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About:
Prevention and treatment of acute lung injury with time-controlled adaptive ventilation: physiologically informed modification of airway pressure release ventilation
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covidontheweb.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Prevention and treatment of acute lung injury with time-controlled adaptive ventilation: physiologically informed modification of airway pressure release ventilation
Creator
Camporota, Luigi
Aiash, Hani
Andrews, Penny
Gatto, Louis
Habashi, Nader
Kollisch-Singule, Michaela
Nieman, Gary
Blair, Sarah
Al-Khalisy, Hassan
Daxon, Benjamin
Madden, Maria
Satalin, Joshua
Source
PMC
abstract
Mortality in acute respiratory distress syndrome (ARDS) remains unacceptably high at approximately 39%. One of the only treatments is supportive: mechanical ventilation. However, improperly set mechanical ventilation can further increase the risk of death in patients with ARDS. Recent studies suggest that ventilation-induced lung injury (VILI) is caused by exaggerated regional lung strain, particularly in areas of alveolar instability subject to tidal recruitment/derecruitment and stress-multiplication. Thus, it is reasonable to expect that if a ventilation strategy can maintain stable lung inflation and homogeneity, regional dynamic strain would be reduced and VILI attenuated. A time-controlled adaptive ventilation (TCAV) method was developed to minimize dynamic alveolar strain by adjusting the delivered breath according to the mechanical characteristics of the lung. The goal of this review is to describe how the TCAV method impacts pathophysiology and protects lungs with, or at high risk of, acute lung injury. We present work from our group and others that identifies novel mechanisms of VILI in the alveolar microenvironment and demonstrates that the TCAV method can reduce VILI in translational animal ARDS models and mortality in surgical/trauma patients. Our TCAV method utilizes the airway pressure release ventilation (APRV) mode and is based on opening and collapsing time constants, which reflect the viscoelastic properties of the terminal airspaces. Time-controlled adaptive ventilation uses inspiratory and expiratory time to (1) gradually “nudge” alveoli and alveolar ducts open with an extended inspiratory duration and (2) prevent alveolar collapse using a brief (sub-second) expiratory duration that does not allow time for alveolar collapse. The new paradigm in TCAV is configuring each breath guided by the previous one, which achieves real-time titration of ventilator settings and minimizes instability induced tissue damage. This novel methodology changes the current approach to mechanical ventilation, from arbitrary to personalized and adaptive. The outcome of this approach is an open and stable lung with reduced regional strain and greater lung protection.
has issue date
2020-01-06
(
xsd:dateTime
)
bibo:doi
10.1186/s13613-019-0619-3
bibo:pmid
31907704
has license
cc-by
sha1sum (hex)
7f45468609cea65308db7f7b36d0cd9503261543
schema:url
https://doi.org/10.1186/s13613-019-0619-3
resource representing a document's title
Prevention and treatment of acute lung injury with time-controlled adaptive ventilation: physiologically informed modification of airway pressure release ventilation
has PubMed Central identifier
PMC6944723
has PubMed identifier
31907704
schema:publication
Ann Intensive Care
resource representing a document's body
covid:7f45468609cea65308db7f7b36d0cd9503261543#body_text
is
schema:about
of
named entity 'supportive'
named entity 'reduced'
named entity 'describe'
named entity 'attenuated'
named entity 'delivered'
named entity 'lung'
named entity 'mechanical'
named entity 'acute lung injury'
named entity 'instability'
named entity 'HOMOGENEITY'
named entity 'ANIMAL'
named entity 'OUTCOME'
named entity 'TO DESCRIBE'
named entity 'REFLECT'
named entity 'GROUP'
named entity 'OPEN'
named entity 'DOES NOT'
named entity 'OUR'
named entity 'HIGH RISK OF'
named entity 'NOVEL'
named entity 'IMPACTS'
named entity 'LUNG INJURY'
named entity 'COLLAPSING'
named entity 'EXAGGERATED'
named entity 'ARDS'
named entity 'CONTROLLED'
named entity 'TIME'
named entity 'ventilation'
named entity 'Thus'
named entity 'maintain'
named entity 'nudge'
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named entity 'animal'
named entity 'damage'
named entity 'ventilator'
named entity 'lung'
named entity 'microenvironment'
named entity 'mode'
named entity 'airway pressure release ventilation'
named entity 'acute respiratory distress syndrome'
named entity 'lung injury'
named entity 'ARDS'
named entity 'lung'
named entity 'alveoli'
named entity 'mechanical ventilation'
named entity 'risk of death'
named entity 'tissue damage'
named entity 'APRV'
named entity 'greater'
named entity 'stable'
named entity 'trauma'
named entity 'alveolar'
named entity 'volumetric strain'
named entity 'CPAP'
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named entity 'lung collapse'
named entity 'PEEP'
named entity 'neonatal'
named entity 'lung tissue'
named entity 'T Low'
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named entity 'alveolar'
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named entity 'ARDS'
named entity 'alveolar'
named entity 'normal range'
named entity 'desaturate'
named entity 'CPAP'
named entity 'lung tissue'
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