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Detection of Relative Afferent Pupillary Defects Using Eye Tracking and a VR Headset

PURPOSE: The purpose of this study was to assess the feasibility of detecting relative afferent pupillary defects (RAPDs) using a commercial virtual reality headset equipped with an eye tracker. METHODS: This is a cross-sectional study in which we compare the new computerized RAPD test with the trad...

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Autores principales: Bruegger, Dominik, Grabe, Hilary M., Vicini, Rino, Dysli, Muriel, Lussi, David, Abegg, Mathias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10309159/
https://www.ncbi.nlm.nih.gov/pubmed/37367721
http://dx.doi.org/10.1167/tvst.12.6.22
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author Bruegger, Dominik
Grabe, Hilary M.
Vicini, Rino
Dysli, Muriel
Lussi, David
Abegg, Mathias
author_facet Bruegger, Dominik
Grabe, Hilary M.
Vicini, Rino
Dysli, Muriel
Lussi, David
Abegg, Mathias
author_sort Bruegger, Dominik
collection PubMed
description PURPOSE: The purpose of this study was to assess the feasibility of detecting relative afferent pupillary defects (RAPDs) using a commercial virtual reality headset equipped with an eye tracker. METHODS: This is a cross-sectional study in which we compare the new computerized RAPD test with the traditional clinical standard using the swinging flashlight test. Eighty-two participants including 20 healthy volunteers aged 10 to 88 years were enrolled in this study. We present a bright/dark stimulus alternating between the eyes every 3 seconds using a virtual reality headset, and we simultaneously record changes in pupil size. To determine the presence of an RAPD, we developed an algorithm analyzing the pupil size differences. For the assessment of the performance of the automated and the manual measurement a post hoc impression based on all available data is created. The accuracy of the manual clinical evaluation and the computerized method is compared using confusion matrices and the gold standard of the post hoc impression. The latter is based on all available clinical information. RESULTS: We found that the computerized method detected RAPD with a sensitivity of 90.2% and an accuracy of 84.4%, as compared to the post hoc impression. This was not significantly different from the clinical evaluation with a sensitivity of 89.1% and an accuracy of 88.3%. CONCLUSIONS: The presented method offers an accurate, easy to use, and fast method to measure an RAPD. In contrast to today's clinical practice, the measures are quantitative and objective. TRANSLATIONAL RELEVANCE: Computerized testing of Relative Afferent Pupillary Defects (RAPD) using a VR-headset and eye-tracking reaches non-inferior performance compared with senior neuro-ophthalmologists.
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spelling pubmed-103091592023-06-30 Detection of Relative Afferent Pupillary Defects Using Eye Tracking and a VR Headset Bruegger, Dominik Grabe, Hilary M. Vicini, Rino Dysli, Muriel Lussi, David Abegg, Mathias Transl Vis Sci Technol Neuro-Ophthalmology PURPOSE: The purpose of this study was to assess the feasibility of detecting relative afferent pupillary defects (RAPDs) using a commercial virtual reality headset equipped with an eye tracker. METHODS: This is a cross-sectional study in which we compare the new computerized RAPD test with the traditional clinical standard using the swinging flashlight test. Eighty-two participants including 20 healthy volunteers aged 10 to 88 years were enrolled in this study. We present a bright/dark stimulus alternating between the eyes every 3 seconds using a virtual reality headset, and we simultaneously record changes in pupil size. To determine the presence of an RAPD, we developed an algorithm analyzing the pupil size differences. For the assessment of the performance of the automated and the manual measurement a post hoc impression based on all available data is created. The accuracy of the manual clinical evaluation and the computerized method is compared using confusion matrices and the gold standard of the post hoc impression. The latter is based on all available clinical information. RESULTS: We found that the computerized method detected RAPD with a sensitivity of 90.2% and an accuracy of 84.4%, as compared to the post hoc impression. This was not significantly different from the clinical evaluation with a sensitivity of 89.1% and an accuracy of 88.3%. CONCLUSIONS: The presented method offers an accurate, easy to use, and fast method to measure an RAPD. In contrast to today's clinical practice, the measures are quantitative and objective. TRANSLATIONAL RELEVANCE: Computerized testing of Relative Afferent Pupillary Defects (RAPD) using a VR-headset and eye-tracking reaches non-inferior performance compared with senior neuro-ophthalmologists. The Association for Research in Vision and Ophthalmology 2023-06-27 /pmc/articles/PMC10309159/ /pubmed/37367721 http://dx.doi.org/10.1167/tvst.12.6.22 Text en Copyright 2023 The Authors https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License.
spellingShingle Neuro-Ophthalmology
Bruegger, Dominik
Grabe, Hilary M.
Vicini, Rino
Dysli, Muriel
Lussi, David
Abegg, Mathias
Detection of Relative Afferent Pupillary Defects Using Eye Tracking and a VR Headset
title Detection of Relative Afferent Pupillary Defects Using Eye Tracking and a VR Headset
title_full Detection of Relative Afferent Pupillary Defects Using Eye Tracking and a VR Headset
title_fullStr Detection of Relative Afferent Pupillary Defects Using Eye Tracking and a VR Headset
title_full_unstemmed Detection of Relative Afferent Pupillary Defects Using Eye Tracking and a VR Headset
title_short Detection of Relative Afferent Pupillary Defects Using Eye Tracking and a VR Headset
title_sort detection of relative afferent pupillary defects using eye tracking and a vr headset
topic Neuro-Ophthalmology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10309159/
https://www.ncbi.nlm.nih.gov/pubmed/37367721
http://dx.doi.org/10.1167/tvst.12.6.22
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