• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于 GPU 加速的软组织热损伤建模。

Modeling of soft tissue thermal damage based on GPU acceleration.

机构信息

School of Engineering, RMIT University , Bundoora , Australia.

Robotics and Mechatronics Research Laboratory, Department of Mechanical and Aerospace Engineering, Monash University , Clayton , Australia.

出版信息

Comput Assist Surg (Abingdon). 2019 Oct;24(sup1):5-12. doi: 10.1080/24699322.2018.1557891. Epub 2019 Jul 24.

DOI:10.1080/24699322.2018.1557891
PMID:31340685
Abstract

Hyperthermia treatments require precise control of thermal energy to form the coagulation zones which sufficiently cover the tumor without affecting surrounding healthy tissues. This has led modeling of soft tissue thermal damage to become important in hyperthermia treatments to completely eradicate tumors without inducing tissue damage to surrounding healthy tissues. This paper presents a methodology based on GPU acceleration for modeling and analysis of bio-heat conduction and associated thermal-induced tissue damage for prediction of soft tissue damage in thermal ablation, which is a typical hyperthermia therapy. The proposed methodology combines the Arrhenius Burn integration with Pennes' bio-heat transfer for prediction of temperature field and thermal damage in soft tissues. The problem domain is spatially discretized on 3-D linear tetrahedral meshes by the Galerkin finite element method and temporally discretized by the explicit forward finite difference method. To address the expensive computation load involved in the finite element method, GPU acceleration is implemented using the High-Level Shader Language and achieved via a sequential execution of compute shaders in the GPU rendering pipeline. Simulations on a cube-shape specimen and comparison analysis with standalone CPU execution were conducted, demonstrating the proposed GPU-accelerated finite element method can effectively predict the temperature distribution and associated thermal damage in real time. Results show that the peak temperature is achieved at the heat source point and the variation of temperature is mainly dominated in its direct neighbourhood. It is also found that by the continuous application of point-source heat energy, the tissue at the heat source point is quickly necrotized in a matter of seconds, while the entire neighbouring tissues are fully necrotized in several minutes. Further, the proposed GPU acceleration significantly improves the computational performance for soft tissue thermal damage prediction, leading to a maximum reduction of 55.3 times in computation time comparing to standalone CPU execution.

摘要

热疗需要精确控制热能以形成凝固区域,这些区域应充分覆盖肿瘤,同时不影响周围的健康组织。这使得软组织热损伤建模在热疗中变得非常重要,因为其目的是在不引起周围健康组织损伤的情况下彻底消灭肿瘤。本文提出了一种基于 GPU 加速的方法,用于建模和分析生物热传导以及相关的热诱导组织损伤,以预测热消融中的软组织损伤,这是一种典型的热疗方法。所提出的方法将 Arrhenius Burn 积分与 Pennes 生物传热相结合,用于预测软组织中的温度场和热损伤。问题域在三维线性四面体网格上通过 Galerkin 有限元方法离散化,在时间上通过显式向前有限差分方法离散化。为了解决有限元方法中涉及的昂贵计算负载,使用高级着色语言在 GPU 上实现了 GPU 加速,并通过在 GPU 渲染管道中顺序执行计算着色器来实现。在立方体形状的样本上进行了模拟,并与独立的 CPU 执行进行了比较分析,结果表明,所提出的 GPU 加速有限元方法可以有效地实时预测温度分布和相关的热损伤。结果表明,峰值温度出现在热源点,温度的变化主要由其直接邻域决定。还发现,通过连续施加点源热能,热源点处的组织在几秒钟内迅速坏死,而整个邻近组织在几分钟内完全坏死。此外,所提出的 GPU 加速方法显著提高了软组织热损伤预测的计算性能,与独立的 CPU 执行相比,计算时间最多减少了 55.3 倍。

相似文献

1
Modeling of soft tissue thermal damage based on GPU acceleration.基于 GPU 加速的软组织热损伤建模。
Comput Assist Surg (Abingdon). 2019 Oct;24(sup1):5-12. doi: 10.1080/24699322.2018.1557891. Epub 2019 Jul 24.
2
Fast computation of soft tissue thermal response under deformation based on fast explicit dynamics finite element algorithm for surgical simulation.基于手术模拟快速显式动力学有限元算法的软组织变形下的热响应快速计算。
Comput Methods Programs Biomed. 2020 Apr;187:105244. doi: 10.1016/j.cmpb.2019.105244. Epub 2019 Nov 27.
3
Towards real-time finite-strain anisotropic thermo-visco-elastodynamic analysis of soft tissues for thermal ablative therapy.用于热消融治疗的软组织实时有限应变各向异性热粘弹动力学分析
Comput Methods Programs Biomed. 2021 Jan;198:105789. doi: 10.1016/j.cmpb.2020.105789. Epub 2020 Oct 8.
4
Neural network methodology for real-time modelling of bio-heat transfer during thermo-therapeutic applications.神经网络方法在热疗应用中实时模拟生物传热过程。
Artif Intell Med. 2019 Nov;101:101728. doi: 10.1016/j.artmed.2019.101728. Epub 2019 Sep 30.
5
Simulating thermal effects of MR-guided focused ultrasound in cortical bone and its surrounding tissue.模拟磁共振引导聚焦超声在皮质骨及其周围组织中的热效应。
Med Phys. 2018 Feb;45(2):506-519. doi: 10.1002/mp.12704. Epub 2017 Dec 25.
6
A numerical study on dual-phase-lag model of bio-heat transfer during hyperthermia treatment.热疗过程中生物传热双相滞后模型的数值研究。
J Therm Biol. 2015 Apr-May;49-50:98-105. doi: 10.1016/j.jtherbio.2015.02.008. Epub 2015 Feb 17.
7
A study on thermal damage during hyperthermia treatment based on DPL model for multilayer tissues using finite element Legendre wavelet Galerkin approach.基于有限元勒让德小波伽辽金方法的多层组织双光子光声层析成像模型热疗过程热损伤研究
J Therm Biol. 2016 Dec;62(Pt B):170-180. doi: 10.1016/j.jtherbio.2016.06.020. Epub 2016 Jul 2.
8
Thermal-mechanical deformation modelling of soft tissues for thermal ablation.用于热消融的软组织热-机械变形建模
Biomed Mater Eng. 2014;24(6):2299-310. doi: 10.3233/BME-141043.
9
Non-Fourier based thermal-mechanical tissue damage prediction for thermal ablation.基于非傅里叶的热消融热机械组织损伤预测
Bioengineered. 2017 Jan 2;8(1):71-77. doi: 10.1080/21655979.2016.1227609. Epub 2016 Sep 30.
10
Coupled thermo-electro-mechanical models for thermal ablation of biological tissues and heat relaxation time effects.生物组织热消融的热电-力学耦合模型及热弛豫时间效应。
Phys Med Biol. 2019 Dec 13;64(24):245008. doi: 10.1088/1361-6560/ab4cc5.

引用本文的文献

1
Optimization of laser dosimetry based on patient-specific anatomical models for the ablation of pancreatic ductal adenocarcinoma tumor.基于个体化解剖模型的胰腺导管腺癌肿瘤消融激光剂量学优化。
Sci Rep. 2023 Jul 8;13(1):11053. doi: 10.1038/s41598-023-37859-7.