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Posterior Scleritis: Analysis of Epidemiology, Clinical Factors, and Risk of Recurrence in a Cohort of 114 Patients

医学 巩膜炎 流行病学 回顾性队列研究 入射(几何) 多发性关节炎 队列 外科 痹症科 系统性血管炎 肉芽肿伴多发性血管炎 上巩膜炎 内科学 儿科 疾病 血管炎 眼科 关节炎 葡萄膜炎 物理 光学
作者
Alenka Lavrič,Dhananjay Raje,Parthopratim Dutta Majumder,Nishat Bansal,Jyotirmay Biswas,Carlos Pavésio,Rupesh Agrawal
出处
期刊:Ocular Immunology and Inflammation [Informa]
卷期号:24 (1): 6-15 被引量:84
标识
DOI:10.3109/09273948.2015.1005240
摘要

AbstractPurpose: To describe the clinical and epidemiological characteristics of patients with posterior scleritis, and to analyze the response to treatment and time to relapse.Methods: Retrospective study of 114 cases of posterior scleritis from two tertiary care, university-affiliated, referral centers in the United Kingdom and India between 2004 and 2013. Data included sociodemographic factors, medical history, clinical, laboratory and ultrasound findings, therapies, and outcomes. LogMAR visual acuity at presentation and final visit and time to relapse were the main outcome measures.Results: The mean age was 45.9 ± 16.8 years, 71.1% were women, and 18 (15.8%) patients had bilateral disease; 71 (62.3%) cases were idiopathic. Rheumatoid polyarthritis (12.28%), systemic lupus erythematous (4.38%) and pANCA+ systemic vasculitis (5.26%) were the most frequent systemic associations. VA improved by 0.24 ± 0.36 LogMAR between presentation and last follow up (p < 0.001). The median time to remission was 210 days (95% CI: 184–256 days). Recurrences after remission were observed in 36.63%. The observed incidence rate of posterior scleritis relapse after remission was 15.81% per person-year (95% CI: 11.78–20.77%). Systemic disease was present significantly in patients more than 50 years of age (OR = 2.29; 95% CI: 1.01–5.17; p = 0.044).Conclusion: Posterior scleritis is an uncommon disease causing pain and visual loss. In around 40% of the cases, it can be associated with other systemic diseases. Median time to relapse was 210 days. Relapses may occur in around 1 in 3 patients, with an incidence rate of 15.81% per person/year.KeywordsAnkylosing spondylitisimmunosuprressionposterior scleritisrheumatoid arthritisscleral diseasescleritissystemic disease“T” signThis article refers to:Posterior Scleritis and Necrobiotic Xanthogranuloma Declaration of interestThe authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper. This work was supported by the National Institute for Health Research (NIHR) Biomedical Research Centre based at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health. JJGL is a PhD candidate at the Departamento de Cirugía, Facultad de Medicina, Universidad de Alcalá, Madrid, Spain. RA was on NMRC overseas research training fellowship at Moorfields Eye Hospital and Institute of Ophthalmology, London, UK.
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