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Authordc.contributor.authorRobinson, Thompson G. 
Authordc.contributor.authorWang, Xia 
Authordc.contributor.authorArima, Hisatomi 
Authordc.contributor.authorBath, Philip M. 
Authordc.contributor.authorBillot, Laurent 
Authordc.contributor.authorBroderick, Joseph P. 
Authordc.contributor.authorDemchuk, Andrew M. 
Authordc.contributor.authorDonnan, Geoffery A. 
Authordc.contributor.authorKim, Jong S. 
Authordc.contributor.authorLavados Germain, Pablo Manuel 
Authordc.contributor.authorLee, Tsong Hai 
Authordc.contributor.authorLindley, Richard I. 
Authordc.contributor.authorMartins, Sheila C. O. 
Authordc.contributor.authorOlavarria, Veronica V. 
Authordc.contributor.authorPandian, Jeyaraj D. 
Authordc.contributor.authorParsons, Mark W. 
Authordc.contributor.authorPontes Neto, Octavio M. 
Authordc.contributor.authorRicci, Stefano 
Authordc.contributor.authorSato, Shoichiro 
Authordc.contributor.authorSharma, Vijay K. 
Authordc.contributor.authorNguyen, Thang H. 
Authordc.contributor.authorWang, Ji Guang 
Authordc.contributor.authorWoodward, Mark 
Authordc.contributor.authorChalmers, John 
Authordc.contributor.authorAnderson, Craig S. 
Admission datedc.date.accessioned2018-05-22T16:19:29Z
Available datedc.date.available2018-05-22T16:19:29Z
Publication datedc.date.issued2017
Cita de ítemdc.identifier.citationStroke. 2017;48:1877-1883es_ES
Identifierdc.identifier.other10.1161/STROKEAHA.116.016274
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/148023
Abstractdc.description.abstractBackground and Purpose-Many patients receiving thrombolysis for acute ischemic stroke are on prior antiplatelet therapy (APT), which may increase symptomatic intracerebral hemorrhage risk. In a prespecified subgroup analysis, we report comparative effects of different doses of intravenous alteplase according to prior APT use among participants of the international multicenter ENCHANTED study (Enhanced Control of Hypertension and Thrombolysis Stroke Study). Methods-Among 3285 alteplase-treated patients (mean age, 66.6 years; 38% women) randomly assigned to low-dose (0.6 mg/kg) or standard-dose (0.9 mg/kg) intravenous alteplase within 4.5 hours of symptom onset, 752 (22.9%) reported prior APT use. Primary outcome at 90 days was the combined end point of death or disability (modified Rankin Scale [mRS] scores, 2-6). Other outcomes included mRS scores 3 to 6, ordinal mRS shift, and symptomatic intracerebral hemorrhage by various standard criteria. Results-There were no significant differences in outcome between patients with and without prior APT after adjustment for baseline characteristics and management factors during the first week; defined by mRS scores 2 to 6 (adjusted odds ratio [OR], 1.01; 95% confidence interval [CI], 0.81-1.26; P=0.953), 3 to 6 (OR, 0.95; 95% CI, 0.75-1.20; P=0.662), or ordinal mRS shift (OR, 1.03; 95% CI, 0.87-1.21; P=0.770). Alteplase-treated patients on prior APT had higher symptomatic intracerebral hemorrhage (OR, 1.82; 95% CI, 1.00-3.30; P=0.051) according to the safe implementation of thrombolysis in stroke-monitoring study definition. Although not significant (P-trend, 0.053), low-dose alteplase tended to have better outcomes than standard-dose alteplase in those on prior APT compared with those not using APT (mRS scores of 2-6; OR, 0.84; 95% CI, 0.62-1.12 versus OR, 1.16; 95% CI, 0.99-1.36). Conclusions-Low-dose alteplase may improve outcomes in thrombolysis-treated acute ischemic stroke patients on prior APT, but this requires further evaluation in a randomized controlled trial.es_ES
Patrocinadordc.description.sponsorshipNational Health and Medical Research Council of Australia / Stroke Association of the United Kingdom / Ministry of Health of Brazil, 467322/2014-7, 402388/2013-5 / National Council for Scientific and Technological Development of Brazil, 467322/2014-7, 402388/2013-5 / Ministry for Health, Welfare, and Family Affairs of the Republic of Korea, HI14C1985es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherLippincott Williams & Wilkinses_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Sourcedc.sourceStrokees_ES
Keywordsdc.subjectAspirines_ES
Keywordsdc.subjectBrain infarctiones_ES
Keywordsdc.subjectHypertensiones_ES
Keywordsdc.subjectIntracranial hemorrhageses_ES
Keywordsdc.subjectTissue plasminogen activatores_ES
Títulodc.titleLow-versus standard-dose alteplase in patients on prior antiplatelet therapy: the Enchanted trial (enhanced control of hypertension and thrombolysis stroke study)es_ES
Document typedc.typeArtículo de revista
dcterms.accessRightsdcterms.accessRightsAcceso abierto
Catalogueruchile.catalogadortjnes_ES
Indexationuchile.indexArtículo de publicación ISIes_ES


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile