Please use this identifier to cite or link to this item:
http://hdl.handle.net/10553/120757
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Demelo-Rodriguez, P | en_US |
dc.contributor.author | Galeano-Valle, F | en_US |
dc.contributor.author | Ordieres-Ortega, L | en_US |
dc.contributor.author | Siniscalchi, C | en_US |
dc.contributor.author | Del Pozo, MM | en_US |
dc.contributor.author | Fidalgo, A | en_US |
dc.contributor.author | Gil Díaz, Aída | en_US |
dc.contributor.author | Lobo, JL | en_US |
dc.contributor.author | De Ancos, C | en_US |
dc.contributor.author | Monreal, M | en_US |
dc.date.accessioned | 2023-02-27T19:07:54Z | - |
dc.date.available | 2023-02-27T19:07:54Z | - |
dc.date.issued | 2021 | en_US |
dc.identifier.issn | 1999-4915 | en_US |
dc.identifier.uri | http://hdl.handle.net/10553/120757 | - |
dc.description.abstract | Introduction: 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.language | eng | en_US |
dc.relation.ispartof | Viruses | en_US |
dc.source | Viruses [ISSN 1999-4915], v. 13 (11) 2278 (Noviembre 2021) | en_US |
dc.subject | 32 Ciencias médicas | en_US |
dc.subject | 320505 Enfermedades infecciosas | en_US |
dc.subject.other | Anticoagulants | en_US |
dc.subject.other | COVID-19 | en_US |
dc.subject.other | VTE prophylaxis | en_US |
dc.subject.other | Bleeding risk | en_US |
dc.subject.other | Prognosis | en_US |
dc.title | Validation of a Prognostic Score to Identify Hospitalized Patients with COVID-19 at Increased Risk for Bleeding | en_US |
dc.type | info:eu-repo/semantics/Article | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.3390/v13112278 | en_US |
dc.identifier.pmid | 34835085 | - |
dc.identifier.scopus | 2-s2.0-85120039831 | - |
dc.identifier.isi | WOS:000792953300026 | - |
dc.contributor.orcid | 0000-0002-3096-4711 | - |
dc.contributor.orcid | 0000-0003-1321-6866 | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | 0000-0002-9626-3408 | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | 0000-0002-0494-0767 | - |
dc.identifier.issue | 11 | - |
dc.relation.volume | 13 | en_US |
dc.investigacion | Ciencias de la Salud | en_US |
dc.type2 | Artículo | en_US |
dc.description.numberofpages | 10 | en_US |
dc.utils.revision | Sí | en_US |
dc.date.coverdate | Noviembre 2021 | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.contributor.buulpgc | BU-MED | en_US |
dc.description.sjr | 1,463 | |
dc.description.jcr | 5,818 | |
dc.description.sjrq | Q1 | |
dc.description.jcrq | Q2 | |
dc.description.scie | SCIE | |
dc.description.miaricds | 10,6 | |
item.grantfulltext | open | - |
item.fulltext | Con texto completo | - |
crisitem.author.dept | Departamento de Ciencias Médicas y Quirúrgicas | - |
crisitem.author.orcid | 0000-0002-9626-3408 | - |
crisitem.author.fullName | Gil Díaz, Aída | - |
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