En face swept-source optical coherence tomography detecting thinning of inner retinal layers as an indicator of capillary nonperfusion

Eur J Ophthalmol. 2015 Mar-Apr;25(2):153-8. doi: 10.5301/ejo.5000514. Epub 2014 Sep 12.

Abstract

Purpose: To report en face swept-source optical coherence tomography (SS-OCT) as a noninvasive detection modality for regions of retinal layer thinning that are potential indicators of retinal nonperfusion areas (NPAs) in patients with branch retinal vein occlusion (BRVO).

Methods: Thirty-one eyes of 46 patients with BRVO showing a definite retinal NPA larger than 1 disc in diameter within the vascular arcades were included in this study. We calculated the overlapping correspondence ratio between presumed NPA, which appeared as a dark area in en face SS-OCT, and definite NPA in corresponding fluorescein angiography (FA) images. The correlation between brightness in en face SS-OCT images and corresponding ganglion cell complex (GCC) thickness determined by SD-OCT GCC maps was evaluated as well.

Results: Measured NPA size in FA and presumed NPA size in en face SS-OCT showed strong correlation (r = 0.746, p<0.001) and colocalization. Reliable agreement between the 2 methods was confirmed by size comparisons (p = 0.11), with an overlapping correspondence ratio of 0.73.

Conclusions: The results suggest that en face SS-OCT is a noninvasive and relatively reliable method for delineating retinal thinning as an indicator of NPAs in eyes with BRVO. Because SS-OCT can be performed without mydriasis, this procedure may be an option for evaluating NPAs on a screening basis and during follow-up to reduce the number of FA examinations that carry very rare, but potentially fatal, allergic side effects.

MeSH terms

  • Aged
  • Capillaries / pathology
  • Capillary Permeability
  • Female
  • Fluorescein Angiography
  • Humans
  • Male
  • Middle Aged
  • Retina / pathology*
  • Retinal Vein / pathology*
  • Retinal Vein Occlusion / diagnosis*
  • Retrospective Studies
  • Tomography, Optical Coherence / methods*