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Discrimination of pain intensity level and side effects of postoperative pain using parameters extracted from the evoked pain pattern

机译:使用从诱发的疼痛模式中提取的参数来区分疼痛强度水平和术后疼痛的副作用

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摘要

The value of evoked potentials (EPs) in the clinical assessment of physiological function has been recognized for some time by those with specialized neurophysiological interests. Based on this concept, we have applied this novel technique for discrimination of pain intensity level and side effects using time-domain parameters extracted from the evoked pain pattern (EPP) in postoperative pain via patient-controlled analgesia (PCA). In conventional PCA systems, each delivery is similar to evoked pain stimulation, and we then count the following demands in a lockout interval. Therefore, the EPP is calculated and averaged from several lockout intervals in a period of time. From this calculation, the evoked parameters of area, latency, and amplitude of each period of time can be easily extracted. A total of 741 cases from 1519 patients at a medical center have been screened and compared with these three parameters using different visual analog scales (VAS) and side effects (SE). The results indicate that the area parameter is a good indicator for higher VAS patients and the variance of latency parameter is a better outcome for interpreting the patients with SE. However, the amplitude parameter shows no significant differences in both VAS and SE groups. Using massive information from clinical trials and a novel technique of evoked pain stimulation algorithm, we demonstrate that evoked parameters (i.e. area and latency) can serve as indicators to assess various clinical evidences, such as VAS and SE associated with postoperative pain.
机译:具有专门的神经生理学兴趣的人已经认识到诱发电位(EPs)在生理功能临床评估中的价值已有一段时间。基于此概念,我们已使用这种新技术,通过从患者自控镇痛(PCA)术后疼痛中诱发的疼痛模式(EPP)提取的时域参数来区分疼痛强度水平和副作用。在传统的PCA系统中,每次传递类似于诱发的疼痛刺激,然后我们在锁定间隔中计算以下需求。因此,根据一段时间内的几个锁定间隔来计算EPP并将其平均。从该计算中,可以容易地提取每个时间段的面积,等待时间和幅度的诱发参数。从医疗中心的1519名患者中筛选出741例病例,并使用不同的视觉模拟量表(VAS)和副作用(SE)与这三个参数进行比较。结果表明,面积参数是较高VAS患者的良好指标,潜伏期参数的变化是解释SE患者的较好结果。但是,幅度参数在VAS和SE组中均没有显示出显着差异。使用来自临床试验的大量信息和诱发疼痛刺激算法的新技术,我们证明诱发参数(即面积和潜伏期)可以用作评估各种临床证据的指标,例如与术后疼痛相关的VAS和SE。

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