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首页> 外文期刊>Neuromuscular disorders: NMD >Comparison of maximal voluntary isometric contraction and hand-held dynamometry in measuring muscle strength of patients with progressive lower motor neuron syndrome.
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Comparison of maximal voluntary isometric contraction and hand-held dynamometry in measuring muscle strength of patients with progressive lower motor neuron syndrome.

机译:最大自愿等距收缩法与手持测功法在进行性下运动神经元综合征患者肌肉力量测量中的比较。

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Context. Maximal voluntary isometric contraction, a method quantitatively assessing muscle strength, has proven to be reliable, accurate and sensitive in amyotrophic lateral sclerosis. Hand-held dynamometry is less expensive and more quickly applicable than maximal voluntary isometric contraction. Objective. To investigate if hand-held dynamometry is as reliable and valid as maximal voluntary isometric contraction in measuring muscle strength in patients with an adult-onset, non-hereditary progressive lower motor neuron syndrome. Design. Two testers performed maximal voluntary isometric contraction and hand-held dynamometry measurements in six muscle groups bilaterally in patients with progressive lower motor neuron syndrome to assess reliability and validity of both the methods. Setting. Outpatient units of an academic medical center. Patients. A consecutive sample of 19 patients with non-hereditary progressive lower motor neuron syndrome (median disease duration 32.5 months, range 10-84) was tested. Outcome measures. Comparison between maximal voluntary strength contractions as measured by hand-held dynamometry and maximal voluntary isometric contraction. Results. Low intra- and interrater variation in all muscle groups were found, intraclass correlation coefficients vary between 0.86 and 0.99 for both methods. Both methods correlated well in all muscle groups with Pearson's correlation coefficients ranged between 0.78 and 0.98. Scatter plots indicated a trend to under-estimate muscle strength above 250 N by hand-held dynamometry as compared with maximal voluntary isometric contraction. Conclusions. For longitudinal evaluation of muscle strength in patients with progressive lower motor neuron syndrome (i.e. between 0 and 250 N), muscle strength can be accurate quantified with both hand-held dynamometry and maximal voluntary isometric contraction. Hand-held dynamometry has the advantage of being cheap and quickly applicable. However, our results indicate that hand-held dynamometry is less sensitive than maximal voluntary isometric contraction in detecting subnormal muscle strength in strong muscle groups (i.e. >250 N), due to limited strength of the tester.
机译:上下文。最大自愿等距收缩是一种定量评估肌肉力量的方法,已被证明在肌萎缩性侧索硬化症中是可靠,准确和敏感的。手持测功机比最大自愿等距收缩更便宜,应用更迅速。目的。调查手持测功器在测量成人发作,非遗传性进行性下运动神经元综合征患者的肌肉力量方面是否与最大自愿等距收缩法一样可靠和有效。设计。两名测试者在进行性下运动神经元综合征患者的双侧六个肌肉群中进行了最大的自愿等距收缩和手持测功测量,以评估这两种方法的可靠性和有效性。设置。学术医疗中心的门诊部。耐心。连续样本19例非遗传性进行性下运动神经元综合征(中位病程32.5个月,范围10-84)进行了测试。成果措施。通过手持式测功机测量的最大自愿力量收缩与最大自主等长收缩之间的比较。结果。发现所有肌肉组的内和间差异均较低,两种方法的组内相关系数均在0.86至0.99之间变化。两种方法在所有肌肉群中的相关性都很好,皮尔森相关系数在0.78至0.98之间。散点图表明,与最大自主等距收缩相比,通过手持测功器低估了250 N以上肌肉强度的趋势。结论为了对进行性下运动神经元综合征(即0到250 N)的患者的肌肉力量进行纵向评估,可以通过手持测功和最大自主等距收缩来准确量化肌肉力量。手持测功机的优点是价格便宜且可快速使用。但是,我们的结果表明,由于测试仪的力量有限,手持测功仪在检测强壮肌肉组(即> 250 N)中的低于正常的肌肉强度时,不如最大自愿等距收缩敏感。

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