March 2012
Volume 53, Issue 14
Free
ARVO Annual Meeting Abstract  |   March 2012
In vivo Identification and Classification of the Schlemm’s Canal-Collector Channel Junctions in Normal Eyes Using Serial High Definition Anterior Segment Fourier-domain OCT
Author Affiliations & Notes
  • Alfredo R. Castillejos
    Ophthal (Glaucoma Services), HOL - New York Eye & Ear Infirmary, Mexico City, Mexico
  • Sung Chul Park
    Department of Ophthalmology, New York Eye and Ear Infirmary, New York, New York
  • Carlos G. De Moraes
    Ophthalmology, New York Univ School of Med, New York, New York
  • Jeffrey M. Liebmann
    Ophthalmology, NYU School of Medicine, New York, New York
  • Robert Ritch
    Ophthalmology, New York Eye & Ear Infirmary, New York, New York
  • Footnotes
    Commercial Relationships  Alfredo R. Castillejos, None; Sung Chul Park, None; Carlos G. De Moraes, None; Jeffrey M. Liebmann, Alcon laboratories Inc., Allergan Inc., Carl Zeiss Meditec Inc., Dyopsis Inc., Pfizer Inc, Topcon Medical Systems Inc (C), Dyopsis Inc., Topcon Medical Systems Inc. (F); Robert Ritch, Diopsys Inc, Pfizer Inc, Topcon Medical Systems Inc (C), Diopsys Inc, Topcon Medical Systems Inc. (F)
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science March 2012, Vol.53, 3277. doi:
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      Alfredo R. Castillejos, Sung Chul Park, Carlos G. De Moraes, Jeffrey M. Liebmann, Robert Ritch; In vivo Identification and Classification of the Schlemm’s Canal-Collector Channel Junctions in Normal Eyes Using Serial High Definition Anterior Segment Fourier-domain OCT. Invest. Ophthalmol. Vis. Sci. 2012;53(14):3277.

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

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Abstract
 
Purpose:
 

To describe, evaluate and classify in vivo the areas of junction between Schlemm’s canal (SC) and the collector channels (CC) in normal adult human eyes using a novel technique of serial high definition anterior segment Fourier-domain OCT imaging (ASFDOCT).

 
Methods:
 

20 normal subjects (mean age: 25±4.0 years) were imaged using ASFDOCT scans over the right temporal limbus. The area was first inspected for CCs. When a clearly visible SC-CC junction was identified, a standardized protocol of serial radial and tangential scans was performed. The highest quality image of each set capturing the ostium of the same CC in both scan orientations was selected for quantitative assessment. The serial scans were used to create composite images which were qualitatively evaluated.

 
Results:
 

In the radial scans, we evaluated SC cross sectional area (9,248±2,500 µm²), maximum width (28±10 µm) and length (365±46 µm) as well as CC maximum lumen diameter (12±4 µm). The ostium diameter (18±8 µm) and SC maximum (28±9 µm) and minimum width (12±6 µm) in a 500 µm long section around the junction were evaluated in the tangential scans. Based on their morphometry, CC were classified into small or large; based on their course, they were divided in anterior and posterior CC.

 
Conclusions:
 

The anatomy of the SC-CC junctions can be objectively measured with real-time, high resolution ASFDOCT and is enhanced by the use of serial radial and tangential imaging. We propose a classification of the CC based on their in vivo anatomy.  

 

 
Keywords: imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) • outflow: trabecular meshwork • aqueous 
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