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Clinical utility of intravitreal fluocinolone acetonide (Iluvien®) implant in the management of patients with chronic diabetic macular edema: a review of the current literature

  • Habiba Saedon*
  • , Astha Anand
  • , Yang C. Yit
  • *Corresponding author for this work
    • Royal Wolverhampton NHS Trust

    Research output: Contribution to journal › Review article › peer-review

    8140 Downloads (Pure)

    Abstract

    The first-line therapy for patients with center-involving diabetic macular edema (DME) is with intravitreal anti-vascular endothelial growth factor (VEGF) agents, with or without adjunctive macular laser treatment. However, a significant proportion of patients have persistent and recurrent edema despite repeated anti-VEGF injections. The fluocinolone acetonide (FA) 190 μg intravitreal implant has been shown in pivotal clinical trials to be efficacious for the treatment of DME and has been approved in many countries for use in patients who have not responded to first-line therapy. In this report, we have collated the latest data from the increasing number of studies to illustrate the pattern of usage of the Iluvien FA implant for DME during the current anti-VEGF era. We have shown that there is now a wealth of published evidence from real-world studies to support the clinical utility of the FA implant in achieving further resolution of edema and improving visual acuity outcomes in this challenging group of patients.

    Original languageEnglish
    Pages (from-to)583-590
    Number of pages8
    JournalClinical Ophthalmology
    Volume11
    DOIs
    Publication statusPublished - 27 Mar 2017

    Bibliographical note

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    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • diabetic macular edema
    • fluocinolone acetonide
    • Iluvien

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