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dc.contributor.authorMartí-Fàbregas, J.
dc.contributor.authorMedrano-Martorell, S.
dc.contributor.authorMerino, E.
dc.contributor.authorPrats-Sánchez, L.
dc.contributor.authorMarín, R.
dc.contributor.authorDelgado-Mederos, R.
dc.contributor.authorMartínez-Domeño, A.
dc.contributor.authorCamps-Renom, P.
dc.contributor.authorJiménez-Xarrié, E.
dc.contributor.authorZedde, M.
dc.contributor.authorGómez-Choco, M.
dc.contributor.authorLara, L.
dc.contributor.authorBoix, A.
dc.contributor.authorCalleja, A.
dc.contributor.authorDe Arce-Borda, A. M.
dc.contributor.authorBravo, Y.
dc.contributor.authorFuentes, B.
dc.contributor.authorHernández-Pérez, M.
dc.contributor.authorCánovas, D.
dc.contributor.authorLlull, L.
dc.contributor.authorZandio, B.
dc.contributor.authorFreijo, M.
dc.contributor.authorCasado-Naranjo, I.
dc.contributor.authorSanahuja, J.
dc.contributor.authorCocho, D.
dc.contributor.authorKrupinski, J.
dc.contributor.authorRodríguez-Campello, A.
dc.contributor.authorPalomeras, E.
dc.contributor.authorDe Felipe, A.
dc.contributor.authorSerrano, M.
dc.contributor.authorZapata-Arriaza, E.
dc.contributor.authorZaragoza-Brunet, J.
dc.contributor.authorDíaz-Maroto, I.
dc.contributor.authorFernández-Domínguez, J.
dc.contributor.authorLago, A.
dc.contributor.authorMaestre, J.
dc.contributor.authorRodríguez Yáñez, Manuel 
dc.contributor.authorGich, I.
dc.date.accessioned2021-10-14T07:33:30Z
dc.date.available2021-10-14T07:33:30Z
dc.date.issued2019
dc.identifier.issn0028-3878
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/31004066
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541433/pdf/NEUROLOGY2018931774.pdf
dc.identifier.urihttp://hdl.handle.net/20.500.11940/15499
dc.description.abstractOBJECTIVE: We tested the hypothesis that the risk of intracranial hemorrhage (ICH) in patients with cardioembolic ischemic stroke who are treated with oral anticoagulants (OAs) can be predicted by evaluating surrogate markers of hemorrhagic-prone cerebral angiopathies using a baseline MRI. METHODS: Patients were participants in a multicenter and prospective observational study. They were older than 64 years, had a recent cardioembolic ischemic stroke, and were new users of OAs. They underwent a baseline MRI analysis to evaluate microbleeds, white matter hyperintensities, and cortical superficial siderosis. We collected demographic variables, clinical characteristics, risk scores, and therapeutic data. The primary endpoint was ICH that occurred during follow-up. We performed bivariate and multivariate Cox regression analyses. RESULTS: We recruited 937 patients (aged 77.6 +/- 6.5 years; 47.9% were men). Microbleeds were detected in 207 patients (22.5%), moderate/severe white matter hyperintensities in 419 (45.1%), and superficial siderosis in 28 patients (3%). After a mean follow-up of 23.1 +/- 6.8 months, 18 patients (1.9%) experienced an ICH. In multivariable analysis, microbleeds (hazard ratio 2.7, 95% confidence interval [CI] 1.1-7, p = 0.034) and moderate/severe white matter hyperintensities (hazard ratio 5.7, 95% CI 1.6-20, p = 0.006) were associated with ICH (C index 0.76, 95% CI 0.66-0.85). Rate of ICH was highest in patients with both microbleed and moderate/severe WMH (3.76 per 100 patient-years, 95% CI 1.62-7.4). CONCLUSION: Patients taking OAs who have advanced cerebral small vessel disease, evidenced by microbleeds and moderate to severe white matter hyperintensities, had an increased risk of ICH. Our results should help to determine the risk of prescribing OA for a patient with cardioembolic stroke. CLINICALTRIALSGOV IDENTIFIER: NCT02238470.
dc.titleMRI predicts intracranial hemorrhage in patients who receive long-term oral anticoagulation
dc.typeArtigoes
dc.contributor.authorcorpHERO study investigators
dc.authorsophosRodríguez Yáñez, Manuel
dc.identifier.doi10.1212/WNL.0000000000007532
dc.identifier.pmid31004066
dc.identifier.sophos30855
dc.issue.number21
dc.journal.titleNEUROLOGY
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago de Compostela - Complexo Hospitalario Universitario de Santiago de Compostela::Neuroloxía
dc.page.initiale2432es
dc.page.finale2443es
dc.subject.keywordCHUS
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)
dc.typesophosArtículo Original
dc.volume.number92


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