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变形性痉挛性轻瘫的损伤系数

Coefficients of impairment in deforming spastic paresis.

作者信息

Gracies J-M

机构信息

Service de rééducation neurolocomotrice, laboratoire analyse et restauration du mouvement, université Paris-Est, hôpitaux universitaires Henri-Mondor, AP-HP, 51, avenue du Maréchal-de-Lattre-de-Tassigny, 94010 Créteil, France.

出版信息

Ann Phys Rehabil Med. 2015 Jun;58(3):173-8. doi: 10.1016/j.rehab.2015.04.004. Epub 2015 May 28.

Abstract

This position paper introduces an assessment method using staged calculation of coefficients of impairment in spastic paresis, with its rationale and proposed use. The syndrome of deforming spastic paresis superimposes two disorders around each joint: a neural disorder comprising stretch-sensitive paresis in agonists and antagonist muscle overactivity, and a muscle disorder ("spastic myopathy") combining shortening and loss of extensibility in antagonists. Antagonist muscle overactivity includes spastic cocontraction (misdirected descending command), spastic dystonia (tonic involuntary muscle activation, at rest) and spasticity (increased velocity-dependent reflexes to phasic stretch, at rest). This understanding of various types of antagonist resistance as the key limiting factors in paretic movements prompts a stepwise, quantified, clinical assessment of antagonist resistances, elaborating on the previously developed Tardieu Scale. Step 1 quantifies limb function (e.g. ambulation speed in lower limb, Modified Frenchay Scale in upper limb). The following four steps evaluate various angles X of antagonist resistance, in degrees all measured from 0°, position of minimal stretch of the tested antagonist. Step 2 rates the functional muscle length, termed XV1 (V1, slowest stretch velocity possible), evaluated as the angle of arrest upon slow and strong passive muscle stretch. XV1 is appreciated with respect to the expected normal passive amplitude, XN, and reflects combined muscle contracture and residual spastic dystonia. Step 3 determines the angle of catch upon fast stretch, termed XV3 (V3, fastest stretch velocity possible), reflecting spasticity. Step 4 measures the maximal active range of motion against the antagonist, termed XA, reflecting agonist capacity to overcome passive (stiffness) and active (spastic cocontraction) antagonist resistances over a single movement. Finally, Step 5 rates the residual active amplitude after 15 seconds of maximal amplitude rapid alternating movements, XA15. Amplitude decrement from XA to XA15 reflects fatigability. Coefficients of shortening (XN-XV1)/XN, spasticity (XV1-XV3)/XV1, weakness (XV1-XA)/XV1 and fatigability (XA-XA15)/XA are derived. A high (e.g., >10%) coefficient of shortening prompts aggressive treatment of the muscle disorder--e.g., by stretch programs, such as prolonged stretch postures -, while high coefficients of weakness or fatigability prompt addressing the neural motor command disorder, e.g. using training programs such as repeated alternating movements of maximal amplitude.

摘要

本立场文件介绍了一种使用痉挛性麻痹损伤系数的阶段性计算的评估方法,及其原理和建议用途。变形性痉挛性麻痹综合征在每个关节周围叠加了两种障碍:一种神经障碍,包括主动肌的牵张敏感麻痹和拮抗肌的过度活动;另一种肌肉障碍(“痉挛性肌病”),表现为拮抗肌的缩短和伸展性丧失。拮抗肌的过度活动包括痉挛性共同收缩(下行指令错误)、痉挛性肌张力障碍(静息时的强直性非自愿肌肉激活)和痉挛(静息时对相位牵张的速度依赖性反射增加)。将各种类型的拮抗肌阻力视为麻痹性运动的关键限制因素的这种理解,促使对拮抗肌阻力进行逐步、量化的临床评估,这是在先前开发的塔迪厄量表基础上进行的详细阐述。第一步量化肢体功能(如下肢的步行速度、上肢的改良弗伦奇量表)。接下来的四个步骤评估拮抗肌阻力的各个角度X,所有角度均从0°开始测量,即测试拮抗肌最小伸展位置。第二步评估功能性肌肉长度,称为XV1(V1,可能的最慢伸展速度),通过缓慢而有力的被动肌肉伸展时的制动角度来评估。相对于预期的正常被动幅度XN评估XV1,它反映了肌肉挛缩和残余痉挛性肌张力障碍的综合情况。第三步确定快速伸展时的捕捉角度,称为XV3(V3,可能的最快伸展速度),反映痉挛情况。第四步测量对抗拮抗肌的最大主动运动范围,称为XA,反映主动肌在单个运动中克服被动(僵硬)和主动(痉挛性共同收缩)拮抗肌阻力的能力。最后,第五步评估最大幅度快速交替运动15秒后的残余主动幅度XA15。从XA到XA15的幅度减小反映疲劳性。得出缩短系数(XN - XV1)/XN、痉挛系数(XV1 - XV3)/XV1、无力系数(XV1 - XA)/XV1和疲劳系数(XA - XA15)/XA。高缩短系数(例如,>10%)促使积极治疗肌肉障碍,例如通过伸展程序,如长时间伸展姿势;而高无力系数或疲劳系数则促使解决神经运动指令障碍,例如使用最大幅度的重复交替运动等训练程序。

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