Tocilizumab in COVID-19: Factors Associated With Mortality Before and After Treatment.

dc.contributor.authorSarabia De Ardanaz, Luis
dc.contributor.authorAndreu-Ubero, Jose M
dc.contributor.authorNavidad-Fuentes, Miriam
dc.contributor.authorFerrer-González, Miguel Ángel
dc.contributor.authorRuíz Del Valle, Victor
dc.contributor.authorSalcedo-Bellido, Inmaculada
dc.contributor.authorBarrios-Rodríguez, Rocío
dc.contributor.authorCáliz-Cáliz, Rafael
dc.contributor.authorRequena, Pilar
dc.date.accessioned2025-01-07T14:23:02Z
dc.date.available2025-01-07T14:23:02Z
dc.date.issued2021-07-01
dc.description.abstractTocilizumab (TCZ) has been administered in SARS-CoV-2 pneumonia but the factors associated with mortality before and after treatment remain unclear. Cox regression models were used to estimate the predictors of time to death in a cohort of hospitalized patients with COVID-19 receiving TCZ. In addition, the mean differences between discharged and deceased patients in laboratory parameters measured before and 3, 6 and 9 days after TCZ administration were estimated with weighted generalized estimation equations. The variables associated with time to death were immunosuppression (Hazard Ratio-HR 3.15; 95% confidence interval-CI 1.17, 8.51), diabetes mellitus (HR 2.63; 95% CI 1.23-5.64), age (HR 1.05; 95% CI 1.02-1.09), days since diagnosis until TCZ administration (HR 1.05, 95% CI 1.00-1.09), and platelets (HR 0.27; 95% CI: 0.11, 0.69). In the post-TCZ analysis and compared to discharged patients, deceased patients had more lactate dehydrogenase (p = 0.013), troponin I (p = 0.013), C-reactive protein (p = 0.013), neutrophils (p = 0.024), and fewer platelets (p = 0.013) and lymphocytes (p = 0.013) as well as a lower average PaO2/FiO2 ratio. In conclusion, in COVID-19 diagnosed patients receiving TCZ, early treatment decreased the risk of death, while age, some comorbidities and baseline lower platelet counts increased that risk. After TCZ administration, lower platelet levels were again associated with mortality, together with other laboratory parameters.
dc.identifier.doi10.3389/fphar.2021.620187
dc.identifier.issn1663-9812
dc.identifier.pmcPMC8281134
dc.identifier.pmid34276355
dc.identifier.pubmedURLhttps://pmc.ncbi.nlm.nih.gov/articles/PMC8281134/pdf
dc.identifier.unpaywallURLhttps://www.frontiersin.org/articles/10.3389/fphar.2021.620187/pdf
dc.identifier.urihttps://hdl.handle.net/10668/26338
dc.journal.titleFrontiers in pharmacology
dc.journal.titleabbreviationFront Pharmacol
dc.language.isoen
dc.organizationSAS - Hospital Universitario Virgen de las Nieves
dc.organizationInstituto de Investigación Biosanitaria de Granada (ibs.GRANADA)
dc.page.number620187
dc.pubmedtypeJournal Article
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCOVID-19
dc.subjectimmunosupression
dc.subjectmortality
dc.subjectplatelet
dc.subjectrisk factor
dc.subjecttocilizumab
dc.titleTocilizumab in COVID-19: Factors Associated With Mortality Before and After Treatment.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number12

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