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A randomized pilot trial of brief versus prolonged heparin after successful reperfusion in acute myocardial infarction

dc.contributor.authorKander, Nathan H.en_US
dc.contributor.authorHolland, Kurt J.en_US
dc.contributor.authorPitt, Bertramen_US
dc.contributor.authorTopol, Eric J.en_US
dc.date.accessioned2006-04-10T13:51:22Z
dc.date.available2006-04-10T13:51:22Z
dc.date.issued1990-01-15en_US
dc.identifier.citationKander, Nathan H., Holland, Kurt J., Pitt, Bertram, Topol, Eric J. (1990/01/15)."A randomized pilot trial of brief versus prolonged heparin after successful reperfusion in acute myocardial infarction." The American Journal of Cardiology 65(3): 139-142. <http://hdl.handle.net/2027.42/28755>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T10-4C70971-15P/2/3dfc40c3c128e4cbefd1651a4b295cb7en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/28755
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2404389&dopt=citationen_US
dc.description.abstractControversy exists as to whether and how long heparin treatment is necessary after infarct vessel recanalization. To determine the role of heparin, patients with suitable angiographic features after reperfusion therapy were randomly allocated to receive a brief infusion of intravenous heparin for =72 hours (group 2), using the same titration mechanism. Patients were excluded for complex intimal dissections, large residual filling defects, less than Thrombolysis in Myocardial Infarction grade 3 flow pattern or &gt;50% residual stenosis. Heparin was sustained except for discontinuation 2 to 4 hours before periaccess sheath removal, or if significant bleeding (&gt;=2 units blood transfusion) occurred. The primary endpoints were 1-week patency determined by repeat catheterization or recurrent ischemia, or both, and the incidence of bleeding complications. Fifty patients were randomized, 25 in both groups. Baseline variables were similar; 14 group 1 and 15 group 2 patients received thrombolytic treatment; 20 patients in each group had coronary angioplasty. Two documented reoclusions occurred in both groups. Significant bleeding complications occurred in 0 of 25 (0%) group 1 versus 6 of 25 (24%) group 2 patients (p 24 hours does not appear to be justified in low-risk patients with successful reperfusion.en_US
dc.format.extent479937 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleA randomized pilot trial of brief versus prolonged heparin after successful reperfusion in acute myocardial infarctionen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Michigan, U.S.A.en_US
dc.contributor.affiliationumDivision of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Michigan, U.S.A.en_US
dc.contributor.affiliationumDivision of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Michigan, U.S.A.en_US
dc.contributor.affiliationumDivision of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Michigan, U.S.A.en_US
dc.identifier.pmid2404389en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/28755/1/0000585.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0002-9149(90)90074-Ben_US
dc.identifier.sourceThe American Journal of Cardiologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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