April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Quantitative In Vivo Corneal Elastography by Doppler Shear Wave Imaging
Author Affiliations & Notes
  • Matthew R Ford
    Ophthalmic Research, Cleveland Clinic Cole Eye Institute, Cleveland, OH
    Biomedical Engineering, Case Western Reserve University, Cleveland, OH
  • Andrew M Rollins
    Biomedical Engineering, Case Western Reserve University, Cleveland, OH
  • William J Dupps
    Ophthalmic Research, Cleveland Clinic Cole Eye Institute, Cleveland, OH
  • Footnotes
    Commercial Relationships Matthew Ford, Cleveland Clinic Innovations (P); Andrew Rollins, Cleveland Clinic Innovations (P); William Dupps, Avedro (F), Cleveland Clinic Innovations (P)
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 3724. doi:
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    • Get Citation

      Matthew R Ford, Andrew M Rollins, William J Dupps; Quantitative In Vivo Corneal Elastography by Doppler Shear Wave Imaging. Invest. Ophthalmol. Vis. Sci. 2014;55(13):3724.

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

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Abstract
 
Purpose
 

To quantitatively measure the in vivo biomechanical properties of the cornea to provide assistance with disease diagnosis and aid in intervention planning.

 
Methods
 

Utilizing a custom built 1310nm Fourier Domain Optical Coherence Tomography (FDOCT) Anterior Segment Imaging system, a volunteer's healthy cornea was imaged while a shear wave was applied to the eyelid. The shear wave magnitude was maintained at less than the 4um limit specified by the FDA for acoustic retinal imaging. A standard Doppler algorithm (sometimes referred to as Phase Sensitive OCT) was then applied to the acquired data to visualize the shear wave in the tissue. A series of fast Fourier transform windows were applied perpendicular to the direction of the wave’s travel to measure the frequency of the wave in the tissue. The shear wave speed was then calculated by means of the Doppler shift between the applied wave and the measured wave passing through the tissue given by C=Vf0/(f-f0) where C is the speed of the shear wave in the tissue, V is the scan velocity, f0 is the applied wave form frequency, and f is the measured waveform frequency . The Shear Modulus and Young’s Modulus of the tissue were then calculated by G=(C/ρ)1/2, and E=3G where G is the Shear Modulus, C is the velocity of the wave in tissue, ρ is the density of the tissue, and E is Young’s Modulus.

 
Results
 

Figure 1 shows the three steps in the image processing sequence. Image A is the acquired FDOCT image of the cornea. Image B is the Doppler (phase sensitive) data from the FDOCT image data, and image C is the Young’s modulus map calculated from the Doppler data. The cornea shown here has a Shear Modulus of 177kPa with a standard deviation of 93kPa, and a Young’s Modulus of 530kPa and a standard deviation of 270kPa.

 
Conclusions
 

We successfully demonstrated the ability to quantitatively measure Young’s modulus in an in vivo setting without significant hardware modifications to an existing FDOCT system. The low cost, speed, comfort, and simplicity of this technique make it ideal for use in a clinical setting. Further work is planned to assess the performance of the technique in characterizing disease states and the effect of clinical interventions.

 
 
Figure 1) A) Filtered magnitude image of the central 2mm of human cornea. B) Doppler (radians) image of the shear wave passing through the cornea. C) Map of Youngs (kPa) modulus of the cornea as calculated from B.
 
Figure 1) A) Filtered magnitude image of the central 2mm of human cornea. B) Doppler (radians) image of the shear wave passing through the cornea. C) Map of Youngs (kPa) modulus of the cornea as calculated from B.
 
Keywords: 552 imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) • 421 anterior segment • 480 cornea: basic science  
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