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1 General aspects (0)   1.1 Epidemiology (6)   1.2 Population genetics (1)   1.3 Pathogenesis (0)   1.4 Quality of life (1)   1.5 Glaucomas as cause of blindness (4)   1.6 Prevention and screening (2) 2 Anatomical structures in glaucoma (0)   2.1 Conjunctiva (1)   2.2 Cornea (2)   2.3 Sclera (0)   2.4 Anterior chamber angle (2)   2.5 Meshwork (1)     2.5.1 Trabecular meshwork (16)     2.5.2 Schlemms canal (0)     2.5.3 Scleral outlet channels (0)   2.6 Aqueous humor dynamics (0)     2.6.1 Production (2)     2.6.2 Outflow (2)       2.6.2.1 Trabecular meshwork (2)       2.6.2.2 Uveoscleral (1)     2.6.3 Compostion (0)   2.7 Episcleral veins and venous pressure (0)   2.8 Iris (0)   2.9 Ciliary body (1)   2.10 Lens (0)   2.11 Vitreous body (0)   2.12 Choroid, peripapillary choroid, peripapillary atrophy (1)   2.13 Retina and retinal nerve fibre layer (8)   2.14 Optic disc (11)   2.15 Optic nerve (1)   2.16 Chiasma and retrochiasmal central nervous system (0)   2.17 Stem cells (0)   2.20 Other (1) 3 Laboratory methods (0)   3.1 Microscopy (0)   3.2 Electron microscopy (0)   3.3 Immunohistochemistry (11)   3.4 Molecular genetics (3)     3.4.1 Linkage studies (6)     3.4.2 Gene studies (7)   3.5 Molecular biology incl. 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with intraocular tumors (0)     9.4.9 Glaucomas associated with elevated episcleral venous pressure (2)       9.4.10 Glaucomas associated with hemorrhage (0)     9.4.11 Glaucomas following intraocular surgery (0)       9.4.11.1 Ciliary block (malignant) glaucoma (0)       9.4.11.2 Glaucomas in aphakia and pseudophakia (0)       9.4.11.3 Epithelial, fibrous, and endothelial proliferation (0)       9.4.11.4 Glaucomas associated with corneal surgery (0)       9.4.11.5 Glaucomas associated with vitreoretinal surgery (0)     9.4.15 Glaucoma in relation to systemic disease (4)     9.4.20 Other (1) 10 Differential diagnosis e.g. anterior and posterior ischemic optic neuropathy (6) 11 Medical treatment (0)   11.1 General management, indication (6)   11.2 Cholinergic drugs (0)   11.3 Adrenergic drugs (0)     11.3.1 Epinephrine (0)     11.3.2 Thymoxamine, dapiprazole (0)     11.3.3 Apraclonidine, brimonidine (5)     11.3.4 Betablocker (14)     11.3.5 Other (2)   11.4 Prostaglandins (22)   11.5 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tube implant (5)     12.8.2 With tube implant or other drainage devices (8)     12.8.3 Non-perforating (12)     12.8.4 Using laser (0)     12.8.5 Other (0)     12.8.10 Woundhealing antifibrosis (14)     12.8.11 Complications, endophthalmitis (3)   12.9 Trabeculotomy, goniotomy (2)   12.10 Cyclodestruction (4)   12.11 Cyclodialysis (0)   12.12 Cataract extraction (0)     12.12.1 Intracapsular (0)     12.12.2 Extracapsular (0)     12.12.3 Phacoemulsification (3)   12.14 Combined cataract extraction and glaucoma surgery (0)     12.14.1 Intracapsular (0)     12.14.2 Extracapsular (0)     12.14.3 Phacoemulsification (0)   12.15 Capsulotomy (0)   12.16 Vitrectomy (0)   12.17 Anesthesia (2)   12.20 Other (3) 13 Therapeutic prognosis and outcome (0)   13.1 Prognostic factors (0)   13.2 Outcome (0)     13.2.1 IOP (0)     13.2.2 Visual field (0)       13.2.2.1 Progression (0)       13.2.2.2 Improvement (0)     13.2.3 Other (0) 14 Costing studies; pharmacoeconomics (3) 15 Miscellaneous (4)

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Abstract #9772 Published in IGR 5-3

Multifocal electroretinogram in branch retinal vein occlusion

Hvarfner C; Andreasson S; Larsson J
American Journal of Ophthalmology 2003; 136: 1163-1165

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PURPOSE: To describe the response from multifocal electroretinography in branch retinal vein occlusion. DESIGN: Prospective observational case control series. METHODS: Multifocal electroretinography was recorded in 15 patients with temporal branch retinal vein occlusion and 21 control subjects using a visual evoked response imaging system. RESULTS: There were significant differences in mean amplitude (p = 0.01) and latency (p = 0.001) between thrombotic and nonthrombotic retina in the same eyes, as well as in patients compared with control subjects. CONCLUSIONS: Responses from multifocal electroretinography demonstrate retinal dysfunction in branch retinal vein occlusion; additional studies will demonstrate whether multifocal electroretinography has a prognostic value.

Dr. C. Hvarfner, Department of Ophthalmology, Lund University Hospital, Lund, Sweden. charlotte.hvarfner@oft.lu.se

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Classification:

6.7 Electro-ophthalmodiagnosis (Part of: 6 Clinical examination methods)

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