Rayos, K.- Rodas, F..  21 year old student  CC: Loss of vision OS and eye aches associated with movement.  PMH: Similar episode in the OD three years.

Slides:



Advertisements
Similar presentations
Medical Retina and Macular Diseases
Advertisements

بسم الله الرحمن الرحيم Fluorescein & ICG Angiography F. Kianersi MD
2 cases of hypertension Year 1 Michaelmas term 2006.
Evan (Jake) Waxman MD PhD
Debilitating Eye Diseases
DIABETIC RETINOPATHY Diabetic retinopathy is a frequent cause of blindness. The exact cause of diabetic microvascular disease is unknown.
Fundoscopic examination
DIABETIC RETINOPATHY.
Fundoscopic Examination
M.R.AKHLAGHI MD  It is based on ophthalmoscopic signs.
Mitral Stenosis. Etiology Most cases of mitral stenosis are due to rheumatic fever The rheumatic process causes immobility and thickening of the mitral.
VISUAL LOSS IN THE ELDERLY
Leo Semes, OD Professor, Optometry UAB, Birmingham, AL.
Systemic diseases and Eye diseases The 4th Affilitated Hospital of China Medical University Eye Hospital of China Medical University.
Ophthalmology for Finals
Fluorescein Angiography & OCT in Diabetic Retinopathy
Thrombus (stationary clot) occludes a branch of the central retinal vein Blockage causes bleeding from that branch Concerned about neovascularization.
DIABETES AND EYE DISEASE: LEARNING OBJECTIVES
Topic assignment : medical ophthalmology
 70yo woman presents with sudden onset loss of vision in her right eye half hour ago  No improvement since  No previous ophthalmic history  What are.
Neuro-ophthalmology Abdulrahman Al-Muammar College of Medicine King Saud University.
Cardiovascular practical Block Part I Shaesta Naseem.
Occlusive vascular disorders of the retina Ayesha S abdullah
HYPERTENSIVE RETINOPATHY DR AJAY DUDANI DR YASHESH MANIAR.
Arterial and Venous Occlusive Disease of the Retina Dr.M NAQEEB Assistant professor Um Al-Qura university.
Retinal vascular diseases 2
Update on Hypertensive Retinopathy
What is funduscopy? And… Why is it important to you?
FFA Dr Aaron Ng. FFA Principles Fluorescence – Stimulated by light of shorter wavelength – Emission of light of longer wavelength Flurescein – Excitation.
 Using the direct opthalmoscope  Visualization of retinal structures  Differentiating arteries from veins  Locating Optic disc,Macula and Fovea  Identifying.
Mobility Program Information on eye diseases and disorders was obtained at the St. Lukes Eye Clinic Website
Diabetes and the Eyes Kenyon Anderson, O.D.. Blindness Risk Diabetic eye disease, caused by diabetes, is a leading cause of blindness and vision loss.
Ocular Ischaemic Syndrome Dr Gulrez Ansari Department of Ophthalmology Watford General Hospital 3 rd November 2004.
Diabetic Retinopathy (DR) Ayesha S Abdullah
Direct Ophthalmoscopy
Diabetic Retinopathy.
Direct Ophthalmoscope
FUNDOSCOPY IN PIH RETINA FUNDOSCOPY PIH
Hypertensive Retinopathy
1 Benign Nephrosclerosis Definition: renal changes in benign hypertension It is always associated with hyaline arteriolosclerosis. mild benign nephrosclerosis.
An Introduction to Examination of the EYE CSP
Ocular Manifestations of Systemic Diseases Dalman.
An 80 year old women complains of a very painful eye along with a feeling of nausea of 2 days duration. On examination the eye is red. 1.What condition.
Diabetic Retinopathy (DR) Ayesha S Abdullah
Elsevier items and derived items © 2009 by Saunders, an imprint of Elsevier Inc. Coronary Artery Disease Coronary artery disease: A condition involving.
Grand Rounds Conference
Chronic Visual Loss. CHRONIC VISUAL LOSS 1. Measure intraocular pressure with a tonometer 2. Evaluate the nerve head 3. Evaluate the clarity of the lens.
Amusing Slide 2013 WTD OPHTH ®.
Pathological changes of the fundus in general diseases .
Cardiovascular Pathology
RETINA Dr. G. Rajasekhar D.N.B, FRCS (Glasgow). RETINA  ARTERY OCCLUSIONS  VEIN OCCLUSIONS  DIABETIC RETINOPATHY  CENTRAL SEROUS RETINOPATHY  HYPERTENSIVE.
Retina and Vitreous Retina.
BRVO. Present by Sattar Heidari MD General ophthalmologist.
RETINAL VASCULAR DISEASES
HYPERTENSIVE RETINOPATHY
OVD of the retina CRAO Hypertensive retinopathy Ayesha S abdullah
Hypertensive retinopathy
Systemic Diseases.
DIABETIC RETINOPATHY Süleyman ÖZEN.
Direct Ophthalmoscopy
Ophthalmoscopy.
Age Related macular degeneratIon-ClassIfIcatIon
Copyright © 2006 American Medical Association. All rights reserved.
Central Retinal Artery Occlusion
Direct Ophthalmoscopy
January 16, 2019.
Hypertensive retinopathy
Pathology Of Hypertension
Retinal vascular disease
Presentation transcript:

