Reduction of major adverse cardiac events with intracoronary compared with intravenous bolus application of abciximab in patients with acute myocardial infarction or unstable angina undergoing coronary angioplasty

被引:112
作者
Wöhrle, J [1 ]
Grebe, OC [1 ]
Nusser, T [1 ]
Al-Khayer, E [1 ]
Schaible, S [1 ]
Kochs, M [1 ]
Hombach, V [1 ]
Höher, M [1 ]
机构
[1] Univ Ulm, D-89081 Ulm, Germany
关键词
angioplasty; stents; glycoproteins; myocardial infarction;
D O I
10.1161/01.CIR.0000066852.98038.D1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-In patients with acute myocardial infarction or unstable angina undergoing coronary angioplasty, abciximab reduces major adverse cardiac events (MACE). Clinical trials have studied intravenous administration only. Intracoronary bolus application of abciximab causes very high local drug concentrations and may be more effective. We studied whether intracoronary bolus administration of abciximab is associated with a reduced MACE rate compared with the standard intravenous bolus application. Methods and Results-We stratified 403 consecutive patients with acute myocardial infarction or unstable angina undergoing coronary angioplasty according to the type of application of abciximab. A 20-mg bolus of abciximab was given intravenously in 109 patients and intracoronarily in 294 patients. There were no differences between the groups with regard to diabetes mellitus, cardiogenic shock, successful intervention, or preprocedural and postprocedural TIMI flow. At 30 days, the incidence of MACE (death, myocardial infarction, urgent revascularization) was significantly lower in the patients with intracoronary compared with intravenous administration of abciximab (10.2% versus 20.2%; P<0.008), which was independent from stenting in multivariate analysis. The effect was most pronounced in patients with preprocedural TIMI 0/1 flow (MACE: intracoronary 11.8% versus intravenous 27.5%, P<0.002; n=273). Conclusions-In patients with acute myocardial infarction or unstable angina undergoing emergency coronary angioplasty, intracoronary bolus application of abciximab is associated with a reduction of MACE compared with the standard intravenous bolus application of abciximab. Prospective, randomized trials are warranted to further assess intracoronary application of abciximab.
引用
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页码:1840 / 1843
页数:4
相关论文
共 10 条
[1]  
Bailey SR, 1997, CATHETER CARDIO DIAG, V42, P181, DOI 10.1002/(SICI)1097-0304(199710)42:2<181::AID-CCD18>3.0.CO
[2]  
2-R
[3]   Reduced thrombus burden with abciximab delivered locally before percutaneous intervention saphenous vein grafts [J].
Barsness, GW ;
Buller, C ;
Ohman, M ;
Schechter, E ;
Pucillo, A ;
Taylor, MA ;
Miller, MJ ;
Reiner, JS ;
Churchill, D ;
Chandler, AB ;
Gonzalez, M ;
Smith, J ;
Tommaso, C ;
Berdan, LG ;
Wildermann, NM ;
Hasdai, D ;
Holmes, DR .
AMERICAN HEART JOURNAL, 2000, 139 (05) :824-829
[4]   Platelet glycoprotein IIb/IIIa inhibition with coronary stenting for acute myocardial infarction. [J].
Montalescot, G ;
Barragan, P ;
Wittenberg, O ;
Ecollan, P ;
Elhadad, S ;
Villain, P ;
Boulenc, JM ;
Morice, MC ;
Maillard, L ;
Pansiéri, M ;
Choussat, R ;
Pinton, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (25) :1895-1903
[5]   Impact of different platelet glycoprotein IIb/IIIa receptor inhibitors among diabetic patients undergoing percutaneous coronary intervention - Do tirofiban and ReoPro give similar efficacy outcomes trial (TARGET) 1-year follow-up [J].
Roffi, M ;
Moliterno, DJ ;
Meier, B ;
Powers, ER ;
Grines, CL ;
DiBattiste, PM ;
Herrmann, HC ;
Bertrand, M ;
Harris, KE ;
Demopoulos, LA ;
Topol, EJ .
CIRCULATION, 2002, 105 (23) :2730-2736
[6]   7E3 monoclonal antibody directed against the platelet glycoprotein IIb/IIIa cross-reacts with the leukocyte integrin Mac-1 and blocks adhesion to fibrinogen and ICAM-1 [J].
Simon, DI ;
Xu, H ;
Ortlepp, S ;
Rogers, C ;
Rao, NK .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (03) :528-535
[7]  
Simoons ML, 2001, LANCET, V357, P1915
[8]   Comparison of angioplasty with stenting, with or without abciximab, in acute myocardial infarction. [J].
Stone, GW ;
Grines, CL ;
Cox, DA ;
Garcia, E ;
Tcheng, JE ;
Griffin, JJ ;
Guagliumi, G ;
Stuckey, T ;
Turco, M ;
Carroll, JD ;
Rutherford, BD ;
Lansky, AJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (13) :957-966
[9]  
Thuraisingham S, 1999, INT J CLIN PRACT, V53, P604
[10]   Randomised placebo-controlled and balloon-angioplasty-controlled trial to assess safety of coronary stenting with use of platelet glycoprotein-IIb/IIIa blockade [J].
Topol, EJ ;
Lincoff, AM ;
Califf, RM ;
Tcheng, JE ;
Kleiman, NS ;
Adelman, AG ;
Burton, JR ;
Talley, JD ;
Ivanhoe, RJ ;
Ducas, C ;
Cheung, PK ;
Schick, U ;
Badard, D ;
Kramer, J ;
Leary, J ;
Snyder, H ;
Wilson, R ;
Dearen, M ;
Caramori, P ;
Webber, S ;
Taylor, J ;
Ferrando, T ;
Cohen, E ;
Balleza, L ;
Rouse, C ;
Hogg, N ;
Kelly, T ;
Alston, S ;
Webb, J ;
Buller, E ;
Ricci, DR ;
Mockman, S ;
Tanguay, JF ;
Poitras, AM ;
Timis, G ;
Davey, D ;
Coleman, P ;
Herrold-Runge, P ;
O'Neill, BJ ;
Foshey, K ;
Fitzgerald, N ;
Almond, D ;
Kostuk, W ;
White, J ;
Oskalns, R ;
Gottlieb, R ;
Koren, P ;
Palazzo, D ;
Azrin, M ;
Barry, MB .
LANCET, 1998, 352 (9122) :87-92