• DocumentCode
    3094635
  • Title

    Investigation of the mechanism of ARFI-based Color Doppler feedback of histotripsy tissue fractionation

  • Author

    Miller, Ryan M. ; Xi Zhang ; Maxwell, Andrew D. ; Tzu-Yin Wang ; Fowlkes, J. Brian ; Cain, Charles ; Zhen Xu

  • Author_Institution
    Dept. of Biomed. Eng., Univ. of Michigan, Ann Arbor, MI, USA
  • fYear
    2013
  • fDate
    21-25 July 2013
  • Firstpage
    934
  • Lastpage
    937
  • Abstract
    Histotripsy controls cavitating bubble clouds to fractionate tissue using high pressure ultrasound pulses. Over the histotripsy treatment, the tissue is increasingly fractionated and eventually liquefied. This process can be monitored in real time using color Doppler synchronized with histotripsy pulses, but the mechanism is not fully understood. We hypothesize that there are two motion phases after each histotripsy pulse: 1) chaotic motion due to cavitation followed by 2) coherent motion induced by acoustic radiation force impulse (ARFI) from the histotripsy pulse. By delaying the Doppler acquisition after the chaotic motion phase, color Doppler can be used to detect the ARFI-induced motion in the treatment tissue, providing real-time feedback for histotripsy tissue fractionation. The residual nuclei from cavitation can persist after the collapse to provide strong acoustic scatterers for Doppler. An agarose tissue phantom was treated with 2-cycle pulses at > 30 MPa using a 500 kHz phased array transducer. Ultrasound acquisitions and high-speed optical images were acquired for 19 ms after every 10th therapy pulse to estimate the motion of the residual cavitation nuclei (the only scatterers in the phantom). PIV and Doppler results showed a brief period of chaotic motion (0.5-2.0 ms depending on the fractionation level) followed by coherent motion first moving away from the transducer (3-6 ms) and then rebounding back (up to 19 ms). Over the course of the treatment in both phantom and ex vivo porcine liver, the duration of the push and rebound increased with increasing number of therapy pulses, and eventually peaked. Using an appropriate delay between the Doppler and the histotripsy pulse to monitor the ARFI motion, the Doppler velocity increased with the number of therapy pulses and peaked, likely when the tissue was liquefied. The results support our hypothesis that appropriately timed color Doppler can measure the coherent ARFI-induced motion in the tissue tre- ted with histotripsy without cavitation inference, providing real-time therapy feedback.
  • Keywords
    biological tissues; biomedical optical imaging; biomedical transducers; biomedical ultrasonics; cavitation; chaos; high-pressure effects; high-speed optical techniques; liver; medical image processing; patient treatment; phantoms; ultrasonic imaging; ultrasonic transducers; 2-cycle pulses; ARFI-based color Doppler feedback mechanism; ARFI-induced motion; Doppler acquisition; Doppler pulse; Doppler velocity; acoustic radiation force impulse; agarose tissue phantom; cavitation; chaotic motion; chaotic motion phase; coherent ARFI-induced motion; coherent motion; ex vivo porcine liver; frequency 500 kHz; high pressure ultrasound pulses; high-speed optical imaging; histotripsy control cavitating bubble clouds; histotripsy pulses; histotripsy tissue fractionation; histotripsy treatment; phased array transducer; pulse therapy; real-time therapy feedback; residual cavitation nuclei; tissue treatment; ultrasound acquisitions; Acoustics; Doppler effect; Fractionation; Image color analysis; Medical treatment; Phantoms; Ultrasonic imaging; Doppler elastography; histotripsy; therapy feedback;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Ultrasonics Symposium (IUS), 2013 IEEE International
  • Conference_Location
    Prague
  • ISSN
    1948-5719
  • Print_ISBN
    978-1-4673-5684-8
  • Type

    conf

  • DOI
    10.1109/ULTSYM.2013.0240
  • Filename
    6724944