TY - JOUR
T1 - A novel method of artery stenosis diagnosis using transfer function and support vector machine based on transmission line model
T2 - A numerical simulation and validation study
AU - Xiao, Hanguang
AU - Avolio, Alberto
AU - Huang, Decai
PY - 2016/6/1
Y1 - 2016/6/1
N2 - Background and objective: Transfer function (TF) is an important parameter for the analysis and understanding of hemodynamics when arterial stenosis exists in human arterial tree. Aimed to validate the feasibility of using TF to diagnose arterial stenosis, the forward problem and inverse problem were simulated and discussed. Methods: A calculation method of TF between ascending aorta and any other artery was proposed based on a 55 segment transmission line model (TLM) of human artery tree. The effects of artery stenosis on TF were studied in two aspects: stenosis degree and position. The degree of arterial stenosis was specified to be 10-90% in three representative arteries: carotid, aorta and iliac artery, respectively. In order to validate the feasibility of diagnosis of artery stenosis using TF and support vector machine (SVM), a database of TF was established to simulate the real conditions of artery stenosis based on the TLM model. And a diagnosis model of artery stenosis was built by using SVM and the database. Results: The simulating results showed the modulus and phase of TF were decreasing sharply from frequency 2 to 10 Hz with the stenosis degree increasing and displayed their unique and nonlinear characteristics when frequency is higher than 10 Hz. The diagnosis results showed the average accuracy was above 76% for the stenosis from 10% to 90% degree, and the diagnosis accuracies of moderate (50%) and serious (90%) stenosis were 87% and 99%, respectively. When the stenosis degree increased to 90%, the accuracy of stenosis localization reached up to 94% for most of arteries. Conclusions: The proposed method of combining TF and SVM is a theoretically feasible method for diagnosis of artery stenosis.
AB - Background and objective: Transfer function (TF) is an important parameter for the analysis and understanding of hemodynamics when arterial stenosis exists in human arterial tree. Aimed to validate the feasibility of using TF to diagnose arterial stenosis, the forward problem and inverse problem were simulated and discussed. Methods: A calculation method of TF between ascending aorta and any other artery was proposed based on a 55 segment transmission line model (TLM) of human artery tree. The effects of artery stenosis on TF were studied in two aspects: stenosis degree and position. The degree of arterial stenosis was specified to be 10-90% in three representative arteries: carotid, aorta and iliac artery, respectively. In order to validate the feasibility of diagnosis of artery stenosis using TF and support vector machine (SVM), a database of TF was established to simulate the real conditions of artery stenosis based on the TLM model. And a diagnosis model of artery stenosis was built by using SVM and the database. Results: The simulating results showed the modulus and phase of TF were decreasing sharply from frequency 2 to 10 Hz with the stenosis degree increasing and displayed their unique and nonlinear characteristics when frequency is higher than 10 Hz. The diagnosis results showed the average accuracy was above 76% for the stenosis from 10% to 90% degree, and the diagnosis accuracies of moderate (50%) and serious (90%) stenosis were 87% and 99%, respectively. When the stenosis degree increased to 90%, the accuracy of stenosis localization reached up to 94% for most of arteries. Conclusions: The proposed method of combining TF and SVM is a theoretically feasible method for diagnosis of artery stenosis.
UR - http://www.scopus.com/inward/record.url?scp=84961838036&partnerID=8YFLogxK
U2 - 10.1016/j.cmpb.2016.03.005
DO - 10.1016/j.cmpb.2016.03.005
M3 - Article
C2 - 27084322
AN - SCOPUS:84961838036
SN - 0169-2607
VL - 129
SP - 71
EP - 81
JO - Computer Methods and Programs in Biomedicine
JF - Computer Methods and Programs in Biomedicine
ER -