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Angioarchitecture and hemodynamics of microvascular arterio-venous malformations
INTRODUCTION: Arteriovenous malformations (AVMs) are characterized by pathological high flow, low resistance connections between arteries and veins. Treatment is critically dependent on correct interpretation of angioarchitectural features. However, some microfistular AVMs do not match the character...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128518/ https://www.ncbi.nlm.nih.gov/pubmed/30192812 http://dx.doi.org/10.1371/journal.pone.0203368 |
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author | Frey, Sabrina Cantieni, Tarcisi Vuillemin, Nicolas Haine, Axel Kammer, Rafael von Tengg-Kobligk, Hendrik Obrist, Dominik Baumgartner, Iris |
author_facet | Frey, Sabrina Cantieni, Tarcisi Vuillemin, Nicolas Haine, Axel Kammer, Rafael von Tengg-Kobligk, Hendrik Obrist, Dominik Baumgartner, Iris |
author_sort | Frey, Sabrina |
collection | PubMed |
description | INTRODUCTION: Arteriovenous malformations (AVMs) are characterized by pathological high flow, low resistance connections between arteries and veins. Treatment is critically dependent on correct interpretation of angioarchitectural features. However, some microfistular AVMs do not match the characteristics described in current AVM classification systems. Therefore, we propose a new subgroup of microfistular AVMs, composed of enlarged, fistulous paths on the venous half of capillaries and/or dilated draining venules (hyperdynamic, capillary-venulous malformation [CV-AVM]). CV-AVMs still ensure arterial flow to the periphery and fistulous venous drainage is less pronounced than in classical AVMs such that these lesions are often misinterpreted as venous malformations. MATERIALS AND METHODS: We developed a computational model to study the effects of microvascular anomalies on local hemodynamics, as well as their impact on angiographic contrast propagation. Flow rates and pressures were computed with a lumped parameter description, while contrast propagation was determined by solving the 1D advection-diffusion equation. RESULTS AND CONCLUSIONS: For the newly proposed CV-AVM angioarchitecture, the computational model predicts increased arterio-venous contrast agent transit times and highly dispersive transport characteristics, compared to microfistular, interstitial type IV AVMs and high flow type II and III AVMs. We related these findings to time-contrast intensity curves sampled from clinical angiographies and found that there is strong evidence for the existence of CV-AVM. |
format | Online Article Text |
id | pubmed-6128518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-61285182018-09-15 Angioarchitecture and hemodynamics of microvascular arterio-venous malformations Frey, Sabrina Cantieni, Tarcisi Vuillemin, Nicolas Haine, Axel Kammer, Rafael von Tengg-Kobligk, Hendrik Obrist, Dominik Baumgartner, Iris PLoS One Research Article INTRODUCTION: Arteriovenous malformations (AVMs) are characterized by pathological high flow, low resistance connections between arteries and veins. Treatment is critically dependent on correct interpretation of angioarchitectural features. However, some microfistular AVMs do not match the characteristics described in current AVM classification systems. Therefore, we propose a new subgroup of microfistular AVMs, composed of enlarged, fistulous paths on the venous half of capillaries and/or dilated draining venules (hyperdynamic, capillary-venulous malformation [CV-AVM]). CV-AVMs still ensure arterial flow to the periphery and fistulous venous drainage is less pronounced than in classical AVMs such that these lesions are often misinterpreted as venous malformations. MATERIALS AND METHODS: We developed a computational model to study the effects of microvascular anomalies on local hemodynamics, as well as their impact on angiographic contrast propagation. Flow rates and pressures were computed with a lumped parameter description, while contrast propagation was determined by solving the 1D advection-diffusion equation. RESULTS AND CONCLUSIONS: For the newly proposed CV-AVM angioarchitecture, the computational model predicts increased arterio-venous contrast agent transit times and highly dispersive transport characteristics, compared to microfistular, interstitial type IV AVMs and high flow type II and III AVMs. We related these findings to time-contrast intensity curves sampled from clinical angiographies and found that there is strong evidence for the existence of CV-AVM. Public Library of Science 2018-09-07 /pmc/articles/PMC6128518/ /pubmed/30192812 http://dx.doi.org/10.1371/journal.pone.0203368 Text en © 2018 Frey et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Frey, Sabrina Cantieni, Tarcisi Vuillemin, Nicolas Haine, Axel Kammer, Rafael von Tengg-Kobligk, Hendrik Obrist, Dominik Baumgartner, Iris Angioarchitecture and hemodynamics of microvascular arterio-venous malformations |
title | Angioarchitecture and hemodynamics of microvascular arterio-venous malformations |
title_full | Angioarchitecture and hemodynamics of microvascular arterio-venous malformations |
title_fullStr | Angioarchitecture and hemodynamics of microvascular arterio-venous malformations |
title_full_unstemmed | Angioarchitecture and hemodynamics of microvascular arterio-venous malformations |
title_short | Angioarchitecture and hemodynamics of microvascular arterio-venous malformations |
title_sort | angioarchitecture and hemodynamics of microvascular arterio-venous malformations |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128518/ https://www.ncbi.nlm.nih.gov/pubmed/30192812 http://dx.doi.org/10.1371/journal.pone.0203368 |
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