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dc.contributor.authorRodríguez Baño, Jesúses_ES
dc.contributor.authorPachón, Jerónimoes_ES
dc.contributor.authorCarratalá Fernández, Jordies_ES
dc.contributor.authorRyan, Pabloes_ES
dc.contributor.authorJarrín, Inmaculadaes_ES
dc.contributor.authorYllescas, Maríaes_ES
dc.contributor.authorArribas, José Ramónes_ES
dc.contributor.authorBerenguer, Juanes_ES
dc.contributor.authorSAM-COVID Study Groupes_ES
dc.contributor.authorFariñas Álvarez, María del Carmen es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2022-04-19T15:36:58Z
dc.date.available2022-04-19T15:36:58Z
dc.date.issued2021es_ES
dc.identifier.issn1198-743Xes_ES
dc.identifier.issn1469-0691es_ES
dc.identifier.urihttp://hdl.handle.net/10902/24612
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). Conclusions: Tocilizumab might be useful in COVID-19 patients with a hyperinflammatory state and should be prioritized for randomized trials in this situationes_ES
dc.format.extent10 p.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceClin Microbiol Infect . 2021 Feb;27(2):244-252es_ES
dc.titleTreatment with tocilizumab or corticosteroids for COVID-19 patients with hyperinflammatory state: a multicentre cohort study (SAM-COVID-19)es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1016/j.cmi.2020.08.010es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1016/j.cmi.2020.08.010es_ES
dc.type.versionacceptedVersiones_ES


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Attribution-NonCommercial-NoDerivatives 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution-NonCommercial-NoDerivatives 4.0 International