VR Disorders; Clinical presentation, classification and RD Ayesha S Abdullah
Learning outcomes By the end of the lecture the students would be able to: Identify the symptoms of VR disorders and correlate them with underlying pathophysiological mechanisms. Classify VR disorders into broad categories. Describe the clinical presentation and epidemiology of RD Correlate the mechanism of retinal detachment with the development (RD) of the eye Classify RD Identify major causes of RD Outline the principles of management
Common symptoms of VR diseases Blurred vision/decreased vision Distorted vision ( metamorphopsia) Difficulty in near work difficulty in recognizing faces Something blocking central vision ( positive scotoma) Minified image/micoropsia-spreading apart of foveal cones Magnification of images/ macropsia-crowding of cones at fovea
Problems with colour vision Difficulty in dark adaptation Field loss Seeing sparkilign bright lights/ photopsia Seeing webs/ black dots -floaters Difficulty in night vision-nyctalopia Difficulty in day vision-hemeralopia
Common signs Decreased visual acuity RAPD Opacities in the vitreous Liquified vitreous gel Cells in the vitreous Signs in the retina specific to the specific disease entity Self-reported Amsler grid Nystagmus
Classification of VR disorders Diseases of the vitreous Retinal Detachment Vascular retinopahties Vitreoretinal degenerations Inflammatory & infective disorders Tumours of the retina
DEVELOPMENT OF THE EYE
What is RD? Separation of the sensory retina from the retinal pigment epithelium by the subretinal fluid
Rhegmatogenous RD Non- rhegmatogenous –Exudative RD –Tractional TYPES
RRD-some anatomical considerations Vitreo-retinal adhesions disc, ora, blood vessels & at fovea Potential subretinal space
RRD RD secondary to a break in the retina
Causes & risk factors In 15% of cases with Posterior vitreous detachment (PVD) a tear develops in the retina 60% of tears develop in peripheral retina with retinal degenerations like Lattice degeneration 40% of the RD occur in myopic eyes; the higher the error the greater the risk Post- Cataract surgery (pseudophakia) ; especially in eyes with retinal degeneration and myopia can develop retinal tears and RRD
Clinical presentation –symptoms Flashes of light Floaters Visual loss Visual field loss Usually an acute event History of predisposing factors, myopia, cataract surgery, trauma etc
Field loss
Clinical examination –signs Visual acuity Anterior segment examination Pupils, (RAPD) Posterior segment examination Vitreous- tobacco dust Retinal signs IOP ( may be low)
Clinical examination –signs Direct ophthalmoscopy
Indirect Ophthalmoscopy
Normal fundus
Rtinal detachment with tear
RD
RD with giant tear
Tractional retina detachment
Principles of management External temponade/ scleral buckling –Seal the break –Create a buckle –Drain the SRF-if required Internal temponade/
Management
Prophylaxis of RRD Photocoagulation of the risky lesions with laser So patients with risk facotrs should be referred for treatment/ consideration of the treatment
Let us Summarize