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The responsiveness of the Action Research Arm test and the Fugl-Meyer Assessment scale in chronic stroke patients.

机译:行动研究臂测试和Fugl-Meyer评估量表对慢性卒中患者的反应性。

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The responsiveness of the Action Research Arm (ARA) test and the upper extremity motor section of the Fugl-Meyer Assessment (FMA) scale were compared in a cohort of 22 chronic stroke patients undergoing intensive forced use treatment aimed at improvement of upper extremity function. The cohort consisted of 13 men and 9 women, median age 58.5 years, median time since stroke 3.6 years. Responsiveness was defined as the sensitivity of an instrument to real change. Two baseline measurements were performed with a 2-week interval before the intervention, and a follow-up measurement after 2 weeks of intensive forced use treatment. The limits of agreement, according to the Bland-Altman method, were computed as a measure of the test-retest reliability. Two different measures of responsiveness were compared: (i) the number of patients who improved more than the upper limit of agreement during the intervention; (ii) the responsiveness ratio. The limits of agreement, designating the interval comprising 95% of the differences between two measurements in a stable individual, were -5.7 to 6.2 and -5.0 to 6.6 for the ARA test and the FMA scale, respectively. The possible sum scores range from 0 to 57 (ARA) and from 0 to 66 (FMA). The number of patients who improved more than the upper limit were 12 (54.5%) and 2 (9.1%); and the responsiveness ratios were 2.03 and 0.41 for the ARA test and the FMA scale, respectively. These results strongly suggest that the ARA test is more responsive to improvement in upper extremity function than the FMA scale in chronic stroke patients undergoing forced use treatment.
机译:比较了22名接受强力使用治疗以改善上肢功能的慢性卒中患者的行动研究组(ARA)测试和Fugl-Meyer评估(FMA)量表的上肢运动部分的反应能力。该队列由13名男性和9名女性组成,中位年龄为58.5岁,自中风以来的中位时间为3.6年。响应能力定义为工具对真实变化的敏感性。在干预前以2周为间隔进行两次基线测量,在密集使用2周后进行随访测量。根据Bland-Altman方法,计算一致极限作为重新测试信度的度量。比较了两种不同的反应程度:(i)干预期间改善超过协议上限的患者人数; (ii)回应率。 ARA检验和FMA标度的一致性极限(分别表示稳定个体中两次测量之间的差异的95%)指定为-5.7至6.2和-5.0至6.6。可能的总分范围为0到57(ARA)和0到66(FMA)。超过上限的患者人数分别为12(54.5%)和2(9.1%); ARA测试和FMA量表的响应率分别为2.03和0.41。这些结果有力地表明,在接受强制使用治疗的慢性卒中患者中,ARA测试对上肢功能的改善比FMA评分更敏感。

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