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High frame rate 3D tissue velocity imaging using sub-aperture beamforming: A pilot study in vivo

机译:使用子孔径波束形成的高帧速3D组织速度成像:体内先导研究

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Implementation of 3D high frame rate (HFR) tissue Doppler imaging (TDI) typically requires a fully wired matrix probe. However, such probes remain impractical for use in a clinical setting. Therefore, clinical matrix arrays rely on sub-aperture (SAP) beamforming. This makes diverging wave (DW) imaging challenging as side- and grating-lobes arise from the simultaneous reconstruction of image lines with considerably different orientations. We have previously shown in computer simulations that these difficulties could be mitigated by using a sparse transmit sequence. The present study looked at the implementation of this sequence in a clinical system. 3D TDI was acquired in vivo at 610 vol/s and compared against conventional TDI (i.e. focused transmissions). The velocity curves obtained from both methods were similar (cross correlation = 0.90 ± 0.11) and the full left ventricle could be imaged at HFR in a single acquisition using the 3D DW sequence. Overall, this study supports the feasibility of HFR 3D TDI in a clinical system, despite the limitations of SAP beamforming.
机译:3D高帧率(HFR)组织多普勒成像(TDI)的实现通常需要完全有线的矩阵探头。然而,在临床环境中使用这种探针仍然不切实际。因此,临床矩阵阵列依赖于子孔径(SAP)波束成形。这使得发散波(DW)成像具有挑战性,因为旁瓣和光栅瓣是由于方向不同的图像线的同时重建而产生的。我们先前在计算机仿真中已经表明,可以通过使用稀疏的发送序列来减轻这些困难。本研究着眼于该序列在临床系统中的实现。体内以610 vol / s的速度采集了3D TDI,并将其与常规TDI(即聚焦传输)进行了比较。从这两种方法获得的速度曲线相似(互相关= 0.90±0.11),并且可以使用3D DW序列在单次采集中以HFR对左心室成像。总体而言,尽管SAP波束成形存在局限性,但这项研究支持HFR 3D TDI在临床系统中的可行性。

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