2012 Proceedings - International Tissue Elasticity Conference
2012 Proceedings - International Tissue Elasticity Conference
2012 Proceedings - International Tissue Elasticity Conference
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061 SINGLE-HEARTBEAT 2–D MYOCARDIAL ELASTOGRAPHY USING AN UNFOCUSED TRANSMIT<br />
SEQUENCE: AN IN VIVO FEASIBILITY STUDY.<br />
SJ Okrasinski 1 , J Provost 1 , D Legrand 1 , EE Konofagou 1,2 .<br />
1 Biomedical Engineering Department, 2 Radiology Department, Columbia University, 622 W 168th<br />
St, New York, NY, 10025, USA.<br />
Background: Myocardial Elastography (ME) is a radiofrequency (RF) based modality for myocardial strain<br />
imaging. However, the methods previously used required spatial and temporal resolution that could be<br />
accomplished through electrocardiogram (ECG) gating over multiple cardiac cycles and long breath–holding<br />
times.<br />
Aims: For this study, imaging sequences were developed and applied in an in vivo canine model based on<br />
a virtual source sequence to image the strain in the entire left ventricle at very high frame rates (2000 fps)<br />
during free breathing and over a single heartbeat, in both open– and closed–chest configurations.<br />
Methods: In this study, approved by the Columbia Institutional Animal Care and Use Committee, two<br />
male mongrel dogs were anesthetized. Transthoracic images in the short–axis, mid–level view were<br />
acquired using a virtual source sequence with a virtual source located behind the transducer with a<br />
Verasonics system (Verasonics, Redmond, WA) and a 64–element phased array (ATL P4–2). Images were<br />
acquired at 2000fps during 2s, immediately followed by the acquisition of 128–line, 30fps, B–mode<br />
frames during 1.5s. ECGs were acquired simultaneously. Their chests were then opened by lateral<br />
thoracotomy and images using the same protocol were repeated. RF signals were reconstructed from the<br />
element data in a pixel–wise fashion as previously reported [1]. Inter–frame axial and lateral<br />
displacements were estimated at 500Hz motion–estimation rate and at 2000Hz motion–sampling rate<br />
using normalized cross–correlation (window size: 7mm, 90% overlap) and were then accumulated during<br />
systole. Axial and lateral strains were estimated using a least–squares estimator on the axial and lateral<br />
displacements (window size: 10.7mm) and then converted to radial and circumferential strains with a<br />
previously described principal strain method [2].<br />
Results: The maximum axial and lateral cumulative strains during systole in the open–chest<br />
configuration were 35±7% and 30±8%, respectively. The average radial and circumferential strains were<br />
found to be 30±10% and -32±9% respectively, which is consistent with previous studies in normal canine<br />
hearts using conventional beamforming [3]. In the closed–chest (transthoracic) configuration, the<br />
maximum axial and lateral cumulative strains during systole from the open–chest canines were 33±10%<br />
and 35±10%, respectively. The average radial and circumferential strains (see Figure) were found to be<br />
33±11% and –36±12%, respectively.<br />
Conclusions: Myocardial Elastography was concluded to be capable of mapping axial and lateral<br />
displacement and strain in both transthoracic and closed–chest regimes using unfocused transmit beams<br />
over the entire canine left ventricle in vivo at very high frame rates during free breathing in a single<br />
heartbeat.<br />
Acknowledgements: This study was funded in part by NIH–NHLBI R01EB006042.<br />
References:<br />
[1] Provost et al.: Phys. Med. Biol., 57, pp. 1095–1112. Feb <strong>2012</strong>.<br />
[2] Zervantonakis et al.: Phys. Med. Biol., 52, pp. 4063–4080. July 2007.<br />
[3] Lee et al.: Phys. Med. Biol., 56, pp. 1155–1172. Feb 2011.<br />
Figure 1: Radial and circumferential strain in a normal, open–chest canine. Strains were estimated using a virtual<br />
source sequence with a virtual source located behind the transducer face.<br />
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