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Sequential Turning Acquisition and Reconstruction (STAR) method for four-dimensional imaging of cyclically moving structures

机译:循环运动结构的三维成像的顺序转向采集和重建(STAR)方法

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Optical coherence tomography allows for dynamic, three-dimensional (3D+T) imaging of the heart within animal embryos. However, direct 3D+T imaging frame rates remain insufficient for cardiodynamic analysis. Previously, this limitation has been addressed by reconstructing 3D+T representations of the beating heart based on sets of two-dimensional image sequences (2D+T) acquired sequentially at high frame rate and in fixed (and parallel) planes throughout the heart. These methods either require additional hardware to trigger the acquisition of each 2D+T series to the same phase of the cardiac cycle or accumulate registration errors as the slices are synchronized retrospectively by pairs, without a gating signal. Here, we present a sequential turning acquisition and reconstruction (STAR) method for 3D+T imaging of periodically moving structures, which does not require any additional gating signal and is not prone to registration error accumulation. Similarly to other sequential cardiac imaging methods, multiple fast image series are consecutively acquired for different sections but in between acquisitions, the imaging plane is rotated around the center line instead of shifted along the direction perpendicular to the slices. As the central lines of all image-sequences coincide and represent measurements of the same spatial position, they can be used to accurately synchronize all the slices to a single inherent reference signal. We characterized the accuracy of our method on a simulated dynamic phantom and successfully imaged a beating embryonic rat heart. Potentially, this method can be applied for structural or Doppler imaging approaches with any direct space imaging modality such as computed tomography, ultrasound, or light microscopy.
机译:光学相干断层扫描技术可以对动物胚胎内的心脏进行动态的三维(3D + T)成像。但是,直接3D + T成像帧速率仍然不足以进行心脏动力学分析。以前,此限制已通过基于以高帧频顺序并在整个心脏的固定(和平行)平面中顺序获取的二维图像序列(2D + T)组重构跳动心脏的3D + T表示法来解决。这些方法或者需要额外的硬件来触发每个2D + T系列采集到心动周期的同一相位,或者由于切片成对地追溯成对同步而没有门控信号,因此累积了配准错误。在这里,我们提出了一种用于周期性运动结构的3D + T成像的顺序转弯采集和重构(STAR)方法,该方法不需要任何附加的门控信号,并且不容易产生套准误差累积。类似于其他顺序的心脏成像方法,针对不同部分连续获取多个快速图像系列,但是在两次获取之间,成像平面围绕中心线旋转,而不是沿着垂直于切片的方向移动。当所有图像序列的中心线重合并代表相同空间位置的测量值时,它们可用于将所有切片精确同步到单个固有参考信号。我们在模拟的动态体模上表征了我们方法的准确性,并成功成像了跳动的胚胎大鼠心脏。潜在地,该方法可以用于具有任何直接空间成像模态的结构或多普勒成像方法,例如计算机断层扫描,超声或光学显微镜。

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