Modelling the impact of clot fragmentation on the microcirculation after thrombectomy.
Many ischaemic stroke patients who have a mechanical removal of their clot (thrombectomy) do not get reperfusion of tissue despite the thrombus being removed. One hypothesis for this 'no-reperfusion' phenomenon is micro-emboli fragmenting off the large clot during thrombectomy and occludin...
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doaj-3e93e79376c346a7b1817dd39b9283f02021-08-13T04:32:11ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582021-03-01173e100851510.1371/journal.pcbi.1008515Modelling the impact of clot fragmentation on the microcirculation after thrombectomy.Wahbi K El-BouriAndrew MacGowanTamás I JózsaMatthew J GounisStephen J PayneMany ischaemic stroke patients who have a mechanical removal of their clot (thrombectomy) do not get reperfusion of tissue despite the thrombus being removed. One hypothesis for this 'no-reperfusion' phenomenon is micro-emboli fragmenting off the large clot during thrombectomy and occluding smaller blood vessels downstream of the clot location. This is impossible to observe in-vivo and so we here develop an in-silico model based on in-vitro experiments to model the effect of micro-emboli on brain tissue. Through in-vitro experiments we obtain, under a variety of clot consistencies and thrombectomy techniques, micro-emboli distributions post-thrombectomy. Blood flow through the microcirculation is modelled for statistically accurate voxels of brain microvasculature including penetrating arterioles and capillary beds. A novel micro-emboli algorithm, informed by the experimental data, is used to simulate the impact of micro-emboli successively entering the penetrating arterioles and the capillary bed. Scaled-up blood flow parameters-permeability and coupling coefficients-are calculated under various conditions. We find that capillary beds are more susceptible to occlusions than the penetrating arterioles with a 4x greater drop in permeability per volume of vessel occluded. Individual microvascular geometries determine robustness to micro-emboli. Hard clot fragmentation leads to larger micro-emboli and larger drops in blood flow for a given number of micro-emboli. Thrombectomy technique has a large impact on clot fragmentation and hence occlusions in the microvasculature. As such, in-silico modelling of mechanical thrombectomy predicts that clot specific factors, interventional technique, and microvascular geometry strongly influence reperfusion of the brain. Micro-emboli are likely contributory to the phenomenon of no-reperfusion following successful removal of a major clot.https://doi.org/10.1371/journal.pcbi.1008515 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Wahbi K El-Bouri Andrew MacGowan Tamás I Józsa Matthew J Gounis Stephen J Payne |
spellingShingle |
Wahbi K El-Bouri Andrew MacGowan Tamás I Józsa Matthew J Gounis Stephen J Payne Modelling the impact of clot fragmentation on the microcirculation after thrombectomy. PLoS Computational Biology |
author_facet |
Wahbi K El-Bouri Andrew MacGowan Tamás I Józsa Matthew J Gounis Stephen J Payne |
author_sort |
Wahbi K El-Bouri |
title |
Modelling the impact of clot fragmentation on the microcirculation after thrombectomy. |
title_short |
Modelling the impact of clot fragmentation on the microcirculation after thrombectomy. |
title_full |
Modelling the impact of clot fragmentation on the microcirculation after thrombectomy. |
title_fullStr |
Modelling the impact of clot fragmentation on the microcirculation after thrombectomy. |
title_full_unstemmed |
Modelling the impact of clot fragmentation on the microcirculation after thrombectomy. |
title_sort |
modelling the impact of clot fragmentation on the microcirculation after thrombectomy. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS Computational Biology |
issn |
1553-734X 1553-7358 |
publishDate |
2021-03-01 |
description |
Many ischaemic stroke patients who have a mechanical removal of their clot (thrombectomy) do not get reperfusion of tissue despite the thrombus being removed. One hypothesis for this 'no-reperfusion' phenomenon is micro-emboli fragmenting off the large clot during thrombectomy and occluding smaller blood vessels downstream of the clot location. This is impossible to observe in-vivo and so we here develop an in-silico model based on in-vitro experiments to model the effect of micro-emboli on brain tissue. Through in-vitro experiments we obtain, under a variety of clot consistencies and thrombectomy techniques, micro-emboli distributions post-thrombectomy. Blood flow through the microcirculation is modelled for statistically accurate voxels of brain microvasculature including penetrating arterioles and capillary beds. A novel micro-emboli algorithm, informed by the experimental data, is used to simulate the impact of micro-emboli successively entering the penetrating arterioles and the capillary bed. Scaled-up blood flow parameters-permeability and coupling coefficients-are calculated under various conditions. We find that capillary beds are more susceptible to occlusions than the penetrating arterioles with a 4x greater drop in permeability per volume of vessel occluded. Individual microvascular geometries determine robustness to micro-emboli. Hard clot fragmentation leads to larger micro-emboli and larger drops in blood flow for a given number of micro-emboli. Thrombectomy technique has a large impact on clot fragmentation and hence occlusions in the microvasculature. As such, in-silico modelling of mechanical thrombectomy predicts that clot specific factors, interventional technique, and microvascular geometry strongly influence reperfusion of the brain. Micro-emboli are likely contributory to the phenomenon of no-reperfusion following successful removal of a major clot. |
url |
https://doi.org/10.1371/journal.pcbi.1008515 |
work_keys_str_mv |
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