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Predicting and Monitoring Histotripsy Damage With Acoustic Cavitation Emission Signals
Predicting and Monitoring Histotripsy Damage With Acoustic Cavitation Emission Signals
Predicting and Monitoring Histotripsy Damage With Acoustic Cavitation Emission Signals

상세정보

자료유형  
 학위논문 서양
최종처리일시  
20260202105222
ISBN  
9798291566305
DDC  
610
저자명  
Haskell, Scott.
서명/저자  
Predicting and Monitoring Histotripsy Damage With Acoustic Cavitation Emission Signals
발행사항  
[Sl] : University of Michigan, 2025
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2025
형태사항  
159 p
주기사항  
Source: Dissertations Abstracts International, Volume: 87-03, Section: B.
주기사항  
Advisor: Sukovich, Jonathan;Xu, Zhen.
학위논문주기  
Thesis (Ph.D.)--University of Michigan, 2025.
초록/해제  
요약This dissertation outlines the work performed to establish acoustic signal acquisition and analysis techniques to predict the relationship between histotripsy dose and the degree of mechanically-induced tissue disruption. As the applications of histotripsy become more diverse, targeting new cancers and other pathologies, having tools to measure the degree of induced-damage will be important to assist in establishing treatment standards across tissue-types and patient populations. Currently, clinical histotripsy procedures are monitored with b-mode ultrasound to visualize the presence of cavitation activity and localize it spatially. However, b-mode ultrasound does not offer sufficient resolution to measure the intensity of the induced damage. Several alternatives have demonstrated varying levels of effectiveness at the pre-clinical level (e.g. shear-wave elastography, MRI, PAM/PCI), but the need for a robust method to monitor histotripsy-induced damage remains.In Chapter 2, several features of Acoustic Cavitation Emission (ACE) signals were investigated for trends that corresponded with bubble dynamics in tissue mimicking hydrogels. Three types and stiffnesses of hydrogels were exposed to repeated histotripsy-generated cavitation at single-focal-point targets, and the ACE-signals following each pulse were recorded. Bubble dynamics were recorded with high-speed (300kHz) optical imaging. Trends in bubble lifespan, nucleation & collapse shockwave amplitude, rebound characteristics, and broadband noise were all investigated as potential features to analyze for correlation with histotripsy exposure (pulses-per-location, ppl) and bubble dynamics (radius vs. time, radiusmax).In Chapter 3, ACE signal features identified from the previous chapter are compared against histological assessments of mechanically-induced tissue disruption in ex vivo tissue targets. Bulk histotripsy ablations (1.3cm cube) were performed in several types of ex-vivo bovine tissue (liver, kidney, brain), and the corresponding ACE signals were recorded throughout treatment and analyzed. Treated tissue samples were stained using hematoxylin and eosin (H&E) staining, and damage outcomes in the ablation zones were scored by a board-certified pathologist. Trends in normalized bubble lifespan assessed from the ACE signals correlated well with necrosis score.In Chapter 4, an automated technique for the quantification of mechanical tissue-disruption from scans of H&E histology is proposed. It functions in two parts: first, the nuclei identification/filtering, and second, the masking of the tissue-area affected by mechanical disruption. These two parts are used to calculate a normalized nuclei density, as a measure of mechanically-induced tissue disruption. Assessments of H&E histology of histotripsy ablations of ex-vivo bovine tissues by the automated tool correlated well with the quantified assessments by a board-certified pathologist. Chapter 5 describes the application of the previously described ACE-signal feedback techniques to histotripsy ablations performed on in-vivo tissues. Bulk ablations were performed in in-vivo porcine livers and several types of murine tumor models. ACE signals were recorded and analyzed for the features of the bubble dynamics. Following exposure, the animals were euthanized, and the ablation regions were extracted, fixed, H&E stained, and quantified using the methods described in Chapter 4. ACE-signals trends from each of the measured tissues/tumor types are presented, as well as correlations between ACE and H&E based assessments of damage.In Chapter 6, the parameters for efficient (i.e. greatest mL / minute) ablation of large volume clots in an in vitro intracerebral hemorrhage (ICH) model are investigated, along with the potential efficacy of ACE-signal feedback for transcranial applications. A range of pulse-repetition-frequencies (PRF) and pulses-per-location (ppl) within the steering volume were applied to generate 4cm diameter spherical lesions in a transcranial hematoma model. Then, the degree of damage was measured as the liquid volume that could be extracted with a syringe attached to a ventriculostomy catheter from the phantom after histotripsy exposure. Following the identification of the optimal PRF/ppl pair with the greatest ablation efficiency (i.e. mL / minute), that histotripsy protocol was applied to clots of variable age (i.e. stiffness) to assess their efficacy in clots with varying viscoelastic properties. Ablation rate and ACE-signal feedback-predictions were correlated against clot stiffness.Chapter 7 is a summary of the primary findings of this dissertation and potential future work for the improvement and/or expansion of ACE-signal based feedback for histotripsy ablation.