Rayos, K.- Rodas, F.

 21 year old student  CC: Loss of vision OS and eye aches associated with movement.  PMH: Similar episode in the OD three years ago with spontaneous resolution. Also, a history of right sided numbness made better with ‘hilot’.  Vision: Right 20/20-2 Left 20/40-1  IOP: OU 15mm Hg (Normal IOP: 15.5 mmHg with fluctuations of 2.75)

 Hypertensive Retinopathy

 Characterized by a variety of retinal vascular signs in individuals with elevated BP  Causes blurring of vision  Bilateral, symmetrical  End organ manifestation

 Funduscopic findings: o Focal attentuation of a major retinal arteriole o Broadening of the arteriolar light reflex o Arteriovenous crossing changes o Hemorrhages o Retinal infarcts (Cotton-wool spots) o Choroidal infarcts (Elschnig’s spots) o Serous dettachment of the retina o Severe disk edema

– Arteriolar narrowing that is almost always bilateral Grade I - 3/4 normal caliber Grade II - 1/2 normal caliber Grade III - 1/3 normal caliber Grade IV - thread-like or invisible – Arterio-venous crossing changes (aka “AV nicking") with venous constriction and banking“ – Arteriolar color changes Copper wire arterioles are those arterioles in which the central light reflex occupies most of the width of the arteriole. Silver wire arterioles are those arterioles in which the central light reflex occupies all of the width of the arteriole.

Grade 1 – general narrowing of arterioles Grade 2- Narrowing of arterioles plus arteriolar spasm Grade 3 – Grade 2 changes plus hemorrhage and exudates - Flame-shaped (splinter hemorrhages)- seen in the nerve fiber layer - Cotton wool spots – result of microinfarction of NFL which produces aggregates of Cytoid bodies - Hard waxy exudates may be seen (lipophilic exudates located in Outer plexiform Inner Nuclear layer)

 Grade 4- All grade 3 changes with optic disc edema, necrosis, thinning, clumping and proliferation of Retinal pigment epithelium  May also occur as a result of obliterative changes in the choriocapillary in malignant hypertension.

 Arteriolar narrowing o A:V- 2:3  AV crossing changes  Grading o I- Leakage o II- Blood and hemorrhage o III- Cotton wool spots o IV- Optic disc swelling, subretinal exudates

Other retinopathies that are known complications of high blood pressure are called:  Diabetic retinopathy  Ischemic optic neuropathy  Retinal artery occlusion  Retinal emboli  Retinal vein occlusion

 Capillaries develop: o Microaneurysms o Thickening of the BM o Dec # of pericytes  Classification based on severity : o Mild o Atleast 1 microaneurysm o Moderate o Extensive microaneurysm o Intraretinal hemorrhages o Venous beading o Cotton wool spots o Severe o Cotton wool spots o Venous beading o Intraretinal microvascular abnormalities (IRMA)

 Presence of neovascularization on optic disk  Bleeding of vessels  Massive vitreous hemorrhage o Sudden visual loss

Age: older age groups – Nonarteritic: late 40s and older – Arteritic: >50 y/o Gender predilection: F>M History: painless visual loss upon awakening – Early: malaise, weight loss, fever, vague abdominal or GI pains, and anorexia – Late: abdominal aortic aneurysm Clinical Findings: – Nonarteritic: visual loss and field loss, small cup disc ratio, sectorial disc edema, pale and swollen optic disc – Arteritic: chalky white, pale, and swollen optic disc; quite prominent, ropey, and tender temporal arteries; oral, tongue, or scalp ulcer

