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                  <mods:namePart>Zapata-Wainberg, G</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Quintas, S</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Ximenez-Carrillo Rico, A</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Benavente Fernandez, L</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Masjuan Vallejo, J</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Gallego Cullere, Jaime</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Freijo Guerrero, Maria del Mar</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Egido, Jose</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Gomez Sanchez, JC</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Martinez Domeno, A</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
                  </mods:role>
                  <mods:namePart>Purroy, F</mods:namePart>
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               <mods:name>
                  <mods:role>
                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Vives Pastor, Barbara</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Rodriguez Yanez, M</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
                  </mods:role>
                  <mods:namePart>Vivancos, J</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Grp Investigadores Estudio TAC</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-09-06T09:56:43Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2018-09</mods:dateIssued>
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               <mods:identifier type="citation">Zapata-Wainberg G, Quintas S, Ximenez-Carrillo Rico A, Benavente Fernandez L, Masjuan Vallejo J, Gallego Cullere J, et al. Prognostic factors and analysis of mortality due to brain haemorrhages associated with vitamin K antagonist oral anticoagulants. Results from the TAC registry. Neurologia. 2018 Sep;33(7):419-26. Epub 2016 Sep 16.</mods:identifier>
               <mods:identifier type="doi">10.1016/j.nrl.2016.07.005</mods:identifier>
               <mods:identifier type="e-issn">1578-1968</mods:identifier>
               <mods:identifier type="issn">0213-4853</mods:identifier>
               <mods:identifier type="journal">Neurologia</mods:identifier>
               <mods:identifier type="other">http://hdl.handle.net/20.500.13003/17449</mods:identifier>
               <mods:identifier type="pubmedID">27645776</mods:identifier>
               <mods:identifier type="pui">L613216120</mods:identifier>
               <mods:identifier type="scopus">2-s2.0-84994772128</mods:identifier>
               <mods:identifier type="uri">https://hdl.handle.net/20.500.12105/22629</mods:identifier>
               <mods:identifier type="wos">444418800001</mods:identifier>
               <mods:abstract>Introduction: Intracranial haemorrhages (ICH) represent a severe and frequently lethal complication in patients treated with vitamin K antagonists (VKA). The purpose of our study is to describe the factors and clinical features associated with mortality in these patients. Methods: We conducted an observational, retrospective, multi-centre study based on prospective stroke registries in Spain. We included all patients admitted to neurology departments during a one-year period who met the following inclusion criteria: being 18 or older, having a diagnosis of ICH, and receiving VKA. Clinical and radiological parameters and 3-month outcomes were analysed. Results: A total of 235 patients from 21 hospitals were included. Mortality rate at 90 days was 42.6%. Bivariate analysis showed a significant association between death and the following factors: median NIHSS score at admission (5 [IQR = 9] vs 17 [IQR = 14] points, P &lt; .01) and presence of an extensive hemispheric haemorrhage (4.9% vs 35%, P &lt; .01; chi(2)). Extensive hemispheric haemorrhages, in addition to being the most lethal type, were associated with a shorter time to death (mean of 16.5 days; 95% CI: 7.1-26). A logistic regression model showed that only baseline NIHSS scores independently predicted death (odds ratio =1.13 [95% CI: 1.08-1.17] for each point in the scale). Conclusion: ICH in patients treated with VKA is associated with high mortality rates; mortality in these patients is mainly and independently associated with the clinical situation at stroke onset.</mods:abstract>
               <mods:language>
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               <mods:subject>
                  <mods:topic>Intracranial haemorrhage</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Oral anticoagulants</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Acenocoumarol</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Warfarin</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Mortality</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>Prognostic factors and analysis of mortality due to brain haemorrhages associated with vitamin K antagonist oral anticoagulants. Results from the TAC registry</mods:title>
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               <mods:genre>research article</mods:genre>
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