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一项关于中风后治疗中复杂运动的纵向肌电图研究。1:尽管临床评估持续改善,但仍存在异质性变化。

A Longitudinal Electromyography Study of Complex Movements in Poststroke Therapy. 1: Heterogeneous Changes Despite Consistent Improvements in Clinical Assessments.

作者信息

Hesam-Shariati Negin, Trinh Terry, Thompson-Butel Angelica G, Shiner Christine T, McNulty Penelope A

机构信息

Neuroscience Research Australia, Sydney, NSW, Australia.

School of Medical Science, University of New South Wales, Sydney, NSW, Australia.

出版信息

Front Neurol. 2017 Jul 28;8:340. doi: 10.3389/fneur.2017.00340. eCollection 2017.

DOI:10.3389/fneur.2017.00340
PMID:28804474
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5532386/
Abstract

Poststroke weakness on the more-affected side may arise from reduced corticospinal drive, disuse muscle atrophy, spasticity, and abnormal coordination. This study investigated changes in muscle activation patterns to understand therapy-induced improvements in motor-function in chronic stroke compared to clinical assessments and to identify the effect of motor-function level on muscle activation changes. Electromyography (EMG) was recorded from five upper limb muscles on the more-affected side of 24 patients during early and late therapy sessions of an intensive 14-day program of Wii-based Movement Therapy (WMT) and for a subset of 13 patients at 6-month follow-up. Patients were classified according to residual voluntary motor capacity with low, moderate, or high motor-function levels. The area under the curve was calculated from EMG amplitude and movement duration. Clinical assessments of upper limb motor-function pre- and post-therapy included the Wolf Motor Function Test, Fugl-Meyer Assessment and Motor Activity Log Quality of Movement scale. Clinical assessments improved over time ( < 0.01) with an effect of motor-function level ( < 0.001). The pattern of EMG change by late therapy was complex and variable, with differences between patients with low compared to moderate or high motor-function levels. The area under the curve ( = 0.028) and peak amplitude ( = 0.043) during Wii-tennis backhand increased for patients with low motor-function, whereas EMG decreased for patients with moderate and high motor-function levels. The reductions included movement duration during Wii-golf ( = 0.048, moderate;  = 0.026, high) and Wii-tennis backhand ( = 0.046, moderate;  = 0.023, high) and forehand ( = 0.009, high) and the area under the curve during Wii-golf ( = 0.018, moderate) and Wii-baseball ( = 0.036, moderate). For the pooled data over time, there was an effect of motor-function ( = 0.016) and an interaction between time and motor-function ( = 0.009) for Wii-golf movement duration. Wii-baseball movement duration decreased as a function of time ( = 0.022). There was an effect on Wii-tennis forehand duration for time ( = 0.002), an interaction of time and motor-function ( = 0.005) and an effect of motor-function level on the area under the curve ( = 0.034) for Wii-golf. This study demonstrated different patterns of EMG changes according to residual voluntary motor-function levels, despite heterogeneity within each level that was not evident following clinical assessments alone. Thus, rehabilitation efficacy might be underestimated by analyses of pooled data.

摘要

中风后患侧肌无力可能源于皮质脊髓驱动减少、废用性肌肉萎缩、痉挛和异常协调。本研究调查了肌肉激活模式的变化,以了解与临床评估相比,强化14天基于Wii的运动疗法(WMT)在慢性中风中治疗诱导的运动功能改善情况,并确定运动功能水平对肌肉激活变化的影响。在为期14天的强化Wii运动疗法计划的早期和晚期治疗阶段,对24例患者患侧的5块上肢肌肉进行了肌电图(EMG)记录,并对其中13例患者在6个月随访时进行了记录。根据残余自主运动能力将患者分为低、中、高运动功能水平。根据EMG振幅和运动持续时间计算曲线下面积。治疗前后上肢运动功能的临床评估包括Wolf运动功能测试、Fugl-Meyer评估和运动活动日志运动质量量表。临床评估随时间改善(<0.01),存在运动功能水平的影响(<0.001)。晚期治疗时EMG变化模式复杂且多变,低运动功能水平患者与中、高运动功能水平患者之间存在差异。低运动功能水平患者在Wii网球反手击球时曲线下面积(=0.028)和峰值振幅(=0.043)增加,而中、高运动功能水平患者的EMG降低。降低包括Wii高尔夫(=0.048,中;=0.026,高)和Wii网球反手击球(=0.046,中;=0.023,高)及正手击球(=0.009,高)时的运动持续时间,以及Wii高尔夫(=0.018,中)和Wii棒球(=0.036,中)时的曲线下面积。对于随时间汇总的数据,Wii高尔夫运动持续时间存在运动功能的影响(=0.016)以及时间与运动功能之间的相互作用(=0.009)。Wii棒球运动持续时间随时间减少(=0.022)。Wii网球正手击球持续时间存在时间的影响(=0.002)、时间与运动功能的相互作用(=0.005),且Wii高尔夫曲线下面积存在运动功能水平的影响(=0.034)。本研究表明,根据残余自主运动功能水平,EMG变化模式不同,尽管每个水平内存在异质性,仅通过临床评估并不明显。因此,汇总数据分析可能会低估康复疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc01/5532386/2e43cf4e61b6/fneur-08-00340-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc01/5532386/2aebea3c62fb/fneur-08-00340-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc01/5532386/2aebea3c62fb/fneur-08-00340-g001.jpg
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