Prognostic Modeling of Individual Patient Risk and Mortality Impact of Ischemic and Hemorrhagic Complications Assessment From the Acute Catheterization and Urgent Intervention Triage Strategy Trial

被引:99
作者
Pocock, Stuart J. [1 ]
Mehran, Roxana [2 ,3 ]
Clayton, Tim C.
Nikolsky, Eugenia [2 ,3 ]
Parise, Helen [2 ,3 ]
Fahy, Martin [2 ,3 ]
Lansky, Alexandra J. [2 ,3 ]
Bertrand, Michel E. [4 ]
Lincoff, A. Michael [5 ]
Moses, Jeffrey W. [2 ,3 ]
Ohman, E. Magnus [6 ]
White, Harvey D. [7 ]
Stone, Gregg W. [2 ,3 ]
机构
[1] London Sch Hyg & Trop Med, Med Stat Unit, London WC1E 7HT, England
[2] Cardiovasc Res Fdn, New York, NY USA
[3] Columbia Univ, Med Ctr, New York, NY USA
[4] Hop Cardiol, F-59037 Lille, France
[5] Cleveland Clin, Cleveland, OH 44106 USA
[6] Duke Univ, Med Ctr, Durham, NC USA
[7] Auckland City Hosp, Auckland, New Zealand
关键词
acute coronary syndrome; bleeding; modeling; myocardial infarction; risk score; ACUTE CORONARY SYNDROMES; ACUTE MYOCARDIAL-INFARCTION; ACUITY TRIAL; CLINICAL-OUTCOMES; BIVALIRUDIN; CLOPIDOGREL; ENOXAPARIN; MANAGEMENT; EVENTS; BLOOD;
D O I
10.1161/CIRCULATIONAHA.109.878017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Both ischemic and hemorrhagic complications increase mortality rate in acute coronary syndromes. Their frequency and relative importance vary according to individual patient risk profiles. We sought to develop prognostic models for the risk of myocardial infarction (MI) and major bleeding to assess their impact on risk of death and to examine the manner in which alternative antithrombotic regimens affect these risks in individual patients. Methods and Results-The Acute Catheterization and Urgent Intervention Triage Strategy (ACUITY) trial randomized 13 819 patients with acute coronary syndrome to heparin plus a glycoprotein IIb/IIIa inhibitor, bivalirudin plus a glycoprotein IIb/IIIa inhibitor, or bivalirudin alone. By logistic regression, there were 5 independent predictors of MI within 30 days (n=705; 5.1%) and 8 independent predictors of major bleeding (n=645; 4.7%), only 2 of which were common to both event types. In a covariate-adjusted, time-updated Cox regression model, both MI and major bleeding significantly affected subsequent mortality rate (hazard ratios, 2.7 and 2.9, respectively; both P<0.001). Treatment with bivalirudin versus heparin plus a glycoprotein IIb/IIIa inhibitor was associated with a nonsignificant 8% increase in MI and a highly significant 50% decrease in major bleeding. Given the individual patient risk profiles and the fact that bivalirudin prevented approximate to 6 major bleeds for each MI that might occur from its use, the estimated reduction in bleeding was greater than the estimated increase in MI by bivalirudin alone rather than heparin plus a glycoprotein IIb/IIIa inhibitor for nearly all patients. Conclusions-Consideration of the individual patient risk profile for MI and major bleeding and the relative treatment effects of alternative pharmacotherapies permits personalized decision making to optimize therapy of patients with acute coronary syndrome.
引用
收藏
页码:43 / 51
页数:9
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