Therapeutic Outcomes of Non-Infectious Scleritis Treated with Tumor Necrosis Factor-Alpha Inhibitors

被引:1
|
作者
Brown, Jaime E. [1 ]
Thomas, Akshay S. [2 ]
Armbrust, Karen R. [3 ,4 ]
Boyd, Kelly [1 ]
Berkenstock, Meghan [5 ]
Kopplin, Laura J. [1 ,6 ]
机构
[1] Univ Wisconsin, Dept Ophthalmol & Visual Sci, Madison, WI USA
[2] Tennessee Retina, Nashville, TN USA
[3] Minneapolis Vet Affairs Hlth Care Syst, Dept Ophthalmol, Minneapolis, MN USA
[4] Univ Minnesota, Dept Ophthalmol & Visual Neurosci, Minneapolis, MN USA
[5] Wilmer Eye Inst, Johns Hopkins Sch Med, Ocular Immunol Div, Baltimore, MD USA
[6] Univ Wisconsin, Dept Ophthalmol & Visual Sci, 2870 Univ Ave, Ste 102, Madison, WI 53701 USA
基金
美国国家卫生研究院;
关键词
Adalimumab; biologics; scleritis; systemic autoimmune disease; TNF inhibitor; EPISCLERITIS; ADALIMUMAB; UVEITIS;
D O I
10.1080/09273948.2023.2191712
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: We determine the efficacy of tumor necrosis factor-alpha (TNF) inhibitors in establishing scleritis quiescence. Methods: We conducted a multicenter retrospective chart review of patients with non-infectious scleritis treated with a TNF inhibitor for at least 6 months. The primary endpoint was scleritis quiescence at 6 months. Secondary endpoints included scleritis quiescence at 12 months, TNF inhibitor effects on concurrent doses of systemic corticosteroids and visual acuity outcomes at 6 and 12 months. Results: At 6 months, 82.2% (37/45) of subjects obtained scleritis quiescence with TNF inhibition. At 12 months, 76.2% (32/42) of subjects remained quiescent. Baseline daily corticosteroid use (21.5 +/- 21.6 mg) decreased to 5.4 +/- 8.3 mg by 6 months (p < 0.0001) and 2.8 +/- 6.1 mg by 12 months (p < 0.001). There was no significant difference between the baseline and 6-month BCVA (p = 0.52). Conclusions: TNF inhibitors are an effective scleritis therapy with significant systemic corticosteroid sparing effect.
引用
收藏
页码:1017 / 1023
页数:7
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