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dc.rights.licenseopenen_US
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorBENARD-LARIBIERE, Anne
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorHUCTEAU, Emilie
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorDEBETTE, Stephanie
dc.contributor.authorKIRCHGESNER, Julien
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorBEZIN, Julien
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorPARIENTE, Antoine
IDREF: 13395711X
dc.date.accessioned2022-07-15T13:57:53Z
dc.date.available2022-07-15T13:57:53Z
dc.date.issued2022-06
dc.date.conference2022-06-14
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/140508
dc.descriptionMeeting abstracten_US
dc.description.abstractEnIntroduction: Antidopaminergic antipsychotics have been associated with an increased risk of ischemic stroke. So far, this risk has not been assessed for antidopaminergic antiemetics (ADAs). This study aimed at estimating the risk of ischemic stroke associated with ADA use. Material and methods: Case-time-control study, based on data from the French reimbursement healthcare system (SNDS). Participants: Patients ≥18y with a first ischemic stroke between 2012 and 2016, and at least one ADA reimbursement in the 70 days before stroke. ADA use was self-compared between a risk-period (days [−14, −1] before stroke) and 3 reference periods (days [−70, −57], [−56, −43], and [−42, −29]). Time-trend of ADA use was controlled using a control group of 21,859 randomly selected patients free of the event, individually matched to cases according to age, sex, and risk factors of ischemic stroke. Association between ADA use and the risk of stroke was assessed by estimating the ratio of the odds ratios (OR) of exposure evaluated in i) stroke cases and ii) in controls. Analyses were adjusted for time-varying confounders (anticoagulants, antiplatelets, prothrombotic and vasoconstrictive drugs). Results: Among the 2,612 patients identified with incident stroke, 1,250 were exposed to ADA in the risk-period and 1,060 in the reference ones. The comparison with the 5,128 and 13,165 controls exposed to ADA in the same periods yielded a ratio of adjusted ORs (aORs) of 3.12 (2.85–3.42). Analyses stratified on age, sex, and dementia showed similar results. Ratio of aORs for analyses stratified on drug was 2.51 (2.18–2.88) for domperidone, 3.62 (3.11–4.23) for metopimazine and 3.53 (2.62–4.76) for metoclopramide. Sensitivity analyses suggested the risk would be especially increased in the first days of use. Discussion/Conclusion: This nationwide self-controlled study reported an increased risk of ischemic stroke with recent ADA use. The highest increase was highlighted for metopimazine and metoclopramide use.
dc.language.isoENen_US
dc.title.enRisk of first ischemic stroke and use of antidopaminergic antiemetics: A nationwide case-time-control study
dc.typeArticle de revueen_US
dc.identifier.doi10.1111/fcp.12786en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
bordeaux.journalFundamental and Clinical Pharmacology
bordeaux.page22-23en_US
bordeaux.volume36en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.countryfren_US
bordeaux.title.proceedingAnnual Meeting of French Society of Pharmacology and Therapeutics
bordeaux.teamAHEAD_BPHen_US
bordeaux.teamELEANOR_BPHen_US
bordeaux.conference.cityLilleen_US
bordeaux.peerReviewedouien_US
hal.identifierhal-03724842
hal.version1
hal.date.transferred2022-07-15T21:24:55Z
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
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