PMID- 28890987 OWN - NLM STAT- MEDLINE DCOM- 20180604 LR - 20220408 IS - 1528-8951 (Electronic) IS - 0148-0731 (Linking) VI - 140 IP - 1 DP - 2018 Jan 1 TI - Impact of Patient-Specific Inflow Velocity Profile on Hemodynamics of the Thoracic Aorta. LID - 10.1115/1.4037857 [doi] AB - Computational fluid dynamics (CFD) provides a noninvasive method to functionally assess aortic hemodynamics. The thoracic aorta has an anatomically complex inlet comprising of the aortic valve and root, which is highly prone to different morphologies and pathologies. We investigated the effect of using patient-specific (PS) inflow velocity profiles compared to idealized profiles based on the patient's flow waveform. A healthy 31 yo with a normally functioning tricuspid aortic valve (subject A), and a 52 yo with a bicuspid aortic valve (BAV), aortic valvular stenosis, and dilated ascending aorta (subject B) were studied. Subjects underwent MR angiography to image and reconstruct three-dimensional (3D) geometric models of the thoracic aorta. Flow-magnetic resonance imaging (MRI) was acquired above the aortic valve and used to extract the patient-specific velocity profiles. Subject B's eccentric asymmetrical inflow profile led to highly complex velocity patterns, which were not replicated by the idealized velocity profiles. Despite having identical flow rates, the idealized inflow profiles displayed significantly different peak and radial velocities. Subject A's results showed some similarity between PS and parabolic inflow profiles; however, other parameters such as Flowasymmetry were significantly different. Idealized inflow velocity profiles significantly alter velocity patterns and produce inaccurate hemodynamic assessments in the thoracic aorta. The complex structure of the aortic valve and its predisposition to pathological change means the inflow into the thoracic aorta can be highly variable. CFD analysis of the thoracic aorta needs to utilize fully PS inflow boundary conditions in order to produce truly meaningful results. FAU - Youssefi, Pouya AU - Youssefi P AD - Department of Cardiothoracic Surgery, St. George's Hospital, London SW17 0QT, UK. AD - Department of Biomedical Engineering, King's College London, London SE1 7EH, UK e-mail: . FAU - Gomez, Alberto AU - Gomez A AD - Department of Biomedical Engineering, King's College London, London SE1 7EH, UK e-mail: . FAU - Arthurs, Christopher AU - Arthurs C AD - Department of Biomedical Engineering, King's College London, London SE1 7EH, UK e-mail: . FAU - Sharma, Rajan AU - Sharma R AD - Department of Cardiology, St. George's Hospital, London SW17 0QT, UK e-mail: . FAU - Jahangiri, Marjan AU - Jahangiri M AD - Department of Cardiothoracic Surgery, St. George's Hospital, London SW17 0QT, UK e-mail: . FAU - Alberto Figueroa, C AU - Alberto Figueroa C AD - Department of Biomedical Engineering, King's College London, London SE1 7EH, UK. AD - Departments of Surgery and Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109 e-mail: . LA - eng GR - NH/11/5/29058/BHF_/British Heart Foundation/United Kingdom PT - Journal Article PL - United States TA - J Biomech Eng JT - Journal of biomechanical engineering JID - 7909584 SB - IM MH - Aorta, Thoracic/diagnostic imaging/*physiology MH - *Hemodynamics MH - Humans MH - Imaging, Three-Dimensional MH - Magnetic Resonance Imaging MH - *Patient-Specific Modeling EDAT- 2017/09/12 06:00 MHDA- 2018/06/05 06:00 CRDT- 2017/09/12 06:00 PHST- 2016/07/28 00:00 [received] PHST- 2017/09/12 06:00 [pubmed] PHST- 2018/06/05 06:00 [medline] PHST- 2017/09/12 06:00 [entrez] AID - 2654063 [pii] AID - 10.1115/1.4037857 [doi] PST - ppublish SO - J Biomech Eng. 2018 Jan 1;140(1). doi: 10.1115/1.4037857.