Edelsten Clive, Lee Vickie, Bentley Christopher R, Kanski Jack J, Graham Elizabeth M
Medical Ophthalmology Department, Great Ormond Street Hospital and Prince Charles Eye Unit, King Edward VII Hospital, Windsor, UK.
Br J Ophthalmol. 2002 Jan;86(1):51-6. doi: 10.1136/bjo.86.1.51.
BACKGROUND/AIMS: The clinical course for childhood chronic anterior uveitis can vary from mild, self limiting disease to bilateral blindness. The purpose of this study was to identify those risk factors at onset that predict disease severity.
A retrospective case note review of all patients with painless anterior uveitis diagnosed from 1982 to 1998. Patients were divided into two cohorts based on route of referral, diagnosis, and compliance with treatment. The standard cohort consisted of only those diagnosed from routine screening of juvenile idiopathic arthritis.
Complications-cataract surgery, ocular hypertension treatment, and visual acuity <6/24. Remission: inactive uveitis on no topical treatment for >6 months. Results-163 patients were included. 34 patients (21%) developed at least one complication. The most significant predictor of complications was severe disease at onset (p = 0.001). Other factors included uveitis at the first examination (p = 0.034), membership of the non-standard cohort (p = 0.0001), non-oligoarticular disease (p = 0.02), and late onset arthritis (p = 0.024). Male sex was associated with increased complications in the standard cohort (p = 0.001). Factors predisposing to remission included membership of the standard cohort (p = 0.003), onset after 1990 (p = 0.016), white race (p = 0.015), mild disease onset (p = 0.003), and a long gap between arthritis and uveitis onset (p = 0.015).
It is possible to characterise the severity of those with childhood chronic anterior uveitis at the onset of disease. The majority of patients remit without visually disabling complications. It may be possible to reduce the complication rate by targeting aggressive immunosuppression on high risk patients before complications develop.
背景/目的:儿童慢性前葡萄膜炎的临床病程差异较大,从轻症、自限性疾病到双侧失明不等。本研究旨在确定疾病初发时可预测疾病严重程度的危险因素。
对1982年至1998年诊断为无痛性前葡萄膜炎的所有患者进行回顾性病历审查。根据转诊途径、诊断及治疗依从性将患者分为两个队列。标准队列仅包括那些通过青少年特发性关节炎常规筛查诊断出的患者。
并发症——白内障手术、高眼压治疗及视力<6/24。缓解:未进行局部治疗>6个月时葡萄膜炎不活动。结果——纳入163例患者。34例患者(21%)出现至少一种并发症。并发症的最显著预测因素是疾病初发时病情严重(p = 0.001)。其他因素包括首次检查时存在葡萄膜炎(p = 0.034)、非标准队列成员(p = 0.0001)、非少关节性疾病(p = 0.02)及晚发性关节炎(p = 0.024)。在标准队列中,男性与并发症增加相关(p = 0.001)。易于缓解的因素包括标准队列成员(p = 0.003)、1990年后发病(p = 0.016)、白种人(p = 0.015)、疾病初发时病情较轻(p = 0.003)及关节炎与葡萄膜炎发病间隔时间长(p = 0.015)。
在儿童慢性前葡萄膜炎疾病初发时能够对其严重程度进行特征描述。大多数患者病情缓解且无导致视力残疾的并发症。在并发症发生前对高危患者进行积极免疫抑制治疗,有可能降低并发症发生率。