Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/127520
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dc.contributor.authorSigüenza, Patriciaen_US
dc.contributor.authorLópez Núñez, Juan Joséen_US
dc.contributor.authorFalga Tirado, Concepciónen_US
dc.contributor.authorGómez-Cuervo, Covadongaen_US
dc.contributor.authorRiera-Mestre, Antonien_US
dc.contributor.authorGil Díaz, Aídaen_US
dc.contributor.authorVerhamme, Peteren_US
dc.contributor.authorMontenegro, Ana Cristinaen_US
dc.contributor.authorBarbagelata-López, Cristinaen_US
dc.contributor.authorImbalzano, Egidioen_US
dc.contributor.authorMonreal, Manuelen_US
dc.date.accessioned2023-11-06T15:21:48Z-
dc.date.available2023-11-06T15:21:48Z-
dc.date.issued2023en_US
dc.identifier.issn0340-6245en_US
dc.identifier.otherScopus-
dc.identifier.urihttp://hdl.handle.net/10553/127520-
dc.description.abstractBackground: The optimal therapy of venous thromboembolism (VTE) in cancer patients with renal insufficiency (RI) is unknown. Current guidelines recommend to use low-molecular-weight heparin over direct oral anticoagulants to treat VTE in cancer patients at high-risk for bleeding. Methods: We used the RIETE registry to compare the 6-month incidence rates of: 1) VTE recurrences vs. major bleeding; and 2) fatal pulmonary embolism (PE) vs. fatal bleeding in 3 subgroups (those with mild, moderate, or severe RI) of cancer patients receiving enoxaparin monotherapy. Results: From January 2009 through June 2022, 2,844 patients with RI received enoxaparin for ≥6 months: 1,432 (50%) had mild, 1,168 (41%) moderate, and 244 (8.6%) had severe RI. Overall, 68%, 62% and 12% respectively, received the recommended doses. Among patients with mild RI, the rates of VTE recurrences vs. major bleeding (4.6% vs. 5.4%) and fatal PE vs. fatal bleeding (1.3% vs. 1.2%) were similar. Among patients with moderate RI, VTE recurrences were half as common as major bleeding (3.1% vs. 6.3%), but fatal PE and fatal bleeding were close (1.8% vs. 1.2%). Among patients with severe RI, VTE recurrences were 3-fold less common than major bleeding (4.1% vs. 13%), but fatal PE was 3-fold more frequent than fatal bleeding (2.5% vs. 0.8%). During the first 10 days, fatal PE was 5-fold more common than fatal bleeding (2.1% vs. 0.4%). Conclusions: Among cancer patients with severe RI, fatal PE was 5-fold more common than fatal bleeding. The recommended doses of enoxaparin in these patients should be revisited.en_US
dc.languageengen_US
dc.relation.ispartofThrombosis and Haemostasisen_US
dc.sourceThrombosis and Haemostasis[ISSN 0340-6245], (Octubre 2023)en_US
dc.subject32 Ciencias médicasen_US
dc.subject3208 Farmacodinámicaen_US
dc.subject320713 Oncologíaen_US
dc.subject320506 Nefrologíaen_US
dc.subject.otherVenous thromboembolismen_US
dc.subject.otherCanceren_US
dc.subject.otherRenal insufficiencyen_US
dc.subject.otherHeparinen_US
dc.titleEnoxaparin for the long-term therapy of venous thromboembolism in patients with cancer and renal insufficiencyen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1055/a-2191-7510en_US
dc.identifier.scopus85174926405-
dc.contributor.orcidNO DATA-
dc.contributor.orcid0000-0002-1226-2353-
dc.contributor.orcidNO DATA-
dc.contributor.orcid0000-0003-2294-2229-
dc.contributor.orcidNO DATA-
dc.contributor.orcid0000-0002-9626-3408-
dc.contributor.orcid0000-0001-8698-2858-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.authorscopusid57214229763-
dc.contributor.authorscopusid57203821467-
dc.contributor.authorscopusid6603227553-
dc.contributor.authorscopusid37107427400-
dc.contributor.authorscopusid56711381300-
dc.contributor.authorscopusid18436415700-
dc.contributor.authorscopusid6506229086-
dc.contributor.authorscopusid57170008600-
dc.contributor.authorscopusid14824495400-
dc.contributor.authorscopusid6507712629-
dc.contributor.authorscopusid34877289400-
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.utils.revisionen_US
dc.date.coverdateOctubre 2023en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr1,248
dc.description.jcr5,0
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
dc.description.miaricds11,0
item.grantfulltextnone-
item.fulltextSin 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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