APL-UW

Jeff Thiel

Research Scientist/Engineer II

Email

jthiel@apl.uw.edu

Phone

206-221-4731

Department Affiliation

Center for Industrial & Medical Ultrasound

Education

B.S. Diagnostic Medical Ultrasound, Seattle University, 1992

Videos

Ultrasonic Propulsion of Residual Kidney Stone Framents

Ultrasonic propulsion, an investigational kidney stone treatment for awake un-anesthetized patients, sweeps stone fragments toward the ureter to facilitate their natural passage through the urine.

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9 Sep 2024

Ultrasonic propulsion, an investigational kidney stone treatment for awake un-anesthetized patients, sweeps stone fragments toward the ureter to facilitate their natural passage through the urine.

Nearly half of patients with small residual fragments following kidney stone surgery, relapse within five years.

Repositioning the fragments results in a 70% lower incidence of relapse -- urgent medical visit or a subsequent surgery. Time to relapse was also longer by nearly 1.5 year in the treatment group.

This study, led by University of Washington and Puget Sound VA investigators, was funded by the NIH.

Sorensen, M.D., et al., "Randomized controlled trial of ultrasonic propulsion-facilitated clearance of residual kidney stone fragments versus observation," J. Urol., doi:10.1097/JU.0000000000004186, 2024.
https://www.auajournals.org/doi/10.10...

Publications

2000-present and while at APL-UW

Advancing boiling histotripsy dose in ex vivo and in vivo renal tissues via quantitative histological analysis and shear wave elastography

Ponomarchuk, E., G. Thomas, M. Song, Y.-N. Wang, S. Totten, G. Schade, J. Thiel, M. Bruce, V. Khokhlova, and T. Khokhlova, "Advancing boiling histotripsy dose in ex vivo and in vivo renal tissues via quantitative histological analysis and shear wave elastography," Ultrasound Med. Biol., 50, 1936-1944, doi:10.1016/j.ultrasmedbio.2024.08.022, 2024.

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1 Dec 2024

Objective
In the context of developing boiling histotripsy (BH) as a potential clinical approach for non-invasive mechanical ablation of kidney tumors, the concept of BH dose (BHD) was quantitatively investigated in porcine and canine kidney models in vivo and ex vivo.

Methods
Volumetric lesions were produced in renal tissue using a 1.5-MHz 256-element HIFU-array with various pulsing protocols: pulse duration tp = 1–10 ms, number of pulses per point ppp = 1–15. Two BHD metrics were evaluated: BHD1 = ppp, BHD2 = tp × ppp. Quantitative assessment of lesion completeness was performed by their histological analysis and assignment of damage score to different renal compartments (i.e., cortex, medulla, and sinus). Shear wave elastography (SWE) was used to measure the Young's modulus of renal compartments in vivo vs ex vivo, and before vs after BH treatments.

Results
In vivo tissue required lower BH doses to achieve identical degree of fractionation as compared to ex vivo. Renal cortex (homogeneous, low in collagen) was equal or higher in stiffness than medulla (anisotropic, collagenous), 5.8–12.2 kPa vs 4.7–9.6 kPa, but required lower BH doses to be fully fractionated. Renal sinus (fatty, irregular, with abundant collagenous structures) was significantly softer ex vivo vs in vivo, 4.9–5.1 kPa vs 9.7–15.2 kPa, but was barely damaged in either case with any tested BH protocols. BHD1 was shown to be relevant for planning the treatment of renal cortex (sufficient BHD1 = 5 pulses in vivo and 10 pulses ex vivo), while none of the tested doses resulted in complete fractionation of medulla or sinus. Post-treatment SWE imaging revealed reduction of tissue stiffness ex vivo by 27–58%, increasing with the applied dose, and complete absence of shear waves within in vivo lesions, both indicative of tissue liquefaction.

Conclusion
The results imply that tissue resistance to mechanical fractionation, and hence required BH dose, are not solely determined by tissue stiffness but also depend on its composition and structural arrangement, as well as presence of perfusion. The SWE-derived reduction of tissue stiffness with increasing BH doses correlated with tissue damage score, indicating potential of SWE for post-treatment confirmation of BH lesion completeness.

