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第二代傅里叶域光学相干断层成像术在冠心病患者中的重复性研究及其与血管内超声的比较:应用自动轮廓检测技术的研究。

Interstudy reproducibility of the second generation, Fourier domain optical coherence tomography in patients with coronary artery disease and comparison with intravascular ultrasound: a study applying automated contour detection.

机构信息

Thoraxcenter, Bd 585, Erasmus MC, Dr. Molewaterplein 40, 3015-GD, Rotterdam, The Netherlands.

出版信息

Int J Cardiovasc Imaging. 2013 Jan;29(1):39-51. doi: 10.1007/s10554-012-0067-8. Epub 2012 May 26.

DOI:10.1007/s10554-012-0067-8
PMID:22639296
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3550705/
Abstract

Recently, Fourier domain OCT (FD-OCT) has been introduced for clinical use. This approach allows in vivo, high resolution (15 micron) imaging with very fast data acquisition, however, it requires brief flushing of the lumen during imaging. The reproducibility of such fast data acquisition under intracoronary flush application is poorly understood. To assess the inter-study variability of FD-OCT and to compare lumen morphometry to the established invasive imaging method, IVUS. 18 consecutive patients with coronary artery disease scheduled for PCI were included. In each target vessel a FD-OCT pullback (MGH system, light source 1,310 nm, 105 fps, pullback speed 20 mm/s) was acquired during brief (3 s) injection of X-ray contrast (flow 3 ml/s) through the guiding catheter. A second pullback was repeated under the same conditions after re-introduction of the FD OCT catheter into the coronary artery. IVUS and OCT imaging was performed in random order. FD-OCT and IVUS pullback data were analyzed using a recently developed software employing semi automated lumen contour and stent strut detection algorithms. Corresponding ROI were matched based on anatomical landmarks such as side branches and/or stent edges. Inter-study variability is presented as the absolute difference between the two pullbacks. FD-OCT showed remarkably good reproducibility. Inter-study variability in native vessels (cohort A) was very low for mean and minimal luminal area (0.10 ± 0.38, 0.19 ± 0.57 mm(2), respectively). Likewise inter-study variability was very low in stented coronary segments (cohort B) for mean lumen, mean stent, minimal luminal and minimal stent area (0.06 ± 0.08, 0.07 ± 0.10, 0.04 ± 0.09, 0.04 ± 0.10 mm(2), respectively). Comparison to IVUS morphometry revealed no significant differences. The differences between both imaging methods, OCT and IVUS, were very low for mean lumen, mean stent, minimal luminal and minimal stent area (0.10 ± 0.45, 0.10 ± 0.36, 0.26 ± 0.54, 0.05 ± 0.47 mm(2), respectively). FD-OCT shows excellent reproducibility and very low inter-study variability in both, native and stented coronary segments. No significant differences in quantitative lumen morphometry were observed between FD-OCT and IVUS. Evaluating these results suggest that FD-OCT is a reliable imaging tool to apply in longitudinal coronary artery disease studies.

摘要

最近,傅里叶域光学相干断层扫描(FD-OCT)已被引入临床应用。这种方法允许在体内进行高分辨率(15 微米)成像,并且具有非常快速的数据采集速度,但是在成像过程中需要短暂冲洗管腔。在冠状动脉内冲洗应用下,这种快速数据采集的可重复性尚不清楚。为了评估 FD-OCT 的研究间可重复性,并将管腔形态计量学与已建立的侵入性成像方法 IVUS 进行比较,我们纳入了 18 名计划行 PCI 的冠心病患者。在每个靶血管中,通过引导导管短暂(3 秒)注入 X 射线对比剂(流速 3ml/s),在 FD-OCT 回拉(MGH 系统,光源 1,310nm,105fps,回拉速度 20mm/s)期间获取 FD-OCT 回拉。在将 FD-OCT 导管重新引入冠状动脉后,在相同条件下重复进行第二次回拉。IVUS 和 OCT 成像以随机顺序进行。使用最近开发的软件分析 FD-OCT 和 IVUS 回拉数据,该软件采用半自动管腔轮廓和支架支柱检测算法。基于侧支和/或支架边缘等解剖学标志,将相应的 ROI 匹配。研究间变异性表示两次回拉之间的绝对差异。FD-OCT 显示出极好的可重复性。天然血管(队列 A)的研究间变异性对于平均和最小管腔面积非常低(分别为 0.10±0.38、0.19±0.57mm²)。同样,支架置入的冠状动脉节段(队列 B)的研究间变异性对于平均管腔、平均支架、最小管腔和最小支架面积也非常低(分别为 0.06±0.08、0.07±0.10、0.04±0.09、0.04±0.10mm²)。与 IVUS 形态计量学比较没有发现显著差异。OCT 和 IVUS 两种成像方法之间的差异对于平均管腔、平均支架、最小管腔和最小支架面积非常低(分别为 0.10±0.45、0.10±0.36、0.26±0.54、0.05±0.47mm²)。FD-OCT 在天然和支架置入的冠状动脉节段均显示出极好的可重复性和极低的研究间变异性。FD-OCT 和 IVUS 之间的定量管腔形态计量学没有显著差异。评估这些结果表明,FD-OCT 是一种可靠的成像工具,可应用于冠状动脉疾病的纵向研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5eb7/3550705/93cc7173eed1/10554_2012_67_Fig6_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5eb7/3550705/979ff247a61d/10554_2012_67_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5eb7/3550705/93cc7173eed1/10554_2012_67_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5eb7/3550705/80783c72dc10/10554_2012_67_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5eb7/3550705/07c7266a7995/10554_2012_67_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5eb7/3550705/d14d68929374/10554_2012_67_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5eb7/3550705/121c955046d1/10554_2012_67_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5eb7/3550705/979ff247a61d/10554_2012_67_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5eb7/3550705/93cc7173eed1/10554_2012_67_Fig6_HTML.jpg

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