In Vivo Measurements of Blood Transport Patterns and Stasis in the Human Left Ventricle

Author(s):  
Sahar Hendabadi ◽  
Javier Bermejo ◽  
Yolanda Benito ◽  
Raquel Yotti ◽  
Francisco Fernández-Avilés ◽  
...  

Because the left ventricle (LV) is not completely emptied during systole, oxygenated blood from the left atrium interacts with residual blood from preceding cycles. It is hypothesized that LV flow is optimal for transporting blood under normal conditions; yet proving this remains a challenge. Furthermore, clinical evaluation of LV hemodynamics has tremendous diagnostic importance for patients with cardiomyopathy. We have performed Doppler-echocardiography on 6 patients with dilated cardiomyopathy and 6 healthy volunteers. Using novel processing of the color-Doppler data, bi-directional velocity field maps in the apical long axis plane were derived. Resulting flow data was used to perform Lagrangian coherent structure (LCS) computation, which enabled novel characterization of the transport topology in the LV during filling and ejection. This framework was used to quantify stasis in the LV, which can be used as a surrogate for diagnosing pumping deficiencies and thrombosis risk. This framework also enables characterization of LV vortices, which have previously received much attention using Eulerian characterizations. The framework presented here uncovers the well-defined boundaries to both E-wave and A-wave filling vortices, which has not been previously reported.

2013 ◽  
Vol 41 (12) ◽  
pp. 2603-2616 ◽  
Author(s):  
Sahar Hendabadi ◽  
Javier Bermejo ◽  
Yolanda Benito ◽  
Raquel Yotti ◽  
Francisco Fernández-Avilés ◽  
...  

2016 ◽  
Vol 18 (5) ◽  
Author(s):  
Kyle Fricke ◽  
Filip Konecny ◽  
Alexander El-Warrak ◽  
Chad Hodgson ◽  
Heather Cadieux-Pitre ◽  
...  

Author(s):  
Sahar Hendabadi ◽  
Juan C. del Alamo ◽  
Shawn C. Shadden

It has become increasingly clear that the dynamics of the left ventricle (LV) plays a major role in dictating overall cardiac health. Phase-contrast magnetic resonance imaging (PCMRI) and Doppler-ultrasound echocardiography can measure flow characteristics inside the human left ventricle in vivo, including diagnostic data useful for evaluating pathological conditions such as cardiomyopathies. Studying these flow patterns is a potential avenue for heart failure diagnosis. Traditional studies based on Eulerian measures computed from instantaneous velocity data, e.g. streamlines, vorticity, Q-criterion, etc., can be insufficient or unreliable to fully understand unsteady blood flow behavior. We used the Finite-Time Lyapunov Exponent (FTLE) approach to compute Lagrangian coherent structures (LCS) to gain insight into how blood is transported inside the LV. LCS can be thought of as special moving boundaries in the flow that partition regions with different dynamics, and whose coordinated motion organizes transport and mixing.


2013 ◽  
Vol 46 (4) ◽  
pp. e26
Author(s):  
H. Gao ◽  
B.E. Griffith ◽  
D. Carrick ◽  
C. McComb ◽  
C. Berry ◽  
...  

2020 ◽  
Vol 477 (7) ◽  
pp. 1261-1286 ◽  
Author(s):  
Marie Anne Richard ◽  
Hannah Pallubinsky ◽  
Denis P. Blondin

Brown adipose tissue (BAT) has long been described according to its histological features as a multilocular, lipid-containing tissue, light brown in color, that is also responsive to the cold and found especially in hibernating mammals and human infants. Its presence in both hibernators and human infants, combined with its function as a heat-generating organ, raised many questions about its role in humans. Early characterizations of the tissue in humans focused on its progressive atrophy with age and its apparent importance for cold-exposed workers. However, the use of positron emission tomography (PET) with the glucose tracer [18F]fluorodeoxyglucose ([18F]FDG) made it possible to begin characterizing the possible function of BAT in adult humans, and whether it could play a role in the prevention or treatment of obesity and type 2 diabetes (T2D). This review focuses on the in vivo functional characterization of human BAT, the methodological approaches applied to examine these features and addresses critical gaps that remain in moving the field forward. Specifically, we describe the anatomical and biomolecular features of human BAT, the modalities and applications of non-invasive tools such as PET and magnetic resonance imaging coupled with spectroscopy (MRI/MRS) to study BAT morphology and function in vivo, and finally describe the functional characteristics of human BAT that have only been possible through the development and application of such tools.


1995 ◽  
Vol 74 (02) ◽  
pp. 673-679 ◽  
Author(s):  
C E Dempfle ◽  
S A Pfitzner ◽  
M Dollman ◽  
K Huck ◽  
G Stehle ◽  
...  

SummaryVarious assays have been developed for quantitation of soluble fibrin or fibrin monomer in clinical plasma samples, since this parameter directly reflects in vivo thrombin action on fibrinogen. Using plasma samples from healthy blood donors, patients with cerebral ischemic insult, patients with septicemia, and patients with venous thrombosis, we compared two immunologic tests using monoclonal antibodies against fibrin-specific neo-epitopes, and two functional tests based on the cofactor activity of soluble fibrin complexes in tPA-induced plasminogen activation. Test A (Enzymun®-Test FM) showed the best discriminating power among normal range and pathological samples. Test B (Fibrinostika® soluble fibrin) clearly separated normal range from pathological samples, but failed to discriminate among samples from patients with low grade coagulation activation in septicemia, and massive activation in venous thrombosis. Functional test C (Fibrin monomer test Behring) displayed good discriminating power between normal and pathological range samples, and correlated with test A (r = 0.61), whereas assay D (Coa-Set® Fibrin monomer) showed little discriminating power at values below 10 μg/ml and little correlation with other assays. Standardization of assays will require further characterization of analytes detected.


2007 ◽  
Vol 55 (S 1) ◽  
Author(s):  
W Schiller ◽  
K Spiegel ◽  
T Schmid ◽  
H Rudorf ◽  
S Flacke ◽  
...  

Diabetes ◽  
1990 ◽  
Vol 39 (10) ◽  
pp. 1243-1250 ◽  
Author(s):  
L. Rossetti ◽  
A. Giaccari ◽  
E. Klein-Robbenhaar ◽  
L. R. Vogel

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