Neuroscience Research Group (NEUROS), School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia.
Uveitis Department, Fundación Oftalmológica Nacional (FUNDONAL), Bogotá, Colombia.
Graefes Arch Clin Exp Ophthalmol. 2022 Dec;260(12):3957-3967. doi: 10.1007/s00417-022-05754-y. Epub 2022 Jul 7.
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.
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.
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.
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.
本研究旨在描述哥伦比亚大型患者队列中巩膜炎的临床特征,并确定与临床表现相关的因素。
这是一项回顾性病例系列研究,纳入了 2015 年至 2020 年间来自哥伦比亚 7 家葡萄膜炎转诊中心的巩膜炎患者。排除了诊断为表层巩膜炎的患者。
我们评估了 389 例巩膜炎患者(509 只眼)。女性占主导地位(75.6%),平均年龄为 51±15 岁。大多数病例为非传染性(94.8%)和单侧(69.2%)。最常见的炎症类型为弥漫性前部巩膜炎(41.7%),其次为结节性巩膜炎(31.9%)和坏死性巩膜炎(12.3%)。41.3%的患者存在系统性自身免疫性疾病,最常见的是类风湿关节炎(18.5%)和肉芽肿性多血管炎(5.9%)。10.4%的系统性自身免疫性疾病患者存在多器官自身免疫。最常见的治疗方法是全身皮质类固醇(50.9%),其次是全身非甾体抗炎药(32.4%)。49.1%的患者需要皮质类固醇保留免疫抑制治疗。坏死性巩膜炎和年龄大于 40 岁的患者更常见系统性自身免疫性疾病。在坏死性巩膜炎和伴有葡萄膜炎、眼压升高或年龄大于 40 岁的患者中,就诊时最佳矫正视力为 20/80 或更差的情况更为常见。
这是哥伦比亚的第一项研究,也是拉丁美洲最大的一项研究,描述了巩膜炎的临床特征和表现模式。最常见的表现是女性单侧前部非传染性弥漫性巩膜炎。系统性自身免疫性疾病和多器官自身免疫较为常见,需要皮质类固醇保留免疫抑制治疗。年龄大于 40 岁和坏死性巩膜炎与更有可能存在系统性自身免疫性疾病和就诊时视力更差相关。