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Predictors of Relapse after Discontinuing Systemic Treatment in Childhood Autoimmune Chronic Uveitis.儿童自身免疫性慢性葡萄膜炎全身治疗停药后复发的预测因素
J Rheumatol. 2017 Jun;44(6):822-826. doi: 10.3899/jrheum.161336. Epub 2017 Apr 1.
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Prevalence of Noninfectious Uveitis in the United States: A Claims-Based Analysis.美国非感染性葡萄膜炎的患病率:基于索赔数据的分析
JAMA Ophthalmol. 2016 Nov 1;134(11):1237-1245. doi: 10.1001/jamaophthalmol.2016.3229.
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Adalimumab in Patients with Active Noninfectious Uveitis.阿达木单抗治疗活动性非感染性葡萄膜炎患者的疗效。
N Engl J Med. 2016 Sep 8;375(10):932-43. doi: 10.1056/NEJMoa1509852.
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Adalimumab for prevention of uveitic flare in patients with inactive non-infectious uveitis controlled by corticosteroids (VISUAL II): a multicentre, double-masked, randomised, placebo-controlled phase 3 trial.阿达木单抗预防皮质类固醇控制的非感染性活动性葡萄膜炎患者的葡萄膜炎发作(VISUAL II):一项多中心、双盲、随机、安慰剂对照的 3 期临床试验。
Lancet. 2016 Sep 17;388(10050):1183-92. doi: 10.1016/S0140-6736(16)31339-3. Epub 2016 Aug 16.
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Current evidence of anti-tumor necrosis factor α treatment efficacy in childhood chronic uveitis: a systematic review and meta-analysis approach of individual drugs.目前抗肿瘤坏死因子 α 治疗儿童慢性葡萄膜炎疗效的证据:个体药物的系统评价和荟萃分析方法。
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尽管甲氨蝶呤存在,仍要考虑在儿童慢性非感染性前葡萄膜炎中适时起始英夫利昔单抗和阿达木单抗治疗。

Timing of infliximab and adalimumab initiation despite methotrexate in children with chronic non-infectious anterior uveitis.

机构信息

Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.

Department of Ophthalmology, Emory University School of Medicine, Atlanta, GA, USA.

出版信息

Eye (Lond). 2019 Apr;33(4):629-639. doi: 10.1038/s41433-018-0283-0. Epub 2018 Nov 28.

DOI:10.1038/s41433-018-0283-0
PMID:30487588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6461976/
Abstract

AIMS

Methotrexate (MTX) is standard treatment in pediatric chronic anterior uveitis (CAU). Addition of tumor necrosis factor-α inhibitors (TNFi) is often needed. We describe the timing and risk factors for TNFi use in children with CAU on MTX.

METHODS

In this retrospective study, we reviewed 51 records, and 46 met inclusion criteria. Primary outcome was the addition of TNFi due to active CAU per Standardization of Uveitis Nomenclature criteria. Time to TNFi and factors associated with their addition were assessed using survival analysis models.

RESULTS

Of 46 children treated with MTX for uveitis (36 juvenile idiopathic arthritis-associated uveitis, 10 idiopathic CAU), 72% had ocular complications. MTX was started a median of 5.0 months, and TNFi 43 months from uveitis diagnosis. Kaplan-Meier estimates suggest that cumulatively, 12% (95% CI: 4-23%) start TNFi within 6 months of MTX, 21% (12-37%) within 1 year, and 39% (24-54%) within 2 years. On Cox Proportional Hazard regression analysis, children with idiopathic CAU required TNFi earlier in their uveitis course (at 3 months (Hazard Ratio 6.06; 95% confidence interval (1.25-29.41))). Females appeared less likely to require TNFi early. Children treated in 2012 and later were more likely to receive TNFi earlier than those treated before 2012.

CONCLUSION

Little is known about optimal time to initiate treatment or factors associated with the need to add TNFi in children on MTX. Children with idiopathic CAU and males required TNFi earlier in their course. Factors associated with these potential risk factors for TNFi warrant further investigation.

摘要

目的

甲氨蝶呤(MTX)是儿童慢性前葡萄膜炎(CAU)的标准治疗方法。通常需要添加肿瘤坏死因子-α抑制剂(TNFi)。我们描述了 MTX 治疗儿童 CAU 时 TNFi 的使用时机和相关风险因素。

方法

在这项回顾性研究中,我们回顾了 51 份记录,其中 46 份符合纳入标准。主要结局是根据葡萄膜炎命名标准,因 CAU 活动而添加 TNFi。使用生存分析模型评估 TNFi 的添加时间和相关因素。

结果

46 例接受 MTX 治疗的儿童中有 36 例为幼年特发性关节炎相关葡萄膜炎,10 例为特发性 CAU,72%有眼部并发症。MTX 起始中位时间为 5.0 个月,TNFi 起始时间为葡萄膜炎诊断后 43 个月。Kaplan-Meier 估计表明,12%(95%CI:4-23%)的患者在 MTX 治疗后 6 个月内开始使用 TNFi,21%(12-37%)在 1 年内,39%(24-54%)在 2 年内。Cox 比例风险回归分析显示,特发性 CAU 患儿在葡萄膜炎病程中更早需要 TNFi(3 个月时(危险比 6.06;95%置信区间(1.25-29.41)))。女性似乎不太可能早期需要 TNFi。2012 年及以后治疗的患儿比 2012 年以前治疗的患儿更早接受 TNFi。

结论

关于 MTX 治疗儿童的最佳起始治疗时间或与需要添加 TNFi 相关的因素知之甚少。特发性 CAU 患儿和男性在病程中更早需要 TNFi。这些 TNFi 潜在风险因素的相关因素值得进一步研究。