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Automatic stent strut detection in intravascular OCT images using image processing and classification technique

机译:使用图像处理和分类技术自动检测血管内OCT图像中的支架撑杆

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Intravascular OCT (iOCT) is an imaging modality with ideal resolution and contrast to provide accurate in vivo assessments of tissue healing following stent implantation. Our Cardiovascular Imaging Core Laboratory has served >20 international stent clinical trials with >2000 stents analyzed. Each stent requires 6-16hrs of manual analysis time and we are developing highly automated software to reduce this extreme effort. Using classification technique, physically meaningful image features, forward feature selection to limit overtraining, and leave-one-stent-out cross validation, we detected stent struts. To determine tissue coverage areas, we estimated stent "contours" by fitting detected struts and interpolation points from linearly interpolated tissue depths to a periodic cubic spline. Tissue coverage area was obtained by subtracting lumen area from the stent area. Detection was compared against manual analysis of 40 pullbacks. We obtained recall = 90±3% and precision = 89±6%. When taking struts deemed not bright enough for manual analysis into consideration, precision improved to 94±6%. This approached inter-observer variability (recall = 93%, precision = 96%). Differences in stent and tissue coverage areas are 0.12 ± 0.41 mm2 and 0.09 ± 0.42 mm2, respectively. We are developing software which will enable visualization, review, and editing of automated results, so as to provide a comprehensive stent analysis package. This should enable better and cheaper stent clinical trials, so that manufacturers can optimize the myriad of parameters (drug, coverage, bioresorbable versus metal, etc.) for stent design.
机译:血管内OCT(iOCT)是一种具有理想分辨率和对比度的成像方式,可为支架植入后的组织愈合提供准确的体内评估。我们的心血管成像核心实验室已为> 20项国际支架临床试验提供了服务,分析了> 2000例支架。每个支架需要6到16个小时的手动分析时间,我们正在开发高度自动化的软件以减少这种繁琐的工作。使用分类技术,具有物理意义的图像特征,前向特征选择以限制过度训练以及留出一个支架的交叉验证,我们检测到了支架撑杆。为了确定组织覆盖面积,我们通过将检测到的支柱和从线性内插组织深度到周期性三次样条的内插点进行拟合来估计支架的“轮廓”。通过从支架面积减去管腔面积获得组织覆盖面积。将检测与手动分析40个回调进行了比较。我们得出的召回率= 90±3%,精度= 89±6%。当考虑到不足以进行手动分析的亮度的支柱时,精度提高到94±6%。这接近了观察者之间的差异(召回率= 93%,精度= 96%)。支架和组织覆盖面积的差异分别为0.12±0.41 mm2和0.09±0.42 mm2。我们正在开发可实现自动化结果的可视化,查看和编辑的软件,以提供全面的支架分析软件包。这将使更好,更便宜的支架临床试验成为可能,以便制造商可以优化支架设计的众多参数(药物,覆盖率,可生物吸收性与金属性等)。

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