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Visupac

Manufactured by Zeiss
Sourced in Japan

Visupac is a compact and automated benchtop instrument designed for the purpose of measuring and analyzing visual acuity. It provides objective and standardized assessment of visual function.

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2 protocols using visupac

1

Retrospective Glaucoma Registry Analysis

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This was a retrospective study that used cross-sectional data from the Duke Glaucoma Registry, a database of electronic medical and research records at the Vision, Imaging, and Performance Laboratory at Duke University. The Duke Health Institutional Review Board approved this study, and a waiver of informed consent was granted due to the retrospective nature of this work. All methods adhered to the tenets of the Declaration of Helsinki for research involving human subjects and the study was conducted in accordance with regulations of the Health Insurance Portability and Accountability Act.
The visual field tests were performed using SAP with the 24-2 Swedish Interactive Threshold Algorithm (Carl Zeiss Meditec, Inc., Dublin, CA) protocol. Unreliable tests with more than 33% fixation losses or 15% false-positive errors were excluded. RNFL thickness measurements were obtained from peripapillary circle scans, acquired using the Spectralis SDOCT (Heidelberg Engineering, GmbH, Dossenheim, Germany). According to manufacturer recommendations, tests with a quality score lower than 15 were excluded. The fundus photos present in the database were acquired from two different cameras: Nidek 3DX (Nidek, Japan) and Visupac (Carl Zeiss Meditec, Inc., Dublin, CA). The image was retained if the optic disc was entirely visible in the photo, and if no artifacts were present.
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2

Multimodal Diabetic Maculopathy Grading

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FP images were viewed using Zeiss VISUPAC software with its available image manipulation tools applied if needed. MC (including the individual blue, green and infrared reflectance images) and SD-OCT images were viewed using Heidelberg Eye Explorer with its image manipulation tools used as necessary.
The MC and FP images were delinked. The diabetic maculopathy was graded based on exudate criteria as described by the DES on both MC and FP in a blind fashion independently by two graders (OK and SP). Infrared reflectance, green reflectance, blue reflectance and MC composite were assessed individually to decide on the presence of exudates (figure 2). An image was deemed ungradable if the detail of the third order retinal vessels from the superior and inferior vascular arcades was not discernible.
On SD-OCT, an exudate was defined as a homogenous hyper-reflective focus of ≥63 µm at, or internal to the outer plexiform layer with no inner hyporeflectivity. M1 maculopathy based on exudate criteria as outlined by the DES was not assessed systematically using SD-OCT as the spacing between the B-scans was >63 µm and the scan did not cover the entire macular as defined by the DES. However, any exudate seen on SD-OCT was recorded and correlated with FP and MC findings.
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