Evaluation of Sustained Intraocular Pressure Elevations Across Antivascular Endothelial Growth Factor Agents.

IF 0.5 Q4 OPHTHALMOLOGY
Neil A Rana, Meghana Chalasani, Jonathan Markle, Matthew W Russell, Ang Li, Katherine E Talcott, Rishi P Singh, Sumit Sharma
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引用次数: 0

Abstract

Purpose: To evaluate the effect of antivascular endothelial growth factor (anti-VEGF) agents on the development of sustained intraocular pressure (IOP) elevations. Methods: This single-center retrospective cohort study included eyes receiving anti-VEGF injections for various indications along with nontreated fellow eyes from 2012 to 2022. Patients were grouped according to treatment with bevacizumab, ranibizumab, or aflibercept. Trends in IOP were recorded after treatment initiation for 1 year. The development of sustained IOP elevations (defined as an increase of 5 mm Hg or greater than baseline for 4 or more weeks) and glaucoma manifestations were recorded. Results: The analysis included 1604 eyes (injection cohort, 907; control cohort, 697). The mean age of the injection cohort was 83.3 years; 56.9% were women and 82.0% were White. Injections were for neovascular age-related macular degeneration (498 [54.9%]), diabetic retinopathy (219 [24.1%]), retinal vein occlusion (161 [17.8%]), and other indications (29 [3.2%)]. Bevacizumab was used in 521 eyes (57.4%), ranibizumab in 129 eyes (14.2%), and aflibercept in 257 eyes (28.3%). The mean age in the control cohort was 81.6 years; 56.1% were women and 84.1% were White. Sustained IOP elevations developed in 97 (6.0%) of 1604 eyes throughout the study. Compared with controls, treated eyes overall did not have an increased rate of sustained IOP elevations (P = .38) or glaucoma progression (P = .51), although patients treated with bevacizumab had a significantly greater incidence of IOP elevation than controls (relative risk, 1.81; 95% CI, 1.18-2.78). The mean number of injections to sustained IOP elevation was 5.4 and did not differ between agents (P > .05). Conclusions: Although not all anti-VEGF agents are associated with IOP-related adverse effects, bevacizumab carries an increased risk for sustained IOP elevation. Further investigation into the long-term effects of bevacizumab on IOP and glaucoma and a comparison with other anti-VEGF agents may be warranted.

评估抗血管内皮生长因子药物的持续眼压升高。
目的:评估抗血管内皮生长因子(anti-VEGF)药物对眼压(IOP)持续升高的影响。方法:这是一项单中心回顾性队列研究:这项单中心回顾性队列研究纳入了 2012 年至 2022 年期间因各种适应症接受抗血管内皮生长因子注射的眼睛以及未接受治疗的同组眼睛。根据贝伐单抗、雷尼单抗或阿弗利贝赛普的治疗情况对患者进行分组。在治疗开始后的一年内记录眼压变化趋势。还记录了眼压持续升高(定义为比基线升高5毫米汞柱或更高,持续4周或更长时间)和青光眼表现。结果分析包括 1604 只眼睛(注射组 907 只;对照组 697 只)。注射组的平均年龄为 83.3 岁;56.9% 为女性,82.0% 为白人。注射对象包括新生血管性老年黄斑变性(498 例 [54.9%])、糖尿病视网膜病变(219 例 [24.1%])、视网膜静脉闭塞(161 例 [17.8%])和其他适应症(29 例 [3.2%])。521只眼睛(57.4%)使用了贝伐单抗,129只眼睛(14.2%)使用了雷尼单抗,257只眼睛(28.3%)使用了阿弗利贝赛普。对照组的平均年龄为 81.6 岁,56.1% 为女性,84.1% 为白人。在整个研究过程中,1604 只眼睛中有 97 只(6.0%)眼压持续升高。与对照组相比,接受治疗的眼睛眼压持续升高(P = .38)或青光眼进展(P = .51)的发生率总体上没有增加,但接受贝伐珠单抗治疗的患者眼压升高的发生率明显高于对照组(相对风险为 1.81;95% CI,1.18-2.78)。眼压持续升高的平均注射次数为 5.4 次,不同药物之间没有差异(P > .05)。结论:虽然并非所有抗血管内皮生长因子药物都与眼压相关的不良反应有关,但贝伐单抗会增加眼压持续升高的风险。可能需要进一步研究贝伐珠单抗对眼压和青光眼的长期影响,并与其他抗血管内皮生长因子药物进行比较。
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来源期刊
CiteScore
1.20
自引率
16.70%
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0
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