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http://hdl.handle.net/11452/31740
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DC Field | Value | Language |
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dc.date.accessioned | 2023-03-27T05:16:48Z | - |
dc.date.available | 2023-03-27T05:16:48Z | - |
dc.date.issued | 2018-10-05 | - |
dc.identifier.citation | Tai, P. vd. (2019). ''Outcomes of patients presenting with mild acute respiratory distress syndrome insights from the lung safe study''. Anesthesiology, 130(2), 263-283. | en_US |
dc.identifier.issn | 0003-3022 | - |
dc.identifier.issn | 1528-1175 | - |
dc.identifier.uri | https://doi.org/10.1097/ALN.0000000000002508 | - |
dc.identifier.uri | https://pubs.asahq.org/anesthesiology/article/130/2/263/20088/Outcomes-of-Patients-Presenting-with-Mild-Acute | - |
dc.identifier.uri | http://hdl.handle.net/11452/31740 | - |
dc.description | Çalışmada 868 yazar bulunmaktadır. Bu yazarlardan sadece Bursa Uludağ Üniversitesi mensuplarının girişleri yapılmıştır. | tr_TR |
dc.description.abstract | Background: 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. | en_US |
dc.description.sponsorship | European Society of Intensive Care Medicine (ESICM) | en_US |
dc.language.iso | en | en_US |
dc.publisher | Lippincott Williams & Wilkins | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.rights | Atıf Gayri Ticari Türetilemez 4.0 Uluslararası | tr_TR |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | Anesthesiology | en_US |
dc.subject | End-expiratory pressure | en_US |
dc.subject | Intensive-care units | en_US |
dc.subject | Mechanical ventilation | en_US |
dc.subject | Hospital mortality | en_US |
dc.subject | Sofa score | en_US |
dc.subject | Injury | en_US |
dc.subject | Ards | en_US |
dc.subject | Epidemiology | en_US |
dc.subject | Subphenotypes | en_US |
dc.subject | Definitions | en_US |
dc.title | Outcomes of patients presenting with mild acute respiratory distress syndrome insights from the lung safe Study | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000466747200013 | tr_TR |
dc.identifier.scopus | 2-s2.0-85060572037 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Bursa Uludağ Üniversitesi/Tıp Fakültesi/Cerrahi Tıp Bilimleri/Anesteziyoloji ve Reanimasyon Anabilim Dalı. | tr_TR |
dc.identifier.startpage | 263 | tr_TR |
dc.identifier.endpage | 283 | tr_TR |
dc.identifier.volume | 130 | tr_TR |
dc.identifier.issue | 2 | tr_TR |
dc.relation.journal | Anesthesiology | en_US |
dc.contributor.buuauthor | Ceylan, İlkay | - |
dc.contributor.buuauthor | Girgin, Nermin Kelebek | - |
dc.contributor.researcherid | AAH-7250-2019 | tr_TR |
dc.relation.collaboration | Yurt dışı | tr_TR |
dc.relation.collaboration | Sanayi | tr_TR |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.identifier.pubmed | 30499850 | tr_TR |
dc.subject.wos | Anesthesiology | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q1 | en_US |
dc.contributor.scopusid | 57200337923 | tr_TR |
dc.contributor.scopusid | 55663009300 | tr_TR |
dc.subject.scopus | Adult Respiratory Distress Syndrome; Acute Lung Injury; Artificial Ventilation | en_US |
dc.subject.emtree | Adult | en_US |
dc.subject.emtree | Adult respiratory distress syndrome | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Artificial ventilation | en_US |
dc.subject.emtree | Body weight | en_US |
dc.subject.emtree | Chronic liver failure | en_US |
dc.subject.emtree | Comorbidity | en_US |
dc.subject.emtree | Diabetes mellitus | en_US |
dc.subject.emtree | Disease course | en_US |
dc.subject.emtree | Disease severity | en_US |
dc.subject.emtree | Evolution | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Hospital mortality | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Immunosuppressive treatment | en_US |
dc.subject.emtree | Intensive care unit | en_US |
dc.subject.emtree | Lung alveolus oxygen tension | en_US |
dc.subject.emtree | Lung injury | en_US |
dc.subject.emtree | Major clinical study | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Middle aged | en_US |
dc.subject.emtree | Observational study | en_US |
dc.subject.emtree | Partial pressure | en_US |
dc.subject.emtree | Pneumonia | en_US |
dc.subject.emtree | Population | en_US |
dc.subject.emtree | Positive end expiratory pressure | en_US |
dc.subject.emtree | Priority journal | en_US |
dc.subject.emtree | Prospective study | en_US |
dc.subject.emtree | Risk factor | en_US |
dc.subject.emtree | Sequential organ failure assessment score | en_US |
dc.subject.emtree | Survival rate | en_US |
dc.subject.emtree | Tidal volume | en_US |
dc.subject.emtree | Treatment duration | en_US |
dc.subject.emtree | Treatment outcome | en_US |
dc.subject.emtree | Ventilated patient | en_US |
Appears in Collections: | PubMed Scopus Web of Science |
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