Rohan Amare, Danielle Stolley, Steve Parrish, Megan Jacobsen, Rick Layman, Chimamanda Santos, Beatrice Riviere, Natalie Fowlkes, David Fuentes, Erik Cressman
{"title":"1D Thermoembolization Model Using CT Imaging Data for Porcine Liver","authors":"Rohan Amare, Danielle Stolley, Steve Parrish, Megan Jacobsen, Rick Layman, Chimamanda Santos, Beatrice Riviere, Natalie Fowlkes, David Fuentes, Erik Cressman","doi":"arxiv-2409.06811","DOIUrl":null,"url":null,"abstract":"Objective: Innovative therapies such as thermoembolization are expected to\nplay an important role in improvising care for patients with diseases such as\nhepatocellular carcinoma. Thermoembolization is a minimally invasive strategy\nthat combines thermal ablation and embolization in a single procedure. This\napproach exploits an exothermic chemical reaction that occurs when an acid\nchloride is delivered via an endovascular route. However, comprehension of the\ncomplexities of the biophysics of thermoembolization is challenging.\nMathematical models can aid in understanding such complex processes and\nassisting clinicians in making informed decisions. In this study, we used a\nHagen Poiseuille 1D blood flow model to predict the mass transport and possible\nembolization locations in a porcine hepatic artery. Method: The 1D flow model was used on in vivo embolization imaging data of\nthree pigs. The hydrolysis time constant of acid chloride chemical reaction was\noptimized for each pig, and LOOCV method was used to test the model's\npredictive ability. Conclusion: This basic model provided a balanced accuracy rate of 66.8% for\nidentifying the possible locations of embolization in the hepatic artery. Use\nof the model provides an initial understanding of the vascular transport\nphenomena that are predicted to occur as a result of thermoembolization.","PeriodicalId":501378,"journal":{"name":"arXiv - PHYS - Medical Physics","volume":"9 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - PHYS - Medical Physics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2409.06811","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: Innovative therapies such as thermoembolization are expected to
play an important role in improvising care for patients with diseases such as
hepatocellular carcinoma. Thermoembolization is a minimally invasive strategy
that combines thermal ablation and embolization in a single procedure. This
approach exploits an exothermic chemical reaction that occurs when an acid
chloride is delivered via an endovascular route. However, comprehension of the
complexities of the biophysics of thermoembolization is challenging.
Mathematical models can aid in understanding such complex processes and
assisting clinicians in making informed decisions. In this study, we used a
Hagen Poiseuille 1D blood flow model to predict the mass transport and possible
embolization locations in a porcine hepatic artery. Method: The 1D flow model was used on in vivo embolization imaging data of
three pigs. The hydrolysis time constant of acid chloride chemical reaction was
optimized for each pig, and LOOCV method was used to test the model's
predictive ability. Conclusion: This basic model provided a balanced accuracy rate of 66.8% for
identifying the possible locations of embolization in the hepatic artery. Use
of the model provides an initial understanding of the vascular transport
phenomena that are predicted to occur as a result of thermoembolization.