Investigative Ophthalmology & Visual Science Cover Image for Volume 60, Issue 9
July 2019
Volume 60, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2019
OCT-Angiography in Vogt Koyanagi Harada Syndrome: A Comparative Cross Sectional Imaging Analysis
Author Affiliations & Notes
  • Justin Yamanuha
    Bascom Palmer Eye Institute, Miami, Florida, United States
  • Janet L Davis
    Bascom Palmer Eye Institute, Miami, Florida, United States
  • Jila Noorikolouri
    Bascom Palmer Eye Institute, Miami, Florida, United States
  • Footnotes
    Commercial Relationships   Justin Yamanuha, None; Janet Davis, Allergan (C), EyePharma (F), NighStar (F); Jila Noorikolouri, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science July 2019, Vol.60, 4553. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Justin Yamanuha, Janet L Davis, Jila Noorikolouri; OCT-Angiography in Vogt Koyanagi Harada Syndrome: A Comparative Cross Sectional Imaging Analysis. Invest. Ophthalmol. Vis. Sci. 2019;60(9):4553.

      Download citation file:


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

      ×
  • Supplements
Abstract

Purpose : Optical coherence tomography angiography (OCT-A) has been shown to identify flow voids in the choriocapillaris and choroid in the acute phase of VKH which correspond to hypo-fluorescent spots on Indocyanine Green Angiography (ICGA).1,2 The purpose of this retrospective, cross sectional study was to compare the sensitivity of OCT-A at detecting flow voids to ICGA and choroidal thickness by EDI OCT in patients with convalescent or chronic VKH treated for various durations.
1. Aggarwal et al. The role of OCT-angiography in the diagnosis and management of acute Vogt-Koyanagi-Harada disease. Ocul Immun Inflamm 2018; 26(1): 142-153
2. Wintergerst MWM et al. OCT-angiography for evaluation of Sattler’s layer in Vogt-Koyanagi-Harada Disease. Ophthalmic Surg Lasers Imaging Retina 2018; 49: 639-642

Methods : This retrospective Institutional Review Board (IRB) approved study was conducted at the Bascom Palmer Eye Institute of the University of Miami. Patients with convalescent or chronic VKH (on systemic immune suppression more than one year after onset) who had same day imaging by EDI OCT, ICGA, and OCT-A between 7/1/18 and 11/23/18 were eligible for inclusion. Pathologic changes were defined as sub-foveal choroidal thickness greater than 300 microns by EDI OCT, hypo-fluorescent spots on ICGA, and flow voids in the choriocapillaris and choroid on OCT-A.

Results : Sixteen eyes of eight patients were included in the analysis. EDI OCT demonstrated choroidal thickening in twelve eyes (75%), ICGA demonstrated hypo-fluorescent spots in sixteen eyes (100%), and OCT-A showed flow voids in fifteen eyes (94%). When co-utilizing modalities, twelve eyes (75%) showed abnormalities on EDI and ICGA, eleven eyes (69%) showed abnormalities on EDI and OCT-A, and fifteen eyes (94%) showed abnormalities on ICGA and OCT-A.

Conclusions : OCT-A flow voids roughly co-localized to areas of ICG hypo-fluorescence which may indicate prior damage rather than active disease in patients receiving immune suppressive therapy in chronic or convalescent VKH. Longitudinal studies correlating changes in immunosuppressive therapy and clinical impression of uveitis activity would help determine whether flow voids on OCT-A represent residual choroidal inflammation in VKH.

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

 

ICGA showing numerous hypo-fluorescent spots.

ICGA showing numerous hypo-fluorescent spots.

 

OCT-A of the same eye showing flow voids in the choroid roughly corresponding to hypo-fluorescent spots on ICGA.

OCT-A of the same eye showing flow voids in the choroid roughly corresponding to hypo-fluorescent spots on ICGA.

×
×

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.

×