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dc.creatorRodríguez-Baño, Jesúses
dc.creatorPachón Díaz, Jerónimoes
dc.creatorCarratalà, Jordies
dc.creatorRyan, Pabloes
dc.creatorJarrín, Inmaculadaes
dc.creatorYllescas, Maríaes
dc.creatorArribas, José Ramónes
dc.creatorBerenguer, Juanes
dc.date.accessioned2022-07-13T10:27:40Z
dc.date.available2022-07-13T10:27:40Z
dc.date.issued2021
dc.identifier.citationRodríguez-Baño, J., Pachón, J., Carratalà, J., Ryan, P., Jarrín, I., Yllescas, M.,...,Berenguer, J. (2021). Treatment with tocilizumab or corticosteroids for COVID-19 patients with hyperinflammatory state: a multicentre cohort study (SAM-COVID-19). Clinical Microbiology and Infection, 27 (2), 244-252.
dc.identifier.issn1198-743Xes
dc.identifier.issn1469-0691 onlinees
dc.identifier.urihttps://hdl.handle.net/11441/135303
dc.description.abstractObjectives The objective of this study was to estimate the association between tocilizumab or corticosteroids and the risk of intubation or death in patients with coronavirus disease 19 (COVID-19) with a hyperinflammatory state according to clinical and laboratory parameters. Methods A cohort study was performed in 60 Spanish hospitals including 778 patients with COVID-19 and clinical and laboratory data indicative of a hyperinflammatory state. Treatment was mainly with tocilizumab, an intermediate-high dose of corticosteroids (IHDC), a pulse dose of corticosteroids (PDC), combination therapy, or no treatment. Primary outcome was intubation or death; follow-up was 21 days. Propensity score-adjusted estimations using Cox regression (logistic regression if needed) were calculated. Propensity scores were used as confounders, matching variables and for the inverse probability of treatment weights (IPTWs). Results In all, 88, 117, 78 and 151 patients treated with tocilizumab, IHDC, PDC, and combination therapy, respectively, were compared with 344 untreated patients. The primary endpoint occurred in 10 (11.4%), 27 (23.1%), 12 (15.4%), 40 (25.6%) and 69 (21.1%), respectively. The IPTW-based hazard ratios (odds ratio for combination therapy) for the primary endpoint were 0.32 (95%CI 0.22–0.47; p < 0.001) for tocilizumab, 0.82 (0.71–1.30; p 0.82) for IHDC, 0.61 (0.43–0.86; p 0.006) for PDC, and 1.17 (0.86–1.58; p 0.30) for combination therapy. Other applications of the propensity score provided similar results, but were not significant for PDC. Tocilizumab was also associated with lower hazard of death alone in IPTW analysis (0.07; 0.02–0.17; p < 0.001).es
dc.formatapplication/pdfes
dc.format.extent9 p.es
dc.language.isoenges
dc.publisherScience Directes
dc.relation.ispartofClinical Microbiology and Infection, 27 (2), 244-252.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectCohort studyes
dc.subjectCorticosteroidses
dc.subjectCOVID-19es
dc.subjectHyperinflammatory statees
dc.titleTreatment with tocilizumab or corticosteroids for COVID-19 patients with hyperinflammatory state: a multicentre cohort study (SAM-COVID-19)es
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Medicinaes
dc.relation.publisherversionhttps://reader.elsevier.com/reader/sd/pii/S1198743X20304924?token=031722D2E384576E74E54CD294E23F8A194DC93334B6531A1847E78C5FF4AB245F31CABC3412B7D5C4AB41DE21023518&originRegion=eu-west-1&originCreation=20220713101841es
dc.identifier.doi10.1016/j.cmi.2020.08.010es
dc.journaltitleClinical Microbiology and Infectiones
dc.publication.volumen27es
dc.publication.issue2es
dc.publication.initialPage244es
dc.publication.endPage252es
dc.contributor.funderInstituto Carlos III (España)es
dc.contributor.funderUnión Europeaes

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