Thrombocytopenia in Patients With an Acute Coronary Syndrome (from the Global Registry of Acute Coronary Events [GRACE])
The incidence of thrombocytopenia after hospital admission, patient and treatment characteristics, and outcomes in patients enrolled in the prospective multinational GRACE were examined. Heparin (unfractionated or low molecular weight) and glycoprotein IIb/IIIa-inhibition can be associated with immu...
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creator | Gore, Joel M., MD Spencer, Frederick A., MD Gurfinkel, Enrique P., MD López-Sendón, José, MD Steg, Ph. Gabriel, MD Granger, Christopher B., MD FitzGerald, Gordon, PhD Agnelli, Giancarlo, MD |
description | The incidence of thrombocytopenia after hospital admission, patient and treatment characteristics, and outcomes in patients enrolled in the prospective multinational GRACE were examined. Heparin (unfractionated or low molecular weight) and glycoprotein IIb/IIIa-inhibition can be associated with immune-mediated thrombocytopenia of clinical importance. The prevalence of thrombocytopenia in patients with acute coronary syndromes (ACSs) in general and specifically related to these therapies and associated outcomes have been studied little outside of clinical trials. Patients with an ACS were stratified into 4 groups of those with heparin-induced thrombocytopenia (HIT), those with glycoprotein IIb/IIIa-associated thrombocytopenia (GAT), those with other thrombocytopenia (not diagnosed as HIT or associated with glycoprotein inhibitors), and those with no thrombocytopenia. From June 2000 to September 2007, a total of 52,647 patients with an ACS and information for platelet count were enrolled in GRACE. Of these, 152 (0.3%) were reported to develop HIT, 324 (0.6%) developed GAT, and 368 (0.7%) developed other thrombocytopenia. Patients with HIT, GAT, or other thrombocytopenia were significantly more likely to die in the hospital versus those without these diseases (adjusted odds ratio [OR] 1.94, 95% confidence interval [CI] 1.07 to 3.53; adjusted OR 3.45, 95% CI 2.35 to 5.05; and adjusted OR 2.83, 95% CI 1.97 to 4.06, respectively). They were also more likely to experience major bleeding, (re)infarction, or stroke. In conclusion, in this large multinational registry, 1.6% of patients with ACS were reported to develop thrombocytopenia, with only 0.3% being HIT. Regardless of whether patients had clinically recognized HIT, GAT, or other thrombocytopenia, all 3 groups had significantly higher rates of major bleeding, recurrent infarction, stroke, and death. |
doi_str_mv | 10.1016/j.amjcard.2008.08.055 |
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Gabriel, MD ; Granger, Christopher B., MD ; FitzGerald, Gordon, PhD ; Agnelli, Giancarlo, MD</creator><creatorcontrib>Gore, Joel M., MD ; Spencer, Frederick A., MD ; Gurfinkel, Enrique P., MD ; López-Sendón, José, MD ; Steg, Ph. Gabriel, MD ; Granger, Christopher B., MD ; FitzGerald, Gordon, PhD ; Agnelli, Giancarlo, MD ; GRACE Investigators</creatorcontrib><description>The incidence of thrombocytopenia after hospital admission, patient and treatment characteristics, and outcomes in patients enrolled in the prospective multinational GRACE were examined. Heparin (unfractionated or low molecular weight) and glycoprotein IIb/IIIa-inhibition can be associated with immune-mediated thrombocytopenia of clinical importance. The prevalence of thrombocytopenia in patients with acute coronary syndromes (ACSs) in general and specifically related to these therapies and associated outcomes have been studied little outside of clinical trials. Patients with an ACS were stratified into 4 groups of those with heparin-induced thrombocytopenia (HIT), those with glycoprotein IIb/IIIa-associated thrombocytopenia (GAT), those with other thrombocytopenia (not diagnosed as HIT or associated with glycoprotein inhibitors), and those with no thrombocytopenia. From June 2000 to September 2007, a total of 52,647 patients with an ACS and information for platelet count were enrolled in GRACE. Of these, 152 (0.3%) were reported to develop HIT, 324 (0.6%) developed GAT, and 368 (0.7%) developed other thrombocytopenia. Patients with HIT, GAT, or other thrombocytopenia were significantly more likely to die in the hospital versus those without these diseases (adjusted odds ratio [OR] 1.94, 95% confidence interval [CI] 1.07 to 3.53; adjusted OR 3.45, 95% CI 2.35 to 5.05; and adjusted OR 2.83, 95% CI 1.97 to 4.06, respectively). They were also more likely to experience major bleeding, (re)infarction, or stroke. In conclusion, in this large multinational registry, 1.6% of patients with ACS were reported to develop thrombocytopenia, with only 0.3% being HIT. Regardless of whether patients had clinically recognized HIT, GAT, or other thrombocytopenia, all 3 groups had significantly higher rates of major bleeding, recurrent infarction, stroke, and death.