Risk of post-injection endophthalmitis peaks within the first three injections of anti-vascular endothelial growth factor therapy: A nationwide registry-based study

IF 3 3区 医学 Q1 OPHTHALMOLOGY Acta Ophthalmologica Pub Date : 2024-06-03 DOI:10.1111/aos.16727
Benjamin Sommer Thinggaard, Frederik Pedersen, Ryo Kawasaki, Jimmi Wied, Yousif Subhi, Jakob Grauslund, Lonny Stokholm
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Abstract

Purpose

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).

Methods

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.

Results

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.

Conclusions

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.

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注射后眼内炎的风险在抗血管内皮生长因子治疗的前三次注射中达到高峰:一项基于全国登记的研究。
目的:报告注射后眼内炎(PIE)的发病率以及与重复注射玻璃体内抗血管内皮生长因子(anti-VEGF)相关的累积风险:我们利用丹麦全国范围内的登记资料,纳入了2007-2022年期间至少接受过一次玻璃体内抗血管内皮生长因子注射的所有年龄≥40岁的人。我们的主要终点 PIE 是通过眼内炎的特定诊断代码和注射前 10 天及注射后 120 天内玻璃体活检的手术代码确定的。根据接受治疗的基础诊断对患者进行分层。根据患者接受注射的次数计算各组间 PIE 的相对风险 (RR):我们共发现了 60 825 例在研究期间接受过玻璃体内抗 VEGF 治疗的患者,中位年龄为 77.2 岁,女性占 58.1%。在随访期间,我们发现 232 例患者在接受了 1 051 549 次注射后出现 PIE,发病率为 0.022% [95% CI 0.019%-0.025%]。尽管抗血管内皮生长因子的年使用量呈线性增长,但从2013年到2022年,发病率仍稳定在0.020% [95% CI 0.017%-0.023%]。与接受 1-3 次注射的患者相比,接受 4-20 次、21-40 次和大于 40 次注射的患者的 RR 分别为 0.46 [95% CI 0.34-0.63]、0.32 [95% CI 0.21-0.50] 和 0.54 [95% CI 0.36-0.81]。不同诊断的结果相似:根据16年的全国登记数据,本研究发现PIE的发病率较低且稳定。值得注意的是,前三次抗血管内皮生长因子注射发生眼内炎的风险最高。
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来源期刊
Acta Ophthalmologica
Acta Ophthalmologica 医学-眼科学
CiteScore
7.60
自引率
5.90%
发文量
433
审稿时长
6 months
期刊介绍: Acta Ophthalmologica is published on behalf of the Acta Ophthalmologica Scandinavica Foundation and is the official scientific publication of the following societies: The Danish Ophthalmological Society, The Finnish Ophthalmological Society, The Icelandic Ophthalmological Society, The Norwegian Ophthalmological Society and The Swedish Ophthalmological Society, and also the European Association for Vision and Eye Research (EVER). Acta Ophthalmologica publishes clinical and experimental original articles, reviews, editorials, educational photo essays (Diagnosis and Therapy in Ophthalmology), case reports and case series, letters to the editor and doctoral theses.
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