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Three single leg standing tests for clinical assessment of chronic plantar heel pain syndrome: static stance, half-squat and heel rise

机译:三个单腿站慢性血小板疼痛综合征临床评估试验:静态,半蹲和脚跟上升

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Abstract Objective To assess reliability and validity of three single leg standing clinical tests in patients with plantar heel pain syndrome (PHPS). Design Cross-sectional reliability study. Participants Forty patients diagnosed with PHPS. Main outcome measures Patients stood on their affected foot in a static stance for up to 30 seconds, a half squat for up to 10 repetitions, and a heel rise for up to 10 repetitions. The first sensation of pain (p1) determined the termination of each test, and established a positive test result. The level of p1 was measured using a visual analogue scale (VAS); time or repetitions for each test were recorded. Prior to performing the tests, all patients completed the Foot & Ankle Computerized Adaptive Test to measure functional status (FS). Results Detection of p1 in each test showed good reliability for inter- and intrarater assessment (Kappa = 0.60 to 0.78 and 0.56 to 0.77, respectively). The intraclass correlation coefficient for the VAS measures was 0.85 to 0.95 for inter-rater assessment and 0.78 to 0.92 for intrarater assessment. However, the Bland and Altman limits of agreement were wide, indicating that these measures were less reliable than the correlation coefficients suggested. Thirty-five patients (88%) experienced a positive pain response to at least one test. Significant correlations were found between the VAS measures in each test and FS ( r = 0.63 to 0.72). Conclusions The static stance, half squat and heel rise tests were easily implemented, and found to be reliable and valid according to one analysis, yet less reliable with another, for pain provocation and VAS levels in patients with PHPS. All three VAS levels correlated well with FS. ]]>
机译:摘要目的评估跖跖疼痛综合征(PHPS)患者三个单腿站立临床试验的可靠性和有效性。设计横截面可靠性研究。参与者诊断患有PHP的患者。主要结果措施患者在受影响的脚上静态脚下持续30秒,半蹲半蹲,最多10次重复,脚跟高达10次重复。疼痛的第一个感觉(P1)确定了每个测试的终止,并建立了阳性测试结果。使用视觉模拟量表(VAS)测量P1的水平;记录每个测试的时间或重复。在进行测试之前,所有患者都完成了足部&脚踝计算机化自适应测试来测量功能状态(FS)。结果检测每次测试中的P1显示出可靠的可靠性,适用于和内部评估(Kappa = 0.60至0.78和0.56至0.77)。对于检测室内评估,VAS措施的腹积相关系数为0.85至0.95,用于检测到0.78至0.92。然而,平淡的协议和Altman限制很大,表明这些措施比表达的相关系数更可靠。三十五名患者(88%)对至少一次测试产生阳性疼痛反应。在每个测试和Fs(r = 0.63至0.72)之间的VAS措施之间发现了显着的相关性。结论静态姿势,半蹲和鞋跟上升试验均可轻松实现,发现根据一种分析,但与其他患者疼痛挑衅和VAS水平不那么可靠,且患有疼痛挑衅和VAS水平可靠且有效。所有三个VAS级别都与FS相关。 ]]>

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