Kasumovic Sanja Sefic, Pavljasevic Suzana, Cabric Emir, Mavija Milka, Dacic-Lepara Sabina, Jankov Mirko
Med Arch. 2014;68(2):113-6. doi: 10.5455/medarh.2014.68.113-116.
The aim of the study was to estimate the diagnostic accuracy of optical coherence tomography parameters in normal, preperimetric, developed perimetric and terminal glaucoma.
180 eyes of 140 consecutive patients were evaluated in this retrospective cross sectional pilot study. Copernicus Spectra--domain optical coherence tomography with resolution of 3 mm obtained through the optic nerve head were included. All examined eyes were divided into four groups (healthy eyes, initial, preperimetric glaucoma, developed perimetric glaucoma and terminal glaucoma).
The highest value of the RIM is noticed in control group 1.44 (1.21-1.70). There is no significant difference in the size of the disc in the eyes with developed open angle glaucoma (1.80 +/- 0.66) compared to normal eyes (p = 0.663), to the eyes with initial glaucoma (p = 0.120), and terminal glaucomatous atrophy (p = 0.068). There is statistically importance of E/D parameter in healthy group 0.17 (0.04-0.27), early glaucomatous group 0.44 (0.35-0.51), developed glaucoma 0.47 (0.39-0.61) respectively p < 0.005. The volume of cup was significantly greater in the eyes with terminal glaucomatous atrophy 1.05 (0.85-1.4) compared to the healthy eyes 0.31 (0.06-0.51) (p < 0.005), significantly greater to initial glaucoma 0.84 (0.58-1.12) (p = 0.007) and significantly higher compared to developed glaucoma 0.82 (0.62-1.07) (p = 0.003). There is no significant difference in the cup between the eyes with early and developed glaucoma (p = 0.912). The eyes with terminal glaucoma had significant lower value of the thickness of retinal nerve fiber layer 56.50 (45.50-71.25) compared to developed glaucoma group 82.5 (72-95.75), initial glaucoma 110.50 (102-123) and healthy eyes 132 (119-150) (p < 0.005).
The SD-OCT scanning should be used to quantify optic nerve head anatomy in human eyes. The changes can be recognized and can indicate as important risk factor in considering glaucoma changes. It also should be considered as an exact model of glaucoma pathology.
本研究旨在评估光学相干断层扫描参数在正常、视野缺损前期、进展期视野缺损及终末期青光眼患者中的诊断准确性。
本回顾性横断面初步研究纳入了140例连续患者的180只眼。采用分辨率为3mm的哥白尼谱域光学相干断层扫描技术获取视神经乳头图像。所有受检眼被分为四组(健康眼、早期、视野缺损前期青光眼、进展期视野缺损青光眼和终末期青光眼)。
对照组的视网膜神经纤维层边缘高度(RIM)最高值为1.44(1.21 - 1.70)。开角型青光眼进展期患者的视盘大小(1.80 ± 0.66)与正常眼(p = 0.663)、早期青光眼患者(p = 0.120)及终末期青光眼萎缩患者(p = 0.068)相比,差异无统计学意义。健康组、早期青光眼组、进展期青光眼组的E/D参数分别为0.17(0.04 - 0.27)、0.44(0.35 - 0.51)、0.47(0.39 - 0.61),差异具有统计学意义(p < 0.005)。终末期青光眼萎缩患者的杯状凹陷体积为1.05(0.85 - 1.4),显著大于健康眼的0.31(0.06 - 0.51)(p < 0.005),也显著大于早期青光眼患者的0.84(0.58 - 1.12)(p = 0.007)以及进展期青光眼患者的0.82(0.62 - 1.07)(p = 0.003)。早期青光眼与进展期青光眼患者的杯状凹陷体积差异无统计学意义(p = 0.912)。终末期青光眼患者的视网膜神经纤维层厚度为56.50(45.50 - 71.25),显著低于进展期青光眼组的82.5(72 - 95.75)、早期青光眼组的110.50(102 - 123)以及健康眼的132(119 - 150)(p < 0.005)。
谱域光学相干断层扫描(SD - OCT)扫描应用于量化人类眼睛的视神经乳头解剖结构。其变化能够被识别,并可作为青光眼病情变化的重要危险因素。它也应被视为青光眼病理学的精确模型。