Randomized controlled trial of ultrasonic propulsion-facilitated clearance of residual kidney stone fragments vs. observation

Sorensen, M.D., and 16 others including B. Dunmire, J. Thiel, B.W. Cunitz, J.C. Kucewicz, and M.R. Bailey, "Randomized controlled trial of ultrasonic propulsion-facilitated clearance of residual kidney stone fragments vs. observation," J. Urol., 6, 811-820, doi:10.1097/JU.0000000000004186, 2024.

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1 Dec 2024

Ultrasonic propulsion is an investigational procedure for awake patients. Our purpose was to evaluate whether ultrasonic propulsion to facilitate residual kidney stone fragment clearance reduced relapse.

This multicenter, prospective, open-label, randomized, controlled trial used single block randomization (1:1) without masking. Adults with residual fragments (individually 5 mm or smaller) were enrolled. Primary outcome was relapse as measured by stone growth, a stone-related urgent medical visit, or surgery by 5 years or study end. Secondary outcomes were fragment passage within 3 weeks and adverse events within 90 days. Cumulative incidence of relapse was estimated using the Kaplan-Meier method. Log-rank test was used to compare the treatment (ultrasonic propulsion) and control (observation) groups.

The trial was conducted from May 9, 2015, through April 6, 2024. Median follow-up (interquartile range) was 3.0 (1.8–3.2) years. The treatment group (n = 40) had longer time to relapse than the control group (n = 42; P < .003). The restricted mean time-to-relapse was 52% longer in the treatment group than in the control group (1530 ± 92 days vs 1009 ± 118 days), and the risk of relapse was lower (hazard ratio 0.30, 95% CI 0.13–0.68) with 8 of 40 and 21 of 42 participants, respectively, experiencing relapse. Omitting 3 participants not asked about passage, 24 treatment (63%) and 2 control (5%) participants passed fragments within 3 weeks of treatment. Adverse events were mild, transient, and self-resolving, and were reported in 25 treated participants (63%) and 17 controls (40%).

A novel 4D volumetric M-mode ultrasound scanning technique for evaluation of intravascular volume and hemodynamic parameters

Patel, S., E. Kao, X. Wang, K. Ringgold, J. Thiel, N. White, S. Aarabi, and D.F. Leotta, "A novel 4D volumetric M-mode ultrasound scanning technique for evaluation of intravascular volume and hemodynamic parameters," WFUMB Ultrasound Open, 2, doi:10.1016/j.wfumbo.2024.100058, 2024.

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25 Jul 2024

Introduction: We use a novel 4-dimensional (4D) volumetric M-mode (VMM) ultrasound (US) technique to assess intravascular volume by monitoring the inferior vena cava (IVC). The VMM method expands the spatial coverage of standard M-mode scanning (depth vs time) by including lateral image direction and adds transducer tilt to cover the region surrounding the IVC. Current ultrasound methods for volume assessment suffer from intra- and inter-operator variability. The VMM technique aims to address these limitations, aiding in early detection of hypovolemia/hemorrhage and guiding resuscitation.
Methods/technical approach: The 4D VMM technique was used on animals that underwent a swine hemorrhagic shock protocol with fluid resuscitation. 2D ultrasound images obtained were formatted in a 3D volume to capture changes over time in vessel size with respiration and volume status. Planes were then extracted from the 3D volume at multiple lateral locations to find and track the IVC. The vessel walls were manually traced on vertical planes (depth vs. time) to determine mean IVC diameter and IVC collapsibility at each measurement time point in the shock/resuscitation protocol. Planes at constant depth (lateral vs. time) were selected to extract respiratory and cardiac cycle data.
Results: Mean IVC diameter in the baseline phase was significantly greater than in the hemorrhage phase (p = 0.020). There was no significant different in mean IVC diameter between baseline and resuscitation (p = 0.064) or hemorrhage and resuscitation phases (p = 0.531). There was no statistically significant difference in mean collapsibility or ΔIVC diameter between protocol phases. The 4D VMM technique effectively measured heart and respiratory rates, consistent with monitored vitals.
Conclusion: 4D VMM identified IVC changes corresponding to blood loss and resuscitation during hemorrhagic shock as well as heart/respiratory rates. This innovative approach holds promise in reducing operator variability and providing actionable information during treatment of shock.

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