Department of Ophthalmology, Odense University Hospital, Odense, Denmark.
Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
Acta Ophthalmol. 2024 Dec;102(8):953-962. doi: 10.1111/aos.16727. Epub 2024 Jun 3.
To report the incidence of post-injection endophthalmitis (PIE) and the cumulative risk associated with repeated injections of intravitreal anti-vascular endothelial growth factor (anti-VEGF).
We employed nationwide registries in Denmark to include all individuals aged ≥40 years who received at least one intravitreal anti-VEGF injection in 2007-2022. Our primary endpoint PIE was identified using specific diagnostic codes for endophthalmitis and procedure codes for vitreous biopsy within 10 days prior to and 120 days post-injection. Patients were stratified according to the underlying diagnoses for which they received the treatment. The relative risk (RR) for PIE was calculated between groups based on the number of injections received by the patients.
We identified 60 825 patients who received intravitreal anti-VEGF treatment during study time, with a median age of 77.2 years and females constituting 58.1%. We identified 232 cases of PIE after 1 051 549 injections during follow-up, resulting in an incidence of 0.022% [95% CI 0.019%-0.025%]. Despite a linear growth in annual anti-VEGF use, the incidence remained stable at 0.020% [95% CI 0.017%-0.023%] from 2013 to 2022. Compared to patients receiving 1-3 injections, RR for patients receiving 4-20, 21-40, and >40 injections were 0.46 [95% CI 0.34-0.63], 0.32 [95% CI 0.21-0.50], and 0.54 [95% CI 0.36-0.81], respectively. Findings were similar across the different diagnoses.
Based on 16 years of nationwide registry data, this study identified a low and stable incidence of PIE. Notably, the highest risk of endophthalmitis was within the first three anti-VEGF injections.
报告玻璃体腔内抗血管内皮生长因子(anti-VEGF)注射后眼内炎(PIE)的发生率及与反复注射相关的累积风险。
我们利用丹麦全国性注册系统,纳入 2007 年至 2022 年期间至少接受过一次玻璃体腔内抗 VEGF 注射的年龄≥40 岁的所有患者。我们通过在注射前 10 天内和注射后 120 天内的特定内眼炎诊断代码和玻璃体活检程序代码,确定了主要结局 PIE。根据患者接受治疗的基础诊断对患者进行分层。根据患者接受的注射次数,计算各组之间 PIE 的相对风险(RR)。
研究期间共纳入 60825 名接受玻璃体腔内抗 VEGF 治疗的患者,中位年龄为 77.2 岁,女性占 58.1%。在随访期间,共发现 1051549 次注射后 232 例 PIE,发生率为 0.022%[95%CI0.019%-0.025%]。尽管抗 VEGF 的年使用量呈线性增长,但 2013 年至 2022 年,发生率仍稳定在 0.020%[95%CI0.017%-0.023%]。与接受 1-3 次注射的患者相比,接受 4-20、21-40 和>40 次注射的患者的 RR 分别为 0.46[95%CI0.34-0.63]、0.32[95%CI0.21-0.50]和 0.54[95%CI0.36-0.81]。不同诊断的结果相似。
基于 16 年的全国性注册数据,本研究发现 PIE 的发生率较低且稳定。值得注意的是,眼内炎的最高风险发生在最初的三次抗 VEGF 注射内。