Multifocal ERG and VEP responses and visual fields: comparing disease-related changes

被引:111
作者
Donald C. Hood
Xian Zhang
机构
[1] Columbia University,Department of Psychology
关键词
electroretinogram (ERG); glaucoma; multifocal; optic neuritis; retinitis pigmentosa (RP); visual evoked; visual evoked potential (VEP);
D O I
10.1023/A:1002727602212
中图分类号
学科分类号
摘要
Static visual perimetry and the multifocal technique both measure the local effects of diseases of the retina and optic tract. The purpose here is to relate the measures obtained from each technique and to describe this relationship in some diseases. It is important to measure both the implicit time and amplitude of the multifocal ERG (mERG) or multifocal VEP (mVEP) responses. Some diseases affect one measure of the responses but not the other. The comparison of either measure to local sensitivity changes measured with static perimetry (e.g. the Humphrey 24-2 and 30-2) presents a problem. Different stimulus displays are employed. Further, the multifocal responses are displayed with arbitrary spacing between the responses. One approach is to measure the amplitude and implicit time of the multifocal responses and display these values on the same coordinates as in the visual field plots. This allows a qualitative comparison of fields and multifocal responses on the same scale. A second approach involves modifying the Humphrey perimeter software so that the test spots are placed in the centers of the multifocal stimuli (e.g. the center of each hexagon of the mERG display). A third approach involves estimating the thresholds for the regions of the multifocal display by interpolating from values at the standard Humphrey locations. The second and third approaches produce a one-to-one mapping of the multifocal and field measures and allow a quantitative comparison between the two. The relationship between visual fields and multifocal responses, determined through one or more of these approaches, is different depending upon whether the disease primarily affects the outer retina (retinitis pigmentosa), ganglion cell (glaucoma), or optic nerve (ischemic optic neuropathy and optic neuritis).
引用
收藏
页码:115 / 137
页数:22
相关论文
共 89 条
[1]  
Sutter EE.(1991)The fast m-transform: a fast computation of cross-correlations with binary m-sequences Soc Ind Appl Math 20 686-94
[2]  
Sutter EE(1992)The field topography of ERG components in man-I. The photopic luminance response Vis Res 32 433-66
[3]  
Tran D.(1994)The topography of visual evoked response properties across the visual field Electroenceph Clin Neurophysiol 90 65-81
[4]  
Baseler HA(1997)A comparison of the components of the multi-focal and full-field ERGs Vis Neurosci 314 533-44
[5]  
Sutter EE(1998)Assessment of local retinal function in patients with retinitis pigmentosa using the multi-focal ERG technique Vis Res 38 163-80
[6]  
Klein SA(2000)An attempt to detect glaucomatous damage to the inner retina with the multifocal ERG Invest Ophthal Vis Sci 41 1570-9
[7]  
Carney T.(2000)An interocular comparison of the multifocal VEP: A possible technique for detecting local damage to the optic nerve Invest Ophthal Vis Sci 41 1580-7
[8]  
Hood DC(2000)Assessing Retinal Function with the Multifocal Technique Prog. Ret Eye Res 19 607-46
[9]  
Seiple W(1998)Implicit time topography of multifocal electroretinograms Invest Ophthal Vis Sci 39 718-23
[10]  
Holopigian K(1998)Multifocal electroretinography in retinitis pigmentosa Amer J Ophthal 125 214-26