Sudden, painless visual loss of moderate degree, initially unilateral, but may become bilateral. Typically occurs in patients 40 to 60 years of age, but well-documented cases have been reported in patients in their teenage years. In younger patients, NAION should be suspected when painless visual loss develops with a contralateral disc at risk (i.e., crowded disc with small or absent optic cup [cup:disc ratio less than 0.3]) and normal MRI scan. The visual deficit may improve. Hyperlipidemia, labile hypertension, and sleep apnea are the common risk factors for younger patients.
(See Figure 10.18.1.)
Afferent pupillary defect, pale disc swelling (often segmental), flame-shaped hemorrhages, normal ESR and CRP.
Nonprogressive NAION: Sudden initial decrease in visual acuity and visual field, which stabilizes.
Progressive NAION: Sudden initial decrease in visual acuity and visual field followed by worsening in visual acuity or visual field days to weeks later. As many as 35% of NAION cases may be progressive.
Reduced color vision, altitudinal or central visual field defect, optic atrophy without cupping (segmental or diffuse) after the edema resolves. Crowded or congenitally anomalous disc with small or absent cup in fellow eye.
Idiopathic: Arteriosclerosis, diabetes, hypertension, hyperlipidemia, hyperhomocysteinemia, anemia, and sleep apnea are associated risk factors, but causation has never been proven. Relative nocturnal hypotension may play a role, especially in patients taking antihypertensive medication. We recommend avoiding antihypertensive medications at night.
Same as 10.17, Arteritic Ischemic Optic Neuropathy (Giant Cell Arteritis).
Consult internist to rule out cardiovascular disease, diabetes, hypertension, and sleep apnea.