Effect of Platelet Inhibition with Cangrelor during PCI on Ischemic Events

被引:654
作者
Bhatt, Deepak L. [1 ,2 ]
Stone, Gregg W. [3 ,4 ]
Mahaffey, Kenneth W. [5 ]
Gibson, C. Michael [6 ]
Steg, P. Gabriel [7 ,8 ]
Hamm, Christian W. [9 ]
Price, Matthew J. [10 ,11 ]
Leonardi, Sergio [12 ]
Gallup, Dianne [5 ]
Bramucci, Ezio [12 ]
Radke, Peter W. [13 ]
Widimsky, Petr [14 ]
Tousek, Frantisek [15 ]
Tauth, Jeffrey [16 ]
Spriggs, Douglas [17 ]
McLaurin, Brent T. [18 ]
Angiolillo, Dominick J. [19 ]
Genereux, Philippe
Liu, Tiepu [20 ]
Prats, Jayne [20 ]
Todd, Meredith [20 ]
Skerjanec, Simona [20 ]
White, Harvey D. [21 ]
Harrington, Robert A. [22 ]
机构
[1] Brigham & Womens Hosp, VA Boston Healthcare Syst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Columbia Univ, Med Ctr, New York, NY USA
[4] Cardiovasc Res Fdn, New York, NY USA
[5] Duke Clin Res Inst, Durham, NC USA
[6] Beth Israel Deaconess Med Ctr, Div Cardiol, Boston, MA 02215 USA
[7] Univ Paris Diderot, INSERM, U698, Paris, France
[8] Hop Bichat Claude Bernard, AP HP, F-75877 Paris, France
[9] Kerckhoff Heart & Thorax Ctr, Bad Nauheim, Germany
[10] Scripps Clin, La Jolla, CA 92037 USA
[11] Scripps Translat Sci Inst, La Jolla, CA USA
[12] Fdn IRCCS Policlin S Matteo, Pavia, Italy
[13] Univ Klinikum Schleswig Holstein, D-23538 Lubeck, Germany
[14] Fak Nemocnice Kralovske Vinohrady, Prague, Czech Republic
[15] Nemocnice Ceske Budejovice, Ceske Budejovice, Czech Republic
[16] Natl Pk Med Ctr, Hot Springs, AR USA
[17] Clearwater Cardiovasc & Intervent Consultants, Clearwater, FL USA
[18] AnMed Hlth, Anderson, SC USA
[19] Univ Florida, Coll Med, Jacksonville, FL USA
[20] Med Co, Parsippany, NJ USA
[21] Green Lane Cardiovasc Serv, Auckland, New Zealand
[22] Stanford Univ, Sch Med, Stanford, CA 94305 USA
关键词
PERCUTANEOUS CORONARY INTERVENTION; ACHIEVE OPTIMAL MANAGEMENT; ANTIPLATELET THERAPY; CLOPIDOGREL PRETREATMENT; CARDIOVASCULAR EVENTS; STANDARD THERAPY; PRASUGREL; METAANALYSIS; TICAGRELOR; STRATEGIES;
D O I
10.1056/NEJMoa1300815
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND The intensity of antiplatelet therapy during percutaneous coronary intervention (PCI) is an important determinant of PCI-related ischemic complications. Cangrelor is a potent intravenous adenosine diphosphate (ADP)-receptor antagonist that acts rapidly and has quickly reversible effects. METHODS In a double-blind, placebo-controlled trial, we randomly assigned 11,145 patients who were undergoing either urgent or elective PCI and were receiving guideline-recommended therapy to receive a bolus and infusion of cangrelor or to receive a loading dose of 600 mg or 300 mg of clopidogrel. The primary efficacy end point was a composite of death, myocardial infarction, ischemia-driven revascularization, or stent thrombosis at 48 hours after randomization; the key secondary end point was stent thrombosis at 48 hours. The primary safety end point was severe bleeding at 48 hours. RESULTS The rate of the primary efficacy end point was 4.7% in the cangrelor group and 5.9% in the clopidogrel group (adjusted odds ratio with cangrelor, 0.78; 95% confidence interval [CI], 0.66 to 0.93; P = 0.005). The rate of the primary safety end point was 0.16% in the cangrelor group and 0.11% in the clopidogrel group (odds ratio, 1.50; 95% CI, 0.53 to 4.22; P = 0.44). Stent thrombosis developed in 0.8% of the patients in the cangrelor group and in 1.4% in the clopidogrel group (odds ratio, 0.62; 95% CI, 0.43 to 0.90; P = 0.01). The rates of adverse events related to the study treatment were low in both groups, though transient dyspnea occurred significantly more frequently with cangrelor than with clopidogrel (1.2% vs. 0.3%). The benefit from cangrelor with respect to the primary end point was consistent across multiple prespecified subgroups. CONCLUSIONS Cangrelor significantly reduced the rate of ischemic events, including stent thrombosis, during PCI, with no significant increase in severe bleeding. (Funded by the Medicines Company; CHAMPION PHOENIX ClinicalTrials.gov number, NCT01156571.)
引用
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页码:1303 / 1313
页数:11
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