Translational Medicine Branch, Division of Intramural Research, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892-1538, USA.
Med Phys. 2011 Jan;38(1):125-41. doi: 10.1118/1.3523621.
In X-ray fused with MRI, previously gathered roadmap MRI volume images are overlaid on live X-ray fluoroscopy images to help guide the clinician during an interventional procedure. The incorporation of MRI data allows for the visualization of soft tissue that is poorly visualized under X-ray. The widespread clinical use of this technique will require fully automating as many components as possible. While previous use of this method has required time-consuming manual intervention to register the two modalities, in this article, the authors present a fully automatic rigid-body registration method.
External fiducial markers that are visible under these two complimentary imaging modalities were used to register the X-ray images with the roadmap MR images. The method has three components: (a) The identification of the 3D locations of the markers from a full 3D MR volume, (b) the identification of the 3D locations of the markers from a small number of 2D X-ray fluoroscopy images, and (c) finding the rigid-body transformation that registers the two point sets in the two modalities. For part (a), the localization of the markers from MR data, the MR volume image was thresholded, connected voxels were segmented and labeled, and the centroids of the connected components were computed. For part (b), the X-ray projection images, produced by an image intensifier, were first corrected for distortions. Binary mask images of the markers were created from the distortion-corrected X-ray projection images by applying edge detection, pattern recognition, and image morphological operations. The markers were localized in the X-ray frame using an iterative backprojection-based method which segments voxels in the volume of interest, discards false positives based on the previously computed edge-detected projections, and calculates the locations of the true markers as the centroids of the clusters of voxels that remain. For part (c), a variant of the iterative closest point method was used to find correspondences between and register the two sets of points computed from MR and X-ray data. This knowledge of the correspondence between the two point sets was used to refine, first, the X-ray marker localization and then the total rigid-body registration between modalities. The rigid-body registration was used to overlay the roadmap MR image onto the X-ray fluoroscopy projections.
In 35 separate experiments, the markers were correctly registered to each other in 100% of the cases. When half the number of X-ray projections was used (10 X-ray projections instead of 20), the markers were correctly registered in all 35 experiments. The method was also successful in all 35 experiments when the number of markers was (retrospectively) halved (from 16 to 8). The target registration error was computed in a phantom experiment to be less than 2.4 mm. In two in vivo experiments, targets (interventional devices with pointlike metallic structures) inside the heart were successfully registered between the two modalities.
The method presented can be used to automatically register a roadmap MR image to X-ray fluoroscopy using fiducial markers and as few as ten X-ray projections.
在 X 射线与 MRI 融合中,先前采集的路标 MRI 体图像被叠加在实时 X 射线透视图像上,以帮助临床医生在介入手术中进行引导。MRI 数据的加入允许显示在 X 射线下难以可视化的软组织。这项技术的广泛临床应用将需要尽可能自动完成尽可能多的组件。虽然以前使用这种方法需要耗时的手动干预来注册两种模式,但在本文中,作者提出了一种完全自动的刚体配准方法。
在这两种互补成像模式下可见的外部基准标记物用于将 X 射线图像与路标 MR 图像配准。该方法有三个组成部分:(a)从完整的 3D MR 体中识别标记物的 3D 位置,(b)从少量 2D X 射线透视图像中识别标记物的 3D 位置,以及(c)找到将两个点集在两个模式中进行配准的刚体变换。对于部分(a),从 MR 数据中定位标记物,将 MR 体图像阈值化,分割连通体并进行标记,并计算连通分量的质心。对于部分(b),通过图像增强器产生的 X 射线投影图像首先进行失真校正。通过应用边缘检测、模式识别和图像形态学操作,从失真校正的 X 射线投影图像中创建标记物的二进制掩模图像。使用基于迭代反向投影的方法在 X 射线框架中定位标记物,该方法分割感兴趣体积中的体素,根据先前计算的边缘检测投影丢弃假阳性,并将真实标记物的位置计算为剩余体素聚类的质心。对于部分(c),使用迭代最近点方法的变体来找到从 MR 和 X 射线数据计算的两个点集之间的对应关系并进行配准。这种对两个点集之间对应关系的了解用于首先改进 X 射线标记物定位,然后改进模态之间的总刚体配准。刚体配准用于将路标 MR 图像叠加到 X 射线透视投影上。
在 35 次单独的实验中,标记物在 100%的情况下正确地相互配准。当使用 X 射线投影数量的一半(从 20 个减少到 10 个)时,在所有 35 个实验中,标记物都正确配准。当标记物数量(事后)减半(从 16 个减少到 8 个)时,该方法在所有 35 个实验中也取得了成功。在一个体模实验中,目标配准误差计算值小于 2.4 毫米。在两项体内实验中,心脏内的介入设备(带有点状金属结构的设备)成功地在两种模式之间进行了配准。
所提出的方法可用于使用基准标记物和少至 10 个 X 射线投影自动将路标 MR 图像配准到 X 射线透视图像。