Improved biomechanical metrics of cerebral vasospasm identified via sensitivity analysis of a 1D cerebral circulation model.


Journal

Journal of biomechanics
ISSN: 1873-2380
Titre abrégé: J Biomech
Pays: United States
ID NLM: 0157375

Informations de publication

Date de publication:
11 Jun 2019
Historique:
received: 08 11 2018
revised: 12 04 2019
accepted: 12 04 2019
pubmed: 9 5 2019
medline: 11 6 2020
entrez: 9 5 2019
Statut: ppublish

Résumé

Cerebral vasospasm (CVS) is a life-threatening condition that occurs in a large proportion of those affected by subarachnoid haemorrhage and stroke. CVS manifests itself as the progressive narrowing of intracranial arteries. It is usually diagnosed using Doppler ultrasound, which quantifies blood velocity changes in the affected vessels, but has low sensitivity when CVS affects the peripheral vasculature. The aim of this study was to identify alternative biomarkers that could be used to diagnose CVS. We used a 1D modelling approach to describe the properties of pulse waves that propagate through the cardiovascular system, which allowed the effects of different types of vasospasm on waveforms to be characterised at several locations within a simulated cerebral network. A sensitivity analysis empowered by the use of a Gaussian process statistical emulator was used to identify waveform features that may have strong correlations with vasospasm. We showed that the minimum rate of velocity change can be much more effective than blood velocity for stratifying typical manifestations of vasospasm and its progression. The results and methodology of this study have the potential not only to improve the diagnosis and monitoring of vasospasm, but also to be used in the diagnosis of many other cardiovascular diseases where cardiovascular waves can be decoded to provide disease characterisation.

Identifiants

pubmed: 31064657
pii: S0021-9290(19)30283-0
doi: 10.1016/j.jbiomech.2019.04.019
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

24-32

Informations de copyright

Crown Copyright © 2019. Published by Elsevier Ltd. All rights reserved.

Auteurs

A Melis (A)

INSIGNEO Institute for in silico Medicine, The University of Sheffield, UK; Department of Mechanical Engineering, The University of Sheffield, UK.

F Moura (F)

Engineering, Modeling and Applied Social Sciences Center, Federal University of ABC, Brazil.

I Larrabide (I)

Pladema-CONICET-UNICEN, Tandil, Argentina.

K Janot (K)

University Hospital of Tours, UMR Imagerie et Cervau, Inserm U930, Université François-Rabelais, Tours, France.

R H Clayton (RH)

INSIGNEO Institute for in silico Medicine, The University of Sheffield, UK; Department of Computer Science, The University of Sheffield, UK.

A P Narata (AP)

University Hospital of Tours, UMR Imagerie et Cervau, Inserm U930, Université François-Rabelais, Tours, France.

A Marzo (A)

INSIGNEO Institute for in silico Medicine, The University of Sheffield, UK; Department of Mechanical Engineering, The University of Sheffield, UK. Electronic address: a.marzo@sheffield.ac.uk.

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Classifications MeSH