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Ventilator dyssynchrony – Detection, pathophysiology, and clinical relevance: A Narrative review

Mortality associated with the acute respiratory distress syndrome remains unacceptably high due in part to ventilator-induced lung injury (VILI). Ventilator dyssynchrony is defined as the inappropriate timing and delivery of a mechanical breath in response to patient effort and may cause VILI. Such...

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Autores principales: Sottile, Peter D., Albers, David, Smith, Bradford J., Moss, Marc M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720746/
https://www.ncbi.nlm.nih.gov/pubmed/33381233
http://dx.doi.org/10.4103/atm.ATM_63_20
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author Sottile, Peter D.
Albers, David
Smith, Bradford J.
Moss, Marc M.
author_facet Sottile, Peter D.
Albers, David
Smith, Bradford J.
Moss, Marc M.
author_sort Sottile, Peter D.
collection PubMed
description Mortality associated with the acute respiratory distress syndrome remains unacceptably high due in part to ventilator-induced lung injury (VILI). Ventilator dyssynchrony is defined as the inappropriate timing and delivery of a mechanical breath in response to patient effort and may cause VILI. Such deleterious patient–ventilator interactions have recently been termed patient self-inflicted lung injury. This narrative review outlines the detection and frequency of several different types of ventilator dyssynchrony, delineates the different mechanisms by which ventilator dyssynchrony may propagate VILI, and reviews the potential clinical impact of ventilator dyssynchrony. Until recently, identifying ventilator dyssynchrony required the manual interpretation of ventilator pressure and flow waveforms. However, computerized interpretation of ventilator waive forms can detect ventilator dyssynchrony with an area under the receiver operating curve of >0.80. Using such algorithms, ventilator dyssynchrony occurs in 3%–34% of all breaths, depending on the patient population. Moreover, two types of ventilator dyssynchrony, double-triggered and flow-limited breaths, are associated with the more frequent delivery of large tidal volumes >10 mL/kg when compared with synchronous breaths (54% [95% confidence interval (CI), 47%–61%] and 11% [95% CI, 7%–15%]) compared with 0.9% (95% CI, 0.0%–1.9%), suggesting a role in propagating VILI. Finally, a recent study associated frequent dyssynchrony-defined as >10% of all breaths-with an increase in hospital mortality (67 vs. 23%, P = 0.04). However, the clinical significance of ventilator dyssynchrony remains an area of active investigation and more research is needed to guide optimal ventilator dyssynchrony management.
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spelling pubmed-77207462020-12-29 Ventilator dyssynchrony – Detection, pathophysiology, and clinical relevance: A Narrative review Sottile, Peter D. Albers, David Smith, Bradford J. Moss, Marc M. Ann Thorac Med Review Article Mortality associated with the acute respiratory distress syndrome remains unacceptably high due in part to ventilator-induced lung injury (VILI). Ventilator dyssynchrony is defined as the inappropriate timing and delivery of a mechanical breath in response to patient effort and may cause VILI. Such deleterious patient–ventilator interactions have recently been termed patient self-inflicted lung injury. This narrative review outlines the detection and frequency of several different types of ventilator dyssynchrony, delineates the different mechanisms by which ventilator dyssynchrony may propagate VILI, and reviews the potential clinical impact of ventilator dyssynchrony. Until recently, identifying ventilator dyssynchrony required the manual interpretation of ventilator pressure and flow waveforms. However, computerized interpretation of ventilator waive forms can detect ventilator dyssynchrony with an area under the receiver operating curve of >0.80. Using such algorithms, ventilator dyssynchrony occurs in 3%–34% of all breaths, depending on the patient population. Moreover, two types of ventilator dyssynchrony, double-triggered and flow-limited breaths, are associated with the more frequent delivery of large tidal volumes >10 mL/kg when compared with synchronous breaths (54% [95% confidence interval (CI), 47%–61%] and 11% [95% CI, 7%–15%]) compared with 0.9% (95% CI, 0.0%–1.9%), suggesting a role in propagating VILI. Finally, a recent study associated frequent dyssynchrony-defined as >10% of all breaths-with an increase in hospital mortality (67 vs. 23%, P = 0.04). However, the clinical significance of ventilator dyssynchrony remains an area of active investigation and more research is needed to guide optimal ventilator dyssynchrony management. Wolters Kluwer - Medknow 2020 2020-10-10 /pmc/articles/PMC7720746/ /pubmed/33381233 http://dx.doi.org/10.4103/atm.ATM_63_20 Text en Copyright: © 2020 Annals of Thoracic Medicine http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Review Article
Sottile, Peter D.
Albers, David
Smith, Bradford J.
Moss, Marc M.
Ventilator dyssynchrony – Detection, pathophysiology, and clinical relevance: A Narrative review
title Ventilator dyssynchrony – Detection, pathophysiology, and clinical relevance: A Narrative review
title_full Ventilator dyssynchrony – Detection, pathophysiology, and clinical relevance: A Narrative review
title_fullStr Ventilator dyssynchrony – Detection, pathophysiology, and clinical relevance: A Narrative review
title_full_unstemmed Ventilator dyssynchrony – Detection, pathophysiology, and clinical relevance: A Narrative review
title_short Ventilator dyssynchrony – Detection, pathophysiology, and clinical relevance: A Narrative review
title_sort ventilator dyssynchrony – detection, pathophysiology, and clinical relevance: a narrative review
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720746/
https://www.ncbi.nlm.nih.gov/pubmed/33381233
http://dx.doi.org/10.4103/atm.ATM_63_20
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