Patterns of glaucomatous visual field progression identified by three progression criteria

被引:68
作者
Boden, C
Blumenthal, EZ
Pascual, J
McEwan, G
Weinreb, RN
Medeiros, F
Sample, PA
机构
[1] Univ Calif San Diego, Dept Ophthalmol, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Hamilton Glaucoma Ctr, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Visual Funct Lab, La Jolla, CA 92093 USA
[4] Hebrew Univ Jerusalem, Hadassah Med Ctr, Dept Ophthalmol, Jerusalem, Israel
关键词
D O I
10.1016/j.ajo.2004.07.003
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE: To determine typical patterns of repeatable glaucomatous visual field progression. DESIGN: Retrospective analysis of data obtained from two prospective studies. METHODS: Included were 72 eyes of 72 patients tested up to six times over 2 years, and 40 eyes of 40 patients followed annually for up to 12 years. Each patient had two abnormal baseline visual fields, abnormal optic nerves, and serial fields. Progression was identified using three methods: by glaucoma change probability using total deviation (GCP-TD) and pattern deviation (GCP-PD) plots and by a clinical criteria. Progression was categorized as deepening or expansion of an existing scotoma, or a new scotoma. RESULTS: The percentage of eyes repeatably progressed ranged from 17% to 27%. The most common pattern of progression was a deepening of an existing scotoma in the annual group, followed by expansion. With two follow, ups required, percentages for deepening only were 20% (clinical classifier). A combination of expansion and deepening was most common for the GCP criteria: 15% (GCP-TD classifier), and 10% (GCP-PD classifier) for the annual group. For the semiannual group, deepening was most common with the clinical criteria (11% of eyes), and deepening with expansion was most common by GCP criteria (14%, GCP-TD and GCP-PD). No eyes showed repeatable new scotomas. CONCLUSIONS: Glaucomatous visual fields progress in the area of the visual field where baseline testing showed an existing scotoma. Follow-up testing might be improved by concentrating on already defective locations and using sparser test patterns or screening algorithms in normal areas of the visual field. (C) 2004 by Elsevier Inc. All rights reserved.
引用
收藏
页码:1029 / 1036
页数:8
相关论文
共 22 条
[1]  
ANDERSON DR, 1999, AUTOMATED STATIC PER, P280
[2]  
Bengtsson B, 1997, ACTA OPHTHALMOL SCAN, V75, P184
[3]   DETERMINING PROGRESSIVE VISUAL-FIELD LOSS IN SERIAL HUMPHREY VISUAL-FIELDS [J].
BIRCH, MK ;
WISHART, PK ;
ODONNELL, NP .
OPHTHALMOLOGY, 1995, 102 (08) :1227-1234
[4]   Evaluating several sources of variability for standard and SWAP visual fields in glaucoma patients, suspects, and normals [J].
Blumenthal, EZ ;
Sample, PA ;
Berry, CC ;
Lee, AC ;
Girkin, CA ;
Zangwill, L ;
Caprioli, J ;
Weinreb, RN .
OPHTHALMOLOGY, 2003, 110 (10) :1895-1902
[5]   DIFFERENTIAL LIGHT THRESHOLD - SHORT-TERM AND LONG-TERM FLUCTUATION IN PATIENTS WITH GLAUCOMA, NORMAL CONTROLS, AND PATIENTS WITH SUSPECTED GLAUCOMA [J].
FLAMMER, J ;
DRANCE, SM ;
ZULAUF, M .
ARCHIVES OF OPHTHALMOLOGY, 1984, 102 (05) :704-706
[6]  
GAASTERLAND DE, 1994, OPHTHALMOLOGY, V101, P1445
[7]  
HEIJL A, 1991, PERIMETRY UPDATE 1990/1991, P303
[8]   Estimating progression of visual field loss in glaucoma [J].
Katz, J ;
Gilbert, D ;
Quigley, HA ;
Sommer, A .
OPHTHALMOLOGY, 1997, 104 (06) :1017-1025
[9]  
Katz J, 1999, ARCH OPHTHALMOL-CHIC, V117, P1137
[10]  
Katz J, 2000, INVEST OPHTH VIS SCI, V41, P1012