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Blanco, P. J.

Publications and source records attributed to Blanco, P. J..

3 recordsLinked to original sources

Foot perfusion. Insights from an anatomically detailed arterial network model

Peripheral artery disease currently affects over 202 million people worldwide. The ankle-brachial index is one of the most used measurements to assess a reduction in blood flow to the foot, but it is not able to characterise tissue perfusion. Information on tissue perfusion can be obtained, among others, through an MRI scan, which is time-consuming and can be painful if induction of ischemia is warranted for the scan. As an alternative, we model foot perfusion during a cuff-induced ischaemia test to characterise how occlusions in foot arteries affect perfusion in foot regions. Simulations are not patient-specific at this stage, and are conducted on a 1D arterial network model which includes 154 foot and calf arterial segments, providing a realistic description of the topology of the foot arterial vasculature. A baseline model characterizes perfusion in angiosomes under healthy conditions, which is then modified to reflect 42 pathological scenarios by introducing occlusions and different levels of collateral impairment. Results show a marked influence of collateral impairment on angiosome perfusion under the condition of a single-artery occlusion, highlighting the role of blood redistribution. If two feeding arteries are occluded, perfusion markedly decreases at all collateral impairment levels due to the severe reduction in incoming blood flow. These results provide a bridge between the angiosome-targeted and "best-vessel" strategies for revascularization, showing that both can be correct depending on collateral sufficiency. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=77 SRC="FIGDIR/small/692561v1_ufig1.gif" ALT="Figure 1"> View larger version (22K): org.highwire.dtl.DTLVardef@10d4da5org.highwire.dtl.DTLVardef@649775org.highwire.dtl.DTLVardef@13b8e4org.highwire.dtl.DTLVardef@cfbb3e_HPS_FORMAT_FIGEXP M_FIG C_FIG HighlightsO_LIWe propose a computational model of foot perfusion during a cuff-induced ischaemia test that allows the assessment of perfusion in each angiosome of the foot C_LIO_LIWe study how occlusions in the main feeding arteries of the foot impact tissue perfusion C_LIO_LIWe highlight the role of collateralization if adequate inflow is maintained C_LIO_LIResults show that both angiosome-targeted and "best-vessel" strategies for revascularization can be correct depending on arch patency and collateral sufficiency C_LI

bioengineering↗

Blood flow modeling under LVAD physiology. From global circulation to local hemodynamics

This document presents the modeling strategy to address the in-silico study of different LVAD patho-physiological scenarios. The proposed approach employs a closed-loop lumped-parameter compartmental representation of the global circulation in the cardiovascular system (CVS). The CVS is coupled to a HeartMate 3 LVAD, and different cardiovascular conditions are proposed by modification of model parameters. Once the simulation for these conditions are performed, the cardiac function is analyzed in detail, and the global circulation model delivers flow rate waveforms which are employed as boundary conditions in a 3D hemodynamic simulation. This local circulation model is built using a patient-specific geometry of the aortic arch, containing 7 inlet/outlet boundaries, namely: LVAD cannula, aortic root, left and right subclavian arteries, left and right common carotid arteries and thoracic aorta. This model is exploited to investigate the impact of global cardiovascular conditions in the local hemodynamic features, particularly the wall shear stress (WSS) in different spatial regions.

bioengineering↗

A modular and reusable model of epithelial transport in the proximal convoluted tubule

We review a collection of published renal epithelial transport models, from which we build a consistent and reusable mathematical model able to reproduce many observations and predictions from the literature. The flexible modular model we present here can be adapted to specific configurations of epithelial transport, and in this work we focus on transport in the proximal convoluted tubule of the renal nephron. Our mathematical model of the epithelial proximal convoluted tubule describes the cellular and subcellular mechanisms of the transporters, intracellular buffering, solute fluxes, and other processes. We provide free and open access to the Python implementation to ensure our multiscale proximal tubule model is accessible; enabling the reader to explore the model through setting their own simulations, reproducibility tests, and sensitivity analyses.

bioengineering↗