Japee Shruti A, Ellis Christopher G, Pittman Roland N
Department of Biomedical Engineering, Medical College of Virginia Campus, Virginia Commonwealth University, Richmond, VA 23298, USA.
Microcirculation. 2004 Jan-Feb;11(1):39-54. doi: 10.1080/10739680490266171.
Video recordings of red blood cell (RBC) flow through capillary networks contain a considerable amount of information pertaining to oxygen transport through the microcirculation. Image analysis of these video recordings has been widely used to determine RBC dynamics (velocity, lineal density and supply rate) and oxygenation (Brunner et al., 2000; Ellis et al., 1990, 1992; Ellsworth et al., 1987; Klyscz et al., 1997; Pries 1988). However, not all capillaries in a given field of view are suitable for image analysis. Typically, capillary segments that are relatively straight and in sharp focus, and exhibit flow of individual RBCs that are well separated by plasma gaps, are good candidates for analysis. We have developed several image processing tools to aid in the selection of such capillaries for analysis and to obtain quick overviews of RBC flow through the microcirculation.
Burgess et al. (Microcirc. 2:75, 1995) and Burkell et al. (Annals Biomed. Eng. 24:1, 1996; J. Vasc. Res. 35:2, 1998) have previously introduced mean and variance images to aid in the selection of capillaries for analysis. We have extended their concept and developed similar two dimensional visualization techniques for studies of RBC flow through capillary networks.
Five new methods of processing video data were developed. The minimum image highlights all capillaries containing RBCs in a given field of view. The maximum image identifies capillaries that exhibit high lineal density or stopped flow. The range image represents the difference between the maximum and minimum light intensity values that occur at a given pixel over a given time period, and helps to identify capillary segments that are in good focus and are perfused by RBCs and plasma. The difference image represents the cumulative sum of the square of differences in intensity values between consecutive frames and gives an indication of the frequency of passage of RBCs separated by plasma gaps. The transition image represents the number of times the intensity at a given pixel crosses a predefined threshold and indicates the number of RBCs (or trains of RBCs) that passes a given location during the observation period.
The above flow visualization techniques are valuable tools to aid in the study of image focus, network geometry, RBC flow paths and dynamics, that can then be used in identifying capillaries for subsequent (separate) detailed analysis to provide quantitative information about RBC flow.
红细胞(RBC)流经毛细血管网络的视频记录包含了大量与通过微循环进行氧运输相关的信息。对这些视频记录进行图像分析已被广泛用于确定红细胞动力学(速度、线性密度和供应率)以及氧合作用(Brunner等人,2000年;Ellis等人,1990年、1992年;Ellsworth等人,1987年;Klyscz等人,1997年;Pries,1988年)。然而,在给定视野中的并非所有毛细血管都适合进行图像分析。通常,相对笔直且聚焦清晰、单个红细胞流被血浆间隙充分分隔的毛细血管段是分析的良好候选对象。我们开发了几种图像处理工具,以帮助选择此类毛细血管进行分析,并快速获取红细胞流经微循环的概况。
Burgess等人(《微循环》2:75,1995年)和Burkell等人(《生物医学工程年鉴》24:1,1996年;《血管研究杂志》35:2,1998年)此前已引入均值和方差图像来帮助选择用于分析的毛细血管。我们扩展了他们的概念,并开发了类似的二维可视化技术用于研究红细胞流经毛细血管网络。
开发了五种处理视频数据的新方法。最小图像突出显示给定视野中所有含有红细胞的毛细血管。最大图像识别出呈现高线密度或血流停滞的毛细血管。范围图像表示在给定时间段内给定像素处出现的最大和最小光强度值之间的差异,并有助于识别聚焦良好且有红细胞和血浆灌注的毛细血管段。差异图像表示连续帧之间强度值差异的平方的累积和,并给出了被血浆间隙分隔的红细胞通过频率的指示。过渡图像表示给定像素处的强度越过预定义阈值的次数,并指示在观察期内通过给定位置的红细胞(或红细胞序列)数量。
上述血流可视化技术是有助于研究图像聚焦、网络几何形状、红细胞流动路径和动力学的宝贵工具,然后可用于识别毛细血管以便后续(单独)进行详细分析,以提供有关红细胞流动的定量信息。