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VISE Summer Seminar: Kenneth B. Bader, PhD

Posted by on Tuesday, July 24, 2018 in News.

VISE Seminar

to be led by

Kenneth B. Bader, Ph.D.
Department of Radiology and the Committee on Medical Physics,
University of Chicago, Chicago, IL

 

 

 

 

 

 

 

 

 

Date: Thursday, July 31, 2018
Location: Stevenson Center 5326
Time: 12:10 p.m. start, 12:00 p.m. lunch

Title:
Passive Cavitation Imaging for Monitoring Histotripsy-Enhanced Thrombolysis

Abstract:
Deep vein thrombosis (DVT) is a major public health problem, affecting 600,000 Americans annually with a healthcare cost of $10 billion and more than 100,000 deaths. The American Heart Association recommends catheter-directed thrombolytics or mechanical interventions for critical obstructions to prevent amputation of the afflicted limb or death. These treatment regimens are not effective for the chronic thrombus components present in 27 to 43% of DVT cases. Our preliminary studies demonstrate synergy between histotripsy, a form of therapeutic ultrasound that  employs the mechanical action of bubble clouds to ablate tissue and induce fluid mixing, and the thrombolytic recombinant tissue plasminogen activator (rt-PA) for enhancing thrombolysis of retracted venous clots in vitro. The bubble clouds are hyperechoic, enabling standard B-mode imaging to be used for image guidance. The volumetric oscillations of the bubbles also generate acoustic emissions proportional to the mechanical activity generated during the histotripsy pulse. Passive cavitation imaging (PCI) utilizes clinical imaging arrays to record and beamform emissions, generating maps of the location and strength of bubble cloud emissions. Here, the utility of PCI to predict histotripsy ablation will be assessed using receiver operating characteristic (ROC) curve analysis and compared to plane wave B-mode imaging in a gel phantom. The area under the ROC curve, accuracy, and sensitivity were greater for PCI relative to B-mode imaging (p < 0.05), albeit with limited passive cavitation image range resolution. Further analysis of histotripsy-generated emissions in an in vitro porcine clot model ascertained no variation in the power or location of bubble cloud activity with or without thrombolytic drugs. However, the thrombolytic efficacy was improved significantly in the presence of rt-PA. Overall, PCI is a promising modality for monitoring histotripsy-enhanced thrombolysis.

 

 

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