Medical Imaging 2021: Physics of Medical Imaging 2021
DOI: 10.1117/12.2580881
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Evaluation of methods to derive blood flow velocity from 1000 fps high-speed angiographic sequences (HSA) using optical flow (OF) and computational fluid dynamics (CFD)

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Cited by 15 publications
(16 citation statements)
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“…Alternative particle tracers, such as ethiodol droplets, can provide higher contrast to noise ratio. 6 However, there are so far no particle tracers that can be used to perform X-PIV in-vivo, and therefore research developing novel particle tracers for 3D-XPIV will be necessary for real-time clinical applications. Further work modelling CFD particle trajectories would offer a direct comparison of trajectories that may partially explain discrepencies between CFD and 3D-XPIV values.…”
Section: Discussionmentioning
confidence: 99%
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“…Alternative particle tracers, such as ethiodol droplets, can provide higher contrast to noise ratio. 6 However, there are so far no particle tracers that can be used to perform X-PIV in-vivo, and therefore research developing novel particle tracers for 3D-XPIV will be necessary for real-time clinical applications. Further work modelling CFD particle trajectories would offer a direct comparison of trajectories that may partially explain discrepencies between CFD and 3D-XPIV values.…”
Section: Discussionmentioning
confidence: 99%
“…Unlike CFD, 3D-XPIV can be performed immediately after HSA image acquisition, requiring less computational power and time. 4…”
Section: Introductionmentioning
confidence: 99%
“…Additional evaluation is required, but based on this analysis, reflux lengths should be limited to low values (controlled by contrast injection rate) if the angiographic acquisition will be at low frame rates. Extremely high frame rate detectors are in development, 37,45 and once made available for clinical use, these would be extremely valuable to any angiographic contrast flow evaluations.…”
Section: Discussionmentioning
confidence: 99%
“…Contrast concentration–time curves have, for example, been parameterized by their first moments, peaks, or slopes and have been fit with various functions (such as lag normal, gamma variate, or exponential) to extract transit‐time/dilution measures or to estimate treatment efficacy 28–31 . Increased computational power and flat‐panel detectors have allowed for pixel‐by‐pixel tracking of contrast intensities and generation of color‐coded parametric maps, use of computational fluid dynamics, and extraction of flow measures using three‐dimensional contrast transport data 30,32–37 . However, the flow estimation accuracy of even these recent techniques seems to be limited to very specific conditions—required observation of cardiac pulsatility in contrast time–concentration curves, imaging of straight vessel segments without any branch overlap, use of ultrahigh image acquisition rates with poor vessel opacification, or observation of high accuracies only in benchtop studies with steady flow in tubes.…”
Section: Introductionmentioning
confidence: 99%
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