June 2022
Volume 63, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2022
Integration of multidimensional data from bedside optical coherence tomography imaging for retinopathy of prematurity examination.
Author Affiliations & Notes
  • Kai Seely
    Duke University Department of Ophthalmology, Durham, North Carolina, United States
  • Shwetha Mangalesh
    Duke University Department of Ophthalmology, Durham, North Carolina, United States
  • Vincent Tai
    Duke University Department of Ophthalmology, Durham, North Carolina, United States
  • Du Tran-viet
    Duke University Department of Ophthalmology, Durham, North Carolina, United States
  • Katrina Winter
    Duke University Department of Ophthalmology, Durham, North Carolina, United States
  • Stephanie J Chiu
    Duke University Department of Ophthalmology, Durham, North Carolina, United States
  • Christian Viehland
    Department of Biomedical Engineering, Duke University, Durham, North Carolina, United States
  • Cynthia A Toth
    Duke University Department of Ophthalmology, Durham, North Carolina, United States
    Department of Biomedical Engineering, Duke University, Durham, North Carolina, United States
  • Footnotes
    Commercial Relationships   Kai Seely Duke University, Code P (Patent); Shwetha Mangalesh None; Vincent Tai Duke University, Code P (Patent); Du Tran-viet None; Katrina Winter Duke University, Code P (Patent); Stephanie Chiu Duke University, Code P (Patent); Christian Viehland Theia Imaging, LLC, Code I (Personal Financial Interest); Cynthia Toth EMMES, Code C (Consultant/Contractor), Theia Imaging, LLC, Code C (Consultant/Contractor), NIH, Code F (Financial Support), Research to Prevent Blindness, Code F (Financial Support), Theia Imaging, LLC, Code O (Owner), Alcon, Code R (Recipient)
  • Footnotes
    Support  NIH/NEI Grant EY025009, NIH/NEI Grant EY005722, NIH/NEI Grant EY028227, NIH Grant TR002555, Research to Prevent Blindness Stein Innovation Award
Investigative Ophthalmology & Visual Science June 2022, Vol.63, 3130. doi:
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      Kai Seely, Shwetha Mangalesh, Vincent Tai, Du Tran-viet, Katrina Winter, Stephanie J Chiu, Christian Viehland, Cynthia A Toth; Integration of multidimensional data from bedside optical coherence tomography imaging for retinopathy of prematurity examination.. Invest. Ophthalmol. Vis. Sci. 2022;63(7):3130.

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

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Abstract

Purpose : To describe a method for rapid optical coherence tomography (OCT) image capture and multidimensional visualization of retinopathy of prematurity (ROP) in preterm infants in BabySTEPS2.

Methods : We developed retinal OCT imaging protocols for use with an investigational 400kHz, 1060nm swept-source system with a 700g handheld, noncontact probe in preterm infants at risk for ROP. Two imaging protocols were used at the bedside, the day of clinical ROP screening, without sedation or use of an eyelid speculum: Scan 1 (0.7 sec, 1900 A-scans/B-scan, 128 B-scans per 10x10mm volume, with pairs of adjacent A-scans summed producing 950 A-scans/B-scan) for cross-sectional assessment of retinal layers; and Scan 2 (1.4 sec, 640 A-scans/B-scan and 640 B-scans per 10x10mm isodense volume) for en face retinal vascular assessment. For multidimensional visualization, we developed infant-specific software (DOCTRAP v66.2) to optimize automatic segmentation of OCT volumes from Scan 1 and generate total retina thickness maps. We extracted en face retinal vessel maps from maximum pixel intensity at each A-scan position from Scan 2. With auto-montaging software (i2k Retina; DualAlign, Inc.), we created a single posterior pole vessel map per eye and overlaid corresponding thickness maps for comparison to color fundus photos.

Results : We were able to capture, integrate, and visualize multidimensional data from high-speed investigational bedside OCT imaging of preterm infant retinas. This included: depth-resolved analysis of retinal microanatomy at locations of interest (e.g., at the foveal center and vascular-avascular junction); intensity maps of total retinal layer thicknesses; and retinal vessel maps (Figure 1). These data demonstrated important ROP pathology (e.g., retinal neovascularization and plus disease) and in contrast to color photographs, enabled integrated assessment of the developing preterm retina (e.g., retinal layer thicknesses and presence of macular edema).

Conclusions : This method for multidimensional data analysis will be used by human graders and analyzed by semi-automated software (i.e., ROPtool) in BabySTEPS2, and may be integrated into future artificial intelligence-based ROP screening methods.

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

 

Multidimensional research OCT data (A-B) and clinical fundus photo (C) in a preterm eye with ROP. Asterisk, fovea. Arrow, neovascularization. Black line, B-scan location.

Multidimensional research OCT data (A-B) and clinical fundus photo (C) in a preterm eye with ROP. Asterisk, fovea. Arrow, neovascularization. Black line, B-scan location.

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