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玻璃体内注射阿柏西普治疗新生血管性青光眼的有效性和安全性:中国一项单中心、回顾性、观察性研究

Effectiveness and safety of intravitreal aflibercept injection for neovascular glaucoma: A single-center, retrospective, observational study in China.

作者信息

Fan Xiang, Gao Shuang, Wang Haikun, Yang Fan

机构信息

Department of Ophthalmology, Peking University Third Hospital, Beijing, China.

Beijing Key Laboratory of Restoration of Damaged Ocular Nerve, Peking University Third Hospital, Beijing, China.

出版信息

Medicine (Baltimore). 2025 Feb 28;104(9):e41538. doi: 10.1097/MD.0000000000041538.

Abstract

This study evaluates the effectiveness and safety of intravitreal aflibercept injections in Chinese patients with neovascular glaucoma (NVG). We conducted a single-center, retrospective, observational study that identified adult Chinese patients diagnosed with NVG who received intravitreal aflibercept between January 1, 2018, and June 30, 2022, by reviewing medical records. The patients were followed-up for a month. Changes in intraocular pressure (IOP) levels and improvements in neovascularization of the iris (NVI) grades at weeks 1 and 4 compared to baseline were the main outcomes for effectiveness. Safety was assessed on the basis of the occurrence of adverse ocular events. Subgroup analysis was performed for patients with high baseline IOP (>21 mm Hg) and scheduled surgery within the follow-up period. A sum of 42 eyes from 42 patients were included in the full analysis. The included eyes had improved NVI grades by at least 1 level in 84.00% of the eyes after a week and in 91.67% after a month. The mean decline of IOP in 11 eyes that were measured at week 4 was -6.29 mm Hg compared to baseline. Similar trends were observed in the subgroups. Intravitreal aflibercept injection is safe and effective in lowering IOP and inducing NVI regression in Chinese patients, as measured by improvements in NVI grades.

摘要

本研究评估玻璃体内注射阿柏西普在中国新生血管性青光眼(NVG)患者中的有效性和安全性。我们进行了一项单中心、回顾性观察性研究,通过查阅病历,确定了2018年1月1日至2022年6月30日期间接受玻璃体内注射阿柏西普的成年中国NVG患者。对患者进行了为期1个月的随访。与基线相比,第1周和第4周时眼压(IOP)水平的变化以及虹膜新生血管(NVI)分级的改善情况是有效性的主要观察指标。基于眼部不良事件的发生情况评估安全性。对基线眼压高(>21 mmHg)且在随访期内计划进行手术的患者进行亚组分析。共有来自42例患者的42只眼纳入全分析。纳入的眼在1周后84.00%的眼和1个月后91.67%的眼NVI分级至少改善1级。与基线相比,在第4周测量的11只眼中眼压平均下降-6.29 mmHg。亚组中观察到类似趋势。通过NVI分级的改善衡量,玻璃体内注射阿柏西普在中国患者中降低眼压和诱导NVI消退是安全有效的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f87/11875622/dfb7794c075f/medi-104-e41538-g001.jpg

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