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Early bacterial identification among intubated patients with COVID-19 or influenza pneumonia

dc.contributor.authorcoVAPid Study Group
dc.contributor.institutionNOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)
dc.contributor.pblAmerican Thoracic Society; 1998
dc.date.accessioned2021-11-04T04:59:44Z
dc.date.available2021-11-04T04:59:44Z
dc.date.issued2021-09-01
dc.descriptionFunding Information: Supported in part by a grant from the French government through the Programme Investissement d’Avenir (I-SITE ULNE) managed by the Agence Nationale de la Recherche (coVAPid project). I.M.-L. has been supported by Science Foundation Ireland grant number 20/COV/0038. The funders of the study had no role in the study design, data collection, analysis, interpretation, writing of the report, or decision to submit for publication. Publisher Copyright: Copyright © 2021 by the American Thoracic Society
dc.description.abstractRationale: Early empirical antimicrobial treatment is frequently prescribed to critically ill patients with coronavirus disease (COVID-19) based on Surviving Sepsis Campaign guidelines. Objectives: We aimed to determine the prevalence of early bacterial identification in intubated patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pneumonia, as compared with influenza pneumonia, and to characterize its microbiology and impact on outcomes. Methods: A multicenter retrospective European cohort was performed in 36 ICUs. All adult patients receiving invasive mechanical ventilation > 48 hours were eligible if they had SARS-CoV-2 or influenza pneumonia at ICU admission. Bacterial identification was defined by a positive bacterial culture within 48 hours after intubation in endotracheal aspirates, BAL, blood cultures, or a positive pneumococcal or legionella urinary antigen test. Measurements and Main Results: A total of 1,050 patients were included (568 in SARS-CoV-2 and 482 in influenza groups). The prevalence of bacterial identification was significantly lower in patients with SARS-CoV-2 pneumonia compared with patients with influenza pneumonia (9.7 vs. 33.6%; unadjusted odds ratio, 0.21; 95% confidence interval [CI], 0.15-0.30; adjusted odds ratio, 0.23; 95% CI, 0.16-0.33; P,0.0001). Gram-positive cocci were responsible for 58% and 72% of coinfection in patients with SARS-CoV-2 and influenza pneumonia, respectively. Bacterial identification was associated with increased adjusted hazard ratio for 28-day mortality in patients with SARS-CoV-2 pneumonia (1.57; 95% CI, 1.01-2.44; P =0.043). However, no significant difference was found in the heterogeneity of outcomes related to bacterial identification between the two study groups, suggesting that the impact of coinfection on mortality was not different between patients with SARS-CoV-2 and influenza. Conclusions: Bacterial identification within 48 hours after intubation is significantly less frequent in patients with SARSCoV-2 pneumonia than patients with influenza pneumonia.en
dc.description.versionpublishersversion
dc.description.versionpublished
dc.format.extent11
dc.format.extent806206
dc.identifier.doi10.1164/rccm.202101-0030OC
dc.identifier.issn1073-449X
dc.identifier.otherPURE: 34276436
dc.identifier.otherPURE UUID: da475ed3-b3eb-40f0-9007-8a868b221436
dc.identifier.otherScopus: 85114804597
dc.identifier.otherPubMed: 34038699
dc.identifier.otherWOS: 000695758900011
dc.identifier.urihttp://hdl.handle.net/10362/127130
dc.identifier.urlhttps://www.scopus.com/pages/publications/85114804597
dc.language.isoeng
dc.peerreviewedyes
dc.subjectBacterial
dc.subjectInfluenza
dc.subjectIntensive care
dc.subjectMechanical ventilation
dc.subjectSARS-CoV-2
dc.subjectPulmonary and Respiratory Medicine
dc.subjectCritical Care and Intensive Care Medicine
dc.titleEarly bacterial identification among intubated patients with COVID-19 or influenza pneumoniaen
dc.title.subtitleA european multicenter comparative clinical trialen
dc.typejournal article
degois.publication.firstPage546
degois.publication.issue5
degois.publication.lastPage556
degois.publication.titleAmerican Journal Of Respiratory And Critical Care Medicine
degois.publication.volume204
dspace.entity.typePublication
rcaap.rightsopenAccess

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