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The validation of a new actigraphy system for the measurement of periodic leg movements in sleep.

机译:验证了用于测量睡眠中腿部周期性运动的新书法系统的有效性。

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BACKGROUND AND PURPOSE: To determine the accuracy of a new actigraphy system for the measurement of periodic leg movements (PLMs). Continuous measurements of leg movements, made overnight, are essential to diagnose and monitor treatment for PLMs. We have developed the Actiwatch with Cambridge Neuro-Technology Ltd (Cambridge, UK) to detect leg movements consistent with PLMs, to record these movements from both feet over three consecutive nights and to report standard indices of PLMs. We describe three studies designed to validate this device. PATIENTS AND METHODS: The Actiwatch was assessed on a bench model across a range of movement amplitudes. The level of agreement on individual movements between the Actiwatch and bilateral anterior tibialis electromyography (BATEMG) measures was assessed in 199 epochs from five patients with known PLMs. The ability of the Actiwatch to correctly identify patients with PLMs was assessed in a comparison with polysomnography (PSG) in 50 consecutive patients investigatedin the sleep laboratory. RESULTS: The Actiwatch detected all mechanically generated movements (100% sensitivity and 100% specificity) on the bench test. On individual movements BATEMG measurement and the Actiwatch agreed on 94% of epochs. The sensitivity and specificity of the Actiwatch to detect leg movements in severe PLMs as defined by BATEMG (PLMI>/=25) are high (100% sensitive and 97% specific). Our bilateral system gave better agreement with BATEMG than previous systems but the two measures are still not interchangeable. CONCLUSIONS: EMG is only a surrogate measure of limb movement and indices measured in this way correlate poorly with symptoms. We have demonstrated that the Actiwatch faithfully records movement, which offers the potential to reassess the relationships between limb movement indices and symptoms. This which offers a convenient and economical alternative to PSG in the study of large populations to increase our understanding of the epidemiology and clinical significance of PLMs.
机译:背景与目的:确定用于测量周期性腿部运动(PLM)的新书法系统的准确性。一夜之间连续测量腿部运动对于诊断和监测PLM的治疗至关重要。我们与剑桥神经技术有限公司(英国剑桥)合作开发了Actiwatch,以检测与PLM一致的腿部运动,记录连续三个晚上双脚的这些运动,并报告PLM的标准指标。我们描述了旨在验证该设备的三项研究。患者和方法:Actiwatch在台式模型上评估了一系列运动幅度。在5个已知PLM患者的199个时期中,评估了Actiwatch和双侧胫前肌肌电图(BATEMG)措施之间个体运动的一致性水平。在睡眠实验室调查的50位连续患者中,与多导睡眠图(PSG)进行了比较,评估了Actiwatch正确识别PLM患者的能力。结果:Actiwatch在台式试验中检测到所有机械产生的运动(灵敏度为100%,特异性为100%)。在个人机芯上,BATEMG测量和Actiwatch达成了94%的纪元。如BATEMG(PLMI> / = 25)所定义,Actiwatch在严重PLM中检测腿部运动的灵敏度和特异性很高(灵敏性为100%,特异性为97%)。与以前的系统相比,我们的双边系统与BATEMG的协议更好,但是这两项措施仍然不能互换。结论:肌电图只是肢体运动的替代指标,以这种方式测量的指标与症状的相关性很差。我们已经证明Actiwatch忠实地记录了运动,这提供了重新评估肢体运动指标和症状之间关系的潜力。这为大人群研究提供了一种便捷,经济的替代PSG的方法,以加深我们对PLM的流行病学和临床意义的了解。

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