Computational Assessment of Hemodynamics in Asymmetric-Type Lesion of Idealized Coronary Stenoses

dc.contributor.author Oyejide, A.J.
dc.contributor.author Abodunrin, O.D.
dc.contributor.author Ige, E.O.
dc.contributor.author Awonusi, A.A.
dc.date.accessioned 2025-12-15T15:38:31Z
dc.date.available 2025-12-15T15:38:31Z
dc.date.issued 2025
dc.description.abstract Purpose: Coronary artery stenosis, characterized by the narrowing of the arterial lumen, significantly alters blood flow and contributes to the progression of cardiovascular diseases. This study investigates the hemodynamic effects of different stenosis morphologies, all maintaining an 80% lumen reduction, to determine how variations in shape influence flow behavior and mechanical stresses. Methods: We employed computational fluid dynamics (CFD) to analyze five idealized stenosis geometries with the following asymmetric and symmetric configurations: C1 (10% and 70%), C2 (20% and 60%), C3 (30% and 50%), C4 (40% and 40%), and C5 (0% and 80%). Using physiological pulsatile flow conditions, we evaluated key hemodynamic parameters, including velocity profiles, wall shear stress, and pressure distribution. Results: Despite having the same degree of lumen reduction, each stenosis configuration produced distinct hemodynamic profiles. Asymmetric stenoses, particularly the C1 and C2 cases, exhibited pronounced flow disturbances, higher wall shear stress at the stenosis throat, and increased post-stenotic turbulence. In contrast, symmetric stenoses, such as C4, demonstrated more uniform flow and reduced vortex formation. These findings suggest that stenosis morphology plays a crucial role in determining local flow dynamics. Conclusion: Our findings challenge the common practice of generalizing results across stenosis configurations without considering morphological variations, which is prevalent in many CFD studies using idealized models. This study emphasizes the need for stenosis-specific assessments in CFD analyses and clinical interpretations to improve the accuracy of diagnostic tools, optimize personalized treatment strategies, and guide the design of medical devices such as stents. © The Author(s), under exclusive licence to The Brazilian Society of Biomedical Engineering 2025. en_US
dc.identifier.doi 10.1007/s42600-025-00440-4
dc.identifier.issn 2446-4732
dc.identifier.scopus 2-s2.0-105021006387
dc.identifier.uri https://doi.org/10.1007/s42600-025-00440-4
dc.identifier.uri https://hdl.handle.net/20.500.12469/7664
dc.language.iso en en_US
dc.publisher Springer Science and Business Media Deutschland GmbH en_US
dc.relation.ispartof Research on Biomedical Engineering en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Atherosclerosis en_US
dc.subject CFD en_US
dc.subject Coronary Artery en_US
dc.subject Hemodynamics en_US
dc.subject Idealized Geometry en_US
dc.subject Lumen en_US
dc.subject Stenosis en_US
dc.title Computational Assessment of Hemodynamics in Asymmetric-Type Lesion of Idealized Coronary Stenoses en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.scopusid 58000882000
gdc.author.scopusid 57223873517
gdc.author.scopusid 57195775695
gdc.author.scopusid 57808781200
gdc.description.department Kadir Has University en_US
gdc.description.departmenttemp [Oyejide] Ayodele James, Department of Biomedical Engineering, Afe Babalola University, Ado-Ekiti, Nigeria, Department of Electrical and Electronic Engineering, Kadir Has Üniversitesi, Istanbul, Turkey; [Abodunrin] Oluwatosin David, Department of Biomedical Engineering, Afe Babalola University, Ado-Ekiti, Nigeria, Université Euro-Méditerranéenne de Fès, Fez, Fes-Meknes, Morocco; [Ige] Ebenezer Olubunmi, Kate Gleason College of Engineering, Rochester, NY, United States; [Awonusi] Adetokunbo Andrew, College of Engineering, Architecture and Technology, Stillwater, OK, United States en_US
gdc.description.issue 4 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q3
gdc.description.volume 41 en_US
gdc.description.wosquality N/A
relation.isOrgUnitOfPublication b20623fc-1264-4244-9847-a4729ca7508c
relation.isOrgUnitOfPublication.latestForDiscovery b20623fc-1264-4244-9847-a4729ca7508c

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