Clinical patterns and risk factors in scleritis: a multicentric study in Colombia.
de-la-Torre Alejandra, Cabrera-Pérez Mariana, Durán Claudia, García Sandra, Cuevas Miguel, Carreño Néstor, Rangel Carlos M, Pachón-Suárez Diana Isabel, Martínez-Ceballos María Alejandra, Mejía María Elisa
AI Summary
This Colombian study found scleritis predominantly affects females, often unilateral and noninfectious. Systemic autoimmune diseases are common, especially in necrotizing cases and older patients, requiring significant immunosuppression.
Abstract
Purpose
This study aims to describe the clinical characteristics of scleritis in a large cohort of Colombian patients and identify factors associated with the clinical presentation.
Methods
Retrospective case series of patients with scleritis from 2015 to 2020. Clinical records were obtained from seven uveitis referral centers in Colombia. Patients with a diagnosis of episcleritis were excluded.
Results
We evaluated 389 patients with scleritis (509 eyes). There was a female predominance (75.6%) with a mean age of 51 ± 15 years. Most cases were noninfectious (94.8%) and unilateral (69.2%). The most frequent type of inflammation was diffuse anterior scleritis (41.7%), followed by nodular scleritis (31.9%) and necrotizing scleritis (12.3%). Systemic autoimmune diseases were found in 41.3% of patients, the most common being rheumatoid arthritis (18.5%) and granulomatosis with polyangiitis (5.9%). Polyautoimmunity was found in 10.4% of those with a systemic autoimmune disease. The most frequent treatment was systemic steroids (50.9%), followed by systemic NSAIDs (32.4%). Steroid-sparing immunosuppression was required in 49.1% of patients. Systemic autoimmune diseases were more common in patients with necrotizing scleritis and those older than 40 years of age. Best-corrected visual acuity of 20/80 or worse at presentation was more common in necrotizing scleritis and subjects with associated uveitis, ocular hypertension, or who were over 40 years of age.
Conclusions
This is the first study in Colombia and the largest in Latin America describing the clinical characteristics and presentation patterns of scleritis. The most common presentation was in females, with unilateral, anterior diffuse noninfectious scleritis. Systemic autoimmune diseases and polyautoimmunity were frequent, as was the need for steroid-sparing immunosuppression. Age over 40 and necrotizing scleritis were associated with higher odds of having a systemic autoimmune disease and worse visual acuity at presentation.
MeSH Terms
Shields Classification
Key Concepts6
In a retrospective case series of 389 patients with scleritis (509 eyes) from Colombia, there was a female predominance (75.6%) with a mean age of 51 15 years.
In a retrospective case series of 389 patients with scleritis (509 eyes) from Colombia, most cases were noninfectious (94.8%) and unilateral (69.2%).
In a retrospective case series of 389 patients with scleritis (509 eyes) from Colombia, the most frequent type of inflammation was diffuse anterior scleritis (41.7%), followed by nodular scleritis (31.9%) and necrotizing scleritis (12.3%).
In a retrospective case series of 389 patients with scleritis (509 eyes) from Colombia, systemic autoimmune diseases were found in 41.3% of patients, with rheumatoid arthritis (18.5%) and granulomatosis with polyangiitis (5.9%) being the most common.
In a retrospective case series of 389 patients with scleritis (509 eyes) from Colombia, systemic steroids (50.9%) and systemic NSAIDs (32.4%) were the most frequent treatments, with steroid-sparing immunosuppression required in 49.1% of patients.
In a retrospective case series of 389 patients with scleritis (509 eyes) from Colombia, systemic autoimmune diseases were more common in patients with necrotizing scleritis and those older than 40 years of age.
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