Friling Ronit, Kramer Michal, Snir Moshe, Axer-Siegel Ruth, Weinberger D, Mukamel Masza
Pediatric Ophthalmology Unit, Schneider Children's Medical Center of Israel, Petah Tikva, Israel.
J AAPOS. 2005 Aug;9(4):379-82. doi: 10.1016/j.jaapos.2005.04.005.
We sought to evaluate the clinical course, complications, and visual outcome of pediatric uveitis.
Our sample included 38 consecutive children with uveitis treated between 1986 and 2002: 15 with idiopathic uveitis, 10 with Behcet disease, 9 with juvenile rheumatoid arthritis, 4 with other diagnoses. The last group was excluded from the analysis because of its small size. Appropriate ophthalmologic and laboratory examinations were obtained. Treatment consisted of topical, periocular, or systemic steroids with or without immunosuppression.
Complications occurred in all 3 groups, although they tended to be more severe in the patients with juvenile rheumatoid arthritis. Visual acuity improved from presentation to final examination; the difference was statistically significant for the patients with idiopathic uveitis (P < 0.0005) and Behcet disease (P = 0.004).
These findings support an intensive treatment approach to childhood uveitis. The visual prognosis is good even in patients with a severe clinical course.
我们试图评估儿童葡萄膜炎的临床病程、并发症及视力转归。
我们的样本包括1986年至2002年间连续治疗的38例葡萄膜炎患儿:15例特发性葡萄膜炎,10例白塞病,9例幼年型类风湿关节炎,4例其他诊断。最后一组因样本量小被排除在分析之外。进行了适当的眼科和实验室检查。治疗包括局部、眼周或全身使用类固醇,可联合或不联合免疫抑制治疗。
所有3组均出现并发症,不过幼年型类风湿关节炎患者的并发症往往更严重。从初诊到最终检查视力有所改善;特发性葡萄膜炎患者(P < 0.0005)和白塞病患者(P = 0.004)的差异具有统计学意义。
这些发现支持对儿童葡萄膜炎采取强化治疗方法。即使临床病程严重的患者视力预后也良好。