Investigative Ophthalmology & Visual Science Cover Image for Volume 65, Issue 7
June 2024
Volume 65, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2024
Ultra-Wide Field (UWF) Fluorescein Angiographic Non-Perfusion Status After Endolaserless Vitrectomy and Aflibercept Monotherapy for Eyes with Proliferative Diabetic Retinopathy (PDR)-related Vitreous Hemorrhage (VH)
Author Affiliations & Notes
  • Luke Qin
    Ophthalmology, Augusta University, Augusta, Georgia, United States
  • Venkatkrish Manohar Kasetty
    Ophthalmology, Henry Ford Hospital, Detroit, Michigan, United States
  • Starnes Davis
    Ophthalmology, Southeast Retina Center, Augusta, Georgia, United States
  • Barbara A Blodi
    Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison, Wisconsin, United States
  • Dennis M Marcus
    Ophthalmology, Southeast Retina Center, Augusta, Georgia, United States
    Ophthalmology, Augusta University, Augusta, Georgia, United States
  • Footnotes
    Commercial Relationships   Luke Qin None; Venkatkrish Kasetty None; Starnes Davis None; Barbara Blodi None; Dennis Marcus Regeneron Pharmaceuticals, Code C (Consultant/Contractor)
  • Footnotes
    Support  Research Grants: Regeneron Pharmaceuticals.
Investigative Ophthalmology & Visual Science June 2024, Vol.65, 1754. doi:
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      Luke Qin, Venkatkrish Manohar Kasetty, Starnes Davis, Barbara A Blodi, Dennis M Marcus; Ultra-Wide Field (UWF) Fluorescein Angiographic Non-Perfusion Status After Endolaserless Vitrectomy and Aflibercept Monotherapy for Eyes with Proliferative Diabetic Retinopathy (PDR)-related Vitreous Hemorrhage (VH). Invest. Ophthalmol. Vis. Sci. 2024;65(7):1754.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : The effect of anti-vascular endothelial growth factor (anti-VEGF) therapy on retinal non-perfusion in PDR remains ill-defined. We report 3-year UWF fluorescein angiogram (FA) gradings of retinal non-perfusion in eyes randomized in the LASERLESS trial. This provides a unique opportunity to determine the effects of intravitreal aflibercept injection (IAI) monotherapy on retinal ischemia in severe PDR eyes.

Methods : Eligible eyes with PDR-related VH underwent vitrectomy without panretinal photocoagulation (PRP) endolaser with 1 pre- and 1 intraoperative IAI were randomized to postoperative q8- or q16-week IAI monotherapy. Prospectively planned UWFFA’s were performed at 4 weeks (baseline) after vitrectomy and then quarterly throughout the 3-year period. Images were independently graded by the Wisconsin Reading Center for nonperfusion index (NPI), foveal avascular zone integrity, leakage, and neovascularization.

Results : A total of 31 eyes (14 and 17 in q8- and q16-week groups, respectively) were randomized. Through 3 years, q8-week and q16-week eyes received 19 and 12 IAI, respectively. Among all patients, NPI increased from 19.1% at baseline to 22.6%, 27.5%, 31.0% at years 1, 2, and 3, respectively (p=0.086, <0.001, <0.001 for change from baseline, respectively). While NPI increased in both the q8-week and q16-week groups at 3 years, NPI progression was less in q8-week eyes with average increase in NPI of 6.3% compared to 10.3% in q16-week eyes (p=0.283). There is an overall trend toward reduced NPI progression with increased aflibercept injection burden over 3 years.

Conclusions : More frequent aflibercept dosing resulted in reduced proliferative consequences and reduced NPI progression. Although NPI progression was reduced with more frequent IAI, peripheral retinal non-perfusion continues despite persistent anti-VEGF therapy. Our study suggests that anti-VEGF does not reverse retinal ischemia despite a high therapy burden.

This abstract was presented at the 2024 ARVO Annual Meeting, held in Seattle, WA, May 5-9, 2024.

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