Wong Evan N, Morgan William H, Chen Fred K
Centre for Ophthalmology and Visual Science (Incorporating Lions Eye Institute), The University of Western Australia.
Department of Ophthalmology, Sir Charles Gairdner Hospital.
Clin Ophthalmol. 2017 Apr 20;11:745-752. doi: 10.2147/OPTH.S131371. eCollection 2017.
To determine the intersession test-retest variability (TRV) of CenterVue Macular Integrity Assessment (MAIA) microperimeter in glaucoma patients with fixation-threatening field defects.
This is a prospective case-control study of 27 participants consisting of 13 patients with stable primary open-angle glaucoma and 14 control subjects including 5 healthy individuals and 9 retinal patients (5 with non-neovascular age-related macular degeneration and 4 with inherited retinal disease). Each participant underwent three microperimetry tests in one eye at 1-month intervals. Each test used an identical test strategy of 10-2 Cartesian grid and 4-2 staircase algorithm. We investigated TRV by calculating the coefficient of repeatability (CR) for mean sensitivity (MS) and point-wise sensitivity (PWS) for glaucomatous subjects and retinal and normal subjects. 95% confidence intervals (CIs) for CRs were calculated.
There was no significant change in MS, and the median durations of microperimetry sessions were 9'26″, 8'52″, and 8'46″ across the three study visits. The intersession CRs for MS were 1.1, 2.5, and 1.8 dB, and the average CRs for PWS were 3.5, 7.4, and 8.6 dB for healthy controls and retinal and glaucoma patients, respectively. For test loci with 25-34 dB at baseline, CRs for PWS were 8.2 (95% CI: 7.5-8.9) and 4.3 (95% CI: 4.0-4.6) dB for glaucoma and control subjects, respectively.
We found differences in TRV of test loci depending on the baseline sensitivity value. Glaucoma patients had significantly worse TRV for loci that had sensitivity values within the normal range at baseline. The estimated CR has implications for sample size calculation in future glaucoma treatment trials using microperimetry as a clinical endpoint.
确定CenterVue黄斑完整性评估(MAIA)微视野计在有威胁固视的视野缺损的青光眼患者中的检查间隔期重测变异性(TRV)。
这是一项前瞻性病例对照研究,纳入27名参与者,其中包括13例稳定的原发性开角型青光眼患者以及14名对照者,后者包括5名健康个体和9名视网膜疾病患者(5例非新生血管性年龄相关性黄斑变性患者和4例遗传性视网膜疾病患者)。每位参与者的一只眼睛每隔1个月接受三次微视野检查。每次检查均采用相同的10-2笛卡尔网格和4-2阶梯算法的检查策略。我们通过计算青光眼患者、视网膜疾病患者和正常受试者的平均敏感度(MS)和逐点敏感度(PWS)的重复性系数(CR)来研究TRV。计算CR的95%置信区间(CI)。
MS无显著变化,三次研究访视期间微视野检查的中位时长分别为9分26秒、8分52秒和8分46秒。健康对照者、视网膜疾病患者和青光眼患者MS的检查间隔期CR分别为1.1、2.5和1.8 dB,PWS的平均CR分别为3.5、7.4和8.6 dB。对于基线敏感度为25-34 dB的检查位点,青光眼患者和对照者PWS的CR分别为8.2(95% CI:7.5-8.9)和4.3(95% CI:4.0-4.6)dB。
我们发现检查位点的TRV因基线敏感度值而异。对于基线敏感度值在正常范围内的位点,青光眼患者的TRV明显更差。估计的CR对未来以微视野检查作为临床终点的青光眼治疗试验的样本量计算有影响。