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Mechanical power in pediatric acute respiratory distress syndrome: a PARDIE study
BACKGROUND: Mechanical power is a composite variable for energy transmitted to the respiratory system over time that may better capture risk for ventilator-induced lung injury than individual ventilator management components. We sought to evaluate if mechanical ventilation management with a high mec...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722295/ https://www.ncbi.nlm.nih.gov/pubmed/34980228 http://dx.doi.org/10.1186/s13054-021-03853-6 |
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author | Bhalla, Anoopindar K. Klein, Margaret J. Modesto I Alapont, Vicent Emeriaud, Guillaume Kneyber, Martin C. J. Medina, Alberto Cruces, Pablo Diaz, Franco Takeuchi, Muneyuki Maddux, Aline B. Mourani, Peter M. Camilo, Cristina White, Benjamin R. Yehya, Nadir Pappachan, John Di Nardo, Matteo Shein, Steven Newth, Christopher Khemani, Robinder |
author_facet | Bhalla, Anoopindar K. Klein, Margaret J. Modesto I Alapont, Vicent Emeriaud, Guillaume Kneyber, Martin C. J. Medina, Alberto Cruces, Pablo Diaz, Franco Takeuchi, Muneyuki Maddux, Aline B. Mourani, Peter M. Camilo, Cristina White, Benjamin R. Yehya, Nadir Pappachan, John Di Nardo, Matteo Shein, Steven Newth, Christopher Khemani, Robinder |
author_sort | Bhalla, Anoopindar K. |
collection | PubMed |
description | BACKGROUND: Mechanical power is a composite variable for energy transmitted to the respiratory system over time that may better capture risk for ventilator-induced lung injury than individual ventilator management components. We sought to evaluate if mechanical ventilation management with a high mechanical power is associated with fewer ventilator-free days (VFD) in children with pediatric acute respiratory distress syndrome (PARDS). METHODS: Retrospective analysis of a prospective observational international cohort study. RESULTS: There were 306 children from 55 pediatric intensive care units included. High mechanical power was associated with younger age, higher oxygenation index, a comorbid condition of bronchopulmonary dysplasia, higher tidal volume, higher delta pressure (peak inspiratory pressure—positive end-expiratory pressure), and higher respiratory rate. Higher mechanical power was associated with fewer 28-day VFD after controlling for confounding variables (per 0.1 J·min(−1)·Kg(−1) Subdistribution Hazard Ratio (SHR) 0.93 (0.87, 0.98), p = 0.013). Higher mechanical power was not associated with higher intensive care unit mortality in multivariable analysis in the entire cohort (per 0.1 J·min(−1)·Kg(−1) OR 1.12 [0.94, 1.32], p = 0.20). But was associated with higher mortality when excluding children who died due to neurologic reasons (per 0.1 J·min(−1)·Kg(−1) OR 1.22 [1.01, 1.46], p = 0.036). In subgroup analyses by age, the association between higher mechanical power and fewer 28-day VFD remained only in children < 2-years-old (per 0.1 J·min(−1)·Kg(−1) SHR 0.89 (0.82, 0.96), p = 0.005). Younger children were managed with lower tidal volume, higher delta pressure, higher respiratory rate, lower positive end-expiratory pressure, and higher PCO(2) than older children. No individual ventilator management component mediated the effect of mechanical power on 28-day VFD. CONCLUSIONS: Higher mechanical power is associated with fewer 28-day VFDs in children with PARDS. This association is strongest in children < 2-years-old in whom there are notable differences in mechanical ventilation management. While further validation is needed, these data highlight that ventilator management is associated with outcome in children with PARDS, and there may be subgroups of children with higher potential benefit from strategies to improve lung-protective ventilation. Take Home Message: Higher mechanical power is associated with fewer 28-day ventilator-free days in children with pediatric acute respiratory distress syndrome. This association is strongest in children <2-years-old in whom there are notable differences in mechanical ventilation management. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-021-03853-6. |
format | Online Article Text |
