April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
Large Field-of-View Cellular Resolution Mapping of in vivo Retinas by Ultra-High Resolution Adaptive Optics - Optical Coherence Tomography (uhr-ao-oct)
Author Affiliations & Notes
  • R. J. Zawadzki
    Department of Ophthalmology & Vison Science, University of California Davis, Sacramento, California
  • J. W. Evans
    Department of Ophthalmology & Vison Science, University of California Davis, Sacramento, California
  • S. S. Choi
    Department of Ophthalmology & Vison Science, University of California Davis, Sacramento, California
    Department of Vision Science, The New England College of Optometry, Boston, Massachusetts
  • A. R. Fuller
    Department of Computer Science, University of California Davis, Davis, California
  • B. Hamann
    Department of Computer Science, University of California Davis, Davis, California
  • J. S. Werner
    Department of Ophthalmology & Vison Science, University of California Davis, Sacramento, California
  • Footnotes
    Commercial Relationships  R.J. Zawadzki, None; J.W. Evans, None; S.S. Choi, None; A.R. Fuller, None; B. Hamann, None; J.S. Werner, None.
  • Footnotes
    Support  National Eye Institute EY 014743 (JSW), Research to Prevent Blindness (RPB)
Investigative Ophthalmology & Visual Science April 2009, Vol.50, 1057. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      R. J. Zawadzki, J. W. Evans, S. S. Choi, A. R. Fuller, B. Hamann, J. S. Werner; Large Field-of-View Cellular Resolution Mapping of in vivo Retinas by Ultra-High Resolution Adaptive Optics - Optical Coherence Tomography (uhr-ao-oct). Invest. Ophthalmol. Vis. Sci. 2009;50(13):1057.

      Download citation file:


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

      ×
  • Supplements
Abstract

Purpose: : To test the feasibility of UHR-AO-OCT for creating large field-of-view cellular-resolution retinal volumes.

Methods: : An ultra-high resolution AO-FdOCT system (axial resolution, ~3.5 µm; lateral resolution, ~3.5 µm; acquisition speed: 18,000A-scans/s) constructed at UC Davis, was used for in vivo retinal imaging. The maximum lateral extent of a single UHR-AO-OCT volume acquired with this system is 1 mm (3 deg) due to the limited isoplanatic field with adaptive optics and instrument design. To overcome this limitation and to create retinal volumes that are similar in size to those of clinical FD-OCT systems, we acquired sets of UHR-AO-OCT sub-volumes at different retinal eccentricities with two different focus positions (one on inner retina and one on outer retina). Custom visualization software was used to stitch these sub-volumes in three dimensions into one large cellular resolution volume and then to co-register it with fundus photography.

Results: : As an example, a 5x5 mm lateral size cellular resolution volume was constructed from 50 (5x5x2) single UHR-AO-OCT volumes. This large volume uses ~2.5 million A-scans (5000x500) and offers exceptional detail within large volumetric structures of living retina.

Keywords: imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) • imaging/image analysis: clinical • retina 
×
×

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.

×