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Impact of Gender and Antithrombin Strategy on Early and Late Clinical Outcomes in Patients With Non–ST-Elevation Acute Coronary Syndromes (from the ACUITY Trial)
Women with non–ST-elevation acute coronary syndrome are at increased risk for ischemic and bleeding complications compared with men. We examined the impact of gender and antithrombotic therapy for non–ST-elevation acute coronary syndrome on outcomes in patients in the ACUITY trial. Patients were ran...
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Published in: | The American journal of cardiology 2009-05, Vol.103 (9), p.1196-1203 |
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container_title | The American journal of cardiology |
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creator | Lansky, Alexandra J., MD Mehran, Roxana, MD Cristea, Ecatarina, MD Parise, Helen, ScD Feit, Frederick, MD Ohman, E. Magnus, MD White, Harvey D., MD Alexander, Karen P., MD Bertrand, Michel E., MD Desmet, Walter, MD Hamon, Martial, MD Stone, Gregg W., MD |
description | Women with non–ST-elevation acute coronary syndrome are at increased risk for ischemic and bleeding complications compared with men. We examined the impact of gender and antithrombotic therapy for non–ST-elevation acute coronary syndrome on outcomes in patients in the ACUITY trial. Patients were randomized to heparin (unfractionated or enoxaparin) plus a glycoprotein IIb/IIIa inhibitor (GPI), bivalirudin plus a GPI, or bivalirudin alone. We compared major bleeding unconnected to coronary artery bypass grafting, composite ischemia (death, myocardial infarction, or revascularization), and net clinical outcome (composite ischemia or bleeding) in (1) men versus women overall and undergoing percutaneous coronary intervention (PCI) and (2) women overall and undergoing PCI by antithrombotic strategy. Of 13,819 patients enrolled, 4,157 were women (30.1%). Women had similar 30-day composite ischemia (7% vs 8%, p = 0.07) but greater 30-day rates of major bleeding (8% vs 3% p |
doi_str_mv | 10.1016/j.amjcard.2009.01.030 |
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Magnus, MD ; White, Harvey D., MD ; Alexander, Karen P., MD ; Bertrand, Michel E., MD ; Desmet, Walter, MD ; Hamon, Martial, MD ; Stone, Gregg W., MD</creator><creatorcontrib>Lansky, Alexandra J., MD ; Mehran, Roxana, MD ; Cristea, Ecatarina, MD ; Parise, Helen, ScD ; Feit, Frederick, MD ; Ohman, E. Magnus, MD ; White, Harvey D., MD ; Alexander, Karen P., MD ; Bertrand, Michel E., MD ; Desmet, Walter, MD ; Hamon, Martial, MD ; Stone, Gregg W., MD</creatorcontrib><description>Women with non–ST-elevation acute coronary syndrome are at increased risk for ischemic and bleeding complications compared with men. We examined the impact of gender and antithrombotic therapy for non–ST-elevation acute coronary syndrome on outcomes in patients in the ACUITY trial. Patients were randomized to heparin (unfractionated or enoxaparin) plus a glycoprotein IIb/IIIa inhibitor (GPI), bivalirudin plus a GPI, or bivalirudin alone. We compared major bleeding unconnected to coronary artery bypass grafting, composite ischemia (death, myocardial infarction, or revascularization), and net clinical outcome (composite ischemia or bleeding) in (1) men versus women overall and undergoing percutaneous coronary intervention (PCI) and (2) women overall and undergoing PCI by antithrombotic strategy. Of 13,819 patients enrolled, 4,157 were women (30.1%). Women had similar 30-day composite ischemia (7% vs 8%, p = 0.07) but greater 30-day rates of major bleeding (8% vs 3% p <0.0001) and net clinical outcomes (13% vs 10% p <0.0001) than men. One-year composite ischemia and mortality was similar. In women, bivalirudin compared with heparin + GPI resulted in less 30-day major bleeding (5% vs 10%, p <0.0001) but similar composite ischemia (7% vs 6%, p = 0.15). No differences were observed in rates of 1-year composite ischemia or mortality in women who received bivalirudin versus heparin + GPI. Results were similar in women undergoing PCI. In conclusion, women had similar 30-day mortality and composite ischemia but higher net clinical adverse events due to more bleeding complications than men; 1-year mortality was similar for men and women. In women, bivalirudin monotherapy compared with a GPI-based strategy resulted in significantly decreased bleeding but similar rates of 1-year composite ischemia and mortality.