June 2017
Volume 58, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2017
The sensitivity of OCT in detecting optic neuritis
Author Affiliations & Notes
  • Sarah Chao Ying Xu
    Department of Ophthalmology, Mayo Clinic Hospital, Rochester, Minnesota, United States
  • Jacqueline Leavitt
    Department of Ophthalmology, Mayo Clinic Hospital, Rochester, Minnesota, United States
  • David Hodge
    Department of Biostatistics, Mayo Clinic Hospital, Rochester, Minnesota, United States
  • John J Chen
    Department of Ophthalmology, Mayo Clinic Hospital, Rochester, Minnesota, United States
    Department of Neurology, Mayo Clinic Hospital, Rochester, Minnesota, United States
  • Footnotes
    Commercial Relationships   Sarah Xu, None; Jacqueline Leavitt, None; David Hodge, None; John Chen, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science June 2017, Vol.58, 5120. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Sarah Chao Ying Xu, Jacqueline Leavitt, David Hodge, John J Chen; The sensitivity of OCT in detecting optic neuritis. Invest. Ophthalmol. Vis. Sci. 2017;58(8):5120.

      Download citation file:


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

      ×
  • Supplements
Abstract

Purpose : Correctly identifying prior optic neuritis is critically important because the presence or absence of optic neuritis may confirm or refute a diagnosis of neurologic conditions, such as multiple sclerosis and neuromyelitis optica. Prior studies have suggested that optical coherence tomography (OCT) has a sensitivity of 68% for detecting prior optic neuritis. However, they used two standard deviations below age matched controls as “abnormal”. This can be an insensitive measure because patients have different baseline thicknesses. We believe that looking at inter-eye differences in cases of unilateral optic neuritis would be more sensitive in detecting prior optic neuritis. Thus, we evaluated the sensitivity of Cirrus OCT in detecting prior unilateral optic neuritis.

Methods : We performed a retrospective, observational clinical study of all patients with unilateral optic neuritis who presented between 2014 and 2016. Patients were included if they had unilateral optic neuritis and had OCT done at least 3 months after the optic neuritis (range of 3-44 months). Optic neuritis was confirmed radiographically in 70.5% of patients and the remainder were diagnosed clinically. We compared OCT retinal nerve fiber layer (RNFL) and ganglion cell layer (GCL) thicknesses between the affected and unaffected, contralateral eyes. We excluded patients with concomitant glaucoma or other optic neuropathies. Paired T-test was used to compare RNFL and GCL thicknesses between eyes. In calculating sensitivity, thinning was considered significant if the RNFL or GCL was at least 6µm less in the affected eye compared to the unaffected.

Results : A total of forty-four patients (15 male and 29 female) were included in the study. RNFL and GCL thicknesses were significantly lower in eyes with optic neuritis compared to unaffected eyes (p≤0.002). RNFL was thinner by ≥6µm in 84.1% of optic neuritis eyes compared to the unaffected eye. GCL was thinner by ≥6µm in 95.2% optic neuritis eyes. The sensitivity of OCT in detecting prior optic neuritis was 97.7% when using both average RNFL and GCL thicknesses. When using a cutoff of ≥2 standard deviations below age-matched controls, sensitivities were 59.1% for RNFL, 81.0% for GCL, and 81.8% for either GCL or RNFL thicknesses.

Conclusions : OCT is a highly sensitive modality in detecting prior optic neuritis, which is made more robust by using inter-eye differences to approximate change and combining GCL and RNFL data.

This is an abstract that was submitted for the 2017 ARVO Annual Meeting, held in Baltimore, MD, May 7-11, 2017.

×
×

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.

×