Retrospective Ultrasound Doppler Quantification Using a Single Acquisition in Healthy Adults.

OBJECTIVE: Using an experimental tool for retrospective ultrasound Doppler quantification-with high temporal resolution and large spatial coverage-simultaneous flow and tissue measurements were obtained. We compared and validated these experimental values against conventional measurements to determine if the experimental acquisition produced trustworthy tissue and flow velocities. METHODS: We included 21 healthy volunteers. The only exclusion criterion was the presence of an irregular heartbeat. Two ultrasound examinations were performed for each participant, one using conventional and one using experimental acquisition. The experimental acquisition used multiple plane wave emissions combined with electrocardiography stitching to obtain continuous data with over 3500 frames per second. With two recordings covering a biplane apical view of the left ventricle, we retrospectively extracted selected flow and tissue velocities. RESULTS: Flow and tissue velocities were compared between the two acquisitions. Statistical testing showed a small but significant difference. We also exemplified the possibility of extracting spectral tissue Doppler from different sample volumes in the myocardium within the imaging sector, showing a decrease in the velocities from the base to the apex. CONCLUSION: This study demonstrates the feasibility of simultaneous, retrospective spectral and color Doppler of both tissue and flow from an experimental acquisition covering a full sector width. The measurements were significantly different between the two acquisitions but were still comparable, as the biases were small compared to clinical practice, and the two acquisitions were not done simultaneously. The experimental acquisition also enabled the study of deformation by simultaneous spectral velocity traces from all regions of the image sector.

Intraventricular Vector Flow Imaging with Blood Speckle Tracking in Adults: Feasibility, Normal Physiology and Mechanisms in Healthy Volunteers.

This study examines the feasibility of blood speckle tracking for vector flow imaging in healthy adults and describes the physiologic flow pattern and vortex formation in relation to the wall motion in the left ventricle. The study included 21 healthy volunteers and quantified and visualized flow patterns with high temporal resolution down to a depth of 10-12 cm without the use of contrast agents. Intraventricular flow seems to originate during the isovolumetric relaxation with a propagation of blood from base to apex. With the E-wave, rapid inflow and vortex formation occurred on both sides of the valve basally. During diastasis the flow gathers in a large vortex before the pattern from the E-wave repeats during the A-wave. In isovolumetric contraction, the flow again gathers in a large vortex that seems to facilitate the flow out in the aorta during systole. No signs of a persistent systolic vortex were visualized. The geometry of the left ventricle and the movement of the AV-plane is important in creating vortices that are favorable for the blood flow and facilitate outflow. The quantitative measurements are in concordance with these findings, but the clinical interpretation must be evaluated in future clinical studies.

Physiological significance of pre- and post-ejection left ventricular tissue velocities and relations to mitral and aortic valve closures.

BACKGROUND: Tissue Doppler shows short duration velocity spikes during pre- and post-ejection (protodiastole). They have been assumed to be isovolumic contraction and relaxation movements, but this is not in accordance with newer studies. METHODS: We examined 22 healthy volunteers. Valve closures and openings were determined from spectral Doppler from LVOT and mitral inflow and transferred to colour tissue Doppler recordings for comparison with tissue velocities, colour M-mode and strain rate (SR). RESULTS: Pre-ejection positive velocity spikes were simultaneous in both walls, starting ca. 24.8 ± 10.1 ms after start QRS, duration 51.5 ± 10.8 ms, ending 10.2 ± 11.5 ms after mitral valve closure (MVC) (p < 0.001). There were corresponding colour tracings and negative strain rate. Protodiastolic lengthening was predominant in the septum. Negative velocity spikes had a duration of 35.5 ± 10.7 ms, ending 9.5 ± 14.7 ms after aortic valve closure (AVC, p < 0.001) in septum. During isovolumic relaxation, strain rate showed apical lengthening (Peak SR-0.72 ± 0.50 s-1 ) and basal shortening (Peak SR 0.44 ± 0.63 s-1 ). CONCLUSION: Electromechanical activation of the LV is simultaneous in septum and lateral wall, occurs before MVC, is terminated by MVC itself and is thus not isovolumic. Protodiastole is a short event of lengthening, predominantly in the septum. It may be the mechanism for valve closure and ends by AVC itself. Isovolumic relaxation occurs after this velocity spike, and is characterized by elongation of the apex, shortening of the base, thus showing a volume shift from base towards apex.