Short-term intraocular pressure changes after intravitreal aflibercept 2 mg, aflibercept 8 mg and faricimab: a prospective, comparative study

IF 3.7 2区 医学 Q1 OPHTHALMOLOGY British Journal of Ophthalmology Pub Date : 2024-11-12 DOI:10.1136/bjo-2024-326053
Arianna Paris, Giulio Volpe, Kathrin Perruchoud-Ader, Alex Casanova, Moreno Menghini, Gabriela Grimaldi
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Abstract

Background/aims Intravitreal injection (IVT) of anti-vascular endothelial growth factor agents is the standard of care for several retinal diseases but can cause intraocular pressure (IOP) elevations. This study investigates short-term postinjection IOP changes following aflibercept 8 mg and faricimab, compared with aflibercept 2 mg. Methods This observational, prospective study included 90 patients with age-related macular degeneration or diabetic macular oedema, divided into three groups, receiving aflibercept 2 mg, aflibercept 8 mg or faricimab. IOP was measured using an iCare IC200-tonometer preinjection (T0) and at 30 s (T1), 5 min (T2) and 15 min (T3) postinjection. Primary outcomes included IOP changes at the four time points within and between treatment groups. The incidence of transient visual loss requiring paracentesis was recorded. Results All groups experienced a significant IOP increase at T1, with mean IOP increase being 41.47±12.95 mm Hg for aflibercept 2 mg, 43.46±8.97 mm Hg for aflibercept 8 mg and 32.19±11.06 mm Hg for faricimab. By T2, IOP differences were not significant, and by T3, mean IOP returned within normal limits across all groups. Faricimab showed a smaller initial IOP spike than both aflibercept formulations, but this difference was not statistically significant at T2 and T3. Conclusion Transient IOP spikes are observed post-IVT of aflibercept 8 mg and faricimab, with similar trends to aflibercept 2 mg. The initial IOP elevation normalised within 15 min. Faricimab had a lower initial spike, but overall IOP profiles were comparable across different agents. Data are available on reasonable request.
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玻璃体内阿弗利百普 2 毫克、阿弗利百普 8 毫克和法利西单抗治疗后的短期眼压变化:一项前瞻性比较研究
背景/目的 抗血管内皮生长因子药物的玻璃体内注射(IVT)是治疗多种视网膜疾病的标准方法,但会导致眼压(IOP)升高。与阿弗利百普 2 毫克相比,本研究调查了阿弗利百普 8 毫克和法尼单抗注射后眼压的短期变化。方法 这项前瞻性观察研究包括90名老年性黄斑变性或糖尿病性黄斑水肿患者,分为三组,分别接受aflibercept 2毫克、aflibercept 8毫克或法尼单抗治疗。在注射前(T0)、注射后30秒(T1)、5分钟(T2)和15分钟(T3)使用iCare IC200眼压计测量眼压。主要结果包括治疗组内和治疗组间四个时间点的眼压变化。记录需要进行旁路穿刺的一过性视力下降的发生率。结果 所有治疗组在T1时的眼压都明显升高,阿夫利百普2毫克、阿夫利百普8毫克和法尼单抗的平均眼压分别为41.47±12.95毫米汞柱、43.46±8.97毫米汞柱和32.19±11.06毫米汞柱。到了T2,眼压差异不显著,到了T3,所有组的平均眼压都恢复到正常范围内。与两种阿弗利百普制剂相比,法利单抗的初始眼压峰值较小,但在 T2 和 T3 阶段,这种差异没有统计学意义。结论 aflibercept 8 毫克和法利西单抗在静脉滴注后会出现短暂的眼压峰值,其趋势与 aflibercept 2 毫克相似。最初的眼压升高在15分钟内恢复正常。法利西单抗的初始峰值较低,但不同药物的总体眼压情况相当。如有合理要求,可提供相关数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.30
自引率
2.40%
发文量
213
审稿时长
3-6 weeks
期刊介绍: The British Journal of Ophthalmology (BJO) is an international peer-reviewed journal for ophthalmologists and visual science specialists. BJO publishes clinical investigations, clinical observations, and clinically relevant laboratory investigations related to ophthalmology. It also provides major reviews and also publishes manuscripts covering regional issues in a global context.
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