A method of enhanced shear wave elastography based on Chirp coded excitation.

Shear Wave Elastography (SWE) is an imaging technique that detects shear waves generated by tissue excited by Acoustic Radiation Force (ARF), and characterizes the mechanical properties of soft tissue by analyzing the propagation velocity of shear wave. ARF induces a change in energy density through the nonlinear propagation of ultrasound waves, which drives the tissue to generate shear waves. However, the amplitude of shear waves generated by ARF is weak, and the shear waves are strongly attenuated in vivo. Furthermore, the shear waves are usually drowned out by noise at deep locations, which presents a challenge in the detection of shear waves and low signal-to-noise ratios. In this paper, we investigate the feasibility of applying the Chirp coded signal for shear wave excitation (Chirp-SWE) in ARF-based shear wave elastography. The use of Chirp coded excitation of push waveforms was employed to enhance the action of ARF, thereby effectively exciting shear waves. Comparative experiments were carried out with conventional sine long pulses (SWE) and the Barker coded signal (Barker-SWE). The analysis of theoretical and simulation results revealed that Chirp-SWE could increase the excitation energy by approximately 10% compared to conventional SWE and Barker-SWE. The results of the elastic phantom experiments demonstrated that the average peak axial particle velocity obtained by Chirp-SWE was approximately 30%-50% higher, which facilitated the formation of a more stable shear wave. Additionally, it exhibited a higher signal-to-noise ratio during elasticity measurements. The in vitro liver experiments further validated the feasibility of implementing Chirp-SWE in tissues. The results demonstrated the feasibility and advantages of Chirp coded excitation of push waveforms in improving shear wave elastography results. It is expected that this will enhance the accuracy and robustness of soft tissue elastography.