June 2022
Volume 63, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2022
Phase Decorrelation OCT for Monitoring Accelerated Crosslinking: Depth Resolution and Improved Scan Area
Author Affiliations & Notes
  • Brecken Blackburn
    Case Western Reserve University, Cleveland, Ohio, United States
  • Matthew McPheeters
    Case Western Reserve University, Cleveland, Ohio, United States
  • Michael W Jenkins
    Case Western Reserve University, Cleveland, Ohio, United States
  • William J Dupps
    Cleveland Clinic, Cleveland, Ohio, United States
    Case Western Reserve University, Cleveland, Ohio, United States
  • Andrew M. Rollins
    Case Western Reserve University, Cleveland, Ohio, United States
  • Footnotes
    Commercial Relationships   Brecken Blackburn None; Matthew McPheeters None; Michael Jenkins None; William Dupps None; Andrew Rollins None
  • Footnotes
    Support  NIH NEI R01EY028667. This study was supported in part by the NIH-NEI P30 Core Grant (IP30EY025585), Unrestricted Grants from The Research to Prevent Blindness, Inc., and Cleveland Eye Bank Foundation awarded to the Cole Eye Institute.
Investigative Ophthalmology & Visual Science June 2022, Vol.63, 1830. doi:
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    • Get Citation

      Brecken Blackburn, Matthew McPheeters, Michael W Jenkins, William J Dupps, Andrew M. Rollins; Phase Decorrelation OCT for Monitoring Accelerated Crosslinking: Depth Resolution and Improved Scan Area. Invest. Ophthalmol. Vis. Sci. 2022;63(7):1830.

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

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Abstract

Purpose : For assessing corneal biomechanics, resolving spatial heterogeneity both in depth and over a wide lateral field of view is advantageous to observe the effects of crosslinking procedures and diseases such as keratoconus – both of which vary as a function of corneal depth and lateral position. Phase decorrelation optical coherence tomography (PhD-OCT) is able to resolve the varying depth-dependent effects of different corneal crosslinking protocols and, through the use of a conical scanner, an improved ability to scan a wide field of view.

Methods : Ex vivo porcine corneas were imaged with both a typical telecentric scanner and the conical scan sample arm (following Beer et al., 2017) in conjunction with a 1310nm spectral domain OCT system. M-B scans were acquired and processed to extract the short-time complex decorrelation, as described in prior work (Blackburn et al., 2019). Crosslinking protocols were applied, including the Dresden protocol and accelerated protocols.

Results : Using the conical scanning system, there is no substantial degradation of image quality in the periphery and thus no corresponding degradation of the decorrelation signal. The preserved signal quality allows for decorrelation analysis further from the central cornea. Differences in the depth-profiles that were observed between varying crosslinking protocols correspond well with theory. The use of supplemental oxygen in accelerated protocols enhanced the crosslinking effect.

Conclusions : Conical focal plane scanners offer significant advantages for noise-sensitive OCT processing methods such as PhD-OCT to reliably extend their reach into the periphery of the cornea. PhD-OCT is demonstrated to provide depth-dependent information about crosslinking state.

This abstract was presented at the 2022 ARVO Annual Meeting, held in Denver, CO, May 1-4, 2022, and virtually.

 

PhD-OCT normalized depth profiles for CXL, accelerated CXL, accelerated CXL with supplemental oxygen, and sham-treated corneas. Pointwise averages are plotted in depth +/- standard error.

PhD-OCT normalized depth profiles for CXL, accelerated CXL, accelerated CXL with supplemental oxygen, and sham-treated corneas. Pointwise averages are plotted in depth +/- standard error.

 

5mm B-scans of a porcine cornea, acquired with both a telecentric scanner (top) and a conical scanner (bottom). In the intensity images (colorscale a.u.) acquired with a telecentric scanner, the signal drop-off towards the periphery is apparent. In the decorrelation images (colorscale s-1), this corresponds to a high noise region. With the conical scanner, there is no periphery drop off or degradation of the decorrelation signal, allowing for analysis farther from the central cornea.

5mm B-scans of a porcine cornea, acquired with both a telecentric scanner (top) and a conical scanner (bottom). In the intensity images (colorscale a.u.) acquired with a telecentric scanner, the signal drop-off towards the periphery is apparent. In the decorrelation images (colorscale s-1), this corresponds to a high noise region. With the conical scanner, there is no periphery drop off or degradation of the decorrelation signal, allowing for analysis farther from the central cornea.

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