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Dania Al-Nuaimi
Lecture Outline
Anatomy Approach to the Ophthalmic Patient The Red Eye Loss of Vision
Sudden Gradual
Quiz
Surface Anatomy
Ophthalmic History
Presenting Complaint History of Presenting Complaint Past Ophthalmic History
Previous surgery, trauma, refractive error
Family History
genetic/congenital conditions, glaucoma,cataract
Social History
Smoking, alcohol, can they put eye drops in themselves?
Examination
Visual Acuity Pupils External Eye Examination
Lids Conjunctiva Episclera Sclera Cornea Anterior Chamber Lens
Fundoscopy
Systematic Approach
Lids Conjunctiva Episclera Sclera Cornea Anterior Chamber
Lids
Blepharitis
itching, burning, FB sensation tearing crusting swollen lids conjunctival injection Blocked Meibomian glands
Chalazion
Conjunctiva
Subconjunctival Haemorrhage Conjunctivitis
Bacterial Viral Allergic
Subconjunctival Haemorrhage
No pain/mild discomfort Vision normal ? trauma exclude foreign body Well demarcated area No discharge Check
For areas of other bruising history of anticoagulants BP (?Anticoagulant status, FBC)
Conjunctivits - Bacterial
Acute Mild gritty discomfort Mucopurulent discharge Normal Vision No Staining of cornea No Systemic symptoms Commonest pathogens:
Rx antibiotics
Chloramphenicol QDS 1/52
Conjuncitivis - Viral
Acute (7-10/7) Mild Gritty discomfort Slight/moderate photophobia Watery Secretion or discharge Visual acuity normal or sl reduced Lids follicles Corneal opacities subepithelial Systemic symptoms- eg. sore throat or flu like symptoms Pre-auricular lymph node may be swollen Rx conservative
Cool compress Artificial tears
Conjunctivitis - Chlamydial
Subacute onset (2-3/52) Discomfort - gritty Photophobia -Variable Discharge -Watery pus Visual acuity Normal/Slightly Reduced Lid oedema Diffuse conjunctival hyperaemia Cornea
Clear Late: pannus and/or diffuse fibrosis, also of conjunctiva None related to STI
Systemic symptoms: Rx
Conjunctivitis - Allergic
Bilateral Discomfort itching Discharge clear Seasonal Chemosis Papillae/cobblestones Rx avoidance of stimulus, mast cells stabilisers, antihistamines, steroids
Conjunctivitis - Neonatal
Ophthalmia neonatorum
< 1 month old notifiable disease Causative organisms
Commonly acquired from birth canal Immature local immunity Potentially sight threatening May result in serious systemic disease Rx
Gonococcal systemic ceftriaxone Chlamydial systemic erythromycin After counselling refer mother (and partner) to GUM clinic
Episclera
Pingueculum Degenerative yellow-white deposit adjacent to the limbus Reassurance/lubricants May become inflamed Pterygium Triangular sheet of fibrovascular tissue Dry climate/UV light exposure Invades the cornea May become inflamed
Scleritis
Uncommon Sight-threatening inflammation Bilateral (50% cases) Moderate/severe pain classically wakes the patient at night Purplish hue - involvement of the deep episcleral vessels Systemic diseases are present in 50% of patients
Connective tissue diseases
Eg. RA, Wegener s. SLE etc.
Rx NSAIDs or Steroids
Cornea
Abrasion Ulcers
Bacterial Viral
Herpes Simplex
Acanthamoeba
Corneal Abrasion
FB/Trauma Blurred vision Pain Photophobia Watering Usually heals within 48hrs Rx chloramphenicol QDS 1/52
Staph aureus Staph epidermidis Strep pneumonia Pseudomonas aeruginosa (CL) H. Influenzae (children)
Primary episode associated with vesicular rash Recurrent Blurred vision Pain++ Photophobia Watery discharge Reduced corneal sensation Dendritic ulcer highlighted by fluourescein Rx
Topical antiviral zovirax 5x/day then taper If recurrent consider systemic antiviral Do not prescribe topical steroid as can cause geographic ulcer
Cornea - Acanthamoeba
Acanthamoeba = free-living protozoa
Soil, dust, sea, fresh and chlorinated water
History of CL wear Foreign body sensation Blurred vision Photophobia Discharge watery++ Ring infiltrates Symptoms worse and disproportionate to signs Rx topical anti-amoebic agents
Uveitis
Circumcorneal purple + diffuse conjunctival injection Cornea Keratic precipitates Anterior chamber -flare, cells +/- hypopyon Iris - Often hyperaemic Pupil -Contracted +/Synechiae May have activity in posterior chamber and signs in fundus
Visual acuity reduced usually onset 2-3 hours Slight photophobia Watery secretion or discharge Hypermetropia (shallow anterior chamber) Preceded by episodes of blurring pain or haloes for an hour or two in some early evenings for a few weeks
Iris - Oedematous and hyperaemic Pupil - Dilated, oval Pupil light reflex - Absent or reduced IOP- Very high Tenderness - Marked Rx urgent referral to ophthalmologist for acute treatment of pressure
White swollen retina with cherry red spot at macula Afferent pupillary defect Causes: GCA, atherosclerosis/carotid artery disease Associations:
Commoner than arterial occlusion Most occur in age >65 Dilated, tortuous veins, retinal haemorrhages all 4 quadrants, mild optic disc oedema Associations: Diabetes, hypertension, smoking, inflammatory disorders
Retinal Detachment
Cataract
Cataract
Cataract = lens opacity Account for 40% global blindness Can be congenital or acquired Main risk factor = AGE
Cataracts are present in : 16% age 65-69 71% age >85
Glare
oncoming headlights
Myopic shift
second sight
monocular diplopia
when lens changes occur differentially within lens
Cortical Cataract
Clinical Evaluation
What is the cause of the cataract? Does the amount of lens opacity correspond to the degree of visual impairment? Is the patients ability to function sufficiently educed to warrant surgery? What is the prognosis for improvement of vision? Are there any ocular/systemic considerations? Does the patient want surgery
Functional Considerations
Legal or corporate requirements for vision Driving
car bus HGV
Glaucoma
Glaucoma
Group of diseases Primary open angle is the commonest in the UK POAG asymptomatic Often picked up by routine optometric examination May or may not have raised IOP Characterised by optic nerve and visual field changes
Glaucomatous disc
Enlarged cup:disc ratio asymmetry in cup size loss of neuroretinal rim loss of ISNT rule laminar dots bayonetting of vessels Disc margin Haems Peripapillary atrophy
Diabetic Retinopathy
Background Non or preproliferative Proliferative Maculopathy
Microaneurysms, dot and blot haemorrhages, hard exudates, occasional cotton wool spots
Intra-retinal microvascular abnormalities, venous beading/loops, clusters of large blot haemorrhages, multiple cotton wool spots
Diabetic Maculopathy
Macular Degeneration
Visual symptoms
Blurred central vision difficulty reading colour and contrast disturbances metamorphopsia Central scotoma
Dry AMD
Hard Drusen Soft Drusen
Wet AMD
Answers to Quiz
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