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Can the fusion of motion capture and 3D medical imaging reduce the extrinsic variability due to marker misplacements?
In clinical gait analysis, measurement errors impede the reliability and repeatability of the measurements. This extrinsic variability can potentially mislead the clinical interpretation of the analysis and should thus be minimised. Skin marker misplacement has been identified as the largest source...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988975/ https://www.ncbi.nlm.nih.gov/pubmed/31995610 http://dx.doi.org/10.1371/journal.pone.0226648 |
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author | Gasparutto, Xavier Wegrzyk, Jennifer Rose-Dulcina, Kevin Hannouche, Didier Armand, Stéphane |
author_facet | Gasparutto, Xavier Wegrzyk, Jennifer Rose-Dulcina, Kevin Hannouche, Didier Armand, Stéphane |
author_sort | Gasparutto, Xavier |
collection | PubMed |
description | In clinical gait analysis, measurement errors impede the reliability and repeatability of the measurements. This extrinsic variability can potentially mislead the clinical interpretation of the analysis and should thus be minimised. Skin marker misplacement has been identified as the largest source of extrinsic variability between measurements. The goal of this study was to test whether the fusion of motion capture and 3D medical imaging could reduce extrinsic variability due to skin marker misplacement. The fusion method consists in using anatomical landmarks identified with 3D medical imaging to correct marker misplacements. To assess the reduction of variability accountable to the fusion method, skin marker misplacements were voluntarily introduced in the measurement of the pelvis and hip kinematics during gait for two patients scheduled for unilateral hip arthroplasty and two patients that underwent unilateral hip arthroplasty. The root mean square deviation was reduced by -78 ± 15% and the range of variability by -80 ± 16% for the pelvis and hip kinematics in average. These results showed that the fusion method could significantly reduce the extrinsic variability due to skin marker misplacement and thus increase the reliability and repeatability of motion capture measurements. However, the identification of anatomical landmarks via medical imaging is a new source of extrinsic variability that should be assessed before considering the fusion method for clinical applications. |
format | Online Article Text |
id | pubmed-6988975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-69889752020-02-04 Can the fusion of motion capture and 3D medical imaging reduce the extrinsic variability due to marker misplacements? Gasparutto, Xavier Wegrzyk, Jennifer Rose-Dulcina, Kevin Hannouche, Didier Armand, Stéphane PLoS One Research Article In clinical gait analysis, measurement errors impede the reliability and repeatability of the measurements. This extrinsic variability can potentially mislead the clinical interpretation of the analysis and should thus be minimised. Skin marker misplacement has been identified as the largest source of extrinsic variability between measurements. The goal of this study was to test whether the fusion of motion capture and 3D medical imaging could reduce extrinsic variability due to skin marker misplacement. The fusion method consists in using anatomical landmarks identified with 3D medical imaging to correct marker misplacements. To assess the reduction of variability accountable to the fusion method, skin marker misplacements were voluntarily introduced in the measurement of the pelvis and hip kinematics during gait for two patients scheduled for unilateral hip arthroplasty and two patients that underwent unilateral hip arthroplasty. The root mean square deviation was reduced by -78 ± 15% and the range of variability by -80 ± 16% for the pelvis and hip kinematics in average. These results showed that the fusion method could significantly reduce the extrinsic variability due to skin marker misplacement and thus increase the reliability and repeatability of motion capture measurements. However, the identification of anatomical landmarks via medical imaging is a new source of extrinsic variability that should be assessed before considering the fusion method for clinical applications. Public Library of Science 2020-01-29 /pmc/articles/PMC6988975/ /pubmed/31995610 http://dx.doi.org/10.1371/journal.pone.0226648 Text en © 2020 Gasparutto et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Gasparutto, Xavier Wegrzyk, Jennifer Rose-Dulcina, Kevin Hannouche, Didier Armand, Stéphane Can the fusion of motion capture and 3D medical imaging reduce the extrinsic variability due to marker misplacements? |
title | Can the fusion of motion capture and 3D medical imaging reduce the extrinsic variability due to marker misplacements? |
title_full | Can the fusion of motion capture and 3D medical imaging reduce the extrinsic variability due to marker misplacements? |
title_fullStr | Can the fusion of motion capture and 3D medical imaging reduce the extrinsic variability due to marker misplacements? |
title_full_unstemmed | Can the fusion of motion capture and 3D medical imaging reduce the extrinsic variability due to marker misplacements? |
title_short | Can the fusion of motion capture and 3D medical imaging reduce the extrinsic variability due to marker misplacements? |
title_sort | can the fusion of motion capture and 3d medical imaging reduce the extrinsic variability due to marker misplacements? |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988975/ https://www.ncbi.nlm.nih.gov/pubmed/31995610 http://dx.doi.org/10.1371/journal.pone.0226648 |
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