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Dr.Ravi kant Associate Professor Medicine ,AIIMS Rishikesh
Diabetic Retinopathy Dr.Ravi kant Associate Professor Medicine ,AIIMS Rishikesh
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Stages of diabetic Retinopathy
Pathogenesis Stages of diabetic Retinopathy Stage Pathogenesis Cause of Blindness Ischemic Small vessel occlusion capilary leakage, macular (nonproliterative) edema and haemorrhages Ischemia, pericyte degeneration (microaneurysms and arterivenous shunts) Angiogenesis factor release Proliferative Neo vascular prolileration Vitreous haemorrhage C. Fibrotic Vitreous fibrosis traction-included attachment to retina and contraction retinal detachment
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Classification of DR Non- proliferative DR (NPDR) Mild Moderate Severe
Very severe 2. Proliferative DR (PDR) 3. Clinically significant macular oedema (CSME) may exist by itself or along with NPDR and PDR
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Referral to Ophthalmologist
Presence of Risk Factors - Pregnancy - Nephropathy
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Diabetic Retinopathy Diabetic retinopathy is a leading cause of new cases of blindness in people aged 20 to 74 years in the USA Many of the complications of diabetic retinopathy can be prevented or delayed by blood glucose control and timely intervention.
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Ocular Anatomy
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Retinal Anatomy
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Retinal Histology Sclera Choroid RPE Photoreceptor outer segments
inner segment Outer Plexiform layer Bipolar cells Inner plexiform layer Ganglion cells Nerve fiber layer
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Retinal Diagnostic Tests
Fundus Photography Fluorescein Angiography (FA) Optical Coherence Tomography (OCT) Ocular Ultrasonography Electroretinography (ERG)
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Fundus Photography
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Normal FA
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Optical Coherence Tomography (OCT)
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Normal OCT
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Normal Ultrasound
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Pathogenesis of DR Prolonged hyperglycemia is the major etiologic agent in all of the microvascular complications of diabetes, including diabetic retinopathy. The cellular mechanisms through which hyperglycemia acts currently remain unclear
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Pathogenesis of DR Mechanisms that have been proposed are:
1. hyperglycemia may alter the expression of one or more genes, leading to increased (or decreased) amounts of certain gene products that can alter cellular functions. 2. Glycosylated proteins can undergo a series of reactions, leading to considerable alteration of proteins. 3. Chronic hyperglycemia may produce oxidative stress in cells, leading to the formation of an excess of "toxic end products of oxidation" including peroxides, superoxides, nitric oxide, and oxygen free radicals.
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VEGF and DR Vascular Endothelial Growth Factor
Promotes vascular growth and permeability Elevated levels of circulating VEGF in conditions with retinal ischemia
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Anatomic Changes Microanerysms
Damage to endothelial cells leads to dilated capillaries and venules These altered vessels allow serum and blood to leak into the retina
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NPDR
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NPDR FA
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NPDR OCT
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Retinal Ischemia
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PDR
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PDR
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PDR FA
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Vitreous Hemorrhage (VH)
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VH ultrasound
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TRD ultrasound
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Epiretinal Membrane
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PDR Retinal Detachment
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Iris Neovascularization
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Mechanisms of Vision Loss
Retinal ischemia Macular edema Vitreous hemorrhage Epiretinal membrane formation Retinal detachment Neovascular glaucoma
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Prevention Prospective controlled interventional studies have shown that strict control of blood glucose and blood pressure significantly reduces and delays the onset and severity of diabetic retinopathy.
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Screening Type 1 diabetics:
First screen 5 years after onset, then annually. Type 2 diabetics: First screen upon diagnosis and then annually.
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Treatment NPDR without macular edema - Macular edema - Observe
1. Focal/Grid laser photocoagulation 2. Vitrectomy with membrane peeling 3. Intraocular Steroid* 4. Intraocular VEGF inhibitor* * Off-label use, contraversial
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DME laser treatment
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DME laser treatment * * * * * * * * * * * *
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Treatment Vitreous Hemorrhage - Traction Retinal Detachment -
1. Pan-retinal photocoagulation 2. Vitrectomy with laser photocoagulation 3. Intraocular VEGF inhibitor* Traction Retinal Detachment - 1. Observation if not involving the macula 2. Vitrectomy with membrane dissection * Off-label use, contraversial
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Pan-retinal Photocoagulation
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Vitrectomy
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