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    • 1. 发明授权
    • Method and apparatus for providing real-time calculation and display of tissue deformation in ultrasound imaging
    • 用于提供实时计算和显示超声成像组织变形的方法和装置
    • US06352507B1
    • 2002-03-05
    • US09432061
    • 1999-11-02
    • Hans TorpBjorn OlstadAndreas HeimdalSteinar Bjaerum
    • Hans TorpBjorn OlstadAndreas HeimdalSteinar Bjaerum
    • A61B800
    • A61B8/485A61B5/0456A61B5/7239A61B8/488A61B8/543G01S7/52036G01S7/52038G01S7/52042G01S7/52057G01S7/52085G01S7/52095G01S15/584G01S15/8979
    • An ultrasound system and method for calculation and display of tissue deformation parameters are disclosed. An ultrasound acquisition technique that allows a high frame rate in tissue velocity imaging or stain rate imaging is employed. The tissue deformation parameter strain is determined by an accumulation of stain rate estimates for consecutive frames over an interval. The interval may be a triggered interval generated by, for example, an R-wave in an ECG trace. The strain calculation may be improved by moving the sample volume from which the stain rate is accumulated from frame-to-frame according to the relative displacement of the tissue within the original sample volume. The relative displacement of the tissue is defined by the instantaneous tissue velocity of the sample volume. An estimation of strain rate based upon a spatial derivative of tissue velocity is improved by adaptively varying the spatial offset, dr. The spatial offset, dr, can be maximized to cover the entire tissue segment (e.g., heart wall width) while still keeping both of the sample volumes at each end of the offset within the tissue segment. This nay be accomplished by determining whether various parameters (e.g., grayscale value, absolute power estimate, magnitude of the autocorrelation function with unity temporal lag and/or magnitude of strain correlation) of the sample volumes within in the spatial offset are above a given threshold.
    • 公开了用于计算和显示组织变形参数的超声系统和方法。 采用允许组织速度成像或染色率成像中的高帧速率的超声波采集技术。 组织变形参数应变是通过间隔上连续帧的染色率估计的积累来确定的。 该间隔可以是由例如ECG迹线中的R波产生的触发间隔。 通过根据原始样品体积内的组织的相对位移,通过从逐帧移动污染率从其累积的样品体积来改善应变计算。 组织的相对位移由样品体积的瞬时组织速度定义。 通过自适应地改变空间偏移,提高了基于组织速度的空间导数的应变速率的估计。 空间偏移量dr可以最大化以覆盖整个组织段(例如,心脏壁宽度),同时仍保持组织区段内的偏移的每个端部处的两个样本体积。 这可以通过确定在空间偏移内的样本体积的各种参数(例如,灰度值,绝对功率估计,具有单位时间滞后的自相关函数的幅度和/或应变相关的幅度)是否高于给定阈值来实现 。
    • 3. 发明申请
    • Method and apparatus for providing real-time calculation and display of tissue deformation in ultrasound imaging
    • US20050203390A1
    • 2005-09-15
    • US10705087
    • 2003-11-10
    • Hans TorpBjorn OlstadAndreas HeimdalSteinar Bjaerum
    • Hans TorpBjorn OlstadAndreas HeimdalSteinar Bjaerum
    • A61B8/13A61B5/0456A61B8/08G01S7/52G01S15/58G01S15/89A61B8/00
    • A61B8/485A61B5/0456A61B5/7239A61B8/488A61B8/543G01S7/52036G01S7/52038G01S7/52042G01S7/52057G01S7/52085G01S7/52095G01S15/584G01S15/8979
    • An ultrasound system and method for calculation and display of tissue deformation parameters are disclosed. An ultrasound acquisition technique that allows a high frame rate in tissue velocity imaging or strain rate imaging is employed. With this acquisition technique the same ultrasound pulses are used for the tissue image and the Doppler based image. A sliding window technique is used for processing. The tissue deformation parameter strain is also determined by an accumulation of strain rate estimates for consecutive frames over an interval. The interval may be a triggered interval generated by, for example, an R-wave in an ECG trace. The strain calculation may be improved by moving the sample volume from which the strain rate is accumulated from frame-to-frame according to the relative displacement of the tissue within the original sample volume. The relative displacement of the tissue is determined by the instantaneous tissue velocity of the sample volume. An estimation of strain rate based upon a spatial derivative of tissue velocity is improved by adaptively varying the spatial offset, dr. The spatial offset, dr, can be maximized to cover the entire tissue segment (e.g., heart wall width) while still keeping both of the sample volumes at each end of the offset within