Editorial: Novel computational fluid dynamics methods for diagnosis, monitoring, prediction, and personalized treatment for cardiovascular disease and cancer metastasis
Notice bibliographique
Résumé
This Research Topic features recent advances in computational hemodynamic methods for diagnosis, prediction, and personalized treatment planning applicable to cardiovascular disease and cancer metastasis. The collection of articles describes novel tools, therapeutic and process improvement methods, and studies exploiting the capability of computational tools to provide quantitative information about hemodynamics and interactions with cells and tissues beyond conventional clinical possibilities.For example, Wang et al present exciting results showing patient specific steady computational fluid dynamics (CFD) simulations following virtual splenectomy that may predict the likelihood of thrombosis 1 . Preoperative imaging data were used for model creation from portal hypertensive patients who underwent splenectomy. Results show the area of low wall shear stress (WSS; defined as <20% of the patient-specific average) can predict post-splenectomy thrombosis with an area under the receiver operating curve of 0.75. Diameter of the splenic vein was correlated with WSS results, which was further validated in another small group of patients. Extension of this work may influence future postoperative management and prophylaxis protocols in this patient population.Assi et al conducted patient-specific CFD with ultimate application to the prediction of thrombosis using simulations with physiologic boundary conditions to characterize hemodynamics from iliac vein compression syndrome patients relative to controls 2 . Their results from this understudied population showed increased shear rate in the left versus right common iliac vein of patients (resulting in a higher ratio), and relative to controls. This work serves as an exciting foundation for shear rate and the shear rate ratio between contralateral iliac veins to serve as potential measures of thrombosis risk in iliac vein compression syndrome patients.Citing alterations in endothelial cell transport based on local WSS distributions, Rahmati and Maftoon used an idealized vessel with variable curvature to simulate the role of WSS from tortuosity on interactions between circulating tumor cells and the vessel wall 3 . Simulation methods included fluid-structure and receptorligand interactions for circulating tumor cell (i.e. deformable body) adhesion within a simulated plasma environment via an immersed boundary approach. Curvature, asymmetrical flow patterns and associated WSS alterations established local adhesion dynamics. Expansion of such methods may ultimately prove useful in assessing the likelihood of metastasis.Colombo et al describe a workflow using in vitro and in silico approaches to further study hemodynamics in the microvasculature and build from prior papers associating WSS alterations with coronary microvascular disease 4 . In short, the workflow created an idealized microvasculature representation based on Murray's law, which was then printed using 3D molds and ultimately seeded with human embryonic kidney cells to study their response to varying degrees of microvascular disease (i.e. impaired flow to several microvasculature model outlets).Lopez-Santana and colleagues employed CFD simulations with multiple inlets, Windkessel outlet boundary conditions, and geometry from a healthy patient to characterize aortic flow patterns resulting from different geometric parameters related to the anastomosis of a left ventricular assist device outflow graft 5 . Specifically the authors vary the angle of insertion, distance along the ascending aorta from the anatomic ventriculoarterial junction, and cardinal position around the aorta (coronal to sagittal) as parameters, and characterize results in terms of WSS, pressure, vorticity and turbulent kinetic energy.Kim et al. quantified differences in left atrial morphology and associated readouts related to the potential for stroke (i.e. velocity and stasis) using models created from phase-contrast as compared to contrast-enhanced magnetic resonance angiography 6 . Results were promising, suggesting their segmentation and registration workflow allows for the use of contrast enhanced imaging data for 4D flow analysis with minimal impact on the readouts assessed.
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Comment cette classification a été obtenuedéplier
Prédiction distillée sur la base complète
Imitation des enseignantsNi prévalence calibrée, ni vérité terrain. Validation humaine à venir. Apprise à partir de 10 348 étiquettes directes de Codex et de 10 348 étiquettes directes de Gemma. Le mode candidate est l'union des têtes enseignantes seuillées; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont ni des étiquettes humaines ni des étiquettes directes de modèles de pointe.
Scores Codex et Gemma par catégorie
| Catégorie | Codex | Gemma |
|---|---|---|
| Métarecherche | 0,000 | 0,000 |
| Méta-épidémiologie (sens strict) | 0,000 | 0,000 |
| Méta-épidémiologie (sens large) | 0,001 | 0,000 |
| Bibliométrie | 0,001 | 0,000 |
| Études des sciences et des technologies | 0,000 | 0,000 |
| Communication savante | 0,000 | 0,000 |
| Science ouverte | 0,000 | 0,000 |
| Intégrité de la recherche | 0,001 | 0,000 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,000 | 0,000 |
Scores machine (provisoires)
Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.
Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.
score_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découleClassification
machine, non validéePrédiction automatique; un appel candidat d’une seule tête enseignante, pas un consensus.
Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».