Tissue characterization with depthresolved attenuation coefficient and backscatter term in intravascular optical coherence tomography images
Shengnan Liu (Leiden University Medical Center)
Yohei Sotomi (Amsterdam UMC)
Jeroen Eggermont (Leiden University Medical Center)
Gaku Nakazawa (Tokai University)
Sho Torii (Tokai University)
Takeshi Ijichi (Tokai University)
Yoshinobu Onuma (Erasmus MC, Cardialysis)
Patrick W. Serruys (Imperial College London)
Boudewijn P.F. Lelieveldt (TU Delft - Electrical Engineering, Mathematics and Computer Science, Leiden University Medical Center)
Jouke Dijkstra (Leiden University Medical Center)
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Abstract
An important application of intravascular optical coherence tomography (IVOCT) for atherosclerotic tissue analysis is using it to estimate attenuation and backscatter coefficients. This work aims at exploring the potential of the attenuation coefficient, a proposed backscatter term, and image intensities in distinguishing different atherosclerotic tissue types with a robust implementation of depth-resolved (DR) approach. Therefore, the DR model is introduced to estimate the attenuation coefficient and further extended to estimate the backscatter-related term in IVOCT images, such that values can be estimated per pixel without predefining any delineation for the estimation. In order to exclude noisy regions with a weak signal, an automated algorithm is implemented to determine the cut-off border in IVOCT images. The attenuation coefficient, backscatter term, and the image intensity are further analyzed in regions of interest, which have been delineated referring to their pathology counterparts. Local statistical values were reported and their distributions were further compared with a two-sample t -test to evaluate the potential for distinguishing six types of tissues. Results show that the IVOCT intensity, DR attenuation coefficient, and backscatter term extracted with the reported implementation are complementary to each other on characterizing six tissue types: mixed, calcification, fibrous, lipid-rich, macrophages, and necrotic core.