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Controlled Clinical Trial
. 2014 Feb;252(2):339-45.
doi: 10.1007/s00417-013-2499-9. Epub 2013 Nov 1.

Intravitreal triamcinolone injections in non-arteritic anterior ischemic optic neuropathy

Affiliations
Controlled Clinical Trial

Intravitreal triamcinolone injections in non-arteritic anterior ischemic optic neuropathy

Corina Radoi et al. Graefes Arch Clin Exp Ophthalmol. 2014 Feb.

Abstract

Background: In non-arteritic anterior ischemic optic neuropathy (NA-AION), no treatments have demonstrated to be effective in recovering visual loss in randomized clinical trials. Oral steroids have been evaluated, and small series of intravitreal triamcinolone acetonide (IVTA) injection in NA-AION have been reported. The purpose of our study was to report the visual outcome and morphological changes in response to a single IVTA injection as a treatment for patients with NA-AION.

Patients and methods: The charts of 36 patients with visual symptoms and optic disc swelling caused by NA-AION were evaluated. Twenty-one patients had received 4 mg IVTA and were compared with 15 non-treated patients. Visual acuity (VA), retinal nerve fiber layer thickness and static visual field were evaluated after 6 months.

Results: VA improvement at 6 months is statistically better in the treated group than in the non-treated group (p = 0.0035). In the treated group, there was a significant inverse correlation between the delay of the injection and the visual acuity achieved at 6 months (p < 0.0083**, r = -0.56). A significant improvement of the visual field was noted in the injected group when compared with the non-treated group at 6 months (p < 0.0028).

Discussion: In this retrospective study, patients receiving IVTA in the acute phase of NA-AION have better improvement of VA and visual field during the follow-up period of 6 months. However, only a large randomized controlled trial may enable to evaluate the benefits of IVTA Injections on visual outcome in NA-AION.

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