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Common causes of failure in retinal detachment repair include missed or poorly sealed retinal breaks, new retinal breaks, and proliferative vitreoretinopathy (PVR). [10] [14] PVR, a condition where scar tissue grows on the retina, occurs in approximately 8–10% of patients undergoing treatment for retinal detachment. [10]
Central retinal artery occlusion: CRAO is characterized by painless, acute vision loss in one eye. [11] Central retinal vein occlusion: CRVO causes sudden, painless vision loss that can be mild to severe. [12] Branch retinal vein occlusion: sudden painless vision loss or visual field defect are the main symptom of BRVO. [13]
A tear in the retina can allow fluids from the eye to leak in behind the retina, which causes retinal detachment. When this occurs, blood from the retinal blood vessels can bleed into the vitreous. [4] Retinal tear accounts for 11.4–44% of vitreous hemorrhage cases. [1]
Retinal tufts increase the risk of a retinal tear or a detached retina, although the risk is not high- 1% of tufts are thought to lead to retinal detachment. [2] [6] In addition if there is retinal thinning near a zonular traction tuft, there is an increased risk of retinal detachment. [5]
In its most severe form, ROP causes retinal detachment, with attendant visual loss. Treatment is aimed mainly at prevention, via laser or Avastin therapy. Stargardt's disease; Uveitis: is a group of 30 intraocular inflammatory diseases [70] caused by infections, systemic diseases, organ-specific autoimmune processes, cancer or trauma. [71]
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Causes: Peripheral (Posterior) vitreous detachment, retinal detachment, age-related macular degeneration, ocular (retinal) migraine / migraine aura, vertebrobasilar insufficiency, optic neuritis, occipital lobe infarction (similar to occipital stroke), sensory deprivation (ophthalmopathic hallucinations) Risk factors
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