Angioarchitecture and hemodynamics of microvascular arterio-venous malformations

PLoS One. 2018 Sep 7;13(9):e0203368. doi: 10.1371/journal.pone.0203368. eCollection 2018.

Abstract

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.

MeSH terms

  • Angiography, Digital Subtraction
  • Arteriovenous Fistula / classification
  • Arteriovenous Fistula / pathology
  • Arteriovenous Fistula / physiopathology
  • Arteriovenous Malformations / classification
  • Arteriovenous Malformations / pathology*
  • Arteriovenous Malformations / physiopathology*
  • Computer Simulation
  • Hemodynamics
  • Humans
  • Microvessels / abnormalities
  • Microvessels / pathology
  • Microvessels / physiopathology
  • Models, Cardiovascular*

Grants and funding

The author(s) received no specific funding for this work.