Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/120757
DC FieldValueLanguage
dc.contributor.authorDemelo-Rodriguez, Pen_US
dc.contributor.authorGaleano-Valle, Fen_US
dc.contributor.authorOrdieres-Ortega, Len_US
dc.contributor.authorSiniscalchi, Cen_US
dc.contributor.authorDel Pozo, MMen_US
dc.contributor.authorFidalgo, Aen_US
dc.contributor.authorGil Díaz, Aídaen_US
dc.contributor.authorLobo, JLen_US
dc.contributor.authorDe Ancos, Cen_US
dc.contributor.authorMonreal, Men_US
dc.date.accessioned2023-02-27T19:07:54Z-
dc.date.available2023-02-27T19:07:54Z-
dc.date.issued2021en_US
dc.identifier.issn1999-4915en_US
dc.identifier.urihttp://hdl.handle.net/10553/120757-
dc.description.abstractIntroduction: Hospitalized patients with COVID-19 are at increased risk for venous thromboembolism (VTE), but also for bleeding. We previously derived a prognostic score including four variables (elevated D-dimer, elevated ferritin, critical illness, and therapeutic-dose anticoagulation) that identified those at increased risk for major bleeding. Methods: We aimed to validate the score in a subsequent cohort of hospitalized patients with COVID-19 receiving standard-, intermediate- or therapeutic doses of VTE prophylaxis. We evaluated its capacity to predict major bleeding, non-major bleeding, and bleeding-related death. Results: The cohort included 972 patients from 29 hospitals, of whom 280 (29%) received standard-; 412 (42%) intermediate-, 157 (16%) therapeutic doses of VTE prophylaxis and 123 (13%) other drugs. Median duration of prophylaxis was 14.7 ± 10.3 days. Major bleeding occurred in 65 patients (6.7%) and non-major bleeding in 67 (6.9%). Thirty patients with major bleeding (46%) died within the first 30 days after bleeding. The prognostic score identified 203 patients (21%) at very low risk, 285 (29%) at low risk, 263 (27%) intermediate-risk and 221 (23%) at high risk for bleeding. Major bleeding occurred in 1.0%, 2.1%, 8.7% and 15.4% of the patients, respectively. Non-major bleeding occurred in 0.5%, 3.5%, 9.5% and 14.2%, respectively. The c-statistics was: 0.74 (95% confidence intervals [CI]: 0.68–0.79) for major bleeding, 0.73 (95% CI: 0.67–0.78) for non-major bleeding and 0.82 (95% CI: 0.76–0.87) for bleeding-related death. Conclusions: In hospitalized patients with COVID-19, we validated that a prognostic score including 4 easily available items may identify those at increased risk for bleeding.en_US
dc.languageengen_US
dc.relation.ispartofVirusesen_US
dc.sourceViruses [ISSN 1999-4915], v. 13 (11) 2278 (Noviembre 2021)en_US
dc.subject32 Ciencias médicasen_US
dc.subject320505 Enfermedades infecciosasen_US
dc.subject.otherAnticoagulantsen_US
dc.subject.otherCOVID-19en_US
dc.subject.otherVTE prophylaxisen_US
dc.subject.otherBleeding risken_US
dc.subject.otherPrognosisen_US
dc.titleValidation of a Prognostic Score to Identify Hospitalized Patients with COVID-19 at Increased Risk for Bleedingen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.3390/v13112278en_US
dc.identifier.pmid34835085-
dc.identifier.scopus2-s2.0-85120039831-
dc.identifier.isiWOS:000792953300026-
dc.contributor.orcid0000-0002-3096-4711-
dc.contributor.orcid0000-0003-1321-6866-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid0000-0002-9626-3408-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid0000-0002-0494-0767-
dc.identifier.issue11-
dc.relation.volume13en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.description.numberofpages10en_US
dc.utils.revisionen_US
dc.date.coverdateNoviembre 2021en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr1,463
dc.description.jcr5,818
dc.description.sjrqQ1
dc.description.jcrqQ2
dc.description.scieSCIE
dc.description.miaricds10,6
item.grantfulltextopen-
item.fulltextCon texto completo-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0002-9626-3408-
crisitem.author.fullNameGil Díaz, Aída-
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