4.6 Article

Wide field of view swept-source optical coherence tomography for peripheral retinal disease

Journal

BRITISH JOURNAL OF OPHTHALMOLOGY
Volume 100, Issue 10, Pages 1377-1382

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/bjophthalmol-2015-307480

Keywords

Imaging; Retina

Categories

Funding

  1. National Institutes of Health (Bethesda, Maryland, USA) [R01-EY024312, R01-EY023039]
  2. Research to Prevent Blindness (New York, New York, USA)

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Background/aims To assess peripheral retinal lesions and the posterior pole in single widefield optical coherence tomography (OCT) volumes. Methods A wide field of view (FOV) swept-source OCT (WFOV SSOCT) system was developed using a commercial swept-source laser and a custom sample arm consisting of two indirect ophthalmic lenses. Twenty-seven subjects with peripheral lesions (choroidal melanomas, choroidal naevi, sclerochoroidal calcification, retinitis pigmentosa, diabetic retinopathy, retinoschisis and uveitis) were imaged with the WFOV SSOCT. Volumes were taken in primary gaze. Using the optic nerve to fovea distance as a reference measurement, comparisons were made between the lateral FOV of the WFOV SSOCT, current generation spectral-domain OCT (SDOCT) and widefield scanning laser ophthalmoscopy (SLO) of the same eyes. Results Peripheral pathologies were captured with WFOV SSOCT in 26 of the 27 subjects. The one not captured was in the far nasal periphery and was not seen in the primary gaze volume. Posterior pole associated pathologies were captured in all subjects. Current generation SDOCT had a mean lateral FOV of 2.080.21 optic nerve to fovea distance units, WFOV SSOCT had an FOV of 4.62 +/- 0.62 units and SLO had an FOV of 9.35 +/- 1.02 units. Conclusions WFOV OCT can be used to examine both peripheral retinal pathology and the posterior pole within a single volume acquisition. SLO had the greatest FOV, but does not provide depth information. Future studies using widefield OCT systems will help further delineate the role of WFOV OCT to quantitatively assess and monitor peripheral retinal disease in three dimensions.

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