July 2019
Volume 60, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2019
 

Treatment of type 3 choroidal neovascularization with intravitreal injections of Aflibercept : a prospective study.

Author Affiliations & Notes
  • Nicolas Leveziel
    CHU Poitiers, Poitiers, France
    University of Poitiers, France
  • Rania Warrak
    CHU Poitiers, Poitiers, France
  • Emilie Bedue
    CHU Poitiers, Poitiers, France
  • Melodie Omar
    CHU Poitiers, Poitiers, France
  • Pierre Ingrand
    CHU Poitiers, Poitiers, France
  • Footnotes
    Commercial Relationships   Nicolas Leveziel, Bayer (F); Rania Warrak, None; Emilie Bedue, None; Melodie Omar, None; Pierre Ingrand, None
  • Footnotes
    Support  Grant from Bayer
Investigative Ophthalmology & Visual Science July 2019, Vol.60, 135. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Nicolas Leveziel, Rania Warrak, Emilie Bedue, Melodie Omar, Pierre Ingrand;  

      Treatment of type 3 choroidal neovascularization with intravitreal injections of Aflibercept : a prospective study.

      . Invest. Ophthalmol. Vis. Sci. 2019;60(9):135.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract

Purpose :
Type 3 choroidal neovascularization (CNV) is a particularly severe form of exudative AMD characterized by an anastomosis between choroidal vascularization and retinal vascularization usually well-defined on indocyanin green angiography by a hot spot.
In this context, we aimed to evaluate the functionnal and anatomical outcomes of a fixed aflibercept intravitreal injections regimen in naive patients with type 3 CNV.

Methods :
Patients with type 3 CNV underwent best-corrected visual acuity (VA) measurement, fundus examination, fluorescein angiography, indocyanin angiography and SD-OCT.
Treatment protocol was 3 monthly intravitreal injections of aflibercept 2 mg followed by bimonthly injections.
The primary endpoint was VA at 12 months. The secondary endpoints were VA at 6 month and anatomical outcomes (sub-retinal or intra-retinal fluids, central macular thickness) at 6 and 12 months.
This study was approved by the ethics committee (ClinicalTrials.gov Identifier: NCT02320474).

Results :
26 naive patients with type 3 CNV were included in the study (18 women vs 8 men).
At inclusion, the mean age was 82,4 ± 7.7 years, the mean VA was 59.8 ± 12.8 ETDRS letters and the mean macular thickness was 432 ± 95 µm on the studied eye.
On SD-OCT scans, intra-retinal cysts were observed in 92% and sub-retinal fluid was reported in 69% of patients.
The final primary and secondary endpoints will be presented during the meeting.

Conclusions :
Type 3 CNV is considered as the most severe form of exudative CNV because of the higher risk of bilaterality and of the importance of exudation associated with this form.
In this context, a fixed treatment regimen could have an advantage compared to a treat and extend protocol, because it could allow earlier detection of a fellow eye involvement.

This abstract was presented at the 2019 ARVO Annual Meeting, held in Vancouver, Canada, April 28 - May 2, 2019.

×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×