Abstract

BackgroundTo explore the association of clinical characteristics and retinal microstructural features on optical coherence tomography in predicting 1-year visual response following intravitreal bevacizumab injections in eyes with visual impairment from center-involved diabetic macular edema (CI-DME).MethodsMedical records of patients with visual impairment from CI-DME, who initiated intravitreal bevacizumab injections between Jan 2012 and Dec 2016 and were followed for a minimum of 12 months were retrospectively reviewed.ResultsThe study included 226 eyes with a mean (SD) baseline visual acuity (VA) of 51.8 (19.1) letters. At week 12, following the three initial treatments, a mean (SD) VA improved to 61.7 (17.8) letters. Visual gain ≥ 10 letters was observed in 109 eyes (48.2%), while a limited early visual gain < 5 letters was noted in 80 eyes (35.4%). At one year, 110 eyes (48.7%) achieved a good VA gain ≥ 10 letters. In addition, eyes with poor baseline VA had a higher proportion of eyes that obtained limited early VA gained at week 12 (< 5 letters) and maintained in this visual response category at moth 12 compared to eyes with better baseline VA (74.1% versus 59.1%). In the multivariable logistic regression, the following factors reduced the probability of 1-year visual gain ≥ 10 letters: elderly (p = 0.040), better baseline vision (p = 0.001), and limited early visual gain < 5 letters at week 12 (p < 0.001). In multivariable linear regression, male (p = 0.010) and eyes with the presence of hyperreflective foci on baseline OCT (p = 0.010) were likely to have higher VA improvement. However, eyes with better baseline VA (p = 0.002), limited early VA gain at week 12 (p < 0.001), and a presence of EZ disruption at week 12 (p = 0.002) were likely to have less VA improvement.ConclusionsAlthough bevacizumab is considered as effective management for CI-DME, variability in treatment responses is expected. This study revealed that baseline characteristics and visual responses at week 12 might help predict the long-term treatment response. Eyes with characteristics at risk of limited long-term visual outcome may require attention in optimizing their individual treatment strategies.

Highlights

  • Diabetic macular edema (DME) is one of the leading causes of central visual impairment in diabetic patients

  • There are several pathophysiologic and biochemical changes contributing to the development of DME; an increase in vascular endothelial growth factor (VEGF) has been reported as a potent related mediator [1, 2]

  • A significantly higher serum VEGF level was found in diabetic patients with more severe diabetic retinopathy (DR), and more severe disruption of photoreceptor outer segments (external limiting membrane (ELM) and ellipsoid zone (EZ)), compared to less severe DR patients and healthy controls

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Summary

Introduction

Diabetic macular edema (DME) is one of the leading causes of central visual impairment in diabetic patients. Based on randomized clinical trials (RCTs), the remarkable improvement in visual and anatomical outcomes following intravitreal anti-VEGF injection for visual impairment from center-involved DME (CI-DME), compared to macular photocoagulation, has been reported [4,5,6,7]. This significant efficacy was highlighted across all three available anti-VEGF agents (bevacizumab, ranibizumab, and aflibercept) and treatment regimens that were used. To explore the association of clinical characteristics and retinal microstructural features on optical coherence tomography in predicting 1-year visual response following intravitreal bevacizumab injections in eyes with visual impairment from center-involved diabetic macular edema (CI-DME)

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