Abstract
Scleritis is a severe, potentially sight-threatening form of ocular inflammation characterised by oedema of the episcleral and scleral tissues with involvement of the deep episcleral vascular plexus. Scleritis may be associated with a systemic autoimmune disorder, or it may be either infectious or idiopathic in origin. A careful history, examination and targeted investigations are essential as scleritis may be the presenting feature of a potentially life-threatening systemic vasculitis. Also, failing to identify an infectious origin will lead to inappropriate therapy. Scleritis remains a therapeutic challenge, particularly in cases associated with a systemic autoimmune disorder. Treatment of scleritis involves a stepped approach. While the majority of patients will respond to oral nonsteroidal anti-inflammatory drugs (NSAIDs) or oral prednisolone, a significant percentage will require second-line immunosuppressive agents. Subconjunctival corticosteroid injection may be an option in non-necrotising noninfectious anterior scleritis, particularly in those who fail to respond to initial systemic therapy. Biologic agents, particularly infliximab and rituximab, may prove useful in refractory cases, but there is currently limited experience in their use in scleritis.
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Hooper, C., McCluskey, P. (2014). Diagnosis and Management of Scleritis. In: Pleyer, U., Alió, J., Barisani-Asenbauer, T., Le Hoang, P., Rao, N. (eds) Immune Modulation and Anti-Inflammatory Therapy in Ocular Disorders. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-54350-0_3
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