Short-term efficacy of intravitreal Aflibercept injections for retinal angiomatous proliferation

  • Hung Da Chou
  • , Wei Chi Wu
  • , Nan Kai Wang
  • , Lan Hsin Chuang
  • , Kuan Jen Chen
  • , Chi Chun Lai*
  • *Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

10 Scopus citations

Abstract

Background: To evaluate the short-term efficacy of intravitreal injections of aflibercept (IVA) to treat retinal angiomatous proliferation (RAP) and identify factors related to functional outcomes. Methods: This retrospective case series consisted of 19 eyes in 19 patients with RAP. All 19 eyes received 3 monthly consecutive IVA. The primary outcome measures were best-corrected visual acuity (BCVA) and central retinal thickness (CRT) after the last IVA. Results: Of the 19 treated eyes, 8 (42%) were pre-treated with 1 dose of bevacizumab one month prior to the initiation of treatment with aflibercept. BCVA was significantly improved and CRT was significantly reduced after 3 consecutive IVAs (P = 0.014 and P = 0.0002, respectively). Stabilization or improvement in BCVA was observed in 17 eyes (90%) treated with IVA. Eyes with baseline fibrovascular pigment epithelial detachment (PED) showed no significant gain in BCVA, and fibrovascular PED was negatively correlated with final BCVA (Spearman's correlation coefficient = - 0.481, P = 0.037). The mean follow-up was 3.5 ± 0.5 months. Conclusions: In this short-term study, three consecutive IVAs showed efficacy for improving vision and reducing retinal edema in RAP patients. Eyes with fibrovascular PED showed poorer responses, and the presence of fibrovascular PED at baseline was negatively correlated with visual outcomes.

Original languageEnglish
Article number104
JournalBMC Ophthalmology
Volume17
Issue number1
DOIs
StatePublished - 27 06 2017

Bibliographical note

Publisher Copyright:
© 2017 The Author(s).

Keywords

  • Aflibercept
  • Age-related macular degeneration
  • Anti-angiogenic agents
  • Choroidal neovascularization
  • Retinal angiomatous proliferation
  • Type 3 neovascularization

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