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Quantifiable identification of flow-limited ventilator dyssynchrony with the deformed lung ventilator model.
Agrawal, Deepak K; Smith, Bradford J; Sottile, Peter D; Hripcsak, George; Albers, David J.
Afiliação
  • Agrawal DK; Department of Biosciences and Bioengineering, Indian Institute of Technology Bombay, Mumbai, Maharashtra, 400076, India; Department of Bioengineering, University of Colorado Denver | Anschutz Medical Campus, Aurora, CO, 80045, USA. Electronic address: dkagrawal@iitb.ac.in.
  • Smith BJ; Department of Bioengineering, University of Colorado Denver | Anschutz Medical Campus, Aurora, CO, 80045, USA; Section of Pulmonary and Sleep Medicine, Department of Pediatrics, University of Colorado Denver, Anschutz Medical Campus, Aurora, CO, 80045, USA.
  • Sottile PD; Division of Pulmonary Sciences and Critical Care Medicine, Department of Medicine, University of Colorado School of Medicine, Aurora, CO, 80045, USA.
  • Hripcsak G; Department of Biomedical Informatics, Columbia University, New York, NY, 10027, USA.
  • Albers DJ; Department of Bioengineering, University of Colorado Denver | Anschutz Medical Campus, Aurora, CO, 80045, USA; Department of Biomedical Informatics, Columbia University, New York, NY, 10027, USA; Department of Biomedical Informatics, Univerisity of Colorado Anschutz Medical Campus, Aurora, CO 80045.
Comput Biol Med ; 173: 108349, 2024 May.
Article em En | MEDLINE | ID: mdl-38547660
ABSTRACT

BACKGROUND:

Ventilator dyssynchrony (VD) can worsen lung injury and is challenging to detect and quantify due to the complex variability in the dyssynchronous breaths. While machine learning (ML) approaches are useful for automating VD detection from the ventilator waveform data, scalable severity quantification and its association with pathogenesis and ventilator mechanics remain challenging.

OBJECTIVE:

We develop a systematic framework to quantify pathophysiological features observed in ventilator waveform signals such that they can be used to create feature-based severity stratification of VD breaths.

METHODS:

A mathematical model was developed to represent the pressure and volume waveforms of individual breaths in a feature-based parametric form. Model estimates of respiratory effort strength were used to assess the severity of flow-limited (FL)-VD breaths compared to normal breaths. A total of 93,007 breath waveforms from 13 patients were analyzed.

RESULTS:

A novel model-defined continuous severity marker was developed and used to estimate breath phenotypes of FL-VD breaths. The phenotypes had a predictive accuracy of over 97% with respect to the previously developed ML-VD identification algorithm. To understand the incidence of FL-VD breaths and their association with the patient state, these phenotypes were further successfully correlated with ventilator-measured parameters and electronic health records.

CONCLUSION:

This work provides a computational pipeline to identify and quantify the severity of FL-VD breaths and paves the way for a large-scale study of VD causes and effects. This approach has direct application to clinical practice and in meaningful knowledge extraction from the ventilator waveform data.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Lesão Pulmonar Limite: Humans Idioma: En Revista: Comput Biol Med Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Lesão Pulmonar Limite: Humans Idioma: En Revista: Comput Biol Med Ano de publicação: 2024 Tipo de documento: Article