Identificador persistente para citar o vincular este elemento:
http://hdl.handle.net/10553/120755
Campo DC | Valor | idioma |
---|---|---|
dc.contributor.author | Siniscalchi, C | en_US |
dc.contributor.author | Muriel, A | en_US |
dc.contributor.author | Caralt, JMS | en_US |
dc.contributor.author | Bikdeli, B | en_US |
dc.contributor.author | Jimenez, D | en_US |
dc.contributor.author | Lobo, JL | en_US |
dc.contributor.author | Amado, C | en_US |
dc.contributor.author | Gil Díaz, Aída | en_US |
dc.contributor.author | Imbalzano, E | en_US |
dc.contributor.author | Monreal, M | en_US |
dc.date.accessioned | 2023-02-27T19:00:40Z | - |
dc.date.available | 2023-02-27T19:00:40Z | - |
dc.date.issued | 2022 | en_US |
dc.identifier.issn | 1538-7933 | en_US |
dc.identifier.uri | http://hdl.handle.net/10553/120755 | - |
dc.description.abstract | Background: Statins possess antithrombotic and profibrinolytic properties. The association between statin use and short-term outcomes in patients with acute pulmonary embolism (PE) remains unknown. Methods: We used the data from the Registro Informatizado de Pacientes con Enfermedad TromboEmbólica registry to compare the 30-day all-cause mortality in patients with acute PE according to the use of statins. Secondary outcome was fatal PE. We used cancer-related mortality as a falsification endpoint. Results: From January 2009 to April 2021, 31 169 patients with PE were recruited. Of these, 5520 (18%) were using statins at baseline: low intensity: 829, moderate: 3636, high intensity: 1055. Statin users were older and had a higher frequency of diabetes, hypertension, or atherosclerotic disease than non-users (P <0.001 for all comparisons). During the first 30 days, 1475 patients died (fatal PE, 255). On multivariable analysis, statin users had a lower risk of all-cause death (odds ratio [OR]: 0.65; 95% confidence interval [CI]: 0.56–0.76) and fatal PE (OR: 0.42; 95% CI: 0.28–0.62) than non-users. The risk for death was lower in patients using either low- (OR: 0.51; 95% CI: 0.34–0.77), moderate- (OR: 0.68; 95% CI: 0.57–0.81), or high-intensity statins (OR: 0.68; 95% CI: 0.51–0.92). Results did not change in mixed effects logistic regression models with hospitals as a random effect. Statins were not associated with a significant chance in cancer mortality (falsification endpoint). Conclusions: PE patients using statins at baseline had a significantly lower risk of dying within the first 30 days than non-users. Randomized trials are needed to confirm these data. | en_US |
dc.language | eng | en_US |
dc.relation.ispartof | Journal of Thrombosis and Haemostasis | en_US |
dc.source | Journal of Thrombosis and Haemostasis [ISSN 1538-7933], v. 20 (8), p. 1839-1851 (Agosto 2022) | en_US |
dc.subject | 32 Ciencias médicas | en_US |
dc.subject | 3205 Medicina interna | en_US |
dc.subject.other | Bleeding | en_US |
dc.subject.other | Death | en_US |
dc.subject.other | Pulmonary embolism | en_US |
dc.subject.other | Statin | en_US |
dc.subject.other | Venous thromboembolism | en_US |
dc.title | Statin use and 30-day mortality in patients with acute symptomatic pulmonary embolism | en_US |
dc.type | info:eu-repo/semantics/article | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1111/jth.15753 | en_US |
dc.identifier.pmid | 35510755 | - |
dc.identifier.scopus | 2-s2.0-85133898266 | - |
dc.identifier.isi | WOS:000800852100001 | - |
dc.contributor.orcid | 0000-0002-0613-1074 | - |
dc.contributor.orcid | 0000-0002-4805-4011 | - |
dc.contributor.orcid | 0000-0001-6814-7963 | - |
dc.contributor.orcid | 0000-0003-1428-879X | - |
dc.contributor.orcid | 0000-0002-4571-7721 | - |
dc.contributor.orcid | 0000-0001-8833-4133 | - |
dc.contributor.orcid | 0000-0003-3186-7048 | - |
dc.contributor.orcid | 0000-0002-9626-3408 | - |
dc.contributor.orcid | 0000-0003-2656-5467 | - |
dc.contributor.orcid | 0000-0002-0494-0767 | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.description.lastpage | 1851 | en_US |
dc.identifier.issue | 8 | - |
dc.description.firstpage | 1839 | en_US |
dc.relation.volume | 20 | en_US |
dc.investigacion | Ciencias de la Salud | en_US |
dc.type2 | Artículo | en_US |
dc.description.numberofpages | 13 | en_US |
dc.utils.revision | Sí | en_US |
dc.date.coverdate | Agosto 2022 | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.contributor.buulpgc | BU-MED | en_US |
dc.description.sjr | 3,086 | |
dc.description.jcr | 10,4 | |
dc.description.sjrq | Q1 | |
dc.description.jcrq | Q1 | |
dc.description.scie | SCIE | |
dc.description.miaricds | 10,8 | |
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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