Feature-maximum-dependency-based fusion diagnosis method for COPD

Chronic Obstructive Pulmonary Disease (COPD) is a chronic lung disease that causes a progressive decline in respiratory function. COPD has become the fourth most lethal disease in the world, and worldwide deaths continue to become more common as a result of COPD. Therefore, it is important to help d...

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Veröffentlicht in:Multimedia tools and applications 2020-06, Vol.79 (21-22), p.15191-15208
Hauptverfasser: Fang, Youli, Wang, Hong, Wang, Lutong, Di, Ruitong, Song, Yongqiang
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Sprache:eng
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Zusammenfassung:Chronic Obstructive Pulmonary Disease (COPD) is a chronic lung disease that causes a progressive decline in respiratory function. COPD has become the fourth most lethal disease in the world, and worldwide deaths continue to become more common as a result of COPD. Therefore, it is important to help doctors diagnose COPD more accurately using big data analytics and effective algorithms. In the past, COPD was mainly studied as follows: applying data to determine the impact of a single feature on the disease, such as the effect of FEV1/FVC (forced expiratory volume in the first second/forced vital capacity), and analyzing a case with simple models, such as logistic regression or a support vector machine. Therefore, there are obviously deficiencies in previous studies. First, the impacts of multi-dimensional features on COPD have not been considered comprehensively. Second, there is no fusion of multiple study methods on the diagnosis and prognosis of COPD. Thus, this paper presents a feature-maximum-dependency-based fusion diagnosis method for COPD. First, the MDF-RS (feature maximum dependency-rough set) algorithm is proposed to extract the optimal combination of multi-dimensional features. Second, the integrated model DSA-SVM (direct search simulated annealing-support vector machine) is presented to classify the disease. Finally, the proposed method is experimentally tested. The results show that the algorithms outperform other classic methods.
ISSN:1380-7501
1573-7721
DOI:10.1007/s11042-018-6876-6