Enoxaparin is superior to unfractionated heparin in patients with ST elevation myocardial infarction undergoing fibrinolysis regardless of the choice of lytic: an ExTRACT-TIMI 25 analysis
dc.contributor.author | Giraldez, Roberto R. | |
dc.contributor.author | Nicolau, Jose Carlos | |
dc.contributor.author | Corbalan, Ramon | |
dc.contributor.author | Gurfinkel, Enrique P. | |
dc.contributor.author | Juarez, Ursulo | |
dc.contributor.author | Lopez Sendon, Jose | |
dc.contributor.author | Parkhomenko, Alexander | |
dc.contributor.author | Molhoek, Peter | |
dc.contributor.author | Mohanavelu, Satishkumar | |
dc.contributor.author | Morrow, David A. | |
dc.contributor.author | Antman, Elliott M. | |
dc.date.accessioned | 2024-01-10T12:05:14Z | |
dc.date.available | 2024-01-10T12:05:14Z | |
dc.date.issued | 2007 | |
dc.description.abstract | Aims We compared outcomes of ST-elevation myocardial infarction (STEMI) patients randomized to a strategy of either enoxaparin or unfractionated heparin (UFH) to support fibrinolysis. Methods and results In the Enoxaparin and Thrombolysis Reperfusion for Acute Myocardial Infarction Treatment-Thrombolysis in Myocardial Infarction Study 25 (ExTRACT-TIMI 25) trial, 20 479 patients undergoing fibrinolysis for STEMI with a fibrin-specific agent (N = 16 283) or streptokinase (SK) IN = 4139) were randomized to enoxaparin throughout their hospitalization or UFH for at [east 48 h. The primary end point of death or nonfatal recurrent MI through 30 days occurred in 12.0% of patients in the UFH and 9.8% in the enoxaparin groups when treated with fibrin-specific lytics [odds ratio(adjusted) (ORadj) 0.78; 95% Cl 0.70-0.87; P < 0.001] and 11.8 vs. 10.2%, respectively, when treated with SK (ORadj 0.83; 95% CI 0.66-1.04; P = 0-10; P-interaction = 0.58). Major bleeding rates including intracranial hemorrhage within the fibrin specific cohort were 1.2 and 2.0% in the UFH and enoxaparin groups, respectively (P < 0.001) and 2.0% in UFH and 2.4% in enoxaparin patients in the SK cohort (P = 0.16). Interaction tests between antithrombin- and lytic-type were non-significant (P = 0.20). Death, nonfatal MI, or major bleeding was significantly reduced with enoxaparin in the fibrin-specific cohort (ORadj 0.82; 95% Cl 0.74-0.91; P < 0.001) and favoured enoxaparin in the SK cohort (ORadj 0.89; 95% Cl 0.72-1.10; P = 0.29; P-interaction = 0.53). Conclusion The benefits of an enoxaparin strategy over UFH were observed in both SK and fibrin -specific-treated STEMI patients. Therefore, an enoxaparin strategy is preferred over UFH to support fibrinolysis for STEMI regardless of lytic agent. | |
dc.fechaingreso.objetodigital | 2024-04-30 | |
dc.format.extent | 8 páginas | |
dc.fuente.origen | WOS | |
dc.identifier.doi | 10.1093/eurheartj/ehm179 | |
dc.identifier.eissn | 1522-9645 | |
dc.identifier.issn | 0195-668X | |
dc.identifier.pubmedid | MEDLINE:17562672 | |
dc.identifier.uri | https://doi.org/10.1093/eurheartj/ehm179 | |
dc.identifier.uri | https://repositorio.uc.cl/handle/11534/75972 | |
dc.identifier.wosid | WOS:000248271600009 | |
dc.information.autoruc | Medicina;Corbalán R;S/I;98700 | |
dc.issue.numero | 13 | |
dc.language.iso | en | |
dc.nota.acceso | contenido parcial | |
dc.pagina.final | 1573 | |
dc.pagina.inicio | 1566 | |
dc.publisher | OXFORD UNIV PRESS | |
dc.revista | EUROPEAN HEART JOURNAL | |
dc.rights | acceso restringido | |
dc.subject | STEMI | |
dc.subject | enoxaparin | |
dc.subject | fibrin-specific lytics | |
dc.subject | streptokinase | |
dc.subject | TISSUE PLASMINOGEN-ACTIVATOR | |
dc.subject | ANTITHROMBIN THERAPY | |
dc.subject | THROMBOLYSIS | |
dc.subject | REPERFUSION | |
dc.subject | ASPIRIN | |
dc.subject | MORTALITY | |
dc.subject.ods | 03 Good Health and Well-being | |
dc.subject.odspa | 03 Salud y bienestar | |
dc.title | Enoxaparin is superior to unfractionated heparin in patients with ST elevation myocardial infarction undergoing fibrinolysis regardless of the choice of lytic: an ExTRACT-TIMI 25 analysis | |
dc.type | artículo | |
dc.volumen | 28 | |
sipa.codpersvinculados | 98700 | |
sipa.index | WOS | |
sipa.index | Scopus | |
sipa.trazabilidad | Carga SIPA;09-01-2024 |
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