Purpose: To compare visual field abnormalities obtained with standard automated perimetry (SAP) to those obtained with the multifocal visual evoked potential (mfVEP) technique in strabismic amblyopes.Methods: Humphrey 24-2 visual fields (HVF) and mfVEPs were obtained from each eye of 12 strabismic amblyopes. For the mfVEP, amplitudes and latencies were analyzed and probability plots derived. Multifocal VEP and HVF hemifields were abnormal if they had clusters of 2 or more contiguous points at p<0.01, or 3 or more contiguous points at p<0.05 with at least one at p<0.01. An eye was abnormal if it had an abnormal hemifield.Results: On SAP, amblyopic eyes had significantly higher foveal thresholds (p=0.003) and lower mean deviation values (p=0.005) than fellow eyes. For the mfVEP, 11 amblyopic and 6 fellow eyes were abnormal. Of the 11 amblyopic eyes, 6 were abnormal on SAP. The deficits extended from the center to mid-periphery. Monocular mfVEP latencies were significantly decreased for amblyopic eyes compared to control eyes (p<0.0002).
Conclusions:Both techniques revealed deficits in visual function across the visual field in strabismic amblyopes, but the mfVEP revealed deficits in fellow eyes and in more amblyopic eyes. In addition, mfVEP response latencies for amblyopic eyes were shorter than normal.Amblyopia is a developmental disorder characterized by decreased vision that cannot be corrected by refractive means and is not accompanied by any overt pathology of the visual system. It is one of the most common causes of decreased vision in childhood. Amblyopia is associated with the presence of strabismus, anisometropia or form deprivation early in life and is characterized by deficits in central visual function such as decreased visual acuity and contrast sensitivity, as well as by visual field deficits. However, there is controversy regarding the extent and depth of these visual field deficits. For example, Phillip and Mayer described visual field deficits in strabismic and ansiometropic amblyopes ranging from central to paracentral scotoma, whereas Sireteanu and Fronius reported finding central defects in For correspondence concerning the manuscript: Vivienne C. Greenstein Ph.D. Department of Ophthalmology Columbia University 630 West 165 th Street New York, NY 10032. Email: vcg17@columbia.edu.. Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.Study Site: Department of Ophthalmology, Columbia University, New York, NY.Presented at the Annual Meeting of the Association for Research in Vision and Ophthalmology, 2005 The authors have no proprietary interests in th...