首页> 外文会议>IEEE Ultrasonics Symposium >Quantification and MRI Validation of Regional Cardiac Contractile Dysfunction in Mice Post Myocardial Infarction Using High Resolution Ultrasound
【24h】

Quantification and MRI Validation of Regional Cardiac Contractile Dysfunction in Mice Post Myocardial Infarction Using High Resolution Ultrasound

机译:使用高分辨率超声术后小鼠区域心脏收缩功能障碍的定量和MRI验证

获取原文

摘要

High resolution 30 MHz ultrasound imaging was performed on the left ventricles (LV) of C57Bl/6 mice post myocardial infarction (MI). Normal (no MI) C57Bl/6 mice were examined as control experiments. Ultrasound imaging was performed at 5-7 short axis slices and 4-5 long axis slices at 1 mm intervals that encompass the LV. Myocardial tissue displacement vectors were measured using a 2D ultrasonic speckle tracking algorithm with sub-pixel resolution. The pixel block window size was approximately 0.4 mm X 0.4 mm and the search region was 0.6 mm X 0.6 mm. The extent of contractile dysfunction and cardiac dyssynchrony were revealed in post-MI mouse LVs by regional myocardial displacement and strain analyses. Strain analyses from the mid-ventricular short axis based upon the ultrasound images were compared to those obtained using MRI, and high levels of correlation were obtained (R velence 0.91 and R velence 0.84 for radial and circumferential strain, respectively). Displacement and strain analyses were conducted on multiple short axis and long axis slices, and 3D displacement vectors were determined at the lines of intersection by summing the vector components derived from each of the orthogonal slices.
机译:在心肌梗死后C57BL / 6小鼠的左心室(LV)上进行高分辨率30MHz超声成像。检查正常(NO MI)C57BL / 6小鼠作为对照实验。超声成像在5-7个短轴切片和4-5个长轴切片处,以1毫米的间隔,包括LV。使用具有子像素分辨率的2D超声波斑点跟踪算法测量心肌组织位移向量。像素块窗口尺寸约为0.4mm×0.4mm,搜索区域为0.6 mm×0.6mm。通过区域心肌位移和应变分析,在MI小鼠LV中揭示了收缩功能障碍和心脏失效程度的程度。将基于超声图像的中间室短轴进行应变分析与使用MRI获得的那些,获得高水平的相关性(分别用于径向和周向rslence 0.84)。位移和应变分析在多个短轴和长轴切片上进行,并且通过求解来自每个正交切片的矢量分量在交叉线上确定3D位移向量。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号