Changes in retinal venous diameter in proliferative diabetic retinopathy patients with diabetic macular edema following faricimab treatment: an observational study - Summary - MDSpire

Changes in retinal venous diameter in proliferative diabetic retinopathy patients with diabetic macular edema following faricimab treatment: an observational study

  • By

  • Hui Zhao

  • Yuanqing Liu

  • Lingchao Zhang

  • Xiaonan Zhao

  • Nan Wang

  • Yuan Tao

  • Hong Wang

  • July 9, 2026

  • 0 min

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Objective:

To evaluate the effect of intravitreal faricimab injections on retinal venous diameter in proliferative diabetic retinopathy (PDR) patients with diabetic macular edema (DME).

Approach:
  • Study Design: Single-center, retrospective cohort study including 46 PDR patients with DME treated with intravitreal faricimab and panretinal photocoagulation.
  • Assessment Parameters: Best-corrected visual acuity (BCVA), central foveal thickness (CFT), microaneurysm (MA) count, hard exudates (HE), neovascularization (NV) area, and retinal venous diameter were assessed at baseline and at 1, 3, and 6 months post-treatment.
Key Findings:
  • Significant improvements in BCVA at 1, 3, and 6 months (P < 0.05).
  • CFT significantly reduced at all time points (P < 0.05).
  • MA count showed no significant reduction at 1 month (P > 0.05) but decreased significantly at 3 and 6 months (P < 0.05).
  • HE area reduction was significant at 6 months (P < 0.05).
  • NV area significantly reduced at all time points (P < 0.05).
  • Retinal venous diameter showed significant reduction at 6 months (P < 0.05).
Interpretation:

Intravitreal faricimab was safe and effective for PDR patients with DME, showing a trend toward morphological reversal of retinal venous diameter at 6 months.

Limitations:
  • Retrospective design may introduce bias.
  • Single-center study limits generalizability.
  • Small sample size may affect statistical power.
Conclusion:

Faricimab may influence retinal microvascular remodeling through dual inhibition of the VEGF-A and Ang-2 pathways.

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