Pan Yuan, Chen Yu-Xi, Lu Yao, Xie Yan-Yan, Xia Yi-Wen, Liang Dan
Department of Ocular Immunology, State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-Sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangdong Provincial Clinical Research Center for Ocular Diseases, No. 54 Xianlie South Road, Guangzhou, 510060, China.
Ophthalmol Ther. 2022 Dec;11(6):2297-2307. doi: 10.1007/s40123-022-00577-w. Epub 2022 Oct 12.
This article aimed to summarize the outcomes of escalating immunosuppressive treatments for patients with recalcitrant noninfectious posterior scleritis (PS).
Clinical records of 16 patients diagnosed with recalcitrant noninfectious PS in the Ocular Immunity and Uveitis Department of Zhongshan Ophthalmic Center from September 2016 to December 2021 were reviewed. Patients were treated with escalating immunosuppressive regimen including corticosteroid, immunosuppressants (IMTs), and adalimumab (ADA). Demographic characteristics and clinical findings at each visit were recorded. The doses of prednisone were analyzed. Main outcomes were corticosteroid-sparing effects, control of inflammation, visual acuity, and safety profile.
Ocular pain was the most common finding (100%), followed by the T sign on the B scan (93.8%) and associated anterior scleritis (75.0%). The average initial dose of prednisone was 25.0 mg/day, and tapered to 11.3 and 5.0 mg/day at month 1 and 3, respectively, with statistical significance (p < 0.05). The median overall periods of prednisone tapering to 10, 5, and 0 mg/day were 1.0, 3.0, and 3.0 months, respectively. There were 93.8% of patients receiving prednisone ≤ 10 mg/day and 68.8% of patients off prednisone at last visit. There were 80% of patients treated with IMT and ADA off prednisone at last visit, reaching the highest percentage compared with others. A best-corrected visual acuity of 1.0 or better at last visit was achieved in 10 eyes (62.5%). The escalating treatments showed good safety profile.
Patients of recalcitrant noninfectious PS benefited from escalating immunosuppressive treatments with favorable visual outcome, in which methotrexate, ciclosporin, and ADA were preferred with good safety.
本文旨在总结对顽固性非感染性后巩膜炎(PS)患者逐步升级免疫抑制治疗的结果。
回顾了2016年9月至2021年12月在中山眼科中心眼免疫与葡萄膜炎科确诊为顽固性非感染性PS的16例患者的临床记录。患者接受了逐步升级的免疫抑制方案治疗,包括皮质类固醇、免疫抑制剂(IMTs)和阿达木单抗(ADA)。记录每次就诊时的人口统计学特征和临床检查结果。分析泼尼松的剂量。主要结果包括皮质类固醇节省效应、炎症控制、视力和安全性。
眼部疼痛是最常见的表现(100%),其次是B超上的T征(93.8%)和相关的前巩膜炎(75.0%)。泼尼松的平均初始剂量为25.0mg/天,在第1个月和第3个月分别减至11.3mg/天和5.0mg/天,差异有统计学意义(p<0.05)。泼尼松减至10mg/天、5mg/天和0mg/天的中位总时间分别为1.0个月、3.0个月和3.0个月。最后一次就诊时,93.8%的患者接受的泼尼松剂量≤10mg/天,68.8%的患者停用了泼尼松。最后一次就诊时,80%接受IMT和ADA治疗的患者停用了泼尼松,这一比例高于其他患者。10只眼(62.5%)在最后一次就诊时最佳矫正视力达到1.0或更好。逐步升级的治疗显示出良好的安全性。
顽固性非感染性PS患者从逐步升级的免疫抑制治疗中获益,视力预后良好,其中甲氨蝶呤、环孢素和ADA安全性良好,为首选。