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首页> 外文期刊>Chiropractic and Manual Therapies >Investigator analytic repeatability of two new intervertebral motion biomarkers for chronic, nonspecific low back pain in a cohort of healthy controls
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Investigator analytic repeatability of two new intervertebral motion biomarkers for chronic, nonspecific low back pain in a cohort of healthy controls

机译:调查仪两种新椎间运动生物标志物的分析重复性慢性,非特异性低腰疼痛在健康对照组

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摘要

Understanding the mechanisms underlying chronic, nonspecific low back pain (CNSLBP) is essential to advance personalized care and identify the most appropriate intervention. Recently, two intervertebral motion biomarkers termed “Motion Sharing Inequality” (MSI) and “Motion Sharing Variability” (MSV) have been identified for CNSLBP using quantitative fluoroscopy (QF). The aim of this study was to conduct intra- and inter-investigator analytic repeatability studies to determine the extent to which investigator error affects their measurement in clinical studies. A cross-sectional cohort study was conducted using the image sequences of 30 healthy controls who received QF screening during passive recumbent flexion motion. Two independent investigators analysed the image sequences for MSI and MSV from October to November 2018. Intra and inter- investigator repeatability studies were performed using intraclass correlations (ICC), standard errors of measurement (SEM) and minimal differences (MD). Intra-investigator ICCs were 0.90 (0.81,0.95) (SEM 0.029) and 0.78 (0.59,0.89) (SEM 0.020) for MSI and MSV, respectively. Inter-investigator ICCs 0.93 (0.86,0.97) (SEM 0.024) and 0.55 (0.24,0.75) (SEM 0.024). SEMs for MSI and MSV were approximately 10 and 30% of their group means respectively. The MDs for MSI for intra- and inter-investigator repeatability were 0.079 and 0.067, respectively and for MSV 0.055 and 0.067. MSI demonstrated substantial intra- and inter-investigator repeatability, suggesting that investigator input has a minimal influence on its measurement. MSV demonstrated moderate intra-investigator reliability and fair inter-investigator repeatability. Confirmation in patients with CNSLBP is now required.
机译:了解慢性慢性的机制,非特异性低腰疼痛(CNSLBP)对于推进个性化护理并确定最合适的干预至关重要。最近,已经使用定量荧光透视(QF)对CNSLBP鉴定出“运动共享不等式”(MSI)和“运动共享变异性”(MSV)的两个椎间运动生物标志物。本研究的目的是进行血内研究所和中间分析重复性研究,以确定研究者误差影响其在临床研究中的测量的程度。使用30个健康对照的图像序列进行横截面队列研究,该序列是在被动斜倚屈曲运动中接受QF筛选的健康对照。两位独立的调查人员分析了MSI和MSV的图像序列于2018年10月至11月。使用脑内相关性(ICC),测量标准误差(SEM)和最小差异(MD)进行帧内和研究员重复性研究。研究内ICC分别为0.90(0.81,0.95)(SEM 0.029)和0.78(0.59,0.89)(SEM 0.020),用于MSI和MSV。 INCOR-ICCS 0.93(0.86,0.97)(SEM 0.024)和0.55(0.24,0.75)(SEM 0.024)。 MSI和MSV的SEM分别约为10%和30%的组手段。用于分别的MSI的MDS用于分别为0.079%和0.067,用于MSV 0.055和0.067。 MSI展示了大量的调查室内和研究员重复性,表明研究者输入对其测量有最小的影响。 MSV展示了中生研究员可靠性和公平的调查室可重复性。现在需要CNSLBP患者的确认。

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