Vascular Tunic: Iris, Ciliary Body, Choroid Flashcards
What is Uveal tract?
- Uveal tract is made up of the iris, ciliary body and choroid
- This is a highly vascular and densely pigmented layer of eyeball between sclera and retina
What are causes of Uveitis?
- Autoimmune: common in IBD, SLE, MS, Behcets, juvenile idiopathic arthritis, rheumatoid disease
- Infections: associated with Herpes zoster virus, CMV
- Iatrogenic/Drug induced: rifabutin, cidofovir, bisphosphonates
- Traumatic: Sympathetic ophthalmia (uveal tissue exposed due to penetrative injury, causes inflammation in good eye)
How is Uveitis classified?
-
Keratitic precipitates
- Granulomatous
- Non-granulomatous
-
Chronicity
- Acute
- Recurrent: more than 3 months apart
- Chronic: frequent but with less than 3 months apart
What are symptoms of Anterior Uveitis?
- Progressive and usually unilateral, painful, redness with blurred vision and photophobia. Loss of vision over hours/days
- Eye pain often worse when trying to read
- Excess tear production
- Headache
- Photophobia
- Ocular discomfort & pain (may increase with use)
- Lacrimaton
- Visual acuity initially normal → impaired
What are signs of anterior uveitis?
-
Small, fixed oval (or irregular) pupil
- stuck to lens because of posterior synechiae which are adhesions between posterior surface of iris and anterior surface of lens capsule
- Remember this usually occurs in late stages of the condition so a normal pupil doesn’t totally exclude anterior uveitis
- Ciliary flush
- Flare and cells seen in slit lamp - imagine in cinemas beam of light with the white things floating)
- Keratitic precipitates - deposits at back of cornea
- Hypopyon - describes pus and inflammatory cells in the anterior chamber, often resulting in a visible fluid level
- Red eye
- Blurred Vision
How is anterior uveitis managed?
Immediate specialist urgent referral required in suspected uveitis
- Topical steroids/subconjunctival steroids – reduce inflammation
- Cycloplegics (eg cyclopentolate, atropine) - relax the spasm of ciliary body, reduce the pain, and relieve photophobia
What are symptoms and signs of intermediate uveitis (affecting viteous and posterior ciliary body)?
Symptoms:
- Blurring of vision
- Floaters
- May not have pain
Signs:
- Cells in vitreous
- Snow balls - clumps of cells in vitreous
- Snowbanking - on retina
- Sheathing of blood vessels
- Macular oedema
What is the management of Intermediate Uveitis?
- Local: Periocular steroids or Intravitreal steroid implants
- Systemic: Pulse therapy, Oral steroids, Immunosuppression, Aetiology-specific drugs
What are symptoms and signs of Posterior Uveitis (inflammation of choroid)?
Symptoms
- Gradual, normally bilateral, visual loss, often with associated floaters
- Occasional photophobia, little or no discomfort or redness
Signs
- Inflammatory lesions/granulomas may be seen on retina or choroid
- Inflammation of retinal blood vessels may occur
- Associated with TB, Sarcoidosis, CMV
What are investigations for Posterior Uveitis?
Imaging may be useful:
- OCT
- Fundus fluorescein angiography
What are the general investigation and management for Uveitis?
- Immediate specialist referral required in suspected uveitis
- Classify based on cause and treat: infectious vs non-infectious?
- If suspecting infection: sample of vitreous for PCR
- Investigate and treat secondary causes as necessary
- Autoimmune: Sarcoid ACE, anti dsDNA for SLE, MRI for MS, HLA for Behcets, HLAB27 for ankylosing spondylitis, psoriasis
What are complications of Uveitis?
- Hypotony (low IOP)
- Glaucoma
- Cataracts
- Posterior synechiae
What are complications of treatment for Uveitis?
- Steroid – may lead to cataract or glaucoma
- Immunosuppressants - side effects such as immunosuppression
What are features associated with Glaucoma?
- Group of conditions – could be caused with or without increased pressure in the eye
- Leads to damage to the optic nerve and loss of retinal ganglion cells forming main cause of irreversible blindness
- Early detection and treatment is important in preventing glaucoma related blindness
- Compliance/adherence to treatment is important
- Affects 0.5% of people over the age of 40
- The prevalence increases with age up to 10% over the age of 80 years. Affects males and females equally
What are types of Glaucoma?
- Open angle – asymptomatic
- Primary Open Angle Glaucoma
- Normal Tension Glaucoma
- Closed angle glaucoma
- Acute
- Primary Angle Closure Glaucoma
- Primary Glaucoma
- Secondary Glaucoma (Inflammatory, Secondary to haemorrhage, Neovascular, Steroid induced, Ocular tumour)
What are risk factors of Primary Open Angle Glaucoma?
