303 research outputs found

    Identification of left ventricular model parameters

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    Simulations with a model of left ventricular pressure generation consisting of time-varying elastance, resistance, series-elastance, and deactivation were fitted to pressure curves measured in the isolated rabbit ventricle. For constant ejection flows, a fit with a RMS error of 2.78 mmHg was obtained provided that deactivation was actually incorporated in the model. Deactivation was assumed to depend linearly on end ejection pressure. Resistance was found to be independent of volum

    Deactivation in the rabbit left ventricle induced by constant ejection flow

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    A study of pressure generated by the left ventricle after ejection with constant flow for different values of the ejection flow, flow duration, time of flow arrest, and ventricular volume is discussed. It was found that pressure after ejection, normalized with respect to isovolumic pressure, is regenerated according to a model consisting of an elastance, a resistance, a series elastance, and an additional deactivation component. Deactivation is defined as the difference between the value 1 and the plateau value of the normalized pressure after constant flow ejection. It is shown that this plateau value is constant after constant flow ejection until the minimum in isovolumic dP/dt, i.e. during physiological systole. The plateau value is uniquely related to the value of the normalized pressure with a time constant of 10.44±0.09 ms which agrees with the series-elastance time constant of 10.35±0.26 m

    Exploiting flow dynamics for super-resolution in contrast-enhanced ultrasound

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    Ultrasound localization microscopy offers new radiation-free diagnostic tools for vascular imaging deep within the tissue. Sequential localization of echoes returned from inert microbubbles with low-concentration within the bloodstream reveal the vasculature with capillary resolution. Despite its high spatial resolution, low microbubble concentrations dictate the acquisition of tens of thousands of images, over the course of several seconds to tens of seconds, to produce a single super-resolved image. %since each echo is required to be well separated from adjacent microbubbles. Such long acquisition times and stringent constraints on microbubble concentration are undesirable in many clinical scenarios. To address these restrictions, sparsity-based approaches have recently been developed. These methods reduce the total acquisition time dramatically, while maintaining good spatial resolution in settings with considerable microbubble overlap. %Yet, non of the reported methods exploit the fact that microbubbles actually flow within the bloodstream. % to improve recovery. Here, we further improve sparsity-based super-resolution ultrasound imaging by exploiting the inherent flow of microbubbles and utilize their motion kinematics. While doing so, we also provide quantitative measurements of microbubble velocities. Our method relies on simultaneous tracking and super-localization of individual microbubbles in a frame-by-frame manner, and as such, may be suitable for real-time implementation. We demonstrate the effectiveness of the proposed approach on both simulations and {\it in-vivo} contrast enhanced human prostate scans, acquired with a clinically approved scanner.Comment: 11 pages, 9 figure

    .Blood flow patterns estimation in the left ventricle with low-rate 2D and 3D dynamic contrast-enhanced ultrasound

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    a b s t r a c t Background and Objective : Left ventricle (LV) dysfunction always occurs at early heart-failure stages, pro- ducing variations in the LV flow patterns. Cardiac diagnostics may therefore benefit from flow-pattern analysis. Several visualization tools have been proposed that require ultrafast ultrasound acquisitions. However, ultrafast ultrasound is not standard in clinical scanners. Meanwhile techniques that can handle low frame rates are still lacking. As a result, the clinical translation of these techniques remains limited, especially for 3D acquisitions where the volume rates are intrinsically low. Methods : To overcome these limitations, we propose a novel technique for the estimation of LV blood velocity and relative-pressure fields from dynamic contrast-enhanced ultrasound (DCE-US) at low frame rates. Different from other methods, our method is based on the time-delays between time-intensity curves measured at neighbor pixels in the DCE-US loops. Using Navier-Stokes equation, we regularize the obtained velocity fields and derive relative-pressure estimates. Blood flow patterns were characterized with regard to their vorticity, relative-pressure changes (dp/dt) in the LV outflow tract, and viscous energy loss, as these reflect the ejection efficiency. Results : We evaluated the proposed method on 18 patients (9 responders and 9 non-responders) who un- derwent cardiac resynchronization therapy (CRT). After CRT, the responder group evidenced a significant (p < 0.05) increase in vorticity and peak dp/dt, and a non-significant decrease in viscous energy loss. No significant difference was found in the non-responder group. Relative feature variation before and after CRT evidenced a significant difference (p < 0.05) between responders and non-responders for vorticity and peak dp/dt. Finally, the method feasibility is also shown with 3D DCE-US. Conclusions : Using the proposed method, adequate visualization and quantification of blood flow patterns are successfully enabled based on low-rate DCE-US of the LV, facilitating the clinical adoption of the method using standard ultrasound scanners. The clinical value of the method in the context of CRT is also shown
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