma from physiological cupping.
Eighty patients with glaucoma or physiological cupping (40 of each) were randomized according to the examination used (GI: color retinography, GII: color retinography + visual field, GIII: color retinography + optical coherence tomography, GIV: color retinography + visual field + optical coherence tomography). Twenty non-specialist ophthalmologists diagnosed glaucoma from PowerPoint slide images, without direct patient examination.
Inter-examiner agreement was good for GII (ĸ: 0.63; 95%CI, 0.53-0.72), moderate for GIII (ĸ: 0.58; 95%CI, 0.48-0.68) and GIV (ĸ: 0.41; 95%CI, 0.31-0.51), and low for GI (ĸ: 0.30; 95%CI, 0.20-0.39) (p<0.001). Diagnostic accuracy was higher in GIII (15.8 ± 1.82) than GI (12.95 ± 1.46, p<0.001) and higher in GII (16.25 ± 2.02) than GI and GIV (14.10 ± 2.24) (both p<0.001). For glaucoma patients only, diagnostic accuracy in GII and GIII was superior to that in GI and GIV (both p<0.001). Sensitivity and specificity were 59% and 70.5% in GI; 86.5% and 76% in GII, 86.5% and 71.5% in GIII; and 68.5% and 72.5% in GIV, respectively. Accuracy was highest in GII (81.3% [95%CI, 77.1-84.8]), followed by GIII (79% [95%CI, 74.7-82.7]), GIV (70,5% [95%CI, 65.9-74.8]), and GI (64.8% [95%CI, 60.0-69.3]).
Non-glaucoma specialists could not differentiate glaucoma from increased physiological cupping when using color retinography assessment alone. Diagnostic accuracy and inter-rater agreement improved significantly with the addition of visual field or optical coherence tomography. However, the use of both modalities did not improve sensitivity/specificity.
比较非青光眼专家使用视野和/或光学相干断层扫描(OCT)联合眼底彩色照相来区分青光眼和生理性杯盘比增大。
将 80 例青光眼或生理性杯盘比增大患者(各 40 例)随机分为 GI 组(眼底彩色照相)、GII 组(眼底彩色照相+视野检查)、GIII 组(眼底彩色照相+OCT 检查)和 GIV 组(眼底彩色照相+视野检查+OCT 检查)。20 名非专科眼科医生通过幻灯片图像诊断青光眼,不进行直接的患者检查。
GII 组(ĸ:0.63;95%CI,0.53-0.72)、GIII 组(ĸ:0.58;95%CI,0.48-0.68)和 GIV 组(ĸ:0.41;95%CI,0.31-0.51)的组间一致性良好,而 GI 组(ĸ:0.30;95%CI,0.20-0.39)的组间一致性较低(p<0.001)。GIII 组(15.8 ± 1.82)的诊断准确性高于 GI 组(12.95 ± 1.46,p<0.001),GII 组(16.25 ± 2.02)的诊断准确性高于 GI 组和 GIV 组(14.10 ± 2.24,均 p<0.001)。仅对青光眼患者进行分析,GII 和 GIII 组的诊断准确性优于 GI 和 GIV 组(均 p<0.001)。GI 组的灵敏度和特异度分别为 59%和 70.5%;GII 组为 86.5%和 76%,GIII 组为 86.5%和 71.5%,GIV 组为 68.5%和 72.5%。GII 组的准确性最高(81.3% [95%CI,77.1-84.8]),其次是 GIII 组(79% [95%CI,74.7-82.7])、GIV 组(70.5% [95%CI,65.9-74.8])和 GI 组(64.8% [95%CI,60.0-69.3])。
非青光眼专家仅使用眼底彩色照相评估时,无法区分青光眼和生理性杯盘比增大。随着视野或光学相干断层扫描的加入,诊断准确性和组间一致性显著提高。然而,两种方法的联合使用并未提高灵敏度/特异性。