- Age
- Genetics: first degree relatives of an open-angle glaucoma patient have a 16% chance of developing the disease
- Black patients
- Myopia
- Hypertension
- Diabetes mellitus
- Corticosteroids
What are symptoms and signs of Primary Open Angle Glaucoma?
- Symptoms
- Characterised by a slow rise in intraocular pressure: symptomless for a long period
- Typically present following an ocular pressure measurement during a routine examination by an optometrist
- Signs
- Peripheral visual field loss - nasal scotomas progressing to ‘tunnel vision’
- Decreased visual acuity
- Optic disc cupping
- Increased intraocular pressure
What are the signs on fundoscopy on Primary Open-Angle Glaucoma?
- Optic disc cupping - cup-to-disc ratio >0.7 (normal = 0.4-0.7), occurs as loss of disc substance makes optic cup widen and deepen
- Optic disc pallor - indicating optic atrophy
- Bayonetting of vessels - vessels have breaks as they disappear into the deep cup and re-appear at the base
- Additional features - Cup notching (usually inferior where vessels enter disc), Disc haemorrhages
What is the process of diagnosis and case finding for Primary Open Angle Glaucoma?
- Case finding and provisional diagnosis is done by an optometrist and if suspected full investigations are performed
- optic nerve head damage visible under the slit lamp
- visual field defect
- IOP > 24 mmHg as measured by Goldmann-type applanation tonometry
- Referral to the ophthalmologist is done via the GP
- Final diagnosis is done by full set of investigations
What are investigations for Primary Open angle glaucoma?
- Automated perimetry to assess visual field
- Slit lamp examination with pupil dilatation to assess optic neve and fundus for a baseline
- Applanation tonometry to measure IOP
- Central corneal thickness measurement
- Gonioscopy to assess peripheral anterior chamber configuration and depth
- Assess risk of future visual impairment, using risk factors such as IOP, central corneal thickness (CCT), family history, life expectancy
How is Primary Open Angle Glaucoma managed?
- Medical Treatment
- First line: prostaglandin analogue (PGA) eyedrop
- Second line: beta-blocker, carbonic anhydrase inhibitor, or sympathomimetic eyedrop
- If more advanced
- Laser
- Selective laser trabeculoplasty (shine into angle to open it up)
- Cylodiode: acts on ciliary body
- Peripheral laser iridotomy: reserved for angle closure glaucoma because it works very quickly
- Surgery
- Trabeculectomy – creates a fistula to increase aqueous outflow. Steroids required every 2 hours post surgery for 2 weeks to prevent scarring and closure of the anastomosis
- Artificial shunts
- Laser
- Reassessment
- Important to exclude progression and visual field loss
- Needs to be done more frequently if: IOP uncontrolled, the patient is high risk, or there is progression
What are factors predisposing to acute angle closure glaucoma?
Rise in Intra-ocular pressure secondary to impairment of aqueous outflow
- Hypermetropia (long-sightedness)
- Pupillary dilatation
- Lens growth associated with age
What are symptoms and signs of Acute Angle Closure Glaucoma?
Symptoms
- Severe pain: may be ocular or headache
- Systemic malaise
- Nausea and vomiting
- Decreased visual acuity
- Symptoms worse with mydriasis (e.g. watching TV in a dark room)
- Blurred vision when loking at lights and haloes around lights
Signs
- Semi-dilated non-reacting pupil
- Corneal oedema results in dull or hazy cornea
- Systemic upset may be seen, such as nausea and vomiting and even abdominal pain
- Hard, red-eye with hazy cornea. Minimally or non light reactve mid-dilated pupil
What is the management of Acute Angle Closure Glaucoma?
- Urgent referral to an ophthalmologist
- Medical management options includes:
- Reducing aqueous secretions with acetazolamide
- Inducing pupillary constriction with topical pilocarpine and phenylephrine in patients with artificial lens
- Beta blockers - topical timolol
- Steroids – prednisolone 15mg every 15 minutes for an hour, then hourly
- Sympathomimetic topically – apraclonidine or brimonidine
- Preventative treatment in other eye too
- Not in patients with sulfonamide allergy or sickle cell disease/trait
- Analgesia and antiemetics as necessary
- Surgical Management
- Peripheral iridotomy – allows for free flow of aqueous to leave and therefore to reduce the pressure (small hole made in the iris)
- Surgical iridectomy – similar procedure but more invasive and prone to complications
- Lensectomy – remove lens in cataractous cause of acute angle closure