Publication:
Extended dual antiplatelet therapy after acute coronary syndrome in Spain: Results from the EPICOR study.

dc.contributor.authorBardaji, Alfredo
dc.contributor.authorLeal, Manuel
dc.contributor.authorArrarte, Vicente
dc.contributor.authorGarcia-Moll, Xavier
dc.contributor.authorPérez de Isla, Leopoldo
dc.contributor.authorBueno, Hector
dc.contributor.funderFundación AstraZeneca
dc.date.accessioned2020-10-29T14:38:03Z
dc.date.available2020-10-29T14:38:03Z
dc.date.issued2017
dc.description.abstractReal-world, country-specific studies of dual antiplatelet therapy (DAPT) duration among survivors of acute coronary syndrome (ACS) are important for improving long-term prognosis. To investigate DAPT duration after hospital discharge for ACS in Spain. Data from patients enrolled in the Spanish cohort of the EPICOR (long-tErm follow-up of antithrombotic management Patterns In acute CORonary syndrome patients) study (NCT01171404) were analyzed for changes to antithrombotic medication up to 2 years postdischarge according to index event diagnosis and patient characteristics. Deaths, coronary events, and bleeding events were analyzed over the same period. Overall, a high proportion of patients remained on DAPT at 2 years (53.1%). Among patients who experienced any on-treatment bleeding event, almost two-thirds remained on DAPT at the end of follow-up. Patients >65 years, diabetic, or those that were medically managed were more likely to continue with DAPT until 2 years following discharge. At 2 years, the incidence of bleeding events requiring hospitalization was low compared with the incidence of coronary events (1.4% vs 6.6%). There was a numerical reduction in coronary events, but no increase in bleeding events, with DAPT continuation compared with single antiplatelet therapy. More than half of patients in this unselected cohort study remained on DAPT at 2 years following discharge for ACS. Continuation with DAPT was greater among patients with additional cardiovascular risk factors, which suggests that treating physicians in Spain prioritizes ischemic risk reduction over bleeding risk in patients with ACS, according to patient's risk profile.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThe EPICOR study was funded by AstraZeneca.es_ES
dc.format.number2es_ES
dc.format.volume35es_ES
dc.identifier.citationCardiovasc Ther. 2017; 35(2):e12237es_ES
dc.identifier.doi10.1111/1755-5922.12237es_ES
dc.identifier.journalCardiovascular therapeuticses_ES
dc.identifier.pubmedID27885830es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/11262
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.relation.publisherversionhttps://doi.org/10.1111/1755-5922.12237es_ES
dc.repisalud.institucionCNICes_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Investigación Cardiovascular Traslacional Multidisciplinariaes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.meshPercutaneous Coronary Interventiones_ES
dc.subject.meshAcute Coronary Syndromees_ES
dc.subject.meshAdministration, Orales_ES
dc.subject.meshAgedes_ES
dc.subject.meshDrug Administration Schedulees_ES
dc.subject.meshDrug Therapy, Combinationes_ES
dc.subject.meshFibrinolytic Agentses_ES
dc.subject.meshFollow-Up Studieses_ES
dc.subject.meshHemorrhagees_ES
dc.subject.meshHumanses_ES
dc.subject.meshMalees_ES
dc.subject.meshMiddle Agedes_ES
dc.subject.meshPatient Dischargees_ES
dc.subject.meshPlatelet Aggregation Inhibitorses_ES
dc.subject.meshPractice Patterns, Physicians'es_ES
dc.subject.meshProspective Studieses_ES
dc.subject.meshRegistrieses_ES
dc.subject.meshRisk Factorses_ES
dc.subject.meshSpaines_ES
dc.subject.meshTime Factorses_ES
dc.subject.meshTreatment Outcomees_ES
dc.titleExtended dual antiplatelet therapy after acute coronary syndrome in Spain: Results from the EPICOR study.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionAMes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication4e417023-fc1f-41d2-8130-485f76466465
relation.isAuthorOfPublication.latestForDiscovery4e417023-fc1f-41d2-8130-485f76466465

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