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NEUROLOGY 1988;38:1767
© 1988 American Academy of Neurology

The pattern electroretinogram

A long-term study in acute optic neuropathy

David I. Kaufman, DO, Robert W. Lorance, MD, Monika Woods, BA and Shirley H. Wray, MD, PhD, FRCP

College of Osteopathic Medicine (Dr. Kaufman), Michigan State University, East Lansing, MI; the Department of Neurology (Dr. Lorance), Loyola School of Medicine, Maywood, IL; and the Department of Neurology (Dr. Wray and Ms. Woods), Massachusetts General Hospital, Boston, MA.

We report a 2-year prospective study of the electroretinographic response to reversal of checkerboard patterns (P-ERG) obtained in 63 eyes with acute optic nerve lesions. The aim of the study was to document the value of P-ERG regarding diagnosis and prognosis of four types of optic neuropathy: optic neuritis, compressive or hereditary optic atrophy, and traumatic optic neuropathy. We documented visual loss by neuro-ophthalmologic examination and recorded pattern-reversal visual evoked potentials (P-VEP). The initial P-ERG was normal to large- and medium-sized checks in 89% and the P-VEP abnormal in 94% of eyes with acute optic nerve lesions. Forty-six eyes were followed for up to 2 years. Two groups emerged. Group A (n = 17) gradually and permanently had significant reduction of the P-ERG to three separate check sizes. All 17 had no improvement in acuity better than 20/100, retained centrocecal scotomas, and developed optic atrophy. In group B (n = 29) the P-ERG remained within normal limits to one or more check sizes. Twenty-two of these eyes recovered acuity to 20/25 or better and had resolution of the field defect. The data showed that P-VEP was superior to P-ERG in diagnosis of acute and chronic optic nerve lesions. However, significant reduction of the b-wave of the P-ERG to three separate check sizes correlated closely with failure of visual recovery and the eventual development of severe optic atrophy, suggesting a prognostic value for P-ERG in optic neuropathy.

Address correspondence and reprint requests to Dr. Kaufman, College of Osteopathic Medicine, Internal Medicine, B 309 West Fee Hall, Michigan State University, East Lansing, MI 48824.

Received May 6, 1987. Accepted for publication in final form May 25, 1988.







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