» Articles » PMID: 15698706

Quantification of Soft Tissue Artefact in Motion Analysis by Combining 3D Fluoroscopy and Stereophotogrammetry: a Study on Two Subjects

Overview
Date 2005 Feb 9
PMID 15698706
Citations 52
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Soft tissue artefact is the most invalidating source of error in human motion analysis using optoelectronic stereophotogrammetry. It is caused by the erroneous assumption that markers attached to the skin surface are rigidly connected to the underlying bones. The quantification of this artefact in three dimensions and the knowledge of how it propagates to relevant joint angles is necessary for the interpretation of gait analysis data.

Methods: Two subjects, treated by total knee replacement, underwent data acquisition simultaneously with fluoroscopy and stereophotogrammetry during stair climbing, step up/down, sit-to-stand/stand-to-sit, and extension against gravity. The reference 3D kinematics of the femur and tibia was reconstructed from fluoroscopy-based tracking of the relevant prosthesis components. Soft tissue artefact was quantified as the motion of a grid of retro-reflecting makers attached to the thigh and shank with respect to the underlying bones, tracked by optoelectronic stereophotogrammetry. The propagation of soft tissue artefact to knee rotations was also calculated.

Findings: The standard deviation of skin marker trajectory in the corresponding prosthesis-embedded anatomical frame was found up to 31 mm for the thigh and up to 21 mm for the shank. The ab/adduction and internal/external rotation angles were the most affected by soft tissue artefact propagation, with root mean square errors up to 192% and 117% of the corresponding range, respectively.

Interpretations: In both the analysed subjects the proximal thigh showed the largest soft tissue artefact. This is subject- and task-specific. However, larger artefact does not necessarily produce larger propagated error on knee rotations. Propagated errors were extremely critical on ab/adduction and internal/external rotation. These large errors can nullify the usefulness of these variables in the clinical interpretation of gait analysis.

Citing Articles

Validation of a 3D Markerless Motion Capture Tool Using Multiple Pose and Depth Estimations for Quantitative Gait Analysis.

DHaene M, Chorin F, Colson S, Guerin O, Zory R, Piche E Sensors (Basel). 2024; 24(22).

PMID: 39598883 PMC: 11597901. DOI: 10.3390/s24227105.


A comparison of lower body gait kinematics and kinetics between Theia3D markerless and marker-based models in healthy subjects and clinical patients.

DSouza S, Siebert T, Fohanno V Sci Rep. 2024; 14(1):29154.

PMID: 39587194 PMC: 11589150. DOI: 10.1038/s41598-024-80499-8.


In-vitro external fixation pin-site model proof of concept: A novel approach to studying wound healing in transcutaneous implants.

McCall B, Rana K, Sugden K, Junaid S Proc Inst Mech Eng H. 2024; 238(4):403-411.

PMID: 38602217 PMC: 11010558. DOI: 10.1177/09544119241234154.


A portable system to measure knee extensor spasticity after spinal cord injury.

De Santis D, Perez M J Neuroeng Rehabil. 2024; 21(1):50.

PMID: 38594696 PMC: 11003160. DOI: 10.1186/s12984-024-01326-9.


Influence of Lateral Sitting Wedges on the Rasterstereographically Measured Scoliosis Angle in Patients Aged 10-18 Years with Adolescent Idiopathic Scoliosis.

Feustel A, Konradi J, Wolf C, Huthwelker J, Westphal R, Chow D Bioengineering (Basel). 2023; 10(9).

PMID: 37760188 PMC: 10525467. DOI: 10.3390/bioengineering10091086.