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A Multichannel Acoustic Approach to Define a Pulmonary Pathology as Combined Pulmonary Fibrosis and Emphysema Syndrome

机译:多通道声学方法,以定义肺部病理学,肺纤维化和肺气肿综合征

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Interstitial lung diseases (ILDs) have been increasing their relevance in loss of lives according to a recent world wide medical information. Idiopathic pulmonary fibrosis (IPF) and combined pulmonary fibrosis and emphysema syndrome (CPFES) belong to ILD class with the latter having a limited survival prognosis. In clinical environment high resolution computed tomography (HRCT) is used to detect CPFE; however, there is still controversy about the amount of emphysema observed in HRCT to declare CPFES. Consequently, to help in the diagnosis of CPFES to develop an alternative technique seems to be attractive. In this study, we propose a multichannel acoustic approach to discriminate between IPF and CPFES parameterizing the multichannel lung sounds information linearly and classifying it by neural networks (NN). The NN performance using different features provided values above 90% in the validation phase. Furthermore, to test the trained NN, the proposed approach was applied on new data from five patients 3 diagnosed by experts as CPFES and 2 with IPF. The univariate autoregressive model obtained the best classification followed by the feature vector formed by the percentile frequencies augmented by the total power of the acoustic information. Results indicate that multichannel acoustic analysis is promising to discern between these two ILDs.
机译:根据最近的全球医疗信息,间质肺病(ILDS)一直在增加其丧失生活中的相关性。特发性肺纤维化(IPF)和肺纤维化和肺气肿综合征(CPFES)属于ILD类,后者存在有限的存活预后。在临床环境中,使用高分辨率计算断层扫描(HRCT)来检测CPFE;但是,关于在HRCT中观察到的呼气液的量仍然存在争议,以宣布CPFES。因此,为了帮助诊断CPFE开发替代技术似乎有吸引力。在这项研究中,我们提出了一种多通道声学方法来区分IPF和CPFES参数,参数化多通道肺部的信息线性和通过神经网络(NN)对其进行分类。使用不同特征的NN性能在验证阶段提供高于90%的值。此外,为了测试培训的NN,将所提出的方法从专家诊断为CPFES和IPF诊断的5例患者3患者的新数据上应用。单变量自动增加模型获得了最佳分类,然后是由百分位频率形成的特征向量,由声信息的总功率增强。结果表明,多通道声学分析在这两个ILD之间具有辨别。

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