</description><identifier>ISSN: 0002-9149</identifier><identifier>EISSN: 1879-1913</identifier><identifier>DOI: 10.1016/j.amjcard.2008.08.055</identifier><identifier>PMID: 19121432</identifier><identifier>CODEN: AJCDAG</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Acute Coronary Syndrome - complications ; Acute Coronary Syndrome - drug therapy ; Acute Coronary Syndrome - mortality ; Acute coronary syndromes ; Aged ; Aged, 80 and over ; Anticoagulants - adverse effects ; Biological and medical sciences ; Cardiology. Vascular system ; Cardiovascular ; Clinical outcomes ; Coronary heart disease ; Drug therapy ; Female ; Heart ; Hematologic and hematopoietic diseases ; Hemorrhage ; Hemorrhage - etiology ; Hemorrhage - mortality ; Heparin - adverse effects ; Humans ; Inhibitor drugs ; Male ; Medical sciences ; Middle Aged ; Myocarditis. Cardiomyopathies ; Platelet diseases and coagulopathies ; Platelet Glycoprotein GPIIb-IIIa Complex - antagonists & inhibitors ; Prospective Studies ; Recurrence ; Registries ; Risk ; Stroke - etiology ; Stroke - mortality ; Thrombocytopenia - chemically induced ; Thrombocytopenia - mortality</subject><ispartof>The American journal of cardiology, 2009-01, Vol.103 (2), p.175-180</ispartof><rights>Elsevier Inc.</rights><rights>2009 Elsevier Inc.</rights><rights>2009 INIST-CNRS</rights><rights>Copyright Elsevier Sequoia S.A. Jan 15, 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-6aa569de9b2dee7a70daba3b85ee974f3081b9cdf1afc68d97d9e8520a2fa2433</citedby><cites>FETCH-LOGICAL-c475t-6aa569de9b2dee7a70daba3b85ee974f3081b9cdf1afc68d97d9e8520a2fa2433</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0002914908015154$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21151486$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19121432$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gore, Joel M., MD</creatorcontrib><creatorcontrib>Spencer, Frederick A., MD</creatorcontrib><creatorcontrib>Gurfinkel, Enrique P., MD</creatorcontrib><creatorcontrib>López-Sendón, José, MD</creatorcontrib><creatorcontrib>Steg, Ph. Gabriel, MD</creatorcontrib><creatorcontrib>Granger, Christopher B., MD</creatorcontrib><creatorcontrib>FitzGerald, Gordon, PhD</creatorcontrib><creatorcontrib>Agnelli, Giancarlo, MD</creatorcontrib><creatorcontrib>GRACE Investigators</creatorcontrib><title>Thrombocytopenia in Patients With an Acute Coronary Syndrome (from the Global Registry of Acute Coronary Events [GRACE])</title><title>The American journal of cardiology</title><addtitle>Am J Cardiol</addtitle><description>The incidence of thrombocytopenia after hospital admission, patient and treatment characteristics, and outcomes in patients enrolled in the prospective multinational GRACE were examined. Heparin (unfractionated or low molecular weight) and glycoprotein IIb/IIIa-inhibition can be associated with immune-mediated thrombocytopenia of clinical importance. The prevalence of thrombocytopenia in patients with acute coronary syndromes (ACSs) in general and specifically related to these therapies and associated outcomes have been studied little outside of clinical trials. Patients with an ACS were stratified into 4 groups of those with heparin-induced thrombocytopenia (HIT), those with glycoprotein IIb/IIIa-associated thrombocytopenia (GAT), those with other thrombocytopenia (not diagnosed as HIT or associated with glycoprotein inhibitors), and those with no thrombocytopenia. From June 2000 to September 2007, a total of 52,647 patients with an ACS and information for platelet count were enrolled in GRACE. Of these, 152 (0.3%) were reported to develop HIT, 324 (0.6%) developed GAT, and 368 (0.7%) developed other thrombocytopenia. Patients with HIT, GAT, or other thrombocytopenia were significantly more likely to die in the hospital versus those without these diseases (adjusted odds ratio [OR] 1.94, 95% confidence interval [CI] 1.07 to 3.53; adjusted OR 3.45, 95% CI 2.35 to 5.05; and adjusted OR 2.83, 95% CI 1.97 to 4.06, respectively). They were also more likely to experience major bleeding, (re)infarction, or stroke. In conclusion, in this large multinational registry, 1.6% of patients with ACS were reported to develop thrombocytopenia, with only 0.3% being HIT. Regardless of whether patients had clinically recognized HIT, GAT, or other thrombocytopenia, all 3 groups had significantly higher rates of major bleeding, recurrent infarction, stroke, and death.