Evidence map›Paper›PMID 39481233›Full record

ArticlePhysics in medicine and biology2024

Treatment envelope of transcranial histotripsy: challenges and strategies to maximize the treatment location profile.

Ning Lu, Ellen M Yeats, Jonathan R Sukovich, Timothy L Hall, Aditya S Pandey, Zhen Xu

Abstract read
In one paragraph

Article in Physics in medicine and biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Focused ultrasound for brain metastases.Neuro-oncology advances · 2026
    Review
  3. Review
  4. Article
  5. Review
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Ning LuDepartment of Radiology, Stanford University, Palo Alto, CA 94304, United States of America.ORCID 0000-0002-8110-9176
Ellen M YeatsDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, United States of America.
Jonathan R SukovichDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, United States of America.
Timothy L HallDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, United States of America.
Aditya S PandeyDepartment of Neurosurgery, University of Michigan, Ann Arbor, MI 48109, United States of America.
Zhen XuDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, United States of America.ORCID 0000-0003-0262-3044

Funding

Novel Ultrasonic Technique for the Treatment of Hemorrhagic StrokeR01NS108042 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PANDEY, ADITYA S · 2018 to 2022
$2.6M
Transcranial Magnetic Resonance guided Histotripsy (tcMRgHt)R01EB028309 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI XU, ZHEN · 2019 to 2022
$2.4M
Acoustic Cavitation Emission (ACE) Feedback Methods for Monitoring Histotripsy-Induced Tissue Fractionation In SituR01EB032772 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SUKOVICH, JONATHAN ROBERT · 2022 to 2025
$2.0M
NIBIB NIH HHS R01 EB028309NIBIB NIH HHS R01 EB032772NINDS NIH HHS R01 NS108042
6 · The paper itself

Abstract

A 750 kHz, 360-element ultrasound array has been built for transcranial histotripsy applications. This study aims to evaluate its performance to determine whether this array is adequate for treating a wide range of brain locations through a human skull. Treatment location profiles in 2 excised human skulls were experimentally characterized based on passive cavitation mapping. Full-wave acoustic simulations were performed in 8 human skulls to analyze the ultrasound propagation at shallow targets in skulls with different properties. Results showed that histotripsy successfully generated cavitation from deep to shallow targets within 5 mm from the skull surface in the skull with high SDR and small thickness, whereas in the skull with low SDR and large thickness, the treatment envelope was limited up to 16 mm from the skull surface. Simulation results demonstrated that the treatment envelope was highly dependent on the skull acoustic properties. Pre-focal pressure hotspots were observed in both simulation and experiments when targeting near the skull. For each skull, the acoustic pressure loss increases significantly for shallow targets compared to central targets due to high attenuation, large incident angles, and pre-focal pressure hotspots. Strategies including array design optimization, pose optimization, and amplitude correction, are proposed to broaden the treatment envelope. This study identifies the capabilities and limitations of the 360-element transcranial histotripsy array and suggests strategies for designing the next-generation transcranial histotripsy array to expand the treatment location profile for a future clinical trial.

Indexed as

SkullHumansUltrasonic Therapyacoustic cavitationhistotripsyphased arraytranscranial brain therapytreatment envelope

Identifiers

PMID39481233
PMCPMC11551913

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.