Department of Electronics and Electrical Engineering, Indian Institute of Technology Guwahati, , Guwahati, India.
J R Soc Interface. 2013 Oct 16;10(89):20130761. doi: 10.1098/rsif.2013.0761. Print 2013 Dec 6.
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.
碎裂 QRS 波(f-QRS)已被证明是多种疾病的有效生物标志物,包括远程和急性心肌梗死、心脏结节病、非缺血性心肌病等。与传统标志物(如 Q 波、ST 段抬高等)相比,它的灵敏度和/或特异性更高,而且这些传统标志物可能会随着时间的推移而消退或消失。患有此类疾病的患者必须接受昂贵且有时需要侵入性的检查来进行诊断。自动检测 f-QRS 并识别其各种形态,以及提取常规心电图特征(如 P、QRS、T 波幅度和持续时间等),将比现有方法更可靠地进行诊断、治疗和疾病预后,因此,无论是在基于医院的远程健康监测环境还是在植入式 ICD 设备中,都具有重要的临床意义。本工作提出了一种从心电图中自动检测 f-QRS 并识别其各种形态的算法,据我们所知,这是此类工作中的首例。使用我们最近提出的基于时域形态和基于梯度的心电图特征提取算法,提取 QRS 复合体,并对其应用一级分解的离散小波变换(DWT),使用“Haar”小波,以检测碎片的存在。观察详细的 DWT 系数来假设检测文献中报道的所有类型形态的假设。为了对算法进行建模和验证,使用了 PhysioNet 的 PTB 数据库。从数据库中随机选择了 40 名患者,由两名有经验的心脏病专家检查他们的心电图,并将结果与算法获得的结果进行比较。在 40 名患者中,有 31 名患者被两名心脏病专家认为适合比较,结果表明,从所选的 31 名患者中,有 334 名患者(89.8%)的导联与我们提出的算法相符。检测 f-QRS 的灵敏度和特异性值分别为 0.897 和 0.899。自动化将加快对碎裂的检测,减少人为错误,并允许将其应用于基于医院的远程监测和 ICD 设备。