{"title":"Higher-order thermal modeling and computational analysis of laser ablation in anisotropic cardiac tissue.","authors":"Federica Bianconi, Massimiliano Leoni, Argyrios Petras, Emiliano Schena, Luca Gerardo-Giorda, Alessio Gizzi","doi":"10.1007/s10237-025-01926-x","DOIUrl":null,"url":null,"abstract":"<p><p>Laser ablation techniques employ fast hyperthermia mechanisms for diseased-tissue removal, characterized by high selectivity, thus preserving the surrounding healthy tissue. The associated modeling approaches are based on classical Fourier-type laws, though a limited predictivity is observed, particularly at fast time scales. Moreover, limited knowledge is available for cardiac tissue compared to radiofrequency approaches. The present work proposes a comprehensive modeling approach for the computational investigation of the key factors involved in laser-based techniques and assessing the outcomes of induced cellular thermal damage in the cardiac context. The study encompasses a comparative finite element study involving various thermal and cellular damage models incorporating optical-thermal couplings, three-state cellular death dynamics, and a second-order heat transfer formulation generalizing the classical Fourier-based heat equation. A parametric investigation of the thermal profiles shows that higher-order models accurately capture temperature dynamics and lesion formation compared with the classical Fourier-based model. The results highlight the critical role of cardiac anisotropy, influencing the shape and extent of thermal damage, while the three-state cell death model effectively describes the transition from reversible to irreversible damage. These findings demonstrate the reliability of higher-order thermal formulations, laying the basis for future investigations of arrhythmia management via in silico approaches.</p>","PeriodicalId":489,"journal":{"name":"Biomechanics and Modeling in Mechanobiology","volume":" ","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2025-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomechanics and Modeling in Mechanobiology","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1007/s10237-025-01926-x","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0
Abstract
Laser ablation techniques employ fast hyperthermia mechanisms for diseased-tissue removal, characterized by high selectivity, thus preserving the surrounding healthy tissue. The associated modeling approaches are based on classical Fourier-type laws, though a limited predictivity is observed, particularly at fast time scales. Moreover, limited knowledge is available for cardiac tissue compared to radiofrequency approaches. The present work proposes a comprehensive modeling approach for the computational investigation of the key factors involved in laser-based techniques and assessing the outcomes of induced cellular thermal damage in the cardiac context. The study encompasses a comparative finite element study involving various thermal and cellular damage models incorporating optical-thermal couplings, three-state cellular death dynamics, and a second-order heat transfer formulation generalizing the classical Fourier-based heat equation. A parametric investigation of the thermal profiles shows that higher-order models accurately capture temperature dynamics and lesion formation compared with the classical Fourier-based model. The results highlight the critical role of cardiac anisotropy, influencing the shape and extent of thermal damage, while the three-state cell death model effectively describes the transition from reversible to irreversible damage. These findings demonstrate the reliability of higher-order thermal formulations, laying the basis for future investigations of arrhythmia management via in silico approaches.
期刊介绍:
Mechanics regulates biological processes at the molecular, cellular, tissue, organ, and organism levels. A goal of this journal is to promote basic and applied research that integrates the expanding knowledge-bases in the allied fields of biomechanics and mechanobiology. Approaches may be experimental, theoretical, or computational; they may address phenomena at the nano, micro, or macrolevels. Of particular interest are investigations that
(1) quantify the mechanical environment in which cells and matrix function in health, disease, or injury,
(2) identify and quantify mechanosensitive responses and their mechanisms,
(3) detail inter-relations between mechanics and biological processes such as growth, remodeling, adaptation, and repair, and
(4) report discoveries that advance therapeutic and diagnostic procedures.
Especially encouraged are analytical and computational models based on solid mechanics, fluid mechanics, or thermomechanics, and their interactions; also encouraged are reports of new experimental methods that expand measurement capabilities and new mathematical methods that facilitate analysis.