Computer model-based injury prediction and evaluation of lung function in mice with acute and ventilator-induced lung injuries.

IF 3.5 2区 医学 Q1 PHYSIOLOGY
Elizabeth Kaye, Alexander Sosa, Katharine Drayton Warner, David J Albers, Peter D Sottile, Bradford J Smith
{"title":"Computer model-based injury prediction and evaluation of lung function in mice with acute and ventilator-induced lung injuries.","authors":"Elizabeth Kaye, Alexander Sosa, Katharine Drayton Warner, David J Albers, Peter D Sottile, Bradford J Smith","doi":"10.1152/ajplung.00248.2025","DOIUrl":null,"url":null,"abstract":"<p><p>Invasive mechanical ventilation is a lifesaving intervention for acute respiratory distress syndrome (ARDS) patients but also causes ventilator-induced lung injury (VILI) that can be challenging to avoid due to inter-patient and temporal heterogeneity. Thus, the aim of this study was to characterize and predict experimental VILI using readily available measures of lung function. Initially healthy (CTL) and hydrochloric acid (HCL) lung-injured mice were ventilated for four hours at PEEP = 1, 3, or 8 cmH<sub>2</sub>O to produce graded VILI severity as measured in lung function, alveolocapillary leak, and inflammation. Optimally protective PEEP was found to be 8 and 3 cmH<sub>2</sub>O in the HCL and CTL groups, respectively. A novel computational model was fit to the data to investigate elastance dynamics described by the \"compliance factor\" (C<sub>F</sub>) which was also used to predict VILI over four subsequent hours of ventilation. The model C<sub>F</sub> is a sensitive measure of injury-induced alterations in the pressure- and pressure-history dependence of lung elastance that are known to correlate with recruitment and derecruitment dynamics. The C<sub>F</sub> was then combined with PEEP and plateau pressures calculated from 10 minutes at the start of prolonged ventilation and used to accurately predict VILI outcomes measured four hours later. This model outperformed other commonly utilized measures of injury such as driving pressure and mechanical power. The computer model provides a new tool for understanding lung dynamics and for predicting VILI. In future work, this approach could be used to guide identification of lung protective ventilation settings.</p>","PeriodicalId":7593,"journal":{"name":"American journal of physiology. Lung cellular and molecular physiology","volume":" ","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2025-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of physiology. Lung cellular and molecular physiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1152/ajplung.00248.2025","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Invasive mechanical ventilation is a lifesaving intervention for acute respiratory distress syndrome (ARDS) patients but also causes ventilator-induced lung injury (VILI) that can be challenging to avoid due to inter-patient and temporal heterogeneity. Thus, the aim of this study was to characterize and predict experimental VILI using readily available measures of lung function. Initially healthy (CTL) and hydrochloric acid (HCL) lung-injured mice were ventilated for four hours at PEEP = 1, 3, or 8 cmH2O to produce graded VILI severity as measured in lung function, alveolocapillary leak, and inflammation. Optimally protective PEEP was found to be 8 and 3 cmH2O in the HCL and CTL groups, respectively. A novel computational model was fit to the data to investigate elastance dynamics described by the "compliance factor" (CF) which was also used to predict VILI over four subsequent hours of ventilation. The model CF is a sensitive measure of injury-induced alterations in the pressure- and pressure-history dependence of lung elastance that are known to correlate with recruitment and derecruitment dynamics. The CF was then combined with PEEP and plateau pressures calculated from 10 minutes at the start of prolonged ventilation and used to accurately predict VILI outcomes measured four hours later. This model outperformed other commonly utilized measures of injury such as driving pressure and mechanical power. The computer model provides a new tool for understanding lung dynamics and for predicting VILI. In future work, this approach could be used to guide identification of lung protective ventilation settings.

基于计算机模型的急性和呼吸机肺损伤小鼠肺功能预测与评价。
有创机械通气是急性呼吸窘迫综合征(ARDS)患者的救命干预手段,但也会导致呼吸机诱发的肺损伤(VILI),由于患者间和时间异质性,这种损伤很难避免。因此,本研究的目的是利用现成的肺功能测量来表征和预测实验性VILI。初始健康(CTL)和盐酸(HCL)肺损伤小鼠在PEEP = 1、3或8 cmH2O下通气4小时,通过测量肺功能、肺泡毛细血管渗漏和炎症来产生分级的VILI严重程度。在HCL和CTL组中,最佳保护性PEEP分别为8和3 cmH2O。一个新的计算模型拟合的数据,以研究弹性动力学描述的“顺应系数”(CF),也用于预测VILI在随后的四个小时的通气。CF模型是损伤引起的肺弹性的压力和压力历史依赖性改变的敏感测量,已知与招募和退出招募动力学相关。然后将CF与延长通气开始时10分钟计算的PEEP和平台压相结合,用于准确预测4小时后测量的VILI结果。该模型优于其他常用的损伤测量方法,如驾驶压力和机械功率。该计算机模型为了解肺动力学和预测VILI提供了新的工具。在未来的工作中,该方法可用于指导肺保护性通气设置的识别。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
9.20
自引率
4.10%
发文量
146
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Lung Cellular and Molecular Physiology publishes original research covering the broad scope of molecular, cellular, and integrative aspects of normal and abnormal function of cells and components of the respiratory system. Areas of interest include conducting airways, pulmonary circulation, lung endothelial and epithelial cells, the pleura, neuroendocrine and immunologic cells in the lung, neural cells involved in control of breathing, and cells of the diaphragm and thoracic muscles. The processes to be covered in the Journal include gas-exchange, metabolic control at the cellular level, intracellular signaling, gene expression, genomics, macromolecules and their turnover, cell-cell and cell-matrix interactions, cell motility, secretory mechanisms, membrane function, surfactant, matrix components, mucus and lining materials, lung defenses, macrophage function, transport of salt, water and protein, development and differentiation of the respiratory system, and response to the environment.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信