Overview
Scleritis is the inflammation of the sclera (the white part of the eye) and may be associated with uveitis. It is a severe condition often requiring systemic treatment and must carefully be differentiated from scleritis as they present similarly, but have significantly different outcomes.
Epidemiology
- Often seen in association with other inflammatory diseases such as rheumatoid arthritis
- Sclerosis may be the first symptom of connective tissue disease
Risk Factors
- Previous personal history
- Associated systemic inflammatory disease e.g. inflammatory bowel disease, connective tissue disease (e.g. rheumatoid arthritis, systemic lupus erythematosus (SLE))
- Syphilis
- Tuberculosis
Presentation
Unlike episcleritis, scleritis is classically painful, but the pain may still be mild. Features are:
- Classically painful red eye – this may be mild
- May be unilateral or bilateral
- Eye watering
- Photophobia
- Gradual reduction in vision
- Injected vessels do not move with gentle pressure, unlike in episcleritis
- Phenylephrine eye drops do not improve redness, unlike in episcleritis
Differential Diagnoses
Anterior uveitis
- Pain – may be worse with use i.e. reading something close by
- Photophobia is more prominent
- Ciliary flush may be present
- Pupil margins may be irregular
- Associated autoimmune disease/infection may be present
Episcleritis
- Classically non-painful red eye but there may be mild pain
- Watering and/or photophobia may be present but milder
- Injected vessels are mobile and move with gentle pressure
- Phenylephrine eye drops improve eye redness
Acute angle-closure glaucoma
- Severe ocular pain/headache
- Associated vomiting
- Blurred vision and halos around light surfaces
Optic neuritis
- There is no red eye
- There is pain in eye movement
- Colour desaturation may be seen – colours appear faded/washed-out
Investigations
Overview
- Slit-lamp examination – shows inflammation in scleritis
- Immediate (within 24 hours) referral to ophthalmology
Other investigations are generally carried out to assess for underlying causes such as:
- FBC
- U&Es
- ESR:
- Elevated in inflammation
- CRP:
- Elevated in infection/inflammation
- Syphilis testing:
- If suspected
- Autoantibodies:
- Examples are rheumatoid factor for rheumatoid arthritis – if suspected
- X-rays:
- If chest pathology/spine or other bony pathology suspected
Management
- Immediate (within 24 hours) referral to ophthalmology
- Management generally involves treating the underlying cause through the use of corticosteroids, immunosuppression, and antibiotics if indicated.
Patient Advice
- Patients should be safety-netted on the symptoms of recurrence and be alerted about the possibility of episodes in the other eye
Complications
- Raised intraocular pressure and glaucoma
- Retinal detachment
- Uveitis
- Cataract
- Anterior globe ischaemia
- Scleral perforation
Prognosis
- The prognosis depends on the presence of an underlying condition and the management of the said condition.
- Early diagnosis and management of scleritis and effective management of any underlying conditions improve the prognosis.