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Lumbar segment-dependent soft tissue artifacts of skin markers during in vivo weight-bearing forward–Backward bending
Lumbar segment-dependent soft tissue artifacts of skin markers during in vivo weight-bearing forward–Backward bending
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Lumbar segment-dependent soft tissue artifacts of skin markers during in vivo weight-bearing forward–Backward bending
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Lumbar segment-dependent soft tissue artifacts of skin markers during in vivo weight-bearing forward–Backward bending
Lumbar segment-dependent soft tissue artifacts of skin markers during in vivo weight-bearing forward–Backward bending

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Lumbar segment-dependent soft tissue artifacts of skin markers during in vivo weight-bearing forward–Backward bending
Lumbar segment-dependent soft tissue artifacts of skin markers during in vivo weight-bearing forward–Backward bending
Journal Article

Lumbar segment-dependent soft tissue artifacts of skin markers during in vivo weight-bearing forward–Backward bending

2022
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Overview
Traditional optical motion capture (OMC) with retroreflective markers is commonly used to measure joint kinematics but was also reported with unavoidable soft tissue artifacts (STAs) when quantifying the motion of the spine. Additionally, the patterns of the STA on the lumbar spine remain unclear. This study aimed to 1) quantify the in vivo STAs of the human lower back in three-dimensional directions during weight-bearing forward–backward bending and 2) determine the effects of the STAs on the calculated flexion angles between the upper and lower lumbar spines and adjacent vertebrae by comparing the skin marker (SM)- and virtual bone marker (VM)-based measurements. Six healthy volunteers were imaged using a biplanar radiographic system, and thirteen skin markers were mounted on every volunteer’s lower back while performing weight-bearing forward–backward bending. The STAs in the anterior/posterior (AP), medial/lateral (ML), and proximal/distal (PD) directions were investigated. The flexion angles between the upper and lower lumbar segments and adjacent intervertebral segments (L2–L5) throughout the cycle were calculated. For all the participants, STAs continuously increased in the AP direction and exhibited a reciprocal trend in the PD direction. During flexion, the STA at the lower lumbar region (L4–L5: 13.5 ± 6.5 mm) was significantly higher than that at the upper lumbar (L1–L3: 4.0 ± 1.5 mm) in the PD direction ( p < 0.01). During extension, the lower lumbar (L4–L5: 2.7 ± 0.7 mm) exhibited significantly less STAs than that exhibited by the upper lumbar region (L1–L3: 6.1 ± 3.3 mm) ( p < 0.05). The STA at the spinous process was significantly lower than that on both sides in the AP direction ( p < 0.05). The present results on STAs, based on dual fluoroscopic measurements in healthy adult subjects, presented an anatomical direction, marker location, and anatomic segment dependency, which might help describe and quantify STAs for the lumbar spine kinematics and thus help develop location- and direction-specific weighting factors for use in global optimization algorithms aimed at minimizing the effects of STAs on the calculation of lumbar joint kinematics in the future.

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