the tissue segment. This may be accomplished by determining whether various parameters (e.g., grayscale value, absolute power estimate, magnitude of the autocorrelation function with unity temporal lag and/or magnitude of strain correlation) of the sample volumes within in the spatial offset are above a given threshold. Strain rate may be estimated using a generalized strain rate estimator that is based on a weighted sum of two-sample strain rate estimators with different spatial offsets. The weights are proportional to the magnitude of the strain rate correlation estimate for each spatial offset, and thus reduce the effect of noisy, i.e. poorly correlated, samples. An improved signal correlation estimator that uses a spatial lag in addition to the usual temporal lag is disclosed. The spatial lag is found from the tissue velocity. The improved signal correlation estimator can be utilized both in the estimation of strain rate and tissue velocity. Tissue velocity may be estimated in a manner that reduces aliasing while maintaining spatial resolution. Three copies of a received ultrasound signal are bandpass filtered at three center frequencies. The middle of the three center frequencies is centered at the second harmonic of the ultrasound signal. A reference tissue velocity is estimated from the two signals filtered at the outside center frequencies. The reference tissue velocity is used to choose a tissue velocity from a number of tissue velocities estimated from the signal centered at the second harmonic. A method to estimate the strain rate in any direction, not necessarily along the ultrasound beam, based on tissue velocity data from a small region of interest around a sample volume is disclosed. Quantitative tissue deformation parameters, such as tissue velocity, tissue velocity integrals, strain rate and/or strain, may be presented as functions of time and/or spatial position for applications such as stress echo. For example, strain rate or strain values for three different stress levels may be plotted together with respect to time over a cardiac cycle. Parameters which are derived from strain rate or strain velocity, such as peak systolic wall thickening percentage, may be plotted with respect to various stress levels,
    • 10. 发明授权
    • Ultrasound display of tissue, tracking and tagging
    • 超声显示组织,跟踪和标记
    • US06863655B2
    • 2005-03-08
    • US10064085
    • 2002-06-10
    • Steinar BjaerumBjorn OlstadKjell Kristoffersen
    • Steinar BjaerumBjorn OlstadKjell Kristoffersen
    • A61B5/0456A61B8/08G01S7/52G01S15/89G06T7/20A61B8/06
    • G06T7/20A61B5/0456A61B8/0883A61B8/463A61B8/485A61B8/488G01S7/52042G01S7/52066G01S7/52071G01S7/52087G01S7/52088G01S15/8979G06T2207/30048
    • An ultrasound machine that generates a pattern of indicia corresponding to tracked moving structure, such as a cardiac wall tissue that is displayed on a monitor. The pattern of indicia is generated by displaying a set of tagging symbols related to the tracked movement of the structure over a time period by an apparatus comprising a front-end that generates received signals in response to backscattered ultrasound waves. A Doppler processor generates a spatial set of signals values representing movement within the structure. A non-Doppler processor generates a set of parameter signals representing a spatial set of B-mode values within the structure. A host processor embodies a tracking function to generate a set of tracked movement parameter profiles and motion parameter profiles over a time period corresponding to anatomical locations associated with the set of tagging symbols. A display processor overlays the set of tagging symbols onto an image of the moving structure on a monitor, such as B-mode, showing a pattern of indicia that allows visualization of the expansion and contraction of the moving structure in real-time over the time period.
    • 一种产生对应于跟踪的运动结构的标记图案的超声机器,例如显示在监视器上的心脏壁组织。 通过包括响应于反向散射超声波产生接收信号的前端的装置,通过显示与一段时间内的结构的跟踪运动相关的一组标签符号来生成标记的图案。 多普勒处理器产生表示结构内移动的空间信号值集合。 非多普勒处理器生成表示该结构内的B模式值的空间集合的一组参数信号。 主机处理器体现跟踪功能,以在对应于与该组标签符号相关联的解剖位置的时间周期内生成一组跟踪运动参数轮廓和运动参数轮廓。 显示处理器将标记符号集合覆盖在诸如B模式的监视器上的移动结构的图像上,示出了标记的图案,其允许在时间上实时地可视化移动结构的扩展和收缩 期。