Background
- NB Uveitis can refer to inflammation of the iris (iritis), ciliary body (cyclitis) and/or choroid (chorioretinitis)
- Anterior uveitis is inflammation of the anterior segment i.e. iritis and iridocyclitis (anterior chamber inflammation)
- Intermediate uveitis is inflammation of the ciliary body, pars plana and anterior vitreous
- Posterior uveitis is inflammation of the choroid or retina
- Panuveitis can also occur
- All can be acute (< 3 months), recurrent or chronic
- Potentially blinding; accounts for 10% of blindness in the developed world; 17-52/100,000/year
Aetiology
- Systemic autoimmune conditions e.g. seronegative spondyloarthropathies (ankylosing spondylitis; Reiter’s/reactive arthritis; inflammatory bowel disease); Behcet’s; Sarcoidosis; Psoriasis; Multiple sclerosis
- Associated with HLA-B27
- Infection e.g. HSV, VZV, CMV, toxoplasmosis (also syphilis and tuberculosis)
- Trauma
Presentation
- Unilateral (usually)
- Pain is the main symptom
- In AU, this is often accompanied by redness; in PU redness may be absent
- Redness is often strongest at the iris border (circumcorneal injection)
- In AU, this is often accompanied by redness; in PU redness may be absent
- Dimished or blurred vision
- Watering of the eye
- Photophobia
- Flashes or floaters may be seen in posterior uveitis
- In chronic cases, there may be an unreactive and/or irregularly shaped pupil due to synechiae (adhesions)
- On examination with a slit-lamp, deposits of white blood cells are often seen in the anterior chamber and are a diagnostic feature
- Often graded (from 0 to +4- >50 cells)
- aqueous may be cloudy (flare)- also graded from 0 to +4 (fibrin deposition)
- Where possible a full examination of inside the eye (slit lamp or fundoscopy) should be attempted to look for evidence of intermediate (cells in vitreous) or posterior (deposits in the retina)
Investigations
- Often clinical diagnosis but investigation of an underlying cause may be useful
- Imaging (OCT or fluorescein angiography) may be helpful too.
Management
- The mainstay of management is eyedrops
- Corticosteroid drops
- Cycloplegic-mydriatic (dilating) drops e.g. cyclopentolate or atropine)
- paralysis the ciliary body, relieving pain and preventing adhesions between the iris and lens
- If there is suspicion of infection, topical antibiotics (chloramphenicol) can also be given
- If an underlying cause e.g. systemic disease, is identified, manage this appropriately to prevent recurrence
- If patients do recur, systemic steroids may be a possibility.