일반주제명  
Biomedical engineering
일반주제명  
Histology
일반주제명  
Health sciences
일반주제명  
Acoustics
키워드  
Histotripsy
키워드  
Damage monitoring
키워드  
Acoustic Cavitation Emission
키워드  
Acoustic signal acquisition
키워드  
Transcranial hematoma model
기타저자  
University of Michigan Biomedical Engineering
기본자료저록  
Dissertations Abstracts International. 87-03B.
전자적 위치 및 접속  
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MARC

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■0820  ▼a610
■1001  ▼aHaskell,  Scott.
■24510▼aPredicting  and  Monitoring  Histotripsy  Damage  With  Acoustic  Cavitation  Emission  Signals
■260    ▼a[Sl]▼bUniversity  of  Michigan▼c2025
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2025
■300    ▼a159  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  87-03,  Section:  B.
■500    ▼aAdvisor:  Sukovich,  Jonathan;Xu,  Zhen.
■5021  ▼aThesis  (Ph.D.)--University  of  Michigan,  2025.
■520    ▼aThis  dissertation  outlines  the  work  performed  to  establish  acoustic  signal  acquisition  and  analysis  techniques  to  predict  the  relationship  between  histotripsy  dose  and  the  degree  of  mechanically-induced  tissue  disruption.  As  the  applications  of  histotripsy  become  more  diverse,  targeting  new  cancers  and  other  pathologies,  having  tools  to  measure  the  degree  of  induced-damage  will  be  important  to  assist  in  establishing  treatment  standards  across  tissue-types  and  patient  populations.  Currently,  clinical  histotripsy  procedures  are  monitored  with  b-mode  ultrasound  to  visualize  the  presence  of  cavitation  activity  and  localize  it  spatially.  However,  b-mode  ultrasound  does  not  offer  sufficient  resolution  to  measure  the  intensity  of  the  induced  damage.  Several  alternatives  have  demonstrated  varying  levels  of  effectiveness  at  the  pre-clinical  level  (e.g.  shear-wave  elastography,  MRI,  PAM/PCI),  but  the  need  for  a  robust  method  to  monitor  histotripsy-induced  damage  remains.In  Chapter  2,  several  features  of  Acoustic  Cavitation  Emission  (ACE)  signals  were  investigated  for  trends  that  corresponded  with  bubble  dynamics  in  tissue  mimicking  hydrogels.  Three  types  and  stiffnesses  of  hydrogels  were  exposed  to  repeated  histotripsy-generated  cavitation  at  single-focal-point  targets,  and  the  ACE-signals  following  each  pulse  were  recorded.  Bubble  dynamics  were  recorded  with  high-speed  (300kHz)  optical  imaging.  Trends  in  bubble  lifespan,  nucleation  &  collapse  shockwave  amplitude,  rebound  characteristics,  and  broadband  noise  were  all  investigated  as  potential  features  to  analyze  for  correlation  with  histotripsy  exposure  (pulses-per-location,  ppl)  and  bubble  dynamics  (radius  vs.  time,  radiusmax).In  Chapter  3,  ACE  signal  features  identified  from  the  previous  chapter  are  compared  against  histological  assessments  of  mechanically-induced  tissue  disruption  in  ex  vivo  tissue  targets.  Bulk  histotripsy  ablations  (1.3cm  cube)  were  performed  in  several  types  of  ex-vivo  bovine  tissue  (liver,  kidney,  brain),  and  the  corresponding  ACE  signals  were  recorded  throughout  treatment  and  analyzed.  Treated  tissue  samples  were  stained  using  hematoxylin  and  eosin  (H&E)  staining,  and  damage  outcomes  in  the  ablation  zones  were  scored  by  a  board-certified  pathologist.  