Wearable sensor systems measure differences in knee laxity between healthy and affected knees during dynamic exercise activities: A systematic review

IF 2 Q2 ORTHOPEDICS Journal of Experimental Orthopaedics Pub Date : 2024-07-24 DOI:10.1002/jeo2.12094
Sander C. van Eijck, Marly M. J. Vugts, Rob P. A. Janssen, Iris Hoogendoorn, Keita Ito, Maria C. van der Steen
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Abstract

Purpose

Knee laxity can be experienced as knee instability which may lead to a limitation in the activity of patients. Current methods to determine knee instability are performed in a static setting, which does not always correlate with dynamic knee laxity during activities. Wearables might be able to measure knee laxity in a dynamic setting and could be of added value in the diagnosis and treatment of excessive knee laxity. Therefore, the aim of this systematic review is to provide an overview of the wearables that have been developed and their ability to measure knee laxity during dynamic activities.

Methods

The PRISMA guidelines for systematic reviews were followed. A literature search was conducted in EMBASE, PubMed and Cochrane databases. Included studies assessed patients with knee instability using a non-invasive wearable sensor system during dynamic activity, with comparison to a reference system or healthy knees. Data extraction was performed by two authors via a predefined format. The risk of bias was assessed by The Dutch checklist for diagnostic tests.

Results

A total of 4734 articles were identified. Thirteen studies were included in the review. The studies showed a great variety of patients, sensor systems, reference tests, outcome measures and performed activities. Nine of the included studies were able to measure differences in patients with knee instability, all including a tri-axial accelerometer. Differences were not measurable in all parameters and activities in these studies.

Conclusions

Wearables, including at least a tri-axial accelerometer, seem promising for measuring dynamic knee laxity in the anterior-posterior and mediolateral direction. At this stage, it remains unclear if the measured outcomes completely reflect the knee instability that patients experience in daily life.

Level of Evidence

Level III.

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可穿戴传感器系统可测量动态运动时健康膝关节和受影响膝关节之间的膝关节松弛差异:系统综述。
目的:膝关节松弛可表现为膝关节不稳定,可能导致患者活动受限。目前确定膝关节不稳的方法都是在静态环境下进行的,并不总是与活动时膝关节的动态松弛相关联。可穿戴设备或许能在动态环境下测量膝关节松弛程度,从而为膝关节过度松弛的诊断和治疗带来附加价值。因此,本系统综述旨在概述已开发的可穿戴设备及其在动态活动中测量膝关节松弛程度的能力:方法:研究遵循了系统性综述的 PRISMA 指南。在 EMBASE、PubMed 和 Cochrane 数据库中进行了文献检索。纳入的研究使用无创可穿戴传感器系统对动态活动中的膝关节不稳定患者进行了评估,并与参考系统或健康膝关节进行了比较。数据提取由两位作者通过预定义格式完成。根据荷兰诊断测试核对表对偏倚风险进行评估:结果:共发现 4734 篇文章。共有 13 项研究被纳入综述。这些研究显示了患者、传感器系统、参考测试、结果测量和执行活动的多样性。所纳入的研究中有九项能够测量膝关节不稳定患者的差异,所有研究都采用了三轴加速度计。在这些研究中,并非所有参数和活动都能测量出差异:可穿戴设备(至少包括三轴加速度计)似乎有望测量膝关节前后和内外侧方向的动态松弛。现阶段,尚不清楚测量结果是否能完全反映患者在日常生活中的膝关节不稳定性:证据等级:三级。
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来源期刊
Journal of Experimental Orthopaedics
Journal of Experimental Orthopaedics Medicine-Orthopedics and Sports Medicine
CiteScore
3.20
自引率
5.60%
发文量
114
审稿时长
13 weeks
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