4.6 Article

Anatomic-Functional Correlates in Lesions of Retinal Vein Occlusion

Journal

Publisher

ASSOC RESEARCH VISION OPHTHALMOLOGY INC
DOI: 10.1167/iovs.62.7.10

Keywords

retina; retinal vein occlusion; RVO; anti-VEGF; vascular endothelial growth factor; macular edema; laser

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Funding

  1. King Abdulaziz University in Rabigh, Saudi Arabia
  2. Saudi Arabian Cultural Bureau in London, United Kingdom [R8384CEM]

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The study aimed to evaluate anatomic-functional associations at sites of retinal lesions in RVO patients. The results showed decreased retinal sensitivity at sites of RVO lesions, with impaired function in ischemic areas not recovering after treatment and even worsened with reperfusion.
PURPOSE. To evaluate anatomic-functional associations at sites of retinal lesions in retinal vein occlusion (RVO). METHODS. This pilot, prospective, observational study was conducted at the Northern Ireland Clinical Research Facility (NICRF) of Queen's University and the Belfast Health and Social Care Trust, Northern Ireland, between August 1, 2018, and September 30, 2019. The study included 10 treatment-naive patients with RVO (10 RVO eyes and 10 fellow eyes). There were 81 points/sites assessed for each eye at baseline; six patients were re-assessed 6 months after anti-vascular endothelial growth factor therapy at the same locations. We investigated associations between retinal sensitivity and presence of structural RVO lesions, including retinal ischemia, hemorrhages, intraretinal fluid (IRF) and subretinal fluid outside the foveal/parafoveal regions. Comparisons were made between RVO eyes and fellow eyes at baseline, and between RVO eyes at baseline and at 6 months after treatment. Regression models were used to investigate anatomic-functional associations. RESULTS. At baseline, strong associations were found between reduced retinal sensitivity and presence of ischemia (estimate = -2.08 dB; P < 0.001), intraretinal fluid (estimate = -7.82 dB; P < 0.001), and subretinal fluid (estimate = -8.66 dB; P < 0.001). Resolution of subretinal fluid but not intraretinal fluid was associated with improved function (estimate = 2.40 dB [P = 0.022]; estimate = 1.16 dB [P = 0.228], respectively). However, reperfusion of ischemic retina, observed in 31 of 486 points (6%) 6 months after antivascular endothelial growth factor therapy, was associated with a further decrease in retinal sensitivity (estimate = -2.34 dB; P = 0.035). CONCLUSIONS. Retinal sensitivity was decreased at sites of RVO lesions. Decreased function at sites of retinal ischemia did not recover after treatment, even when reperfusion occurred.

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