Detection of Progression With 10-2 Standard Automated Perimetry: Development and Validation of an Event-Based Algorithm

被引:14
|
作者
De Moraes, Carlos Gustavo [1 ,2 ]
Paula, Jayter Silva [3 ]
Blumberg, Dana M. [1 ]
Cioffi, George A. [1 ]
Al-Aswad, Lama A. [1 ]
Girkin, Christopher A. [4 ]
Weinreb, Robert N. [5 ,6 ]
Zangwill, Linda M. [5 ,6 ]
Ritch, Robert [7 ]
Susanna, Remo [2 ]
Hood, Donald C. [8 ]
Liebmann, Jeffrey M. [1 ]
机构
[1] Columbia Univ, Edward S Harkness Eye Inst, Dept Ophthalmol, Bernard & Shirlee Brown Glaucoma Res Lab,Med Ctr, New York, NY 10027 USA
[2] Univ Sao Paulo, Dept Ophthalmol, Sch Med, Sao Paulo, Brazil
[3] Univ Sao Paulo, Dept Ophthalmol Otorhinolaryngol & Head Neck Surg, Ribeirao Preto Med Sch, Ribeirao Preto, Brazil
[4] Univ Alabama Birmingham, Dept Ophthalmol, Birmingham, AL 35294 USA
[5] Univ Calif San Diego, Hamilton Glaucoma Ctr, Viterbi Family Dept Ophthalmol, San Diego, CA 92103 USA
[6] Univ Calif San Diego, Shiley Eye Inst, San Diego, CA 92103 USA
[7] New York Eye & Ear Infirm Mt Sinai, Einhorn Clin Res Ctr, Dept Ophthalmol, New York, NY USA
[8] Columbia Univ, Dept Psychol, New York, NY 10027 USA
关键词
VISUAL-FIELD PROGRESSION; QUALITY-OF-LIFE; GLAUCOMA; THRESHOLD; DAMAGE; ASSOCIATION; VARIABILITY; SPECIFICITY; PREVALENCE; FREQUENCY;
D O I
10.1016/j.ajo.2020.03.046
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE: To describe the development of a new algorithm for detecting progressive changes in 10-2 visual field (VF) tests using event-based analysis and to test its validity in a second, independent glaucoma cohort. DESIGN: Prospective cohort study. METHODS: Patients with established open-angle glaucoma from the Macular Assessment and Progression Study (MAPS; development cohort, n = 151), and the African Descent and Glaucoma Evaluation Study (AD-AGES; validation cohort, n = 52) were evaluated. The 10-2 VF results from MAPS were obtained during 4 test-retest sessions within a 4-month period. For the validation analysis, 10-2 VF results from ADAGES performed on at least 5 visits were used. The event-based pointwise changes on 10-2 tests in the validation cohort were determined using 2 progression criteria: at least 3 progressing VF locations on 2 or 3 consecutive tests ("possible" or "likely" progression). Linear mixed-effects models were used to evaluate VF progression. RESULTS: In the validation cohort, the mean (SD) follow-up time was 2.3 (0.7) years. The number of eyes experiencing 10-2 VF progression based on "possible" and "likely" progression was 36 (54.5%) and 11 (16.6%), respectively. Eyes experiencing "possible" progression had MD changes ( - 0.60 dB/year [95% confidence interval (CI): -0.93 to - 0.28]) faster than those not meeting this criterion (P < .001), whereas for those with "likely" progression the difference was -0.91 dB/year (95% CI: -1.26 to -0.56, P < .001). CONCLUSIONS: A new event-based progression algorithm using the 10-2 VF can identify eyes experiencing more rapid MD progression and may be used as a tool to assess progressive macular functional changes in glaucoma. (C) 2020 Published by Elsevier Inc.
引用
收藏
页码:37 / 43
页数:7
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