Scleritis and Episcleritis Flashcards
What is Scleritis?
Inflammation (not usually caused by infection) of the full thickness of the sclera.
Associations of Scleritis (5).
50% of patients have an associated systemic condition e.g. :-
- Rheumatoid Arthritis (strongest association).
- SLE.
- IBD.
- Sarcoidosis.
- Granulomatosis with Polyangiitis.
Epidemiology of Scleritis.
Commoner in middle-aged women.
Most Severe Type of Scleritis.
Necrotising Scleritis - visual impairment but no pain and can lead to perforation of the sclera.
Clinical Features of Scleritis (4).
- Acute Onset.
- 50%. of cases are bilateral.
- Deep Boring Pain.
- Severely Red Eye.
Investigation of Scleritis.
Any patient who presents with red eye with a suspected potentially sight-threatening cause should be referred for same day assessment by an ophthalmologist.
Management of Scleritis (4).
- Further Assessment for an underlying systemic condition.
- NSAIDs (Topical/Systemic).
- Steroids (Topical/Systemic).
- Immunosuppressants (appropriate to the systemic condition e.g. Methotrexate - RA).
Definition of Episcleritis.
Benign and self-limiting inflammation (not infection) of the episclera (outermost layer of sclera, just under conjunctiva).
Epidemiology of Episcleritis.
Commoner in young-middle aged adults.
Differences between SCLERITIS and Episcleritis (4).
- Severity of Pain (No/Mild).
- Ophthalmoplegia.
- Non-Blanching Vessels.
- Diffuse (unlike Segmental - Lateral) Redness.
Clinical Differentiation of Scleritis and Episcleritis (3).
- Phenylephrine Eye Drops.
- Blanches conjunctival and episcleral vessels.
- If redness improves - Episcleritis.
Management of Episcleritis (3).
- No treatment.
- Simple analgesia.
- Cold Compresses.