Noninvasive assessment of airflows by electrical impedance tomography in intubated hypoxemic patients: an exploratory study.
Acute respiratory distress syndrome
Electrical impedance
Mechanical ventilation
Respiratory airflow
Respiratory failure
Spirometry
Journal
Annals of intensive care
ISSN: 2110-5820
Titre abrégé: Ann Intensive Care
Pays: Germany
ID NLM: 101562873
Informations de publication
Date de publication:
22 Jul 2019
22 Jul 2019
Historique:
received:
29
01
2019
accepted:
17
07
2019
entrez:
24
7
2019
pubmed:
25
7
2019
medline:
25
7
2019
Statut:
epublish
Résumé
Noninvasive monitoring of maximal inspiratory and expiratory flows (MIF and MEF, respectively) by electrical impedance tomography (EIT) might enable early recognition of changes in the mechanical properties of the respiratory system due to new conditions or in response to treatments. We aimed to validate EIT-based measures of MIF and MEF against spirometry in intubated hypoxemic patients during controlled ventilation and spontaneous breathing. Moreover, regional distribution of maximal airflows might interact with lung pathology and increase the risk of additional ventilation injury. Thus, we also aimed to describe the effects of mechanical ventilation settings on regional MIF and MEF. We performed a new analysis of data from two prospective, randomized, crossover studies. We included intubated patients admitted to the intensive care unit with acute hypoxemic respiratory failure (AHRF) and acute respiratory distress syndrome (ARDS) undergoing pressure support ventilation (PSV, n = 10) and volume-controlled ventilation (VCV, n = 20). We measured MIF and MEF by spirometry and EIT during six different combinations of ventilation settings: higher vs. lower support during PSV and higher vs. lower positive end-expiratory pressure (PEEP) during both PSV and VCV. Regional airflows were assessed by EIT in dependent and non-dependent lung regions, too. MIF and MEF measured by EIT were tightly correlated with those measured by spirometry during all conditions (range of R EIT provides accurate noninvasive monitoring of MIF and MEF. The present study also generates the hypothesis that EIT could guide PSV and PEEP settings aimed to increase homogeneity of distending and deflating regional airflows.
Sections du résumé
BACKGROUND
BACKGROUND
Noninvasive monitoring of maximal inspiratory and expiratory flows (MIF and MEF, respectively) by electrical impedance tomography (EIT) might enable early recognition of changes in the mechanical properties of the respiratory system due to new conditions or in response to treatments. We aimed to validate EIT-based measures of MIF and MEF against spirometry in intubated hypoxemic patients during controlled ventilation and spontaneous breathing. Moreover, regional distribution of maximal airflows might interact with lung pathology and increase the risk of additional ventilation injury. Thus, we also aimed to describe the effects of mechanical ventilation settings on regional MIF and MEF.
METHODS
METHODS
We performed a new analysis of data from two prospective, randomized, crossover studies. We included intubated patients admitted to the intensive care unit with acute hypoxemic respiratory failure (AHRF) and acute respiratory distress syndrome (ARDS) undergoing pressure support ventilation (PSV, n = 10) and volume-controlled ventilation (VCV, n = 20). We measured MIF and MEF by spirometry and EIT during six different combinations of ventilation settings: higher vs. lower support during PSV and higher vs. lower positive end-expiratory pressure (PEEP) during both PSV and VCV. Regional airflows were assessed by EIT in dependent and non-dependent lung regions, too.
RESULTS
RESULTS
MIF and MEF measured by EIT were tightly correlated with those measured by spirometry during all conditions (range of R
CONCLUSIONS
CONCLUSIONS
EIT provides accurate noninvasive monitoring of MIF and MEF. The present study also generates the hypothesis that EIT could guide PSV and PEEP settings aimed to increase homogeneity of distending and deflating regional airflows.
Identifiants
pubmed: 31332551
doi: 10.1186/s13613-019-0560-5
pii: 10.1186/s13613-019-0560-5
pmc: PMC6646434
doi:
Types de publication
Journal Article
Langues
eng
Pagination
83Subventions
Organisme : Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
ID : Ricerca corrente 2018 - "Rimozione extracorporeal di anidride carbonica (CO2) e modulazione della ventilazione spontanea in pazienti con insufficienza respiratoria acuta (sindrome da distress respiratorio
Organisme : Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
ID : ARDS) e acuta su cronico (broncopneumopatia cronico ostruttiva
Organisme : Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
ID : COPD)"
Références
Anesthesiology. 2004 Sep;101(3):722-8
pubmed: 15329597
Eur Respir J. 2005 Aug;26(2):319-38
pubmed: 16055882
Intensive Care Med. 2009 Jun;35(6):1132-7
pubmed: 19255741
Intensive Care Med. 2009 Aug;35(8):1362-7
pubmed: 19513694
Intensive Care Med. 2009 Nov;35(11):1900-6
pubmed: 19652949
JAMA. 2012 Jun 20;307(23):2526-33
pubmed: 22797452
J Appl Physiol (1985). 2012 Oct;113(7):1154-61
pubmed: 22898553
Crit Care Med. 2013 May;41(5):1296-304
pubmed: 23474677
Crit Care Med. 2013 Jul;41(7):1664-73
pubmed: 23507723
Physiol Meas. 2013 Nov;34(11):N107-14
pubmed: 24150032
Am J Respir Crit Care Med. 2014 Jan 15;189(2):149-58
pubmed: 24261322
BMC Pulm Med. 2014 Apr 29;14:73
pubmed: 24779960
Crit Care Med. 2015 Sep;43(9):1823-31
pubmed: 25985386
Crit Care Med. 2016 Sep;44(9):e838-45
pubmed: 27054894
Am J Physiol Lung Cell Mol Physiol. 2016 Jul 1;311(1):L8-L19
pubmed: 27190067
Physiol Meas. 2016 Jun;37(6):698-712
pubmed: 27203725
Intensive Care Med. 2016 Aug;42(8):1206-13
pubmed: 27318943
Intensive Care Med. 2016 Sep;42(9):1360-73
pubmed: 27334266
Intensive Care Med. 2016 Oct;42(10):1576-1587
pubmed: 27518321
Thorax. 2017 Jan;72(1):83-93
pubmed: 27596161
Am J Respir Crit Care Med. 2017 May 1;195(9):1207-1215
pubmed: 27997805
Crit Care Med. 2017 Apr;45(4):687-694
pubmed: 28107207
Am J Respir Crit Care Med. 2018 Jan 1;197(1):132-136
pubmed: 28557528
Intensive Care Med. 2017 Oct;43(10):1453-1463
pubmed: 28762180
Ann Transl Med. 2017 Jul;5(14):292
pubmed: 28828367
Crit Care. 2017 Dec 28;21(Suppl 3):312
pubmed: 29297365
Am J Respir Crit Care Med. 2018 Nov 1;198(9):1165-1176
pubmed: 29902384
Crit Care. 2018 Sep 21;22(1):221
pubmed: 30236123
Crit Care. 2018 Sep 29;22(1):245
pubmed: 30268138
Intensive Care Med. 2019 May;45(5):674-677
pubmed: 30284639
J Appl Physiol. 1972 Aug;33(2):252-4
pubmed: 5054434