Viterbi Family Department of Ophthalmology, Hamilton Glaucoma Center, Shiley Eye Institute, University of California, San Diego, La Jolla, California, USA; Department of Ophthalmology, Ankara Ulucanlar Eye Training and Research Hospital, Ankara, Turkey.
Viterbi Family Department of Ophthalmology, Hamilton Glaucoma Center, Shiley Eye Institute, University of California, San Diego, La Jolla, California, USA.
Am J Ophthalmol. 2021 Mar;223:229-240. doi: 10.1016/j.ajo.2020.10.015. Epub 2020 Oct 29.
To investigate central visual field (VF) defects among 4 phenotypes of glaucomatous optic discs.
Cross-sectional study.
Optic disc phenotypes were determined in eyes with definite or suspected glaucoma that had a 24-2 VF with mean deviation (MD) better than -12 dB and a 10-2 VF. 10-2 VFs were classified as abnormal based on a cluster criterion. Additionally, the average of the total deviation values at each 10-2 test point was compared by optic disc phenotype.
The following 4 glaucomatous optic disc phenotypes were identified in 448 eyes of 309 patients: focal ischemic (FI) (n = 121); generalized cup enlargement (GE) (n = 109); myopic glaucoma (MY) (n = 66); and senile sclerotic (SS) (n = 152). Although 24-2 VF MD values were similar among optic disc phenotypes, GE eyes had higher 10-2 VF MD (P = .004), as well as lower 24-2 VF pattern standard deviations (PSD) (P < .001) and VF 10-2 PSD (P < .001) than the other phenotypes. The prevalence of an abnormal VF 10-2 was highest in FI eyes (78.5%) and lowest in GE eyes (50.5%) (P < .001). In glaucoma suspects, the prevalence of an abnormal 10-2 VF was highest in the MY eyes (31.2%) and FI eyes (23.5%) and lowest in GE eyes (8.6%). In mild glaucoma, the prevalence of abnormal 10-2 VF test results was highest in FI eyes (79.2%) and lowest in GE eyes (44.4%) (P = .013).
The severity and prevalence of central VF loss varied among different glaucomatous optic disc phenotypes. Glaucomatous eyes with FI and MY optic disc phenotypes are more likely to have 10-2 VF loss, particularly in early disease, and especially may benefit from testing with both 10-2 and 24-2 VF tests.
研究 4 种青光眼视盘表型的中央视野(VF)缺损。
横断面研究。
在视野平均偏差(MD)优于-12dB 且 10-2VF 较好的确诊或疑似青光眼患者的眼中,确定视盘表型。根据聚类标准,将 10-2VF 分类为异常。此外,还比较了每个 10-2 测试点的总偏差值的平均值与视盘表型的关系。
在 309 例患者的 448 只眼中确定了以下 4 种青光眼视盘表型:局灶性缺血(FI)(n=121);普遍性杯扩大(GE)(n=109);近视性青光眼(MY)(n=66);和老年硬化(SS)(n=152)。尽管 24-2VF MD 值在视盘表型之间相似,但 GE 眼的 10-2VF MD 更高(P=0.004),24-2VF 模式标准偏差(PSD)(P<0.001)和 VF 10-2 PSD(P<0.001)均较低。FI 眼的异常 10-2VF 患病率最高(78.5%),而 GE 眼最低(50.5%)(P<0.001)。在青光眼疑似患者中,MY 眼(31.2%)和 FI 眼(23.5%)的异常 10-2VF 患病率最高,而 GE 眼最低(8.6%)。在轻度青光眼患者中,FI 眼(79.2%)异常 10-2VF 测试结果的患病率最高,而 GE 眼(44.4%)最低(P=0.013)。
不同青光眼视盘表型的中央 VF 损失的严重程度和患病率不同。FI 和 MY 视盘表型的青光眼眼更有可能出现 10-2VF 损失,尤其是在早期疾病中,尤其可能受益于 10-2 和 24-2VF 测试的联合测试。