Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/27031
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dc.contributor.authorReis, Aline Mela Dos-
dc.contributor.authorMidega, Thais Dias-
dc.contributor.authorDeliberato, Rodrigo Octavio-
dc.contributor.authorJohnson, Alistair Ew-
dc.contributor.authorBulgarelli, Lucas-
dc.contributor.authorCorrea, Thiago Domingos-
dc.contributor.authorCeli, Leo Anthony-
dc.contributor.authorPelosi, Paolo-
dc.contributor.authorGama De Abreu, Marcelo-
dc.contributor.authorSchultz, Marcus J-
dc.contributor.authorSerpa Neto, Ary-
dc.date.accessioned2021-07-20T03:21:53Z-
dc.date.available2021-07-20T03:21:53Z-
dc.date.issued2021-05-
dc.identifier.citationAnnals of Translational Medicine 2021; 9(9): 783en
dc.identifier.issn2305-5839
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/27031-
dc.description.abstractMechanical ventilation can injure lung tissue and respiratory muscles. The aim of the present study is to assess the effect of the amount of spontaneous breathing during mechanical ventilation on patient outcomes. This is an analysis of the database of the 'Medical Information Mart for Intensive Care (MIMIC)'-III, considering intensive care units (ICUs) of the Beth Israel Deaconess Medical Center (BIDMC), Boston, MA. Adult patients who received invasive ventilation for at least 48 hours were included. Patients were categorized according to the amount of spontaneous breathing, i.e., ≥50% ('high spontaneous breathing') and <50% ('low spontaneous breathing') of time during first 48 hours of ventilation. The primary outcome was the number of ventilator-free days. In total, the analysis included 3,380 patients; 70.2% were classified as 'high spontaneous breathing', and 29.8% as 'low spontaneous breathing'. Patients in the 'high spontaneous breathing' group were older, had more comorbidities, and lower severity scores. In adjusted analysis, the amount of spontaneous breathing was not associated with the number of ventilator-free days [20.0 (0.0-24.2) vs. 19.0 (0.0-23.7) in high vs. low; absolute difference, 0.54 (95% CI, -0.10 to 1.19); P=0.101]. However, 'high spontaneous breathing' was associated with shorter duration of ventilation in survivors [6.5 (3.6 to 12.2) vs. 7.6 (4.1 to 13.9); absolute difference, -0.91 (95% CI, -1.80 to -0.02); P=0.046]. In patients surviving and receiving ventilation for at least 48 hours, the amount of spontaneous breathing during this period was not associated with an increased number of ventilator-free days.en
dc.language.isoeng
dc.subjectMechanical ventilationen
dc.subjectacute respiratory distress syndrome (ARDS)en
dc.subjectpositive end-expiratory pressure (PEEP)en
dc.subjectspontaneous breathingen
dc.subjecttidal volumeen
dc.subjectventilator-induced lung injuryen
dc.titleEffect of spontaneous breathing on ventilator-free days in critically ill patients-an analysis of patients in a large observational cohort.en
dc.typeJournal Articleen
dc.identifier.journaltitleAnnals of Translational Medicineen
dc.identifier.affiliationDepartment of Surgical Sciences and Integrated Diagnostics (DISC), University of Genoa, Genoa, Italyen
dc.identifier.affiliationNuffield Department of Medicine, University of Oxford, Oxford, UKen
dc.identifier.affiliationIRCCS San Martino Policlinico Hospital, Genoa, Italyen
dc.identifier.affiliationDepartment of Critical Care Medicine, Hospital Israelita Albert Einstein, São Paulo, Brazilen
dc.identifier.affiliationDepartment of Intensive Care & 'Laboratory of Experimental Intensive Care and Anesthesiology' (L·E·I·C·A), Academic Medical Center, Amsterdam, The Netherlandsen
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, Australiaen
dc.identifier.affiliationData Analytics Research and Evaluation (DARE) Centreen
dc.identifier.affiliationBig Data Analytics Group, Hospital Israelita Albert Einstein, São Paulo, Brazilen
dc.identifier.affiliationLaboratory for Computational Physiology, Institute for Medical Engineering & Science, MIT, Cambridge, MA, USAen
dc.identifier.affiliationDivision of Pulmonary, Critical Care and Sleep Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USAen
dc.identifier.affiliationPulmonary Engineering Group, Department of Anesthesiology and Intensive Care Medicine, University Hospital Carl Gustav Carus, Technical University Dresden, Dresden, Germanyen
dc.identifier.affiliationMahidol-Oxford Tropical Medicine Research Unit (MORU), Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailanden
dc.identifier.doi10.21037/atm-20-7901en
dc.type.contentTexten
dc.identifier.pubmedid34268396
local.name.researcherSerpa Neto, Ary
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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