</description><identifier>ISSN: 0002-9149</identifier><identifier>EISSN: 1879-1913</identifier><identifier>DOI: 10.1016/j.amjcard.2009.01.030</identifier><identifier>PMID: 19406258</identifier><identifier>CODEN: AJCDAG</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Acute Coronary Syndrome - diagnosis ; Acute Coronary Syndrome - drug therapy ; Acute Coronary Syndrome - mortality ; Acute Coronary Syndrome - therapy ; Acute coronary syndromes ; Adult ; Age Factors ; Aged ; Aged, 80 and over ; Angioplasty, Balloon, Coronary - methods ; Angioplasty, Balloon, Coronary - mortality ; Anticoagulants - therapeutic use ; Antithrombins - therapeutic use ; Biological and medical sciences ; Cardiology ; Cardiology. Vascular system ; Cardiovascular ; Cause of Death ; Clinical outcomes ; Coronary heart disease ; Dose-Response Relationship, Drug ; Drug Administration Schedule ; Drug Therapy, Combination ; Electrocardiography ; Enoxaparin - therapeutic use ; Female ; Follow-Up Studies ; Gender ; Heart ; Heparin - therapeutic use ; Hirudins ; Humans ; Male ; Medical research ; Medical sciences ; Middle Aged ; Myocarditis. Cardiomyopathies ; Patients ; Peptide Fragments - therapeutic use ; Platelet Glycoprotein GPIIb-IIIa Complex - therapeutic use ; Probability ; Proportional Hazards Models ; Recombinant Proteins - therapeutic use ; Reference Values ; Risk Assessment ; Severity of Illness Index ; Sex Factors ; Survival Analysis ; Time Factors ; Treatment Outcome</subject><ispartof>The American journal of cardiology, 2009-05, Vol.103 (9), p.1196-1203</ispartof><rights>Elsevier Inc.</rights><rights>2009 Elsevier Inc.</rights><rights>2009 INIST-CNRS</rights><rights>Copyright Elsevier Sequoia S.A. May 1, 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-922ec7ad9d262affaa8620e8b48072ca9724bb12e122286ba3e59d7aa85af6913</citedby><cites>FETCH-LOGICAL-c475t-922ec7ad9d262affaa8620e8b48072ca9724bb12e122286ba3e59d7aa85af6913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,786,790,27957,27958</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21568331$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19406258$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lansky, Alexandra J., MD</creatorcontrib><creatorcontrib>Mehran, Roxana, MD</creatorcontrib><creatorcontrib>Cristea, Ecatarina, MD</creatorcontrib><creatorcontrib>Parise, Helen, ScD</creatorcontrib><creatorcontrib>Feit, Frederick, MD</creatorcontrib><creatorcontrib>Ohman, E. Magnus, MD</creatorcontrib><creatorcontrib>White, Harvey D., MD</creatorcontrib><creatorcontrib>Alexander, Karen P., MD</creatorcontrib><creatorcontrib>Bertrand, Michel E., MD</creatorcontrib><creatorcontrib>Desmet, Walter, MD</creatorcontrib><creatorcontrib>Hamon, Martial, MD</creatorcontrib><creatorcontrib>Stone, Gregg W., MD</creatorcontrib><title>Impact of Gender and Antithrombin Strategy on Early and Late Clinical Outcomes in Patients With Non–ST-Elevation Acute Coronary Syndromes (from the ACUITY Trial)</title><title>The American journal of cardiology</title><addtitle>Am J Cardiol</addtitle><description>Women with non–ST-elevation acute coronary syndrome are at increased risk for ischemic and bleeding complications compared with men. We examined the impact of gender and antithrombotic therapy for non–ST-elevation acute coronary syndrome on outcomes in patients in the ACUITY trial. Patients were randomized to heparin (unfractionated or enoxaparin) plus a glycoprotein IIb/IIIa inhibitor (GPI), bivalirudin plus a GPI, or bivalirudin alone. We compared major bleeding unconnected to coronary artery bypass grafting, composite ischemia (death, myocardial infarction, or revascularization), and net clinical outcome (composite ischemia or bleeding) in (1) men versus women overall and undergoing percutaneous coronary intervention (PCI) and (2) women overall and undergoing PCI by antithrombotic strategy. Of 13,819 patients enrolled, 4,157 were women (30.1%). Women had similar 30-day composite ischemia (7% vs 8%, p = 0.07) but greater 30-day rates of major bleeding (8% vs 3% p <0.0001) and net clinical outcomes (13% vs 10% p <0.0001) than men. One-year composite ischemia and mortality was similar. In women, bivalirudin compared with heparin + GPI resulted in less 30-day major bleeding (5% vs 10%, p <0.0001) but similar composite ischemia (7% vs 6%, p = 0.15). No differences were observed in rates of 1-year composite ischemia or mortality in women who received bivalirudin versus heparin + GPI. Results were similar in women undergoing PCI. In conclusion, women had similar 30-day mortality and composite ischemia but higher net clinical adverse events due to more bleeding complications than men; 1-year mortality was similar for men and women. In women, bivalirudin monotherapy compared with a GPI-based strategy resulted in significantly decreased bleeding but similar rates of 1-year composite ischemia and mortality.