Practical identifiability analysis of a minimal cardiovascular system model.

Cardiovascular system Mathematical model Parameter identification Practical identifiability

Journal

Computer methods and programs in biomedicine
ISSN: 1872-7565
Titre abrégé: Comput Methods Programs Biomed
Pays: Ireland
ID NLM: 8506513

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 22 12 2015
revised: 01 12 2016
accepted: 16 01 2017
pubmed: 6 2 2017
medline: 10 8 2019
entrez: 4 2 2017
Statut: ppublish

Résumé

Parameters of mathematical models of the cardiovascular system can be used to monitor cardiovascular state, such as total stressed blood volume status, vessel elastance and resistance. To do so, the model parameters have to be estimated from data collected at the patient's bedside. This work considers a seven-parameter model of the cardiovascular system and investigates whether these parameters can be uniquely determined using indices derived from measurements of arterial and venous pressures, and stroke volume. An error vector defined the residuals between the simulated and reference values of the seven clinically available haemodynamic indices. The sensitivity of this error vector to each model parameter was analysed, as well as the collinearity between parameters. To assess practical identifiability of the model parameters, profile-likelihood curves were constructed for each parameter. Four of the seven model parameters were found to be practically identifiable from the selected data. The remaining three parameters were practically non-identifiable. Among these non-identifiable parameters, one could be decreased as much as possible. The other two non-identifiable parameters were inversely correlated, which prevented their precise estimation. This work presented the practical identifiability analysis of a seven-parameter cardiovascular system model, from limited clinical data. The analysis showed that three of the seven parameters were practically non-identifiable, thus limiting the use of the model as a monitoring tool. Slight changes in the time-varying function modeling cardiac contraction and use of larger values for the reference range of venous pressure made the model fully practically identifiable.

Sections du résumé

BACKGROUND AND OBJECTIVE OBJECTIVE
Parameters of mathematical models of the cardiovascular system can be used to monitor cardiovascular state, such as total stressed blood volume status, vessel elastance and resistance. To do so, the model parameters have to be estimated from data collected at the patient's bedside. This work considers a seven-parameter model of the cardiovascular system and investigates whether these parameters can be uniquely determined using indices derived from measurements of arterial and venous pressures, and stroke volume.
METHODS METHODS
An error vector defined the residuals between the simulated and reference values of the seven clinically available haemodynamic indices. The sensitivity of this error vector to each model parameter was analysed, as well as the collinearity between parameters. To assess practical identifiability of the model parameters, profile-likelihood curves were constructed for each parameter.
RESULTS RESULTS
Four of the seven model parameters were found to be practically identifiable from the selected data. The remaining three parameters were practically non-identifiable. Among these non-identifiable parameters, one could be decreased as much as possible. The other two non-identifiable parameters were inversely correlated, which prevented their precise estimation.
CONCLUSIONS CONCLUSIONS
This work presented the practical identifiability analysis of a seven-parameter cardiovascular system model, from limited clinical data. The analysis showed that three of the seven parameters were practically non-identifiable, thus limiting the use of the model as a monitoring tool. Slight changes in the time-varying function modeling cardiac contraction and use of larger values for the reference range of venous pressure made the model fully practically identifiable.

Identifiants

pubmed: 28153466
pii: S0169-2607(15)30457-0
doi: 10.1016/j.cmpb.2017.01.005
pii:
doi:

Types de publication

Evaluation Study Journal Article

Langues

eng

Pagination

53-65

Informations de copyright

Copyright © 2017 Elsevier B.V. All rights reserved.

Auteurs

Antoine Pironet (A)

GIGA-In Silico Medicine, University of Liège, B5a, Quartier Agora, Allée du 6 août, 19, 4000 Liège, Belgium. Electronic address: a.pironet@alumni.ulg.ac.be.

Paul D Docherty (PD)

Department of Mechanical Engineering, University of Canterbury, Private Bag 4800, Christchurch 8140, New Zealand.

Pierre C Dauby (PC)

GIGA-In Silico Medicine, University of Liège, B5a, Quartier Agora, Allée du 6 août, 19, 4000 Liège, Belgium.

J Geoffrey Chase (JG)

Department of Mechanical Engineering, University of Canterbury, Private Bag 4800, Christchurch 8140, New Zealand.

Thomas Desaive (T)

GIGA-In Silico Medicine, University of Liège, B5a, Quartier Agora, Allée du 6 août, 19, 4000 Liège, Belgium.

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