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An automated algorithm for online detection of fragmented QRS and identification of its various morphologies

机译:在线检测碎片QRS并识别其各种形态的自动算法

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摘要

Fragmented QRS (f-QRS) has been proven to be an efficient biomarker for several diseases, including remote and acute myocardial infarction, cardiac sarcoidosis, non-ischaemic cardiomyopathy, etc. It has also been shown to have higher sensitivity and/or specificity values than the conventional markers (e.g. Q-wave, ST-elevation, etc.) which may even regress or disappear with time. Patients with such diseases have to undergo expensive and sometimes invasive tests for diagnosis. Automated detection of f-QRS followed by identification of its various morphologies in addition to the conventional ECG feature (e.g. P, QRS, T amplitude and duration, etc.) extraction will lead to a more reliable diagnosis, therapy and disease prognosis than the state-of-the-art approaches and thereby will be of significant clinical importance for both hospital-based and emerging remote health monitoring environments as well as for implanted ICD devices. An automated algorithm for detection of f-QRS from the ECG and identification of its various morphologies is proposed in this work which, to the best of our knowledge, is the first work of its kind. Using our recently proposed time–domain morphology and gradient-based ECG feature extraction algorithm, the QRS complex is extracted and discrete wavelet transform (DWT) with one level of decomposition, using the ‘Haar’ wavelet, is applied on it to detect the presence of fragmentation. Detailed DWT coefficients were observed to hypothesize the postulates of detection of all types of morphologies as reported in the literature. To model and verify the algorithm, PhysioNet's PTB database was used. Forty patients were randomly selected from the database and their ECG were examined by two experienced cardiologists and the results were compared with those obtained from the algorithm. Out of 40 patients, 31 were considered appropriate for comparison by two cardiologists, and it is shown that 334 out of 372 (89.8%) leads from the chosen 31 patients complied favourably with our proposed algorithm. The sensitivity and specificity values obtained for the detection of f-QRS were 0.897 and 0.899, respectively. Automation will speed up the detection of fragmentation, reducing the human error involved and will allow it to be implemented for hospital-based remote monitoring and ICD devices.
机译:碎片QRS(f-QRS)已被证明是多种疾病的有效生物标志物,包括远端和急性心肌梗塞,心脏结节病,非缺血性心肌病等。它还被证明具有更高的敏感性和/或特异性值比常规标记(例如Q波,ST高度等)随时间变化甚至消失或消失。患有此类疾病的患者必须接受昂贵且有时是侵入性的检查才能诊断。 f-QRS的自动检测,然后识别其除常规ECG功能(例如P,QRS,T幅度和持续时间等)外的各种形态,将比状态更可靠的诊断,治疗和疾病预后先进的方法,因此对于基于医院和新兴的远程健康监控环境以及植入的ICD设备都具有重要的临床意义。在这项工作中,提出了一种用于从ECG中检测f-QRS并识别其各种形态的自动算法,据我们所知,这是同类研究中的第一项工作。使用我们最近提出的时域形态学和基于梯度的ECG特征提取算法,提取QRS复杂度,并使用“ Haar”小波对具有一个分解级别的离散小波变换(DWT)进行检测,以检测是否存在碎片化。观察到了详细的DWT系数,以推测检测文献中报道的所有类型形态的假设。为了建模和验证算法,使用了PhysioNet的PTB数据库。从数据库中随机选择40名患者,由两名经验丰富的心脏病专家检查他们的ECG,并将结果与​​从算法中获得的结果进行比较。在40位患者中,有21位心脏病专家认为31位适合进行比较,结果表明,从所选择的31位患者中的372位中有334位(占89.8%)线索符合我们提出的算法。用于检测f-QRS的灵敏度和特异性值分别为0.897和0.899。自动化将加快碎片检测的速度,减少涉及的人为错误,并将其实现为基于医院的远程监控和ICD设备。

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