Evidence map›Paper›PMID 30192812›Full record

ArticlePloS one2018

Angioarchitecture and hemodynamics of microvascular arterio-venous malformations.

Sabrina Frey, Tarcisi Cantieni, Nicolas Vuillemin, Axel Haine, Rafael Kammer, Hendrik von Tengg-Kobligk, Dominik Obrist, Iris Baumgartner

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Cardiac and Hemodynamic Manifestations of Hereditary Hemorrhagic Telangiectasia.The International journal of angiology : official publication of the International College of Angiology, Inc · 2022
    Review
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Sabrina FreyARTORG Center for Biomedical Engineering Research, University of Bern, Bern, Switzerland.ORCID 0000-0002-3981-4437
Tarcisi CantieniARTORG Center for Biomedical Engineering Research, University of Bern, Bern, Switzerland.
Nicolas VuilleminSwiss Cardiovascular Center, Division of Angiology, University of Bern, Bern University Hospital, Bern, Switzerland.
Axel HaineSwiss Cardiovascular Center, Division of Angiology, University of Bern, Bern University Hospital, Bern, Switzerland.
Rafael KammerSwiss Cardiovascular Center, Division of Angiology, University of Bern, Bern University Hospital, Bern, Switzerland.
Hendrik von Tengg-KobligkDepartment of Diagnostic, Interventional and Pediatric Radiology, University of Bern, Bern University Hospital, Bern, Switzerland.
Dominik ObristARTORG Center for Biomedical Engineering Research, University of Bern, Bern, Switzerland.
Iris BaumgartnerSwiss Cardiovascular Center, Division of Angiology, University of Bern, Bern University Hospital, Bern, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionArteriovenous 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

methodsWe 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

conclusionsFor 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.

Indexed as

Models, CardiovascularAngiography, Digital SubtractionArteriovenous FistulaArteriovenous MalformationsComputer SimulationHemodynamicsHumansMicrovessels

Identifiers

PMID30192812
PMCPMC6128518

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.