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dc.rights.licenseopenen_US
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorALLOUCHERY, Marion
ORCID: 0000-0002-8261-9549
IDREF: 193082543
dc.contributor.authorTOMOWIAK, Cécile
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorSINGIER, Allison
dc.contributor.authorPUYADE, Mathieu
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorDARI, Loubna
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorPAMBRUN, Elodie
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorPARIENTE, Antoine
IDREF: 13395711X
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorBEZIN, Julien
ORCID: 0000-0002-2568-1928
IDREF: 181595710
dc.contributor.authorPÉRAULT-POCHAT, Marie-Christine
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorSALVO, Francesco
IDREF: 221043470
dc.date.accessioned2023-10-17T10:12:05Z
dc.date.available2023-10-17T10:12:05Z
dc.date.issued2023-10-01
dc.identifier.issn1365-2141en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/184465
dc.description.abstractEnData regarding the safety of co-administration of ibrutinib with anticoagulants in real-life settings are scarce. Using a nationwide database, we conducted a nested case-control study in a cohort of new users of ibrutinib to assess the risk of clinically relevant bleeding (CRB) associated with anticoagulation. Cases were patients with a diagnosis of CRB, defined as hospitalization with a diagnosis of bleeding. The date of CRB constituted the index date. Up to four controls were matched on sex, age at index date and duration of follow-up. The risk of CRB associated with anticoagulation in patients receiving ibrutinib was estimated using conditional logistic regression models, providing odds ratios (OR) adjusted for risk factors of bleeding. Among 614 cases and 2407 matched controls, the risk of CRB was significantly higher in patients receiving both ibrutinib and anticoagulants (adjusted OR [aOR] 2.54, confidence interval [CI] 95% [1.94; 3.32]). When considering anticoagulant class, aOR was 1.99 (CI 95% [1.19; 3.33]) for VKA, 2.48 (CI 95% [1.76; 3.47]) for direct oral anticoagulants and 3.40 (CI 95% [2.01; 5.75]) for parenteral anticoagulants. In conclusion, this study found a 2.5-fold increased risk of CRB in patients receiving both ibrutinib and anticoagulants in real-life settings, and similar aOR among oral anticoagulants.
dc.language.isoENen_US
dc.subject.enHumans
dc.subject.enAnticoagulants
dc.subject.enCase-Control Studies
dc.subject.enHemorrhage
dc.subject.enPiperidines
dc.subject.enAdministration
dc.subject.enOral
dc.subject.enAtrial Fibrillation
dc.title.enBleeding risk with concurrent use of anticoagulants and ibrutinib: A population-based nested case-control study
dc.title.alternativeBr J Haematolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1111/bjh.18995en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed37485683en_US
bordeaux.journalBritish Journal of Haematologyen_US
bordeaux.page311-318en_US
bordeaux.volume203en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue2en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamAHEADen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04245909
hal.version1
hal.date.transferred2023-10-17T10:12:06Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=British%20Journal%20of%20Haematology&rft.date=2023-10-01&rft.volume=203&rft.issue=2&rft.spage=311-318&rft.epage=311-318&rft.eissn=1365-2141&rft.issn=1365-2141&rft.au=ALLOUCHERY,%20Marion&TOMOWIAK,%20C%C3%A9cile&SINGIER,%20Allison&PUYADE,%20Mathieu&DARI,%20Loubna&rft.genre=article


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