Department of Ophthalmology, University Vita-Salute, Scientific Institute San Raffaele, Milan, Italy.
Ophthalmologica. 2012;228(4):229-33. doi: 10.1159/000343060. Epub 2012 Oct 3.
To describe our experience in treating recalcitrant and severe cases of noninfectious posterior uveitis with the 0.7-mg dexamethasone intravitreal implant as adjunctive anti-inflammatory treatment.
Retrospective study. Twelve patients (8 females; 4 males; 14 affected eyes, 15 implants) with severe recalcitrant uveitis were treated. Patients had an inadequate control of uveitis despite different immunosuppressants and periocular corticosteroid therapy. Primary outcome measures evaluated were: decrease in uveitis activity, improvement in visual acuity, reduction of macular thickness, and occurrence of adverse events.
Uveitis activity decreased in all patients after the implant. The mean follow-up time from injection was 9 months. Best-corrected visual acuity improved from 20/80 to 20/40 at the end of follow-up. The mean retinal thickness improved from 496 to 226 µm. Adverse events encountered were: 3 eyes with intraocular pressure elevation, 1 vitreous hemorrhage and 1 subconjunctival hemorrhage. Three patients reduced the daily systemic corticosteroid dosage after treatment.
The 0.7-mg dexamethasone intravitreal implant appears to be a novel and promising adjunctive treatment for patients with severe posterior noninfectious uveitis recalcitrant to different immunosuppressive agents.
描述我们使用 0.7mg 地塞米松玻璃体内植入物作为辅助抗炎治疗治疗难治性和严重非感染性后葡萄膜炎的经验。
回顾性研究。12 名患者(8 名女性;4 名男性;14 只受影响的眼睛,15 个植入物)患有严重难治性葡萄膜炎。尽管使用了不同的免疫抑制剂和眼周皮质类固醇治疗,但患者的葡萄膜炎仍无法得到控制。主要评估的结局指标是:葡萄膜炎活动度降低、视力提高、黄斑厚度减少以及不良事件的发生。
所有患者在植入后葡萄膜炎活动度均降低。从注射到随访结束的平均时间为 9 个月。最佳矫正视力从 20/80 提高到随访结束时的 20/40。视网膜平均厚度从 496µm 改善至 226µm。发生的不良事件包括:3 只眼眼压升高,1 只眼玻璃体积血,1 只眼结膜下出血。3 名患者在治疗后减少了每日全身皮质类固醇剂量。
0.7mg 地塞米松玻璃体内植入物似乎是一种新颖且有前途的治疗方法,可用于治疗对不同免疫抑制剂治疗难治的严重非感染性后葡萄膜炎。