</description><subject>Acute Coronary Syndrome - diagnosis</subject><subject>Acute Coronary Syndrome - drug therapy</subject><subject>Acute Coronary Syndrome - mortality</subject><subject>Acute Coronary Syndrome - therapy</subject><subject>Acute coronary syndromes</subject><subject>Adult</subject><subject>Age Factors</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Angioplasty, Balloon, Coronary - methods</subject><subject>Angioplasty, Balloon, Coronary - mortality</subject><subject>Anticoagulants - therapeutic use</subject><subject>Antithrombins - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Cardiology</subject><subject>Cardiology. Vascular system</subject><subject>Cardiovascular</subject><subject>Cause of Death</subject><subject>Clinical outcomes</subject><subject>Coronary heart disease</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Administration Schedule</subject><subject>Drug Therapy, Combination</subject><subject>Electrocardiography</subject><subject>Enoxaparin - therapeutic use</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gender</subject><subject>Heart</subject><subject>Heparin - therapeutic use</subject><subject>Hirudins</subject><subject>Humans</subject><subject>Male</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Myocarditis. Cardiomyopathies</subject><subject>Patients</subject><subject>Peptide Fragments - therapeutic use</subject><subject>Platelet Glycoprotein GPIIb-IIIa Complex - therapeutic use</subject><subject>Probability</subject><subject>Proportional Hazards Models</subject><subject>Recombinant Proteins - therapeutic use</subject><subject>Reference Values</subject><subject>Risk Assessment</subject><subject>Severity of Illness Index</subject><subject>Sex Factors</subject><subject>Survival Analysis</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><issn>0002-9149</issn><issn>1879-1913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkt9qFDEUxgdR7Lb6CEoQFL2YNcn8zU1lWda6sFhht4hXIZM5Y7POJGuSKcxd38FH8M18EjPdoUJvvApJft_HOec7UfSC4DnBJH-_n4tuL4Wt5xRjNsdkjhP8KJqRsmAxYSR5HM0wxjRmJGUn0alz-3AlJMufRieEpTinWTmLfq-7g5AemQZdgK7BIqFrtNBe-WtrukpptPVWePg-IKPRSth2uEM24Q0tW6WVFC267L00HTgU-C_CK9Deoa_BA302-s_tr-0uXrVwE36CyUL2o9ZYo4Ud0HbQtb0Tv23Cifw1oMXyar37hnZWifbds-hJI1oHz6fzLLr6uNotP8Wby4v1crGJZVpkPmaUgixEzWqaU9E0QpQ5xVBWaYkLKgUraFpVhAKhlJZ5JRLIWF0ELBNNHiZ2Fr05-h6s-dmD87xTTkLbCg2mdzwvKE7zIgngqwfg3vRWh9o4TXBSsITmAcqOkLTGOQsNP1jVhYY5wXyMkO_5FCEfI-SY8BBh0L2czPuqg_qfasosAK8nQLgw-8YKLZW752iIuEySsZ0PRw7CzG4UWO5kCEZCrSxIz2uj_lvK-QMHOQX-AwZw900T7ijHfDvu27humIVNG0v9C4Tz0jc</recordid><startdate>20090501</startdate><enddate>20090501</enddate><creator>Lansky, Alexandra J., MD</creator><creator>Mehran, Roxana, MD</creator><creator>Cristea, Ecatarina, MD</creator><creator>Parise, Helen, ScD</creator><creator>Feit, Frederick, MD</creator><creator>Ohman, E. Magnus, MD</creator><creator>White, Harvey D., MD</creator><creator>Alexander, Karen P., MD</creator><creator>Bertrand, Michel E., MD</creator><creator>Desmet, Walter, MD</creator><creator>Hamon, Martial, MD</creator><creator>Stone, Gregg W., 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><scope>7X8</scope></search><sort><creationdate>20090501</creationdate><title>Impact of Gender and Antithrombin Strategy on Early and Late Clinical Outcomes in Patients With Non–ST-Elevation Acute Coronary Syndromes (from the ACUITY Trial)</title><author>Lansky, Alexandra J., MD ; Mehran, Roxana, MD ; Cristea, Ecatarina, MD ; Parise, Helen, ScD ; Feit, Frederick, MD ; Ohman, E. 