June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
Slit-Lamp Adapted Ultra-High Resolution OCT for Imaging of the Retinal Neural Tissue Structure and Vascular Morphology
Author Affiliations & Notes
  • Delia DeBuc
    Ophthalmology, University of Miami, Miami, FL
  • Omaima Nomir
    Ophthalmology, University of Miami, Miami, FL
  • Hong Jiang
    Ophthalmology, University of Miami, Miami, FL
  • Jianhua Wang
    Ophthalmology, University of Miami, Miami, FL
  • Footnotes
    Commercial Relationships Delia DeBuc, NIH/NEI-EY020607 (F), NIH Center Core Grant P30EY014801 (F), NIH R01EY020607S (F), Department of Defense (DOD- Grant#W81XWH-09-1-0675) (F), US 61/139,082 (P); Omaima Nomir, NIH/NEI-EY020607 (F), NIH/NEI-EY020607S (F), NIH Center Core Grant P30EY014801 (F), Research to Prevent Blindness Unrestricted Grant (F), Department of Defense (DOD- Grant#W81XWH-09-1-0675) (F); Hong Jiang, NIH (F); Jianhua Wang, NIH (F), RPB (F)
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 1504. doi:
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    • Get Citation

      Delia DeBuc, Omaima Nomir, Hong Jiang, Jianhua Wang; Slit-Lamp Adapted Ultra-High Resolution OCT for Imaging of the Retinal Neural Tissue Structure and Vascular Morphology. Invest. Ophthalmol. Vis. Sci. 2013;54(15):1504.

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

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Abstract
 
Purpose
 

To demonstrate that Slit-Lamp adapted Ultra-High Resolution OCT (SL-UHR-OCT) along with custom-built image processing methods is capable of imaging and quantitatively characterizing the human retinal neural tissue structure and vascular morphology.

 
Methods
 

SL-UHR-OCT images from two healthy volunteers were acquired using a newly developed SL-UHR-OCT with ~3 μm depth resolution (24,000 A-scans/second). Raster scans were performed to obtain both macular and optic-disk-centered image frames (6x6 mm). After correcting for eye motion and filtering images to reduce speckle noise, selected retinal structures were automatically segmented and maximum intensity projection (MIP) images were generated which further facilitated the segmentation of the local vasculature network. A local self-correlation analysis was implemented on the extracted vessel architecture to characterize the features and integrity of the retinal vasculature network.

 
Results
 

A clear visualization of the retinal neural tissue structure and vasculature morphology was observed (Figure 1). The foveal avascular zone was clearly visible in both subjects’ eyes. The vascular network was comprehensively visible for most of the retinal layers and segments. Vessels oriented in a radial pattern were observed for the RNFL while a random oriented pattern was observed for the GCL-ONL segment and RPE layer. Arterial tree and major blood vessels were characterized by positive autocorrelation (lower fractal dimension) and higher luminance in both subjects.

 
Conclusions
 

We have demonstrated the capability of a SL-UHR-OCT device to image retinal neural tissue structure as well as depth-resolved information of the vascular morphology, which might facilitate the investigation of the neurovascular relationship in the human retina without the need of aligning retinal images acquired with different ophthalmic imaging instruments or at different times.

 
 
Figure 1. Visualization of the retinal neural tissue structure and vasculature morphology. (A) High-definition UHR-SD-OCT's retinal image. (B) En face view of the retina. (C) En face view of the ONH. (D) En face visualization of the RNFL. (E) En face view of the retinal segment GCL-INL. (F) En face visualization of the RPE. (G) Skeleton of F (red lines) superposed on MIP images of the RPE. A positive autocorrelation was obtained for the RPE (Hurst exponent of 0.8049 ± 0.0017).
 
Figure 1. Visualization of the retinal neural tissue structure and vasculature morphology. (A) High-definition UHR-SD-OCT's retinal image. (B) En face view of the retina. (C) En face view of the ONH. (D) En face visualization of the RNFL. (E) En face view of the retinal segment GCL-INL. (F) En face visualization of the RPE. (G) Skeleton of F (red lines) superposed on MIP images of the RPE. A positive autocorrelation was obtained for the RPE (Hurst exponent of 0.8049 ± 0.0017).
 
Keywords: 552 imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) • 549 image processing • 688 retina  
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