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October 20, 2025Journal of VitreoRetinal Diseases4 citations

The Efficacy and Safety of Intravitreal Aflibercept 8 mg in Clinical Practice

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BBBrandon A. BatesHMHana A. MansourHAHasenin Al-khersan

Key Points

  • Intravitreal aflibercept treatment improved best-corrected visual acuity outcomes over multiple injections, and
  • Among treatment-naive eyes, BCVA improved significantly from 0.57 to 0.48 after four injections, indicating effectiveness
  • Review of 20,385 intravitreal aflibercept injections across 22 US retina practices assessed treatment impacts
  • Low rates of intraocular inflammation and endophthalmitis were observed, supporting the safety of intravitreal aflibercept.

Abstract

Purpose: To characterize real-world use of intravitreal aflibercept 8 mg across 22 US retina practices. Methods: Retrospective review of patients who received at least 1 intravitreal aflibercept 8 mg injection for treatment of neovascular age-related macular degeneration, diabetic macular edema, or diabetic retinopathy through April 1, 2024. Data from health records were collected retrospectively, including best-corrected visual acuity (BCVA), interval between treatments, and adverse events. Results: A total of 8323 eyes of 6271 patients received 20 385 intravitreal aflibercept 8 mg injections. A total of 669 eyes (8.0%) were not previously treated. Among treatment-naive eyes, mean logMAR BCVA improved from 0.57 (Snellen equivalent ~20/80) at the time of the first intravitreal aflibercept 8 mg injection, to 0.47 (Snellen equivalent ~20/60) ( P < .001), 0.46 (Snellen equivalent ~20/60) ( P < .001), and 0.48 (Snellen equivalent ~20/60) ( P = .012) at the second, third, and fourth intravitreal aflibercept 8 mg injections, respectively. Among previously treated eyes, mean logMAR BCVA improved from 0.46 (Snellen equivalent ~20/60) at the time of the first intravitreal aflibercept 8 mg injection, to 0.42 (Snellen equivalent ~20/50) ( P < .001), 0.43 (Snellen equivalent ~20/50) ( P < .001), and 0.45 (Snellen equivalent ~20/60) ( P = .70) at the second, third, and fourth intravitreal aflibercept 8 mg injections, respectively. Treatment intervals to time of second, third, and fourth intravitreal aflibercept 8 mg injections increased compared to baseline intervals, by a mean of 2.2 days ( P < .001), 2.5 days ( P < .001), and 13.5 days ( P < .001), respectively. Intraocular inflammation was observed in 11 eyes (1 in 1853 injections). Nine eyes (1 in 2265 injections) developed suspected endophthalmitis. Conclusions: In this real-world clinical setting, intravitreal aflibercept 8 mg treatment demonstrated improvements in BCVA outcomes, with increased intervals between injections. Rates of intraocular inflammation and endophthalmitis were low.

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Cite This Study

Bates et al. (2025) studied this question.

synapsesocial.com/papers/68f5c338e2d8b12842645b7ehttps://doi.org/10.1177/24741264251383384
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