Differentiation between optic disc drusen and optic disc oedema using fundus photography

Acta Ophthalmol. 2017 Jun;95(4):e329-e335. doi: 10.1111/aos.13338. Epub 2017 Jan 13.

Abstract

Purpose: To describe a funduscopic sign that can be used to differentiate between optic disc drusen (ODD) and optic disc oedema (ODE).

Methods: A total of 73 eyes from 73 consecutive subjects with disc margin blurring who had been evaluated using spectral-domain optical coherence tomography (SD-OCT) were included. Final diagnosis was made by SD-OCT; ODD was defined by direct visualization of ODD, while ODE was defined by documentation of retinal nerve fibre layer oedema (nasal retinal nerve fibre layer thickness >78.0 μm). Peripapillary retina was selected as a two-disc-diameter-sized square image from the fundus photograph. Using MATLAB software, colour photographs were converted to indexed image of eight colours. Presence of a smooth contour strip between the nasal disc margin and juxtapapillary retina was defined as a halo. Whether the halo could predict the ODD was analysed retrospectively.

Results: The halo sign was detected in 45 eyes (100%) with ODD including one eye with both ODD and ODE. No eyes with ODE alone showed the halo sign. The halo sign implied the presence of ODD (Cohen's kappa = 1.000, p < 0.001) and the absence of ODE (Cohen's kappa = 0.971, p < 0.001). The halo sign showed a good interobserver reliability [ICC (2, 1) = 0.944, 95% confidence interval 0.912-0.964]. SD-OCT images showed that halos represented retinal elevations above ODD.

Conclusions: In the patients with blurred disc margin, the presence of a halo strongly suggested underlying ODD rather than ODE.

Keywords: halo sign; optic disc drusen; optic disc oedema; spectral-domain optical coherence tomography.

MeSH terms

  • Adult
  • Diagnosis, Differential
  • Female
  • Follow-Up Studies
  • Humans
  • Male
  • Middle Aged
  • Nerve Fibers / pathology*
  • Optic Disk / pathology*
  • Optic Disk Drusen / diagnosis*
  • Papilledema / diagnosis*
  • Photography / methods*
  • Reproducibility of Results
  • Retinal Ganglion Cells / pathology*
  • Retrospective Studies
  • Tomography, Optical Coherence / methods*