Evidence map›Paper›PMID 37055807›Full record

ArticleBiomedical engineering online2023

Monitoring variability in parameter estimates for lumped parameter models of the systemic circulation using longitudinal hemodynamic measurements.

Nikolai L Bjørdalsbakke, Jacob Sturdy, Emma M L Ingeström, Leif R Hellevik

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Article in Biomedical engineering online, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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3 · Its place in the literature

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4 citing papers in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Nikolai L BjørdalsbakkeDepartment of Structural Engineering, Norwegian University of Science and Technology (NTNU), Richard Birkelandsvei 1a, Trondheim, Norway. nikolai.l.bjordalsbakke@ntnu.no.
Jacob SturdyDepartment of Structural Engineering, Norwegian University of Science and Technology (NTNU), Richard Birkelandsvei 1a, Trondheim, Norway.
Emma M L IngeströmDepartment of Circulation and Medical Imaging, Norwegian University of Science and Technology (NTNU), Prinsesse Kristinas gt. 3, Trondheim, Norway.
Leif R HellevikDepartment of Structural Engineering, Norwegian University of Science and Technology (NTNU), Richard Birkelandsvei 1a, Trondheim, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPhysics-based cardiovascular models are only recently being considered for disease diagnosis or prognosis in clinical settings. These models depend on parameters representing the physical and physiological properties of the modeled system. Personalizing these parameters may give insight into the specific state of the individual and etiology of disease. We applied a relatively fast model optimization scheme based on common local optimization methods to two model formulations of the left ventricle and systemic circulation. One closed-loop model and one open-loop model were applied. Intermittently collected hemodynamic data from an exercise motivation study were used to personalize these models for data from 25 participants. The hemodynamic data were collected for each participant at the start, middle and end of the trial. We constructed two data sets for the participants, both consisting of systolic and diastolic brachial pressure, stroke volume, and left-ventricular outflow tract velocity traces paired with either the finger arterial pressure waveform or the carotid pressure waveform.

resultsWe examined the feasibility of separating parameter estimates for the individual from population estimates by assessing the variability of estimates using the interquartile range. We found that the estimated parameter values were similar for the two model formulations, but that the systemic arterial compliance was significantly different ([Formula: see text]) depending on choice of pressure waveform. The estimates of systemic arterial compliance were on average higher when using the finger artery pressure waveform as compared to the carotid waveform.

conclusionsWe found that for the majority of participants, the variability of parameter estimates for a given participant on any measurement day was lower than the variability both across all measurement days combined for one participant, and for the population. This indicates that it is possible to identify individuals from the population, and that we can distinguish different measurement days for the individual participant by parameter values using the presented optimization method.

Indexed as

ArteriesHemodynamicsBlood PressureHeartHumansModels, BiologicalModels, CardiovascularCardiovascular modelingLumped-parameter modelsModel personalizationParameter variability

Identifiers

PMID37055807
PMCPMC10099701

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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.