June 1993
Volume 34, Issue 7
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Articles  |   June 1993
Optic disc morphology in eyes after nonarteritic anterior ischemic optic neuropathy.
Author Affiliations
  • J B Jonas
    Department of Ophthalmology, University Erlangen-Nürnberg, Germany.
  • L Xu
    Department of Ophthalmology, University Erlangen-Nürnberg, Germany.
Investigative Ophthalmology & Visual Science June 1993, Vol.34, 2260-2265. doi:
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      J B Jonas, L Xu; Optic disc morphology in eyes after nonarteritic anterior ischemic optic neuropathy.. Invest. Ophthalmol. Vis. Sci. 1993;34(7):2260-2265.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

PURPOSE: Parapapillary chorioretinal atrophy, neuroretinal rim loss, and a decrease of retinal vessel diameter have been described to occur in glaucomatous eyes. This study was conducted to evaluate the frequency and degree of these signs in nonarteritic anterior ischemic optic neuropathy (AION). METHODS: We evaluated morphometrically and compared stereo color optic disc photographs of 17 patients after AION, 184 patients with primary open-angle glaucoma, and 98 normal subjects. RESULTS: The optic disc area and retinal vessel diameter were significantly smaller and the visibility of the retinal nerve fiber bundles was significantly reduced in patients after nonarteritic AION compared with that of the normal subjects. The optic disc shape, area, and form of zones alpha and beta of the parapapillary chorioretinal atrophy and the size and form of the neuroretinal rim did not differ significantly between these two groups. In the group of eyes with glaucoma, the neuroretinal rim was significantly smaller and the parapapillary chorioretinal atrophy was significantly larger than in the group of eyes with AION. Visibility of the retinal nerve fiber bundles and retinal vessel caliber did not differ statistically between the eyes with AION and those with glaucoma. CONCLUSIONS: These results indicate that the parapapillary chorioretinal atrophy is not larger in eyes after nonarteritic AION compared with normal eyes. They show that the area and shape of the neuroretinal rim, as determined planimetrically, may not markedly change after nonarteritic AION. They confirm previous reports on a small optic disc size as a risk factor for nonarteritic AION. They agree with findings of a reduced retinal vessel caliber in eyes with optic nerve damage, independently of the cause.

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