Preliminary experience with intravenous P2Y12 platelet receptor inhibition as an adjunct to reduced-dose alteplase during acute myocardial infarction:: Results of the Safety, Tolerability and Effect on Patency in Acute Myocardial Infarction (STEP-AMI) angiographic trial

被引:51
作者
Greenbaum, Adam B.
Ohman, E. Magnus
Gibson, C. Michael
Borzak, Steven
Stebbins, Amanda L.
Lu, Mei
Le May, Michel R.
Stankowski, Jill E.
Emanuelsson, Hakan
Weaver, W. Douglas
机构
[1] Henry Ford Hosp, Cardiac Catheterizat Lab, Detroit, MI 48202 USA
[2] Henry Ford Heart & Vasc Inst, Detroit, MI USA
[3] Duke Clin Res Inst, Durham, NC USA
[4] Beth Israel Deaconess Med Ctr, Boston, MA USA
[5] Florida Cardiovasc Res, Atlantis, FL USA
[6] Univ Ottawa, Inst Heart, Ottawa, ON, Canada
[7] AstraZeneca R&D Charnwood, Loughborough, Leics, England
关键词
D O I
10.1016/j.ahj.2007.06.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Fibrinolytic therapy for acute myocardial infarction (AMI) results in normal flow in only about half of patients. Adjunctive treatment with potent antiplatelet and antithrombin agents increases arterial potency but is associated with excessive bleeding. Congrelor (formerly AR-C69931 MX) is a rapidly acting, specific antagonist of platelet aggregation via binding to the adenosine diphosphate P2Y(12) receptor subtype. The aim of this study was to assess the safety and coronary artery patency of congrelor as an adjunct to alteplase (tissue plasminogen activator [t-PA]). Methods Patients with AMI received aspirin, heparin, and an intravenous infusion of either cangrelor alone, full-dose t-PA alone, or I of 3 doses of cangrelor along with half-dose t-PA. The primary end point was Thrombolysis in Myocardial Infarction (TIMI) grade 3 flow at 60 minutes. Secondary end points included TIMI frame count, TIMI myocardial perfusion grade, extent of ST-segment resolution, composite clinical events, and bleeding. Results Ninety-two of planned 180 patients were enrolled. The combination of cangrelor and half-dose t-PA resulted in similar 60-minute patency as full-dose t-PA alone (55% vs 50%, P = not significant) and greater potency than with cangrelor alone (55% vs 18%, P <.05). The percentage of patients achieving >70% ST-segment resolution at 60 minutes tended to be greater with combination therapy than with either cangrelor or t-PA alone (28% vs 13%, P =.13 and 28% vs 14%, P =.30, respectively). Bleeding and adverse clinical events were comparable among the groups. Conclusion This first experience with the intravenous P2Y(12) receptor inhibitor, cangrelor, suggests the potential of this compound as an adjunct to fibrinolysis during treatment of AMI.
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页码:702 / 709
页数:8
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