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High-dose corticosteroid pulse therapy increases the survival rate in COVID-19 patients at risk of hyper-inflammatory response.

dc.contributor.authorLópez Zúñiga, Miguel Ángel
dc.contributor.authorMoreno-Moral, Aida
dc.contributor.authorOcaña-Granados, Ana
dc.contributor.authorPadilla-Moreno, Francisco Andrés
dc.contributor.authorCastillo-Fernández, Alba María
dc.contributor.authorGuillamón-Fernández, Dionisio
dc.contributor.authorRamírez-Sánchez, Carolina
dc.contributor.authorSanchez-Palop, María
dc.contributor.authorMartínez-Colmenero, Justo
dc.contributor.authorPimentel-Villar, María Amparo
dc.contributor.authorBlázquez-Roselló, Sara
dc.contributor.authorMoreno-Sánchez, José Juan
dc.contributor.authorLópez-Vílchez, María
dc.contributor.authorPrior-Sánchez, Inmaculada
dc.contributor.authorJódar-Moreno, Rosario
dc.contributor.authorLópez Ruz, Miguel Ángel
dc.date.accessioned2023-02-09T10:40:36Z
dc.date.available2023-02-09T10:40:36Z
dc.date.issued2021-01-28
dc.description.abstractTest whether high dose corticosteroid pulse therapy (HDCPT) with either methylprednisolone or dexamethasone is associated with increased survival in COVID-19 patients at risk of hyper-inflammatory response. Provide some initial diagnostic criteria using laboratory markers to stratify these patients. This is a prospective observational study, 318 met the inclusion criteria. 64 patients (20.1%) were treated with HDCPT by using at least 1.5mg/kg/24h of methylprednisolone or dexamethasone equivalent. A multivariate Cox regression (controlling for co-morbidities and other therapies) was carried out to determine whether HDCPT (among other interventions) was associated with decreased mortality. We also carried out a 30-day time course analysis of laboratory markers between survivors and non-survivors, to identify potential markers for patient stratification. HDCPT showed a statistically significant decrease in mortality (HR = 0.087 [95% CI 0.021-0.36]; P = 40 pg/ml, and/or two of the following: C-reactive protein > = 100 mg/L, D-dimer > = 1000 ng/ml, ferritin > = 500 ng/ml and lactate dehydrogenase > = 300 U/L). HDCPT can be an effective intervention to increase COVID-19 survival rates in patients at risk of developing a COVID-19 hyper-inflammatory response, laboratory marker tests can be used to stratify these patients who should be given HDCPT. This study is not a randomized clinical trial (RCT). Future RCTs should be carried out to confirm the efficacy of HDCPT to increase the survival rates of COVID-19.
dc.identifier.doi10.1371/journal.pone.0243964
dc.identifier.essn1932-6203
dc.identifier.pmcPMC7842890
dc.identifier.pmid33507958
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7842890/pdf
dc.identifier.unpaywallURLhttps://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0243964&type=printable
dc.identifier.urihttp://hdl.handle.net/10668/17063
dc.issue.number1
dc.journal.titlePloS one
dc.journal.titleabbreviationPLoS One
dc.language.isoen
dc.organizationHospital Universitario San Cecilio
dc.organizationHospital Universitario Virgen de las Nieves
dc.organizationHospital Universitario San Cecilio
dc.organizationHospital Universitario de Jaén
dc.organizationHospital Universitario de Jaén
dc.organizationHospital Universitario Virgen de la Victoria
dc.page.numbere0243964
dc.pubmedtypeJournal Article
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshAdrenal Cortex Hormones
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshCOVID-19
dc.subject.meshCytokine Release Syndrome
dc.subject.meshDexamethasone
dc.subject.meshFemale
dc.subject.meshHospitalization
dc.subject.meshHumans
dc.subject.meshInflammation
dc.subject.meshMale
dc.subject.meshMethylprednisolone
dc.subject.meshMiddle Aged
dc.subject.meshProspective Studies
dc.subject.meshSARS-CoV-2
dc.subject.meshSpain
dc.subject.meshSurvival Rate
dc.subject.meshCOVID-19 Drug Treatment
dc.titleHigh-dose corticosteroid pulse therapy increases the survival rate in COVID-19 patients at risk of hyper-inflammatory response.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number16
dspace.entity.typePublication

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