May 2005
Volume 46, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2005
Progression Detection in Simulated Scanning Laser Polarimetry Images
Author Affiliations & Notes
  • K.A. Vermeer
    Quantitative Imaging Group, Delft University of Technology, Delft, The Netherlands
    Glaucoma Service, Rotterdam Eye Hospital, Rotterdam, The Netherlands
  • B. Lo
    Laser Diagnostic Technologies, Inc., San Diego, CA
  • Q. Zhou
    Laser Diagnostic Technologies, Inc., San Diego, CA
  • F.M. Vos
    Quantitative Imaging Group, Delft University of Technology, Delft, The Netherlands
    Department of Radiology, Academic Medical Center, Amsterdam, The Netherlands
  • A.M. Vossepoel
    Quantitative Imaging Group, Delft University of Technology, Delft, The Netherlands
    Biomedical Imaging Group Rotterdam, Erasmus MC – University Medical Center Rotterdam, Rotterdam, The Netherlands
  • H.G. Lemij
    Glaucoma Service, Rotterdam Eye Hospital, Rotterdam, The Netherlands
  • Footnotes
    Commercial Relationships  K.A. Vermeer, Laser Diagnostic Technologies, Inc. F, R; B. Lo, Laser Diagnostic Technologies, Inc. E; Q. Zhou, Laser Diagnostic Technologies, Inc. E; F.M. Vos, None; A.M. Vossepoel, None; H.G. Lemij, Laser Diagnostic Technologies, Inc. F, R.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science May 2005, Vol.46, 2533. doi:
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    • Get Citation

      K.A. Vermeer, B. Lo, Q. Zhou, F.M. Vos, A.M. Vossepoel, H.G. Lemij; Progression Detection in Simulated Scanning Laser Polarimetry Images . Invest. Ophthalmol. Vis. Sci. 2005;46(13):2533.

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

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Abstract
 
Abstract:
 

To determine the sensitivity and specificity of several related progression detection methods for glaucoma based on real and simulated Scanning Laser Polarimetry images.

 

One eye of 24 normal subjects was imaged three times on four days with a GDx VCC (with ECC). Seven event–based progression detection methods were tested. These methods, based on one or two baseline visits and one to three follow–up visits, related the observed change to the measurement repeatability. They were trained on the real images for a fixed specificity of 97.5%. The sensitivity of these methods for various reproducibilities was determined by a simulation study for either localized (in a 20 degrees sector) or diffuse loss. The reproducibility of measurements of the eyes was modeled as the mean standard deviation across the image.

 

The minimally detectable loss, defined as the minimum loss that resulted in a sensitivity of 90%, for each method is shown in the figure. The first number in the legend shows the number of baseline visits. The second number is the number of follow–up visits and the last two numbers denote the number of passed/total tests to indicate change (e.g., 2/3 means that 2 out of 3 tests have to indicate loss for the eye to be classified as showing significant change).

 

The minimally detectable loss decreases if more visits are available. Likewise, a larger number of required successful tests results in a lower minimally detectable loss, with the exception of tests with three follow–up visits.

 

Progression detection seems feasible when multiple images are acquired per visit, thereby allowing the estimation of the reproducibility of the eye. Depending on the area showing loss, detection of a loss of typically 3 to 15 µm is possible with a specificity of 97.5% and a sensitivity of 90%.

 

 

 
Keywords: computational modeling • image processing • nerve fiber layer 
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