June 2015
Volume 56, Issue 7
Free
ARVO Annual Meeting Abstract  |   June 2015
Phase-variance OCT imaging of Choroidal Perfusion Abnormalities associated with APMPPE and Post-West Nile Virus Chorioretinitis
Author Affiliations & Notes
  • Susanna S Park
    Ophthalmology & Vision Science, Univ of California Davis Eye Ctr, Sacramento, CA
  • Dae Yu Kim
    Ophthalmology & Vision Science, Univ of California Davis Eye Ctr, Sacramento, CA
  • Robert J Zawadzki
    Ophthalmology & Vision Science, Univ of California Davis Eye Ctr, Sacramento, CA
  • John S Werner
    Ophthalmology & Vision Science, Univ of California Davis Eye Ctr, Sacramento, CA
  • Footnotes
    Commercial Relationships Susanna Park, None; Dae Yu Kim, None; Robert Zawadzki, None; John Werner, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2015, Vol.56, 6167. doi:
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      Susanna S Park, Dae Yu Kim, Robert J Zawadzki, John S Werner; Phase-variance OCT imaging of Choroidal Perfusion Abnormalities associated with APMPPE and Post-West Nile Virus Chorioretinitis. Invest. Ophthalmol. Vis. Sci. 2015;56(7 ):6167.

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

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Abstract
 
Purpose
 

Phase-variance OCT (pv-OCT) imaging uses SD-OCT instrumentation to allow non-invasive visualization of the retinal and choroidal flow in three-dimensions in vivo. The purpose of this study was to determine whether pv-OCT imaging can be used to detect choroidal perfusion abnormalities that may be associated with self-limiting inflammatory disorders of the retina and choroid, such as acute posterior multifocal placoid pigment epitheliopathy (APMPPE) and post-West Nile Virus chorioretinitis. These two conditions were studied since transient ischemia of the choriocapillaris from post-viral vasculitis has been postulated as a possible mechanism for pathogenesis of transient vision loss based on angiographic abnormalities.

 
Methods
 

Two eyes (1 subject) with acute APMPPE and two eyes (1 subject) with newly diagnosed post-West Nile chorioretinitis involving the macula were imaged at presentation and serially thereafter with fundus photography, fluorescein angiography, indocyanine green angiography, SD-OCT and research-grade phase-variance OCT until visual function recovered and stabilized.

 
Results
 

At presentation, both subjects had severe loss of vision with best corrected visual acuity of 20/400. Multiple macular lesions were noted in the study eyes. In all eyes studied, patchy hypoperfusion of the choriocapillaris was noted on pv-OCT during the acute presentation. These patches of hypoperfusion corresponded to the areas of hypofluorescence noted on fluorescein and indocyanine green angiography and outer retinal abnormalities noted on SD-OCT. The areas of choroidal hypoperfusion on pv-OCT were not associated with any shadowing artifacts on SD-OCT B-scans. Both patients were treated with oral prednisone with almost complete recovery of vision over the next several weeks. Recovery of choroidal perfusion abnormality detected on pv-OCT preceded recovery of visual acuity and outer retinal abnormalities noted on SD-OCT.

 
Conclusions
 

pv-OCT imaging allows visualization of transient perfusion abnormalities of the choriocapilaris associated with APMPPE and post-West Nile virus chorioretinitis. These transient perfusion changes at the level of the choriocapillaris may play a role in the pathogenesis of vision loss associated with both these inflammatory conditions.

 
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