Please use this identifier to cite or link to this item: https://accedacris.ulpgc.es/handle/10553/120755
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dc.contributor.authorSiniscalchi, Cen_US
dc.contributor.authorMuriel, Aen_US
dc.contributor.authorCaralt, JMSen_US
dc.contributor.authorBikdeli, Ben_US
dc.contributor.authorJimenez, Den_US
dc.contributor.authorLobo, JLen_US
dc.contributor.authorAmado, Cen_US
dc.contributor.authorGil Díaz, Aídaen_US
dc.contributor.authorImbalzano, Een_US
dc.contributor.authorMonreal, Men_US
dc.date.accessioned2023-02-27T19:00:40Z-
dc.date.available2023-02-27T19:00:40Z-
dc.date.issued2022en_US
dc.identifier.issn1538-7933en_US
dc.identifier.urihttps://accedacris.ulpgc.es/handle/10553/120755-
dc.description.abstractBackground: 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.languageengen_US
dc.relation.ispartofJournal of Thrombosis and Haemostasisen_US
dc.sourceJournal of Thrombosis and Haemostasis [ISSN 1538-7933], v. 20 (8), p. 1839-1851 (Agosto 2022)en_US
dc.subject32 Ciencias médicasen_US
dc.subject3205 Medicina internaen_US
dc.subject.otherBleedingen_US
dc.subject.otherDeathen_US
dc.subject.otherPulmonary embolismen_US
dc.subject.otherStatinen_US
dc.subject.otherVenous thromboembolismen_US
dc.titleStatin use and 30-day mortality in patients with acute symptomatic pulmonary embolismen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1111/jth.15753en_US
dc.identifier.pmid35510755-
dc.identifier.scopus2-s2.0-85133898266-
dc.identifier.isiWOS:000800852100001-
dc.contributor.orcid0000-0002-0613-1074-
dc.contributor.orcid0000-0002-4805-4011-
dc.contributor.orcid0000-0001-6814-7963-
dc.contributor.orcid0000-0003-1428-879X-
dc.contributor.orcid0000-0002-4571-7721-
dc.contributor.orcid0000-0001-8833-4133-
dc.contributor.orcid0000-0003-3186-7048-
dc.contributor.orcid0000-0002-9626-3408-
dc.contributor.orcid0000-0003-2656-5467-
dc.contributor.orcid0000-0002-0494-0767-
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dc.description.lastpage1851en_US
dc.identifier.issue8-
dc.description.firstpage1839en_US
dc.relation.volume20en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.description.numberofpages13en_US
dc.utils.revisionen_US
dc.date.coverdateAgosto 2022en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr3,086
dc.description.jcr10,4
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
dc.description.miaricds10,8
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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