1 / 52

Retinal vascular diseases 2

Retinal vascular diseases 2. Dr. Mohammad Shehadeh. Retinal vein occlusion. Classification: Branch retinal vein occlusion Central retinal vein occlusion. Pathogenesis.

collin
Télécharger la présentation

Retinal vascular diseases 2

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Retinal vascular diseases 2 Dr. Mohammad Shehadeh

  2. Retinal vein occlusion Classification: • Branch retinal vein occlusion • Central retinal vein occlusion

  3. Pathogenesis • Atherosclerosis of the retinal arterioles make them rigid and they compress the veins when they cross it causing it to thrombose  causing branch retinal vein occlusion • Central retinal vein and artery share a common adventitial sheath posterior to lamina cribrosa, so that atherosclerosis changes of the artery may compress the vein causing its thrombosis  and cause central retinal vein occlusion

  4. Risk factors of retinal vein occlusion • Old age : 50% over the age of 65 • Systemic conditions: Hypertention, hyperlipidemia, diabetes, smoking and obesity. • Raised intraocular pressure • Inflammatory diseases such as sarcoidosis • Thrombophilic disorders : inherited or aquired

  5. Branch retinal vein occlusion • Presentation: depend on the extent of macular involvement. • If the macula not involved it may be asymptomatic • Sudden onset of blurred vision • Metamorphopsia • Relative visual field defect

  6. signs • Visual acuity: depend on the extent of macular involvement • Fundus signs: • Venous dilatation and tortuousity • Flame shaped hemorrhages • Retinal edema • Cotton wool spots

  7. FA : eary hypofluorescence due to blockage by edema and blood and late hyperfluorescence due to leakage of dye • Prognosis: reasonably good 50% return to visual acuity of 6/12 or better within 6 mounths • Vision threatenin complications of BRVO: 1- chronic macular edema 2- neovascularization: NVD or NVE

  8. Management of BRVO • We review the patient every 6-12 weeks • When the hemorrhages resolve we do FA: • FA shows good macular perfusion and vision is goodno treatment is required • FA shows macular edema with good macular perfusion and vision is 6/12 or worse after 3 months  laser photocoagulation should be considered but if vision is better than 6/12  no treatment is needed • FA shows macular non perfusion and visual acuity is poor  laser treatment will not improve vision. • FA shows 5 or more disc diameters of non perfusion the patient should be reviewed every 4 months for 1-2 years because there is risk of neovascularization

  9. Central retinal vein occlusion • Non-ischemic CRVO : 75% of cases • Ischemic CRVO

  10. Non-ischemic CRVO Clinical features: • Presentation: with sudden blurred vision • Visual impairment : moderate to severe • Afferent pupillary defect (APD): abscent or mild

  11. Fundus features: • Tortuousity and dilatation of all branches of central retinal vein • Retinal dot-blot and flame shaped hemorrhages all over the four retinal quadrant • Occasional cotton wool spots • Mild to moderate optic disc edema and macular edema

  12. FA : shows • Delayed venous return • Good retinal capillary perfusion • Late leakage • Course: Most signs resolve over 6-12 months Conversion to ischemic type can occur in 34% within 3 years

  13. Prognosis: In cases that do not convert to ischemic type, prognosis is good, with return of visual acuity to normal or near normal in about 50% Management: • Follow up should be for years to detect conversion to ischemic CRVO • High intensity laser to create anastomosis between retinal vein and choroidal vein, but it may cause fibrosis at the laser site or hemorrhage from ruptured vein

  14. Ischemic central retinal vein occlusion Clinical features: • Presentation: sudden and severe visual impairment • Visual impairent: severe • APD : severe

  15. Fundus features: • Marked tortuousity and engorgement of all branches of central retinal vein • Extensive dot-blot and flame shaped hemorrhages • Cotton wool spots which may be numerous • Macular edema • Severe optic disc edema

  16. FA: central masking by retinal hemorrhages and extensive areas of capillary non-perfusion • Course: most acute signs resolve over the next 9-12 months • Prognosis: extremely poor due to macular ischemia, rubeosis iridis develop in about 50% of cases usually 2-4 months and there is high risk of neovascular glaucoma

  17. Management: • Follow up monthly for 6 months in order to detect rubeosis iridis and with gonioscopy to detect angle neovascularization • If neovascularization develops , laser PRP should be done without delay

  18. Retinal artery occlusion • Branch retinal artery occlusion (BRAO) • Central retinal artery occlusion (CRAO) • Cilioretinal artery occlusion

  19. Causes: • Atherosclerosis-related thrombosis(most common cause of CRAO) 80% of cases • Carotid embolism • Giant cell arteritis • Cardiac embolism • Priarteritis in cases of systemic vasculitis, such as SLE , Behcet…Etc. • Thrombophilic disorders such as antiphospholipid syndrome

