April 2011
Volume 52, Issue 14
Free
ARVO Annual Meeting Abstract  |   April 2011
Cellular Resolution in vivo Retinal Imaging with Motion Artifact-Free Adaptive Optics - Optical Coherence Tomography
Author Affiliations & Notes
  • John S. Werner
    Dept of Ophthalmology & Vision Science, Univ of California Davis Med Ctr, Sacramento, California
  • Steven M. Jones
    Lawrence Livermore National Laboratory, Livermore, California
  • Qiang Yang
    Montana State University, Bozeman, Montana
  • Arlie Capps
    Dept of Ophthalmology & Vision Science, Univ of California Davis Med Ctr, Sacramento, California
  • Suman Pilli
    Dept of Ophthalmology & Vision Science, Univ of California Davis Med Ctr, Sacramento, California
  • Dae Yu Kim
    Dept of Ophthalmology & Vision Science, Univ of California Davis Med Ctr, Sacramento, California
  • David W. Arathorn
    Montana State University, Bozeman, Montana
  • Curtis R. Vogel
    Montana State University, Bozeman, Montana
  • Scot S. Olivier
    Lawrence Livermore National Laboratory, Livermore, California
  • Robert J. Zawadzki
    Dept of Ophthalmology & Vision Science, Univ of California Davis Med Ctr, Sacramento, California
  • Footnotes
    Commercial Relationships  John S. Werner, None; Steven M. Jones, None; Qiang Yang, None; Arlie Capps, None; Suman Pilli, None; Dae Yu Kim, None; David W. Arathorn, None; Curtis R. Vogel, None; Scot S. Olivier, None; Robert J. Zawadzki, None
  • Footnotes
    Support  NIH Grant EY 014743, Research to Prevent Blindness
Investigative Ophthalmology & Visual Science April 2011, Vol.52, 4064. doi:
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      John S. Werner, Steven M. Jones, Qiang Yang, Arlie Capps, Suman Pilli, Dae Yu Kim, David W. Arathorn, Curtis R. Vogel, Scot S. Olivier, Robert J. Zawadzki; Cellular Resolution in vivo Retinal Imaging with Motion Artifact-Free Adaptive Optics - Optical Coherence Tomography. Invest. Ophthalmol. Vis. Sci. 2011;52(14):4064.

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

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Abstract

Purpose: : To test the feasibility of new instrumentation that reduces retinal motion artifacts present in volumetric data sets acquired with cellular resolution adaptive optics - Fourier-domain optical coherence tomography (AO-OCT) for improved visualization of microscopic retinal structures.

Methods: : An ultra-high-resolution AO-OCT system was combined with an adaptive optics scanning laser ophthalmoscope (AO-SLO) to track retinal motion during in-vivo AO-OCT data acquisition. Both systems share a common AO sub-system and vertical scanner to permit simultaneous acquisition (at 27 frames/s) of retinal images from the two channels. Transverse eye motion was reconstructed from AO-SLO videos, and a motion adjustment vector was assigned to each AO-OCT A-scan to create motion artifact-free retinal volumes. Next, multiple volumes were averaged to reduce speckle contrast present on single B-scans to improve the visibility of microscopic structures in the inner retina.

Results: : Averaged motion-corrected AO-OCT volumes were created for healthy volunteers. For comparison, AO-OCT volumes acquired with a CMOS-based high speed (125 frames/s) stand alone AO-OCT instrument were also acquired at the same eccentricities for the same subjects.

Conclusions: : Eye motion artifacts limit resolution of AO-OCT retinal imaging due to high magnification. Distortion of volumetric structures also restricts the value of image averaging to reduce speckle contrast in OCT data sets. Correction of retinal motion artifacts allows successful application of this image-processing step in AO-OCT. Additionally, motion artifact-free retinal volumes permit monitoring and quantification of retinal structures at the cellular scale. Finally, motion-corrected AO-OCT volumes acquired at standard speed offer an interesting alternative to ultra-high-speed AO-OCT volume acquisition, as the latter method may suffer from insufficient instrument sensitivity to visualize all the retinal structures, especially cells in the inner retina.

Keywords: imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) • retina • optic nerve 
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