</description><subject>Acute Coronary Syndrome - complications</subject><subject>Acute Coronary Syndrome - drug therapy</subject><subject>Acute Coronary Syndrome - mortality</subject><subject>Acute coronary syndromes</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anticoagulants - adverse effects</subject><subject>Biological and medical sciences</subject><subject>Cardiology. Vascular system</subject><subject>Cardiovascular</subject><subject>Clinical outcomes</subject><subject>Coronary heart disease</subject><subject>Drug therapy</subject><subject>Female</subject><subject>Heart</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hemorrhage</subject><subject>Hemorrhage - etiology</subject><subject>Hemorrhage - mortality</subject><subject>Heparin - adverse effects</subject><subject>Humans</subject><subject>Inhibitor drugs</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Myocarditis. Cardiomyopathies</subject><subject>Platelet diseases and coagulopathies</subject><subject>Platelet Glycoprotein GPIIb-IIIa Complex - antagonists & inhibitors</subject><subject>Prospective Studies</subject><subject>Recurrence</subject><subject>Registries</subject><subject>Risk</subject><subject>Stroke - etiology</subject><subject>Stroke - mortality</subject><subject>Thrombocytopenia - chemically induced</subject><subject>Thrombocytopenia - mortality</subject><issn>0002-9149</issn><issn>1879-1913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUlGL1DAQDqJ4e6s_QQmCoA9dk7Rpm5eTZVlX4UC5O_FBJKTJ1E3tNmuSPW7_valbTrgXYWAI833fTL4ZhF5QsqCElu-6hdp1WnmzYITUizE4f4RmtK5ERgXNH6MZIYRlghbiDJ2H0KUnpbx8is5SndEiZzN0d7P1btc4fYxuD4NV2A74i4oWhhjwNxu3WA14qQ8R8Mp5Nyh_xNfHwSQW4DdtSjhuAW9616geX8FPG2KCuPYhaX37V_L75mq5Wv94-ww9aVUf4PmU5-jrh_XN6mN2-XnzabW8zHRR8ZiVSvFSGBANMwCVqohRjcqbmgOIqmhzUtNGaNNS1eqyNqIyAmrOiGKtYkWez9Grk-7eu98HCFF27uCH1FKynOSV4MmIOeInkPYuBA-t3Hu7S1NLSuRot-zkZLcc7ZZjcJ54LyfxQ7MD8481-ZsAryeAClr1rVeDtuEex9I-aFGXCff-hINkxa0FL4NOK9BgrAcdpXH2v6NcPFDQvR1savoLjhDuP01lYJLI6_E2xtMgNUkz8CL_A2WatfM</recordid><startdate>20090115</startdate><enddate>20090115</enddate><creator>Gore, Joel M., MD</creator><creator>Spencer, Frederick A., MD</creator><creator>Gurfinkel, Enrique P., MD</creator><creator>López-Sendón, José, MD</creator><creator>Steg, Ph. Gabriel, MD</creator><creator>Granger, Christopher B., MD</creator><creator>FitzGerald, Gordon, PhD</creator><creator>Agnelli, Giancarlo, MD</creator><general>Elsevier Inc</general><general>Elsevier</general><general>Elsevier Limited</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TS</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7Z</scope><scope>NAPCQ</scope><scope>P64</scope></search><sort><creationdate>20090115</creationdate><title>Thrombocytopenia in Patients With an Acute Coronary Syndrome (from the Global Registry of Acute Coronary Events [GRACE])</title><author>Gore, Joel M., MD ; Spencer, Frederick A., MD ; Gurfinkel, Enrique P., MD ; López-Sendón, José, MD ; Steg, Ph. Gabriel, MD ; Granger, Christopher B., MD ; FitzGerald, Gordon, PhD ; Agnelli, Giancarlo, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-6aa569de9b2dee7a70daba3b85ee974f3081b9cdf1afc68d97d9e8520a2fa2433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Acute Coronary Syndrome - complications</topic><topic>Acute Coronary Syndrome - drug therapy</topic><topic>Acute Coronary Syndrome - mortality</topic><topic>Acute coronary syndromes</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anticoagulants - adverse effects</topic><topic>Biological and medical sciences</topic><topic>Cardiology. Vascular system</topic><topic>Cardiovascular</topic><topic>Clinical outcomes</topic><topic>Coronary heart disease</topic><topic>Drug therapy</topic><topic>Female</topic><topic>Heart</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Hemorrhage</topic><topic>Hemorrhage - etiology</topic><topic>Hemorrhage - mortality</topic><topic>Heparin - adverse effects</topic><topic>Humans</topic><topic>Inhibitor drugs</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Myocarditis. Cardiomyopathies</topic><topic>Platelet diseases and coagulopathies</topic><topic>Platelet Glycoprotein GPIIb-IIIa Complex - antagonists & inhibitors</topic><topic>Prospective Studies</topic><topic>Recurrence</topic><topic>Registries</topic><topic>Risk</topic><topic>Stroke - etiology</topic><topic>Stroke - mortality</topic><topic>Thrombocytopenia - chemically induced</topic><topic>Thrombocytopenia - mortality</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gore, Joel