  20. Branch retinal artery occlusion • BRAO is most frequently caused by embolism • Presentation: with sudden and profound sectoral visual field loss • Fundus features: • retinal cloudining corresponding to the area of occluded artery • narrowing and segmentation of blood column • One or more emboli may be present

  21. FA: • Delay in arterial filling • Masking of background fluorescence by retinal swelling which is confined to the involved sector • Prognosis : Poor unless the obstruction can be relieved within few hours

  22. Central retinal artery occlusion • CRAO is most frequently the result of atherosclerosis • Presentation: sudden and profound loss of vision except when a portion of the papillomacular bundle is supplied by cilioretinal artery, when central vision is preserved • APD is profound or total

  23. Fundus features: • Attenuation of arteries and veins with segmentation of the blood column • Extensive retinal cloudiness • Cherry red spot : which is an red-orange reflex from intact choroid appearing through the thin fovea • In eyes with cilioretinal artery , part of the macula will appear normal in colour

  24. FA: • Shows delay in arterial filling • Masking of background choroidal fluorescence by retinal swelling • A patent cilioretinal artery will fill during the early phase • Prognosis: Is poor due to retinal infarction • Rubeosis iridis may occur and need PRP laser

  25. Cilioretinal artery occlusion • Cilioretinal artery present in 20% of population • It arises from posterior ciliary circulation but supplies the retina, in the area of the macula and papillomacular bundle

  26. Classification: • Isolated: typically affects young patients with an associated systemic vasculitis • Combined with CRVO: has similar prognosis to non-ischemic CRVO • Combined with anterior ischemic optic neuropathy: affects patients with giant cell arteritis and carry a very poor prognosis

  27. Presentation: with acute, severe loss of central vision • Fundus: cloudiness localized to that part of the retina normally perfused by the vessel • FA: shows corresponding filling defect

  28. Treatment of acute retinal artery occlusion • Initial treatment: • Ocular massage: by 3 mirror contact lens, press for 10 seconds then release for 5 seconds. • Sublingual isosorbide dinitrite: to dilate perepheral blood vessles and decrease resistance • Lowering of IOP with intravenous acetazolamide and mannitol

  29. Subsequent treatment If the above mentioned measures are unsuccessful after 20 minutes we can do the following: • Anterior chamber paracentesis • IV streptokinase ( thrombolytic drug ) • Retrobulbar injection of tolazoline to decrease retrobulbar resistance to flow

  30. Hypertensive retinopathy • Hypertension is diagnosed on blood pressure reading on several consecutive occasions 140/90 or over.

  31. Retinal changes: • Arterial narrowing : May be focal or generalized Severe hypertention may lead to obstruction of precapillary arterioles and the development of cotton wool spots • Vascular leakage: Leading to flame shaped retinal hemorrhages, retinal edema , hard exudates and macular star. Swelling of the optic disc is the hallmark of malignant hypertension.

  32. Arteriosclerrosis: Involves thickenning of the vessel wall The most important sign is arteriovenous nipping Grades of arteriosclerosis: Grade 1 : subtle broadening of arteriolar light reflex Grade 2 : bending of veins at arteriovenous crossings Grade 3 : copper wiring Grade 4 : silver wiring

  33. Choroidal changes: Rare and developes in acute hypertensive crisis • Elshing spots: focal choroidal infarcts • Siegrist streaks: fibrinoid necrosis • Exudative retinal detachment: associated with toxemia of pregnancy.

  34. Retinopathy of prematurity (ROP) • It is aproliferative retinopathy affecting pre-term infants of low birth weight who have been exposed to high ambient oxygen concentration • The vessles reach the nasal periphery after 8th month of gestation but do not reach the temporal perephery until 1 month after delivery • The incompletely vascularized temporal retina is particularly susceptible to oxygen damage especially in preterm infants

  35. Active ROP • Severity: determined in terms of (a)location (b)extent (c) stages (d) plus disease (a) Location : It is determined by three zones centered on the optic disc

  36. (b) Extent: determined by the number of clock hours of the retina involved (c) Staging : Stage1: demarcation line Stage 2: ridge Stage 3: ridge with extraretinal fibrovascular proliferation Stage 4: subtotal retinal detachment Stage 5: total retinal detachment

  37. Oher considerations • Plus disease: signifies tendency to progression. Characterized by: 1- failure of pupil to dilate 2- development of vitreous haze 3- dilatated tortuous vessles 4- Preretinal and vitreous hemorrhage

  38. Threshold disease • It is the indication of treatment in ROP. It is the presence of five consequetive hours or 8 non-consequetive hours of stage 3 in zone 1 or 2 associated with plus disease

  39. screening • Babies born at or before 31 weeks or weighing 1500g or less should be screened for ROP • When to screen? At the gestational age 34 or 4 weeks post delivery which ever comes later.

  40. Treatment: • Ablation of immature retina by cryotherapy or laser ( successful in 85% of cases only) • Retinal surgery in cases of retinal detachment

More Related