Schatz Claude Speeg, Uzel Jean Louis, Leininger Laurent, Danner Stéphanie, Terzic Joëlle, Fischbach Michel
Strasbourg University Eye Hospital, BP 426 1 place de l'Hôpital, 67091 Strasbourg, France.
J Pediatr Ophthalmol Strabismus. 2007 Jan-Feb;44(1):28-34. doi: 10.3928/01913913-20070101-03.
To review, with respect to etiology, the efficacy and complications of different immunosuppressants used in a steroid-sparing strategy for children with uveitis.
Forty children with uveitis were observed during a 5-year period, from 1997 to 2002. After complete ocular and physical assessment, routine and specific laboratory investigations were conducted along with radiologic examination. All cases underwent local therapy. Systemic corticosteroids were necessary in 75% of cases. Pediatric staff determined the need for initial association or sequential relay with immunosuppressants, depending on the severity of the uveitis. A steroid-sparing strategy was developed.
The average age was 6.5 years (range, 3 months to 14 years), with a male-to-female ratio of 23 to 17. Uveitis was anterior in 55% of cases, intermediate in 2.5%, posterior in 42.5%, and bilateral in 62.5%. A positive etiology was found in 47.5% of cases, and articular symptoms were present in 25%. Overall, the improvement in visual acuity was 62.2%. Where corticotherapy was associated with azathioprine, a 61% improvement was achieved. Corticosteroid therapy associated with mycophenolate mofetil resulted in a 94% improvement. No complications were present in 42.5% of cases. Ocular complications were present in 57.5% of cases and systemic complications were present in 12.5% of cases, none being directly related to the use of steroids.
The association of systemic corticotherapy and immunosuppressants in pediatric relapsing or steroid-dependent uveitis allows good recovery of visual acuity, fewer complications, and a minimization of side effects, especially those related to systemic corticosteroids. It requires close collaboration between the ophthalmologist and a fully involved pediatrician.
从病因学角度回顾不同免疫抑制剂在儿童葡萄膜炎激素节省策略中的疗效及并发症。
1997年至2002年期间观察了40例儿童葡萄膜炎患者。在完成眼部及全身评估后,进行了常规及特殊实验室检查以及影像学检查。所有病例均接受局部治疗。75%的病例需要全身使用皮质类固醇。儿科工作人员根据葡萄膜炎的严重程度确定是否需要初始联合使用或序贯接力使用免疫抑制剂,从而制定了激素节省策略。
平均年龄为6.5岁(范围3个月至14岁),男女比例为23比17。55%的病例为前葡萄膜炎,2.5%为中间葡萄膜炎,42.5%为后葡萄膜炎,62.5%为双侧葡萄膜炎。47.5%的病例病因明确,25%出现关节症状。总体而言,视力改善率为62.2%。皮质类固醇与硫唑嘌呤联合使用时,视力改善率为61%。皮质类固醇与霉酚酸酯联合使用时,视力改善率为94%。42.5%的病例无并发症。57.5%的病例出现眼部并发症,12.5%的病例出现全身并发症,均与使用类固醇无直接关系。
全身皮质类固醇治疗与免疫抑制剂联合用于儿童复发性或类固醇依赖型葡萄膜炎,可使视力良好恢复,并发症减少,副作用尤其是与全身皮质类固醇相关的副作用最小化。这需要眼科医生与全身心投入的儿科医生密切合作。