Simulating Subject-Specific Aortic Hemodynamic Effects of Valvular Lesions in Rheumatic Heart Disease

dc.contributor.authorCebull, Hannah L.
dc.contributor.authorAremu, Olukayode O.
dc.contributor.authorKulkarni, Radhika S.
dc.contributor.authorZhang, Samuel X.
dc.contributor.authorSamuels, Petronella
dc.contributor.authorJermy, Stephen
dc.contributor.authorNtusi, Ntobeko A. B.
dc.contributor.authorGoergen, Craig J.
dc.contributor.departmentBiomedical Engineering, Purdue School of Engineering and Technology
dc.date.accessioned2024-12-09T16:32:17Z
dc.date.available2024-12-09T16:32:17Z
dc.date.issued2023
dc.description.abstractRheumatic heart disease (RHD) is a neglected tropical disease despite the substantial global health burden. In this study, we aimed to develop a lower cost method of modeling aortic blood flow using subject-specific velocity profiles, aiding our understanding of RHD's consequences on the structure and function of the ascending aorta. Echocardiography and cardiovascular magnetic resonance (CMR) are often used for diagnosis, including valve dysfunction assessments. However, there is a need to further characterize aortic valve lesions to improve treatment options and timing for patients, while using accessible and affordable imaging strategies. Here, we simulated effects of RHD aortic valve lesions on the aorta using computational fluid dynamics (CFD). We hypothesized that inlet velocity distribution and wall shear stress (WSS) will differ between RHD and non-RHD individuals, as well as between subject-specific and standard Womersley velocity profiles. Phase-contrast CMR data from South Africa of six RHD subjects with aortic stenosis and/or regurgitation and six matched controls were used to estimate subject-specific velocity inlet profiles and the mean velocity for Womersley profiles. Our findings were twofold. First, we found WSS in subject-specific RHD was significantly higher (p < 0.05) than control subject simulations, while Womersley simulation groups did not differ. Second, evaluating spatial velocity differences (ΔSV) between simulation types revealed that simulations of RHD had significantly higher ΔSV than non-RHD (p < 0.05), these results highlight the need for implementing subject-specific input into RHD CFD, which we demonstrate how to accomplish through accessible methods.
dc.eprint.versionFinal published version
dc.identifier.citationCebull HL, Aremu OO, Kulkarni RS, et al. Simulating Subject-Specific Aortic Hemodynamic Effects of Valvular Lesions in Rheumatic Heart Disease. J Biomech Eng. 2023;145(11):111003. doi:10.1115/1.4063000
dc.identifier.urihttps://hdl.handle.net/1805/44858
dc.language.isoen_US
dc.publisherASME
dc.relation.isversionof10.1115/1.4063000
dc.relation.journalJournal of Biomechanical Engineering
dc.rightsPublisher Policy
dc.sourcePMC
dc.subjectAorta
dc.subjectAortic valve
dc.subjectBlood flow velocity
dc.subjectHemodynamics
dc.subjectMagnetic resonance imaging
dc.subjectRheumatic heart disease
dc.titleSimulating Subject-Specific Aortic Hemodynamic Effects of Valvular Lesions in Rheumatic Heart Disease
dc.typeArticle
ul.alternative.fulltexthttps://pmc.ncbi.nlm.nih.gov/articles/PMC10405283/
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