From the Department of Ophthalmology and Visual Sciences, University of British Columbia, Vancouver, BC.
From the Department of Ophthalmology and Visual Sciences, University of British Columbia, Vancouver, BC..
Can J Ophthalmol. 2023 Feb;58(1):66-72. doi: 10.1016/j.jcjo.2021.06.025. Epub 2021 Jul 28.
To examine the difference in incidence of ocular hypertension (OHT) following the introduction of filtered anti-vascular endothelial growth factor (anti-VEGF) medication in silicone-free syringes.
Retrospective cohort study.
A retrospective review of consecutive treatment-naive patients receiving intravitreal anti-VEGF injections in a group practice was performed. Data from the cohort receiving nonfiltered anti-VEGF in insulin syringes (IS group) was collected from June 2015. Data from the cohort receiving filtered anti-VEGF in silicone-free syringes (SFS group) was collected from June 2019. Follow up data were collected at 1 year. Exclusion criteria included prior anti-VEGF treatment, known glaucoma or diagnosis of glaucoma suspect before anti-VEGF treatment, neovascular glaucoma, steroid use, or vitrectomy during follow-up. Primary outcome was the cumulative incidence of intraocular pressure (IOP) > 21 mmHg and IOP ≥ 30 mm Hg at any follow-up visit. The use of IOP lowering therapy was also recorded.
The mean age (71 ± 13 years), mean number of injections (9.6 ± 2.7), and median follow-up time (392 ± 57 days) were similar between groups. The incidence of IOP ≥ 21 mm Hg was 34% (34/100) in the IS group and 15% (15/100) in the SFS group (p = 0.025). The incidence of IOP ≥ 30 mm Hg was 8% (8/100) in the IS group and 0% (0/100) in the SFS group (p =0.004). The incidence of IOP-lowering therapy was 13% in the IS group and 0% in the SFS group (p =0.0002).
The incidence of OHT and treatment with IOP-lowering therapy significantly decreased after the introduction of filtered anti-VEGF medication and silicone-free syringes.
研究在使用无硅注射器过滤的抗血管内皮生长因子(anti-VEGF)药物后,眼压升高(OHT)的发生率有何不同。
回顾性队列研究。
对在一个实践小组中接受玻璃体内抗 VEGF 注射的连续未经治疗的患者进行回顾性研究。从 2015 年 6 月开始收集使用胰岛素注射器(IS 组)注射未过滤的抗 VEGF 的患者的数据。从 2019 年 6 月开始收集使用无硅注射器(SFS 组)过滤抗 VEGF 的患者的数据。在 1 年时收集随访数据。排除标准包括:既往抗 VEGF 治疗、在接受抗 VEGF 治疗前有已知青光眼或青光眼疑似诊断、新生血管性青光眼、皮质类固醇使用或在随访期间行玻璃体切除术。主要结局是任何随访时眼压(IOP)>21mmHg 和 IOP≥30mmHg 的累积发生率。还记录了使用降眼压治疗的情况。
两组的平均年龄(71±13 岁)、平均注射次数(9.6±2.7)和中位随访时间(392±57 天)相似。IS 组的 IOP≥21mmHg 发生率为 34%(34/100),SFS 组为 15%(15/100)(p=0.025)。IS 组 IOP≥30mmHg 的发生率为 8%(8/100),SFS 组为 0%(0/100)(p=0.004)。IS 组使用降眼压治疗的发生率为 13%,SFS 组为 0%(p=0.0002)。
在使用过滤的抗 VEGF 药物和无硅注射器后,OHT 的发生率和需要使用降眼压治疗的发生率显著降低。