The advantages of the ultrasonic examination are the immediate availability, the avoidance of radiation and the visualization of movements with dynamic examinations. In contrast to X-ray examination the ultrasonic investigation can provide useful additional information on soft tissue structures.
This paper presents a new method for the visualization of two-dimensional (2-D) blood flow in ultrasound imaging systems called blood flow imaging (BFI). Conventional methods of color flow imaging (CFI) and power Doppler (PD) techniques are limited as the velocity component transversal to the ultrasound beam cannot be estimated from the received Doppler signal. The BFI relies on the preservation and display of the speckle pattern originating from the blood flow scatterer signal, and it provides qualitative information of the blood flow distribution and movement in any direction of the image. By displaying speckle pattern images acquired with a high frame rate in slow motion, the blood flow movement can be visually tracked from frame to frame. The BFI is easily combined with conventional CFI and PD methods, and the resulting display modes have been shown to have several advantages compared to CFI or PD methods alone. Two different display modes have been implemented: one combining BFI with conventional CFI, and one combining BFI with PD. Initial clinical trials have been performed to assess the clinical usefulness of BFI. The method especially has potential in vascular imaging, but it also shows potential in other clinical applications.
OBJECTIVE--The feasibility of color Doppler tissue velocity imaging (c-TVI) with a high time resolution of 10 ms for simultaneous measurement of the temporal characteristics of regional left ventricular (LV) tissue velocities at different LV sites was examined. Methods and results--In 20 subjects with structurally normal hearts, inter- and intraobserver agreement and the beat-to-beat variation were tested in c-TVI profiles from basal and mid-LV segments of the interventricular septum (IS) and of the lateral free wall (LFW). For peak tissue velocities a mean error of less than 1 cm/s was demonstrated. For systolic regional LV velocity time difference, the mean error was +/- 5 ms, with the best agreement when sampling from basal LV sites. For diastolic regional LV velocity time differences, the mean error was +/- 12 ms. The longitudinal LV movement pattern demonstrated a pattern of incremental tissue velocity from basal to mid-LV, and from IS to LFW sites. Conclusion--The c-TVI method has acceptable inter- and intraobserver agreement and is sufficiently accurate to disclose regional time aspects of LV contraction and relaxation.
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