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A Nonlinear Hysteretic Model for Automated Prediction of Lung Mechanics during Mechanical Ventilation
Mechanical ventilation (MV) is core intensive care unit (ICU) therapy during the Covid-19 pandemic. Optimising MV care to a specific patient with respiratory failure is difficult due to inter- and intra- patient variability in lung mechanics and condition. The ability to accurately predict patient-s...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
, IFAC (International Federation of Automatic Control) Hosting by Elsevier Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153200/ http://dx.doi.org/10.1016/j.ifacol.2021.04.177 |
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author | Zhou, Cong Chase, J. Geoffrey Sun, Qianhui Knopp, Jennifer |
author_facet | Zhou, Cong Chase, J. Geoffrey Sun, Qianhui Knopp, Jennifer |
author_sort | Zhou, Cong |
collection | PubMed |
description | Mechanical ventilation (MV) is core intensive care unit (ICU) therapy during the Covid-19 pandemic. Optimising MV care to a specific patient with respiratory failure is difficult due to inter- and intra- patient variability in lung mechanics and condition. The ability to accurately predict patient-specific lung response to a change in MV settings would enable semi-automated care and significantly improve the efficiency of MV monitoring and care. It has particular emphasis when considering MV care required to treat Covid-19 patients, who require longer MV care, where patient-specific care can reduce the time on MV required. This study develops a nonlinear smooth hysteresis loop model (HLM) able to capture the essential lung dynamics in a patient-specific fashion from measured ventilator data, particularly for changes of compliance and infection points of the pressure-volume loop. The automated (no human input) hysteresis loop analysis (HLA) method is applied to identify HLM model parameters, enabling automated digital cloning to create a virtual patient model to accurately predict lung response at a specified positive end expiratory pressure (PEEP) level, as well as in response to the changes of PEEP. The performance of this automated digital cloning approach is assessed using clinical data from 4 patients and 8 recruitment maneuver (RM) arms. Validation results show the HLM-based hysteresis loops identified using HLA match clinical pressure-volume loops very well with root-mean-square (RMS) errors less than 2% for all 8 data sets over 4 patients, validating the accuracy of the developed HLM in capturing the essential lung physiology and respiratory behaviours at different patient conditions. More importantly, the patient-specific digital clones at lower PEEP levels accurately predict lung response at higher PEEP levels with predicted peak inspiratory pressure (PIP) errors less than 2% in average. In addition, the resulted additional lung volume V(frc) obtained with PEEP changes are predicted with average absolute difference of 0.025L. The overall results validate the versatility and potential of the developed HLM for delineating changes of nonlinear lung dynamics, and its capability to create a predictive virtual patient with use of HLA for future treatment personalization and optimisation in MV therapy. |
format | Online Article Text |
id | pubmed-8153200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | , IFAC (International Federation of Automatic Control) Hosting by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81532002021-05-28 A Nonlinear Hysteretic Model for Automated Prediction of Lung Mechanics during Mechanical Ventilation Zhou, Cong Chase, J. Geoffrey Sun, Qianhui Knopp, Jennifer IFAC-PapersOnLine Article Mechanical ventilation (MV) is core intensive care unit (ICU) therapy during the Covid-19 pandemic. Optimising MV care to a specific patient with respiratory failure is difficult due to inter- and intra- patient variability in lung mechanics and condition. The ability to accurately predict patient-specific lung response to a change in MV settings would enable semi-automated care and significantly improve the efficiency of MV monitoring and care. It has particular emphasis when considering MV care required to treat Covid-19 patients, who require longer MV care, where patient-specific care can reduce the time on MV required. This study develops a nonlinear smooth hysteresis loop model (HLM) able to capture the essential lung dynamics in a patient-specific fashion from measured ventilator data, particularly for changes of compliance and infection points of the pressure-volume loop. The automated (no human input) hysteresis loop analysis (HLA) method is applied to identify HLM model parameters, enabling automated digital cloning to create a virtual patient model to accurately predict lung response at a specified positive end expiratory pressure (PEEP) level, as well as in response to the changes of PEEP. The performance of this automated digital cloning approach is assessed using clinical data from 4 patients and 8 recruitment maneuver (RM) arms. Validation results show the HLM-based hysteresis loops identified using HLA match clinical pressure-volume loops very well with root-mean-square (RMS) errors less than 2% for all 8 data sets over 4 patients, validating the accuracy of the developed HLM in capturing the essential lung physiology and respiratory behaviours at different patient conditions. More importantly, the patient-specific digital clones at lower PEEP levels accurately predict lung response at higher PEEP levels with predicted peak inspiratory pressure (PIP) errors less than 2% in average. In addition, the resulted additional lung volume V(frc) obtained with PEEP changes are predicted with average absolute difference of 0.025L. The overall results validate the versatility and potential of the developed HLM for delineating changes of nonlinear lung dynamics, and its capability to create a predictive virtual patient with use of HLA for future treatment personalization and optimisation in MV therapy. , IFAC (International Federation of Automatic Control) Hosting by Elsevier Ltd. 2020 2021-05-26 /pmc/articles/PMC8153200/ http://dx.doi.org/10.1016/j.ifacol.2021.04.177 Text en © 2019, IFAC (International Federation of Automatic Control) Hosting by Elsevier Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Zhou, Cong Chase, J. Geoffrey Sun, Qianhui Knopp, Jennifer A Nonlinear Hysteretic Model for Automated Prediction of Lung Mechanics during Mechanical Ventilation |
title | A Nonlinear Hysteretic Model for Automated Prediction of Lung Mechanics during Mechanical Ventilation |
title_full | A Nonlinear Hysteretic Model for Automated Prediction of Lung Mechanics during Mechanical Ventilation |
title_fullStr | A Nonlinear Hysteretic Model for Automated Prediction of Lung Mechanics during Mechanical Ventilation |
title_full_unstemmed | A Nonlinear Hysteretic Model for Automated Prediction of Lung Mechanics during Mechanical Ventilation |
title_short | A Nonlinear Hysteretic Model for Automated Prediction of Lung Mechanics during Mechanical Ventilation |
title_sort | nonlinear hysteretic model for automated prediction of lung mechanics during mechanical ventilation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153200/ http://dx.doi.org/10.1016/j.ifacol.2021.04.177 |
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