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Hemorrhagic complications associated with the use of intravenous tissue plasminogen activator in treatment of acute myocardial infarction

dc.contributor.authorCaliff, Robert M.en_US
dc.contributor.authorTopol, Eric J.en_US
dc.contributor.authorGeorge, Barry S.en_US
dc.contributor.authorBoswick, Jane M.en_US
dc.contributor.authorAbbottsmith, Charles W.en_US
dc.contributor.authorSigmon, Kristina N.en_US
dc.contributor.authorCandela, Richard J.en_US
dc.contributor.authorMasek, Ramonaen_US
dc.contributor.authorKereiakes, Dean J.en_US
dc.contributor.authorO'Neill, William W.en_US
dc.date.accessioned2006-04-07T20:31:39Z
dc.date.available2006-04-07T20:31:39Z
dc.date.issued1988en_US
dc.identifier.citationCaliff, Robert M., Topol, Eric J., George, Barry S., Boswick, Jane M., Abbottsmith, Charles, Sigmon, Kristina N., Candela, Richard, Masek, Ramona, Kereiakes, Dean, O'Neill, William W. (1988)."Hemorrhagic complications associated with the use of intravenous tissue plasminogen activator in treatment of acute myocardial infarction." The American Journal of Medicine 85(): 353-359. <http://hdl.handle.net/2027.42/27546>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6TDC-4CKFX75-39/2/6c0cf71887be372a2730af69ec44f6b7en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/27546
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3137818&dopt=citationen_US
dc.description.abstract: Little attention has been paid to the importance of clinical factors associated with bleeding complications caused by the use of thrombolytic agents. The goal of our study was to examine clinical and hematologic factors associated with an increased risk of bleeding in a prospectively observed population that received intravenous tissue plasminogen activator for acute myocardial infarction.: Bleeding complications were evaluated in 386 consecutive patients treated with 150 mg of tissue plasminogen activator over six to eight hours for acute myocardial infarction. All patients also underwent immediate cardiac catheterization.: Quantitation of blood loss during the patients' hospital stay included a median drop in hematocrit of 11.4 points, a median nadir hematocrit of 31.2, a 14 percent rate of significant clinically evident bleeding, and a 31 percent rate of transfusion of two or more units of blood. All of these parameters were much more severe in patients treated with coronary artery bypass surgery. Access site hematoma was the most common source of bleeding (45 percent of patients), whereas 8 percent had gastrointestinal bleeding, two patients had retroperitoneal bleeding, and two patients had intracranial bleeding. The median nadir fibrinogen was 1.3 g/liter. Multiple linear regression models were used to investigate the relationship between clinical variables, including multiple hematologic measurements, and measures of the amount of blood loss. The use of coronary artery bypass grafting was the variable most closely associated with hemorrhage. Other invasive procedures (angioplasty and intra-aortic balloon pumping) were also associated with increased bleeding. Among the patient descriptors examined, lighter weight, older age, female sex, and history of hypertension were associated with greater blood loss. Of laboratory coagulation parameters, only nadir fibrinogen levels were significantly associated with more bleeding.: Careful clinical evaluation may improve assessment of the risk/benefit ratio of thrombolytic therapy.en_US
dc.format.extent1003600 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleHemorrhagic complications associated with the use of intravenous tissue plasminogen activator in treatment of acute myocardial infarctionen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelFamily Medicine and Primary Careen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumUniversity of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumUniversity of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationotherno department founden_US
dc.contributor.affiliationotherRiverside Methodist Hospital, Columbus, Ohio, USAen_US
dc.contributor.affiliationotherDivision of Cardiology, Department of Internal Medicine, Duke University Medical Center, Durham, North Carolina, USAen_US
dc.contributor.affiliationotherChrist Hospital, Cincinnati, Ohio, USAen_US
dc.contributor.affiliationotherDivision of Cardiology, Department of Internal Medicine, Duke University Medical Center, Durham, North Carolina, USAen_US
dc.contributor.affiliationotherRiverside Methodist Hospital, Columbus, Ohio, USAen_US
dc.contributor.affiliationotherRiverside Methodist Hospital, Columbus, Ohio, USAen_US
dc.contributor.affiliationotherChrist Hospital, Cincinnati, Ohio, USAen_US
dc.identifier.pmid3137818en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/27546/1/0000590.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0002-9343(88)90586-4en_US
dc.identifier.sourceThe American Journal of Medicineen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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