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2012 Proceedings - International Tissue Elasticity Conference

2012 Proceedings - International Tissue Elasticity Conference

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038 DYNAMIC SHEAR ELASTICITY PROPERTIES OF BLOOD COAGULATION ASSESSED BY<br />

SHEAR WAVE IMAGING AND CLASSIC RHEOLOGY.<br />

Miguel Bernal 1 , Jean–Luc Gennisson 1 , Mathias Fink 1 , Patrice Flaud 2 , Mickael Tanter 1 .<br />

1 Institut Langevin – Ondes et Images, ESPCI ParisTech, CNRS UMR7587, INSERM U979, 1 rue<br />

Jussieu, 75005 Paris, FRANCE; 2 Matière et Systèmes Complexes, CNRS UMR7057, Université<br />

Paris VII Denis Diderot, 10 rue Alice Domon et Léonie Duquet, 75205 Paris Cedex 13, FRANCE.<br />

Background: Millions of people worldwide are affected by deep venous thrombosis (DVT) every year.<br />

Pulmonary embolism, a dangerous complication, affects about 30 to 50% of these patients [1]. This<br />

happens when the thrombus breaks off from veins and blocks the pulmonary arteries. The diagnosis and<br />

treatment of DVT usually depends on the risk of breakage and stability of the clots. The stability has been<br />

related to the age and elasticity of the blood clots [2,3].<br />

Aims: This work describes the use of the Supersonic shear wave imaging (SSI) technique in the study of<br />

dynamic shear elasticity properties of blood coagulation. We compared the results from this technique<br />

with classical rheology studies.<br />

Methods: Blood was collected from pigs and anticoagulated using ethylenediaminetetraacetic acid<br />

(EDTA). Coagulation was initiated using calcium ions. Ultrasound radiation force was used to<br />

generate shear waves with 100μs tone bursts of 8MHz at 3 different locations in the lateral direction.<br />

The shear wave displacements were measured by ultrafast imaging at a repetition rate of 2kHz. Using<br />

a time–of–flight algorithm, shear wave speed (Vs) was recovered giving access to the shear elasticity (μ)<br />

according to μ=ρVs2. Using a Haake Mars II classical rheology (between 0.2 and 25Hz) was done<br />

simultaneously on the same blood sample. Three different types of experiments were done: dual systems<br />

(70 minutes), ultrasound alone (2 hours) and a multi–day experiment (ultrasound alone).<br />

Results: SSI allowed the visualization of two dimensional (2D) maps of elasticity at every time point. The<br />

spatial shear elasticity of aregion of interest (ROI) in the sample varied with time, from a minimum of<br />

67.4±8.7Pa at coagulation (about 5 minutes) to a maximum of 2168.4±326.8 at 91 minutes. It decreased<br />

to 753.5±138.8Pa after 18 hours, 763.1±107.1 after 24 hours and to 708.3±117.41 after 96 hours. In the<br />

dual experiments, using G’ (conservation modulus) and G” (loss modulus) values from the rheology<br />

experiments, we calculated the phase velocities at 25Hz. The values at coagulation and minute 70 were<br />

0.54±0.02m/s and 0.63±0.01m/s, respectively. While the values from the SSI experiments for the<br />

mean phase velocities (50–350Hz) increased from 0.46±0.12m/s at coagulation to 0.76±0.01m/s at<br />

the same time points. Syneresis phenomenon (expulsion of free water from the clot) was visible in the<br />

2 hour B–mode experiment at the bottom of the sample. This affected the shear elasticity and created two<br />

regions in the blood clot. The mean phase velocity values were similar for the two regions at coagulation,<br />

0.56±0.01 and 0.54±0.1m/s, respectively, but differed with time. At minute 15 (beginning of syneresis<br />

viewed by B–mode), the velocities were 0.85±0.04 for the syneresis region and 0.90±0.01m/s for no<br />

syneresis. At minute 120, they were 0.83±0.09 and 1.06±0.06m/s, respectively. The spatial median shear<br />

values for two ROI’s in the two regions of the 2D maps at minute 120 were 748.5±145.1 and<br />

1477.9±465.7Pa.<br />

Conclusions: The phase velocity values obtained with the SSI technique showed good agreement with<br />

those calculated from the classical rheology experiments. SSI proved to be useful mapping the elasticity of<br />

clots in 2D at multiple time points. It allowed the quantification of the mechanical properties of the thrombi<br />

and their heterogeneities, illustrated by the dynamic mapping of syneresis region appearance showing that<br />

this technique has potential use in predicting thrombi breakage. Future studies include in vivo experiments<br />

in small animals and quantifying the viscosity in order to try to estimate thrombus age.<br />

References:<br />

[1] J. Hirsh and J. Hoak: Management of Deep Vein Thrombosis and Pulmonary Embolism. A Statement for<br />

Healthcare Professionals. Council on Thrombosis (in consultation with the Council on Cardiovascular Radiology),<br />

American Heart Association. Circulation, Vol. 93, No. 12, pp. 2212–45, Jun 1996.<br />

[2] S. Y. Emelianov et al.: Triplex Ultrasound: <strong>Elasticity</strong> Imaging to Age Deep Venous Thrombosis. Ultrasound in<br />

Medicine and Biology, Vol. 28, No. 6, pp. 757–767, 2002.<br />

[3] H. Xie et al.: Correspondence of Ultrasound <strong>Elasticity</strong> Imaging to Direct Mechanical Measurement in Aging DVT<br />

in Rats. Ultrasound in Medicine and Biology, Vol. 31, No. 10, pp. 1351–9, Oct 2005.<br />

68<br />

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