High Frame Rate 3D Tissue Velocity Imaging Using Sub-Aperture Beamforming: a Pilot Study In Vivo

被引:0
|
作者
Santos, Pedro [1 ,2 ]
Haugen, Geir [2 ]
Lovstakken, Lasse [2 ,3 ]
Samset, Eigil [2 ,4 ,5 ]
D'hooge, Jan [1 ]
机构
[1] Katholieke Univ Leuven, Dept Cardiovasc Sci, Leuven, Belgium
[2] GE Vingmed Ultrasound AS, Horten, Norway
[3] Norwegian Univ Sci & Technol, Dept Circulat & Med Imaging, Trondheim, Norway
[4] Univ Oslo, Oslo, Norway
[5] Ctr Cardiol Innovat, Oslo, Norway
来源
2016 IEEE INTERNATIONAL ULTRASONICS SYMPOSIUM (IUS) | 2016年
关键词
Tissue Doppler; diverging wave; in vivo; sub-aperture beamforming; myocardial motion; ULTRASOUND;
D O I
暂无
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
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 subaperture (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.
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页数:4
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