Dokuz Eylül University Faculty of Medicine, Department of Ophthalmology, İzmir, Turkey.
Turk J Ophthalmol. 2021 Feb 25;51(1):32-37. doi: 10.4274/tjo.galenos.2020.84042.
To evaluate the functional and anatomical results of patients with non-infectious intraocular inflammation (IOI) following intravitreal anti-vascular endothelial growth factor (anti-VEGF) injection for the treatment of neovascular age-related macular degeneration (nAMD).
The medical records of patients receiving anti-VEGF treatment for nAMD between January 2015 and March 2019 were retrospectively analyzed. Preoperative and postoperative routine ophthalmological examinations, central macular thickness, duration of inflammation, and follow-up time of the patients with non-infectious IOI following anti-VEGF injection were recorded.
Non-infectious IOI was determined in 13 eyes (11 eyes with aflibercept, 2 eyes with ranibizumab) of 1,966 patients who received a total of 12,652 anti-VEGF (4,796 aflibercept and 7,856 ranibizumab) injections. IOI was detected after a mean of 7 injections (2-12 injections). All eyes had both anterior chamber reaction (Tyndall +1/+3) and vitritis (grade 1-3). None of the patients had pain, hypopyon, or fibrin reaction. Visual acuity progressed to baseline levels within 28.3 days. Vitritis continued with a mean of 40 days. All patients recovered with topical steroid therapy. In 11 eyes, injection of the same anti-VEGF agent was continued. No recurrence of IOI was observed in any patients.
Non-infectious IOI following intravitreal anti-VEGF injection typically occurs without pain, conjunctival injection, hypopyon, or fibrin and responds well to topical steroid therapy. Visual acuity returns to baseline levels within weeks according to the severity of inflammation.
评估玻璃体内抗血管内皮生长因子(anti-VEGF)注射治疗新生血管性年龄相关性黄斑变性(nAMD)后非感染性眼内炎症(IOI)患者的功能和解剖学结果。
回顾性分析 2015 年 1 月至 2019 年 3 月接受抗 VEGF 治疗 nAMD 的患者的病历。记录接受抗 VEGF 治疗的患者的术前和术后常规眼科检查、中央黄斑厚度、炎症持续时间和非感染性 IOI 患者的随访时间。
在接受了总共 12652 次抗 VEGF(4796 次阿柏西普和 7856 次雷珠单抗)注射的 1966 例患者中,有 13 只眼(11 只眼使用阿柏西普,2 只眼使用雷珠单抗)被确定为非感染性 IOI。IOI 在平均 7 次注射后被检测到(2-12 次注射)。所有眼均有前房反应(Tyndall +1/+3)和玻璃体炎症(1-3 级)。无患者出现疼痛、前房积脓或纤维蛋白反应。视力在 28.3 天内恢复到基线水平。玻璃体炎症持续平均 40 天。所有患者均通过局部皮质类固醇治疗恢复。在 11 只眼中,继续注射相同的抗 VEGF 药物。任何患者均未观察到 IOI 复发。
玻璃体内抗 VEGF 注射后发生的非感染性 IOI 通常无疼痛、结膜充血、前房积脓或纤维蛋白,对局部皮质类固醇治疗反应良好。根据炎症的严重程度,视力在数周内恢复到基线水平。