M., MD</creatorcontrib><creatorcontrib>Spencer, Frederick A., MD</creatorcontrib><creatorcontrib>Gurfinkel, Enrique P., MD</creatorcontrib><creatorcontrib>López-Sendón, José, MD</creatorcontrib><creatorcontrib>Steg, Ph. Gabriel, MD</creatorcontrib><creatorcontrib>Granger, Christopher B., MD</creatorcontrib><creatorcontrib>FitzGerald, Gordon, PhD</creatorcontrib><creatorcontrib>Agnelli, Giancarlo, MD</creatorcontrib><creatorcontrib>GRACE Investigators</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Physical Education Index</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biochemistry Abstracts 1</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>The American journal of cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gore, Joel M., MD</au><au>Spencer, Frederick A., MD</au><au>Gurfinkel, Enrique P., MD</au><au>López-Sendón, José, MD</au><au>Steg, Ph. Gabriel, MD</au><au>Granger, Christopher B., MD</au><au>FitzGerald, Gordon, PhD</au><au>Agnelli, Giancarlo, MD</au><aucorp>GRACE Investigators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thrombocytopenia in Patients With an Acute Coronary Syndrome (from the Global Registry of Acute Coronary Events [GRACE])</atitle><jtitle>The American journal of cardiology</jtitle><addtitle>Am J Cardiol</addtitle><date>2009-01-15</date><risdate>2009</risdate><volume>103</volume><issue>2</issue><spage>175</spage><epage>180</epage><pages>175-180</pages><issn>0002-9149</issn><eissn>1879-1913</eissn><coden>AJCDAG</coden><abstract>The incidence of thrombocytopenia after hospital admission, patient and treatment characteristics, and outcomes in patients enrolled in the prospective multinational GRACE were examined. Heparin (unfractionated or low molecular weight) and glycoprotein IIb/IIIa-inhibition can be associated with immune-mediated thrombocytopenia of clinical importance. The prevalence of thrombocytopenia in patients with acute coronary syndromes (ACSs) in general and specifically related to these therapies and associated outcomes have been studied little outside of clinical trials. Patients with an ACS were stratified into 4 groups of those with heparin-induced thrombocytopenia (HIT), those with glycoprotein IIb/IIIa-associated thrombocytopenia (GAT), those with other thrombocytopenia (not diagnosed as HIT or associated with glycoprotein inhibitors), and those with no thrombocytopenia. From June 2000 to September 2007, a total of 52,647 patients with an ACS and information for platelet count were enrolled in GRACE. Of these, 152 (0.3%) were reported to develop HIT, 324 (0.6%) developed GAT, and 368 (0.7%) developed other thrombocytopenia. Patients with HIT, GAT, or other thrombocytopenia were significantly more likely to die in the hospital versus those without these diseases (adjusted odds ratio [OR] 1.94, 95% confidence interval [CI] 1.07 to 3.53; adjusted OR 3.45, 95% CI 2.35 to 5.05; and adjusted OR 2.83, 95% CI 1.97 to 4.06, respectively). They were also more likely to experience major bleeding, (re)infarction, or stroke. In conclusion, in this large multinational registry, 1.6% of patients with ACS were reported to develop thrombocytopenia, with only 0.3% being HIT. Regardless of whether patients had clinically recognized HIT, GAT, or other thrombocytopenia, all 3 groups had significantly higher rates of major bleeding, recurrent infarction, stroke, and death.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>19121432</pmid><doi>10.1016/j.amjcard.2008.08.055</doi><tpages>6</tpages></addata></record> |
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subjects | Acute Coronary Syndrome - complications Acute Coronary Syndrome - drug therapy Acute Coronary Syndrome - mortality Acute coronary syndromes Aged Aged, 80 and over Anticoagulants - adverse effects Biological and medical sciences Cardiology. Vascular system Cardiovascular Clinical outcomes Coronary heart disease Drug therapy Female Heart Hematologic and hematopoietic diseases Hemorrhage Hemorrhage - etiology Hemorrhage - mortality Heparin - adverse effects Humans Inhibitor drugs Male Medical sciences Middle Aged Myocarditis. Cardiomyopathies Platelet diseases and coagulopathies Platelet Glycoprotein GPIIb-IIIa Complex - antagonists & inhibitors Prospective Studies Recurrence Registries Risk Stroke - etiology Stroke - mortality Thrombocytopenia - chemically induced Thrombocytopenia - mortality |
title | Thrombocytopenia in Patients With an Acute Coronary Syndrome (from the Global Registry of Acute Coronary Events [GRACE]) |
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