Trends  in  normalized  bubble  lifespan  assessed  from  the  ACE  signals  correlated  well  with  necrosis  score.In  Chapter  4,  an  automated  technique  for  the  quantification  of  mechanical  tissue-disruption  from  scans  of  H&E  histology  is  proposed.  It  functions  in  two  parts:  first,  the  nuclei  identification/filtering,  and  second,  the  masking  of  the  tissue-area  affected  by  mechanical  disruption.  These  two  parts  are  used  to  calculate  a  normalized  nuclei  density,  as  a  measure  of  mechanically-induced  tissue  disruption.  Assessments  of  H&E  histology  of  histotripsy  ablations  of  ex-vivo  bovine  tissues  by  the  automated  tool  correlated  well  with  the  quantified  assessments  by  a  board-certified  pathologist. Chapter  5  describes  the  application  of  the  previously  described  ACE-signal  feedback  techniques  to  histotripsy  ablations  performed  on  in-vivo  tissues.  Bulk  ablations  were  performed  in  in-vivo  porcine  livers  and  several  types  of  murine  tumor  models.  ACE  signals  were  recorded  and  analyzed  for  the  features  of  the  bubble  dynamics.  Following  exposure,  the  animals  were  euthanized,  and  the  ablation  regions  were  extracted,  fixed,  H&E  stained,  and  quantified  using  the  methods  described  in  Chapter  4.  ACE-signals  trends  from  each  of  the  measured  tissues/tumor  types  are  presented,  as  well  as  correlations  between  ACE  and  H&E  based  assessments  of  damage.In  Chapter  6,  the  parameters  for  efficient  (i.e.  greatest  mL  /  minute)  ablation  of  large  volume  clots  in  an  in  vitro  intracerebral  hemorrhage  (ICH)  model  are  investigated,  along  with  the  potential  efficacy  of  ACE-signal  feedback  for  transcranial  applications.  A  range  of  pulse-repetition-frequencies  (PRF)  and  pulses-per-location  (ppl)  within  the  steering  volume  were  applied  to  generate  4cm  diameter  spherical  lesions  in  a  transcranial  hematoma  model.  Then,  the  degree  of  damage  was  measured  as  the  liquid  volume  that  could  be  extracted  with  a  syringe  attached  to  a  ventriculostomy  catheter  from  the  phantom  after  histotripsy  exposure.  Following  the  identification  of  the  optimal  PRF/ppl  pair  with  the  greatest  ablation  efficiency  (i.e.  mL  /  minute),  that  histotripsy  protocol  was  applied  to  clots  of  variable  age  (i.e.  stiffness)  to  assess  their  efficacy  in  clots  with  varying  viscoelastic  properties.  Ablation  rate  and  ACE-signal  feedback-predictions  were  correlated  against  clot  stiffness.Chapter  7  is  a  summary  of  the  primary  findings  of  this  dissertation  and  potential  future  work  for  the  improvement  and/or  expansion  of  ACE-signal  based  feedback  for  histotripsy  ablation.
■590    ▼aSchool  code:  0127.
■650  4▼aBiomedical  engineering
■650  4▼aHistology
■650  4▼aHealth  sciences
■650  4▼aAcoustics
■653    ▼aHistotripsy
■653    ▼aDamage  monitoring
■653    ▼aAcoustic  Cavitation  Emission
■653    ▼aAcoustic  signal  acquisition  
■653    ▼aTranscranial  hematoma  model
■690    ▼a0541
■690    ▼a0566
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■690    ▼a0986
■71020▼aUniversity  of  Michigan▼bBiomedical  Engineering.
■7730  ▼tDissertations  Abstracts  International▼g87-03B.
■790    ▼a0127
■791    ▼aPh.D.
■792    ▼a2025
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17359835▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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