Age: Mean: early in the 7th decade Gender predilection: M>F History: Acute persistent painless loss of vision, complete/sectional visual field defect, history of hypertension or diabetes mellitus, other medical problems (atrial fibrillation), prolonged direct pressure or drug-induced Clinical Findings: – Fundoscopy: afferent pupillary defect, cherry red spot and a ground-glass retina, emboli, whitening of the retina and Boxcar segmentation (BRAO) – PE: can have murmurs, carotid bruits, or other signs of cardiovascular disease

 Most commonly arise from carotid artery disease  In patients younger than 40, a cardiac origin such as atrial fibrillation, mitral valve prolapse or subacute endocarditis is considered Three types: 1. Cholesterol emboli Also called Hollenhorst plaques Usually arise from an atheromatous plaque in the carotid artery and consist of cholesterol and fibrin Lodge at the bifurcation of the retinal arterioles, are refractile and appear larger than the vessel that contains them

2. Calcific emboli ▪ Originates from damaged cardiac valves producing complete occlusion and infarction of the distal retina ▪ Solid and calcified and usually occur in younger patients 3. Platelet fibrin emboli ▪ Account for most cases of amaurosis fugax ▪ Due to the transit of platelet aggregates through the retinal and choroidal circulations ▪ May be reduced by drugs that reduce platelet aggregation like aspirin

 Increased incidence in smokers, hypertension, diabetes mellitus, hyperlipidemia,collagen- vascular disease, chronic renal failure and hyperviscosity syndromes Fundoscopy shows – Dilated tortuous veins with retinal and macular edema – Hemorrhages all over the posterior pole – Cotton wool spots

 Get patient’s Blood Pressure  Ophthalmoscopy  Flourescein angiography

 Used to monitor the blood pressure of the patient Blood Pressure Classification Systolic, mmHg Diastolic, mmHg Normal<120and <80 Prehypertension120–139or 80–89 Stage 1 hypertension140–159or 90–99 Stage 2 hypertension160or 100 Isolated systolic hypertension140and <90 Source: Table Harrison’s Principles of Internal Medicine 17 th ed.

Ophthalmoscope has long been regarded as part of the standard evaluation of persons with hypertension Ophthalmoscope has been shown to have high rates of interobserver variability (20 to 42 percent) and intraobserver variability (10 to 33 percent) when used in persons with mild hypertension few studies have demonstrated associations between hypertensive retinopathy and specific cardiovascular outcomes (e.g., incident stroke and coronary heart disease) or have adequately controlled for relevant confounding factors (e.g., hyperlipidemia and cigarette smoking)

Mild Hypertensive Retinopathy – Opthalmoscopy Figure 1. Examples of Mild Hypertensive Retinopathy. Panel A shows arteriovenous nicking (black arrow) and focal narrowing (white arrow). Panel B shows arteriovenous nicking (black arrows) and widening or accentuation ("copper wiring") of the central light reflex of the arterioles (white arrows).

Panel A shows retinal hemorrhages (black arrows) and a cotton-wool spot (white arrow). Panel B shows cotton-wool spots (white arrows) and arteriovenous nicking (black arrows).

Multiple cotton-wool spots (white arrows), retinal hemorrhages (black arrows), and swelling of the optic disk are visible

 Technique for examining the circulation of the retina using the dye tracing method  Involves injection of sodium fluorescein into the systemic circulation, and then an angiogram is obtained by photographing the fluorescence emitted after illumination of the retina with blue light at a wavelength of 490 nanometers  Can detect diabetic retinopathy, vein occlusions, retinal artery occlusions, edema of the optic disc, and tumors.

CAUSES OF HYPERFLUORESCENCE:  leaking defects (i.e. capillary leakage, aneurysm, neovascularization) pooling defects staining transmission (filling) defects abnormal vasculature CAUSES OF HYPOFLUORESCENCE:  blocking defect (i.e. blood) filling defect (capillary blockage)

Normal

 Control hypertension  Other vision- threatening conditions should also be controlled  Laser  Intravitreal injection of corticosteroids  Anti-vascular endothelial growth factor drugs  monoclonal antibodies such as bevacizumab (Avastin),bevacizumab  antibody derivatives such as ranibizumab (Lucentis), orranibizumab  orally-available small molecules that inhibit the tyrosine kinases stimulated by VEGF: ▪ lapatinib (Tykerb), sunitinib (Sutent), sorafenib (Nexavar), axitinib, and pazopanib lapatinibsunitinibsorafenibaxitinibpazopanib Merck manual online medical library