<?xml version="1.0" encoding="UTF-8" standalone="yes"?><oembed><version><![CDATA[1.0]]></version><provider_name><![CDATA[TBI Rehabilitation]]></provider_name><provider_url><![CDATA[https://tbirehabilitation.wordpress.com]]></provider_url><author_name><![CDATA[Kostas Pantremenos]]></author_name><author_url><![CDATA[https://tbirehabilitation.wordpress.com/author/onganalop/]]></author_url><title><![CDATA[[Abstract] Composite active range of motion (CXA) and relationship with active function in upper and lower limb spastic&nbsp;paresis]]></title><type><![CDATA[link]]></type><html><![CDATA[<div class="sectionInfo abstractSectionHeading">
<h2 class="sectionHeading">Abstract</h2>
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<h2 class="sectionHeading">Objective:</h2>
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<p>The aim of this study is to evaluate a novel composite measure of active range of motion (X<sub>A</sub>) and determine whether this measure correlates with active function.</p>
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<h2 class="sectionHeading">Design:</h2>
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<p>Post hoc analysis of two randomized, placebo-controlled, double-blind studies with open-label extensions exploring changes in active function with abobotulinumtoxinA.</p>
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<h2 class="sectionHeading">Setting:</h2>
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<p>Tertiary rehabilitation centers in Australia, Europe, and the United States.</p>
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<h2 class="sectionHeading">Subjects:</h2>
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<p>Adults with upper (<i>n</i> = 254) or lower (<i>n</i> = 345) limb spastic paresis following stroke or brain trauma.</p>
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<h2 class="sectionHeading">Interventions:</h2>
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<p>AbobotulinumtoxinA (⩽5 treatment cycles) in the upper or lower limb.</p>
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<h2 class="sectionHeading">Main measures:</h2>
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<p>X<sub>A</sub> was used to calculate a novel composite measure (CX<sub>A</sub>), defined as the sum of X<sub>A</sub> against elbow, wrist, and extrinsic finger flexors (upper limb) or soleus and gastrocnemius muscles (lower limb). Active function was assessed by the Modified Frenchay Scale and 10-m comfortable barefoot walking speed in the upper limb and lower limb, respectively. Correlations between CX<sub>A</sub> and active function at Weeks 4 and 12 of open-label cycles were explored.</p>
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<h2 class="sectionHeading">Results:</h2>
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<p>CX<sub>A</sub> and active function were moderately correlated in the upper limb (<i>P</i> &lt; 0.0001–0.0004, <i>r</i> = 0.476–0.636) and weakly correlated in the lower limb (<i>P</i> &lt; 0.0001–0.0284, <i>r</i> = 0.186–0.285) at Weeks 4 and 12 of each open-label cycle. Changes in CX<sub>A</sub> and active function were weakly correlated only in the upper limb (Cycle 2 Week 12, <i>P</i> = 0.0160, <i>r</i> = 0.213; Cycle 3 Week 4, <i>P</i> = 0.0031, <i>r</i> = 0.296). Across cycles, CX<sub>A</sub> improvements peaked at Week 4, while functional improvements peaked at Week 12.</p>
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<h2 class="sectionHeading">Conclusion:</h2>
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<p>CX<sub>A</sub> is a valid measure for functional impairments in spastic paresis. CX<sub>A</sub> improvements following abobotulinumtoxinA injection correlated with and preceded active functional improvements.</p>
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<p>via <a href="https://journals.sagepub.com/doi/abs/10.1177/0269215520911970">Composite active range of motion (CXA) and relationship with active function in upper and lower limb spastic paresis &#8211; Nicolas Bayle, Pascal Maisonobe, Romain Raymond, Jovita Balcaitiene, Jean-Michel Gracies,</a></p>
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