id | pubmed-8722295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87222952022-01-06 Mechanical power in pediatric acute respiratory distress syndrome: a PARDIE study Bhalla, Anoopindar K. Klein, Margaret J. Modesto I Alapont, Vicent Emeriaud, Guillaume Kneyber, Martin C. J. Medina, Alberto Cruces, Pablo Diaz, Franco Takeuchi, Muneyuki Maddux, Aline B. Mourani, Peter M. Camilo, Cristina White, Benjamin R. Yehya, Nadir Pappachan, John Di Nardo, Matteo Shein, Steven Newth, Christopher Khemani, Robinder Crit Care Research BACKGROUND: Mechanical power is a composite variable for energy transmitted to the respiratory system over time that may better capture risk for ventilator-induced lung injury than individual ventilator management components. We sought to evaluate if mechanical ventilation management with a high mechanical power is associated with fewer ventilator-free days (VFD) in children with pediatric acute respiratory distress syndrome (PARDS). METHODS: Retrospective analysis of a prospective observational international cohort study. RESULTS: There were 306 children from 55 pediatric intensive care units included. High mechanical power was associated with younger age, higher oxygenation index, a comorbid condition of bronchopulmonary dysplasia, higher tidal volume, higher delta pressure (peak inspiratory pressure—positive end-expiratory pressure), and higher respiratory rate. Higher mechanical power was associated with fewer 28-day VFD after controlling for confounding variables (per 0.1 J·min(−1)·Kg(−1) Subdistribution Hazard Ratio (SHR) 0.93 (0.87, 0.98), p = 0.013). Higher mechanical power was not associated with higher intensive care unit mortality in multivariable analysis in the entire cohort (per 0.1 J·min(−1)·Kg(−1) OR 1.12 [0.94, 1.32], p = 0.20). But was associated with higher mortality when excluding children who died due to neurologic reasons (per 0.1 J·min(−1)·Kg(−1) OR 1.22 [1.01, 1.46], p = 0.036). In subgroup analyses by age, the association between higher mechanical power and fewer 28-day VFD remained only in children < 2-years-old (per 0.1 J·min(−1)·Kg(−1) SHR 0.89 (0.82, 0.96), p = 0.005). Younger children were managed with lower tidal volume, higher delta pressure, higher respiratory rate, lower positive end-expiratory pressure, and higher PCO(2) than older children. No individual ventilator management component mediated the effect of mechanical power on 28-day VFD. CONCLUSIONS: Higher mechanical power is associated with fewer 28-day VFDs in children with PARDS. This association is strongest in children < 2-years-old in whom there are notable differences in mechanical ventilation management. While further validation is needed, these data highlight that ventilator management is associated with outcome in children with PARDS, and there may be subgroups of children with higher potential benefit from strategies to improve lung-protective ventilation. Take Home Message: Higher mechanical power is associated with fewer 28-day ventilator-free days in children with pediatric acute respiratory distress syndrome. This association is strongest in children <2-years-old in whom there are notable differences in mechanical ventilation management. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-021-03853-6. BioMed Central 2022-01-03 /pmc/articles/PMC8722295/ /pubmed/34980228 http://dx.doi.org/10.1186/s13054-021-03853-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Bhalla, Anoopindar K. Klein, Margaret J. Modesto I Alapont, Vicent Emeriaud, Guillaume Kneyber, Martin C. J. Medina, Alberto Cruces, Pablo Diaz, Franco Takeuchi, Muneyuki Maddux, Aline B. Mourani, Peter M. Camilo, Cristina White, Benjamin R. Yehya, Nadir Pappachan, John Di Nardo, Matteo Shein, Steven Newth, Christopher Khemani, Robinder Mechanical power in pediatric acute respiratory distress syndrome: a PARDIE study |
title | Mechanical power in pediatric acute respiratory distress syndrome: a PARDIE study |
title_full | Mechanical power in pediatric acute respiratory distress syndrome: a PARDIE study |
title_fullStr | Mechanical power in pediatric acute respiratory distress syndrome: a PARDIE study |
title_full_unstemmed | Mechanical power in pediatric acute respiratory distress syndrome: a PARDIE study |
title_short | Mechanical power in pediatric acute respiratory distress syndrome: a PARDIE study |
title_sort | mechanical power in pediatric acute respiratory distress syndrome: a pardie study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722295/ https://www.ncbi.nlm.nih.gov/pubmed/34980228 http://dx.doi.org/10.1186/s13054-021-03853-6 |
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