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Magnus, MD</creatorcontrib><creatorcontrib>White, Harvey D., MD</creatorcontrib><creatorcontrib>Alexander, Karen P., MD</creatorcontrib><creatorcontrib>Bertrand, Michel E., MD</creatorcontrib><creatorcontrib>Desmet, Walter, MD</creatorcontrib><creatorcontrib>Hamon, Martial, MD</creatorcontrib><creatorcontrib>Stone, Gregg W., MD</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><collection>MEDLINE - Academic</collection><jtitle>The American journal of cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lansky, Alexandra J., MD</au><au>Mehran, Roxana, MD</au><au>Cristea, Ecatarina, MD</au><au>Parise, Helen, ScD</au><au>Feit, Frederick, MD</au><au>Ohman, E. Magnus, MD</au><au>White, Harvey D., MD</au><au>Alexander, Karen P., MD</au><au>Bertrand, Michel E., MD</au><au>Desmet, Walter, MD</au><au>Hamon, Martial, MD</au><au>Stone, Gregg W., MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of Gender and Antithrombin Strategy on Early and Late Clinical Outcomes in Patients With Non–ST-Elevation Acute Coronary Syndromes (from the ACUITY Trial)</atitle><jtitle>The American journal of cardiology</jtitle><addtitle>Am J Cardiol</addtitle><date>2009-05-01</date><risdate>2009</risdate><volume>103</volume><issue>9</issue><spage>1196</spage><epage>1203</epage><pages>1196-1203</pages><issn>0002-9149</issn><eissn>1879-1913</eissn><coden>AJCDAG</coden><notes>ObjectType-Article-2</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-News-1</notes><notes>ObjectType-Feature-3</notes><notes>content type line 23</notes><abstract>Women with non–ST-elevation acute coronary syndrome are at increased risk for ischemic and bleeding complications compared with men. We examined the impact of gender and antithrombotic therapy for non–ST-elevation acute coronary syndrome on outcomes in patients in the ACUITY trial. Patients were randomized to heparin (unfractionated or enoxaparin) plus a glycoprotein IIb/IIIa inhibitor (GPI), bivalirudin plus a GPI, or bivalirudin alone. We compared major bleeding unconnected to coronary artery bypass grafting, composite ischemia (death, myocardial infarction, or revascularization), and net clinical outcome (composite ischemia or bleeding) in (1) men versus women overall and undergoing percutaneous coronary intervention (PCI) and (2) women overall and undergoing PCI by antithrombotic strategy. Of 13,819 patients enrolled, 4,157 were women (30.1%). Women had similar 30-day composite ischemia (7% vs 8%, p = 0.07) but greater 30-day rates of major bleeding (8% vs 3% p <0.0001) and net clinical outcomes (13% vs 10% p <0.0001) than men. One-year composite ischemia and mortality was similar. In women, bivalirudin compared with heparin + GPI resulted in less 30-day major bleeding (5% vs 10%, p <0.0001) but similar composite ischemia (7% vs 6%, p = 0.15). No differences were observed in rates of 1-year composite ischemia or mortality in women who received bivalirudin versus heparin + GPI. Results were similar in women undergoing PCI. In conclusion, women had similar 30-day mortality and composite ischemia but higher net clinical adverse events due to more bleeding complications than men; 1-year mortality was similar for men and women. In women, bivalirudin monotherapy compared with a GPI-based strategy resulted in significantly decreased bleeding but similar rates of 1-year composite ischemia and mortality.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>19406258</pmid><doi>10.1016/j.amjcard.2009.01.030</doi><tpages>8</tpages></addata></record> |
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subjects | Acute Coronary Syndrome - diagnosis Acute Coronary Syndrome - drug therapy Acute Coronary Syndrome - mortality Acute Coronary Syndrome - therapy Acute coronary syndromes Adult Age Factors Aged Aged, 80 and over Angioplasty, Balloon, Coronary - methods Angioplasty, Balloon, Coronary - mortality Anticoagulants - therapeutic use Antithrombins - therapeutic use Biological and medical sciences Cardiology Cardiology. Vascular system Cardiovascular Cause of Death Clinical outcomes Coronary heart disease Dose-Response Relationship, Drug Drug Administration Schedule Drug Therapy, Combination Electrocardiography Enoxaparin - therapeutic use Female Follow-Up Studies Gender Heart Heparin - therapeutic use Hirudins Humans Male Medical research Medical sciences Middle Aged Myocarditis. Cardiomyopathies Patients Peptide Fragments - therapeutic use Platelet Glycoprotein GPIIb-IIIa Complex - therapeutic use Probability Proportional Hazards Models Recombinant Proteins - therapeutic use Reference Values Risk Assessment Severity of Illness Index Sex Factors Survival Analysis Time Factors Treatment Outcome |
title | Impact of Gender and Antithrombin Strategy on Early and Late Clinical Outcomes in Patients With Non–ST-Elevation Acute Coronary Syndromes (from the ACUITY Trial) |
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