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Outcomes of patients presenting with mild acute respiratory distress syndrome insights from the lung safe Study

dc.contributor.buuauthorCeylan, İlkay
dc.contributor.buuauthorGirgin, Nermin Kelebek
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentCerrahi Tıp Bilimleri
dc.contributor.departmentAnesteziyoloji ve Reanimasyon Ana Bilim Dalı
dc.contributor.researcheridAAH-7250-2019
dc.contributor.scopusid57200337923
dc.contributor.scopusid55663009300
dc.date.accessioned2023-03-27T05:16:48Z
dc.date.available2023-03-27T05:16:48Z
dc.date.issued2018-10-05
dc.descriptionÇalışmada 868 yazar bulunmaktadır. Bu yazarlardan sadece Bursa Uludağ Üniversitesi mensuplarının girişleri yapılmıştır.
dc.description.abstractBackground: Patients with initial mild acute respiratory distress syndrome are often underrecognized and mistakenly considered to have low disease severity and favorable outcomes. They represent a relatively poorly characterized population that was only classified as having acute respiratory distress syndrome in the most recent definition. Our primary objective was to describe the natural course and the factors associated with worsening and mortality in this population. Methods: This study analyzed patients from the international prospective Large Observational Study to Understand the Global Impact of Severe Acute Respiratory Failure (LUNG SAFE) who had initial mild acute respiratory distress syndrome in the first day of inclusion. This study defined three groups based on the evolution of severity in the first week: " worsening" if moderate or severe acute respiratory distress syndrome criteria were met, " persisting" if mild acute respiratory distress syndrome criteria were the most severe category, and " improving" if patients did not fulfill acute respiratory distress syndrome criteria any more from day 2. Results: Among 580 patients with initial mild acute respiratory distress syndrome, 18% (103 of 580) continuously improved, 36% (210 of 580) had persisting mild acute respiratory distress syndrome, and 46% (267 of 580) worsened in the first week after acute respiratory distress syndrome onset. Global in-hospital mortality was 30% (172 of 576; specifically 10% [10 of 101], 30% [63 of 210], and 37% [99 of 265] for patients with improving, persisting, and worsening acute respiratory distress syndrome, respectively), and the median (interquartile range) duration of mechanical ventilation was 7 (4, 14) days (specifically 3 [2, 5], 7 [4, 14], and 11 [6, 18] days for patients with improving, persisting, and worsening acute respiratory distress syndrome, respectively). Admissions for trauma or pneumonia, higher nonpulmonary sequential organ failure assessment score, lower partial pressure of alveolar oxygen/fraction of inspired oxygen, and higher peak inspiratory pressure were independently associated with worsening. Conclusions: Most patients with initial mild acute respiratory distress syndrome continue to fulfill acute respiratory distress syndrome criteria in the first week, and nearly half worsen in severity. Their mortality is high, particularly in patients with worsening acute respiratory distress syndrome, emphasizing the need for close attention to this patient population.
dc.description.sponsorshipEuropean Society of Intensive Care Medicine (ESICM)
dc.identifier.citationTai, P. vd. (2019). ''Outcomes of patients presenting with mild acute respiratory distress syndrome insights from the lung safe study''. Anesthesiology, 130(2), 263-283.
dc.identifier.doi10.1097/ALN.0000000000002508
dc.identifier.endpage283
dc.identifier.issn0003-3022
dc.identifier.issn1528-1175
dc.identifier.issue2
dc.identifier.pubmed30499850
dc.identifier.scopus2-s2.0-85060572037
dc.identifier.startpage263
dc.identifier.urihttps://doi.org/10.1097/ALN.0000000000002508
dc.identifier.urihttps://pubs.asahq.org/anesthesiology/article/130/2/263/20088/Outcomes-of-Patients-Presenting-with-Mild-Acute
dc.identifier.urihttp://hdl.handle.net/11452/31740
dc.identifier.volume130
dc.identifier.wos000466747200013
dc.indexed.scopusScopus
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherLippincott Williams & Wilkins
dc.relation.collaborationYurt dışı
dc.relation.collaborationSanayi
dc.relation.collaborationYurt içi
dc.relation.journalAnesthesiology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAnesthesiology
dc.subjectEnd-expiratory pressure
dc.subjectIntensive-care units
dc.subjectMechanical ventilation
dc.subjectHospital mortality
dc.subjectSofa score
dc.subjectInjury
dc.subjectArds
dc.subjectEpidemiology
dc.subjectSubphenotypes
dc.subjectDefinitions
dc.subject.emtreeAdult
dc.subject.emtreeAdult respiratory distress syndrome
dc.subject.emtreeArticle
dc.subject.emtreeArtificial ventilation
dc.subject.emtreeBody weight
dc.subject.emtreeChronic liver failure
dc.subject.emtreeComorbidity
dc.subject.emtreeDiabetes mellitus
dc.subject.emtreeDisease course
dc.subject.emtreeDisease severity
dc.subject.emtreeEvolution
dc.subject.emtreeFemale
dc.subject.emtreeHospital mortality
dc.subject.emtreeHuman
dc.subject.emtreeImmunosuppressive treatment
dc.subject.emtreeIntensive care unit
dc.subject.emtreeLung alveolus oxygen tension
dc.subject.emtreeLung injury
dc.subject.emtreeMajor clinical study
dc.subject.emtreeMale
dc.subject.emtreeMiddle aged
dc.subject.emtreeObservational study
dc.subject.emtreePartial pressure
dc.subject.emtreePneumonia
dc.subject.emtreePopulation
dc.subject.emtreePositive end expiratory pressure
dc.subject.emtreePriority journal
dc.subject.emtreeProspective study
dc.subject.emtreeRisk factor
dc.subject.emtreeSequential organ failure assessment score
dc.subject.emtreeSurvival rate
dc.subject.emtreeTidal volume
dc.subject.emtreeTreatment duration
dc.subject.emtreeTreatment outcome
dc.subject.emtreeVentilated patient
dc.subject.scopusAdult Respiratory Distress Syndrome; Acute Lung Injury; Artificial Ventilation
dc.subject.wosAnesthesiology
dc.titleOutcomes of patients presenting with mild acute respiratory distress syndrome insights from the lung safe Study
dc.typeArticle
dc.wos.quartileQ1
dc.wos.quartileQ1
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Cerrahi Tıp Bilimleri/Anesteziyoloji ve Reanimasyon Ana Bilim Dalı
local.indexed.atPubMed
local.indexed.atWOS
local.indexed.atScopus

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