Impact of high loading and maintenance dose of clopidogrel within the first 15 days after percutaneous coronary intervention on patient outcome

被引:59
作者
Lemesle, Gilles [1 ]
Delhaye, Cedric [1 ]
Sudre, Arnaud [1 ]
Broucqsault, Damien [1 ]
Rosey, Guillaume [2 ]
Bauters, Christophe [3 ]
Lablanche, Jean-Marc [1 ]
机构
[1] Hop Cardiol, Serv Cardiol & Hemodynam B, F-59037 Lille, France
[2] Hop Cardiol, Serv Hypertens & Pathol Cardiovasc, F-59037 Lille, France
[3] Hop Cardiol, Serv Cardiol C, F-59037 Lille, France
关键词
STIMULATED PHOSPHOPROTEIN PHOSPHORYLATION; ACUTE MYOCARDIAL-INFARCTION; STENT THROMBOSIS; ANTIPLATELET THERAPY; PLATELET REACTIVITY; ASPIRIN RESISTANCE; CLINICAL-OUTCOMES; CARDIOVASCULAR EVENTS; DRUG-RESISTANCE; ELUTING STENTS;
D O I
10.1016/j.ahj.2008.09.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background An increase in clopidogrel dose results in an improved inhibition of platelet aggregation. However, whether an increase in clopidogrel dose may improve patient outcome is still debated. The aim of this study was to analyze the impact on patient outcome of an increase in clopidogrel loading and maintenance doses within the first 15 days after percutaneous coronary intervention (PCI). Methods Between 2003 and 2007, we included 2,954 consecutive patients who underwent PCI and stent implantation. We compared 2 historical groups. In the "low-dose" group (2003-2005, n = 1,984), patients were pretreated with a 300-mg clopidogrel loading dose followed by 75 mg/d after PCI. In the "high-dose" group (2006-2007, n = 970), patients were pretreated with a 600-mg clopidogrel loading dose followed by 150 mg/d within the first 15 days and 75 mg/d thereafter. The composite primary end point (death, myocardial infarction, stent thrombosis) and bleeding were systematically indexed during the 2-month follow-up period. Results Clinical and most of angiographic characteristics were similar between the 2 groups. By multivariate analysis, high dose of clopidogrel was associated with a decrease in the composite primary end point (hazard ratio 0.694, 95% Cl 0.485-0.993, P =.046). The other predictors were age, left ventricular ejection fraction, diabetes, renal failure, and acute coronary syndrome. Major bleeding was similar in the low- and high-dose groups (2.8% vs 3.4%, respectively, P =.379). After propensity score matching, the high-dose group was still associated with a significant clinical benefit. Conclusion Our results show that a 600-mg loading dose followed by a 150-mg maintenance dose of clopidogrel within the first 15 days after PCI is independently associated with a decrease in the composite death-myocardial infarction-stent thrombosis at 2 months without increase in hemorrhagic complications. (Am Heart J 2009;157:375-82.)
引用
收藏
页码:375 / 382
页数:8
相关论文
共 36 条
[1]  
Albiero R, 1997, CIRCULATION, V95, P1145
[2]   Resistance to thienopyridines: Clinical detection of coronary stent thrombosis by monitoring of vasodilator-stimulated phosphoprotein phosphorylation [J].
Barragan, P ;
Bouvier, JL ;
Roquebert, PO ;
Macaluso, G ;
Commeau, P ;
Comet, B ;
Lafont, A ;
Camoin, L ;
Walter, U ;
Eigenthaler, M .
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS, 2003, 59 (03) :295-302
[3]   Randomized multicenter comparison of conventional anticoagulation versus antiplatelet therapy in unplanned and elective coronary stenting - The full anticoagulation versus aspirin and ticlopidine (FANTASTIC) study [J].
Bertrand, ME ;
Legrand, V ;
Boland, J ;
Fleck, E ;
Bonnier, J ;
Emmanuelson, H ;
Vrolix, M ;
Missault, L ;
Chierchia, S ;
Casaccia, M ;
Niccoli, L ;
Oto, A ;
White, C ;
Webb-Peploe, M ;
Van Belle, E ;
McFadden, EP .
CIRCULATION, 1998, 98 (16) :1597-1603
[4]   Adjusted clopidogrel loading doses according to vasodilator-stimulated phosphoprotein phosphorylation index decrease rate of major adverse cardiovascular events in patients with clopidogrel resistance: A multicenter randomized prospective study [J].
Bonello, Laurent ;
Camoin-Jau, Laurence ;
Arques, Stephane ;
Boyer, Christian ;
Panagides, Dimitri ;
Wittenberg, Olivier ;
Simeoni, Marie-Claude ;
Barragan, Paul ;
Dignat-George, Francoise ;
Paganelli, Franck .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2008, 51 (14) :1404-1411
[5]   Early potent antithrombotic effect with combined aspirin and a loading dose of clopidogrel on experimental arterial thrombogenesis in humans [J].
Cadroy, Y ;
Bossavy, JP ;
Thalamas, C ;
Sagnard, L ;
Sakariassen, K ;
Boneu, B .
CIRCULATION, 2000, 101 (24) :2823-2828
[6]   Aspirin resistance and adverse clinical events in patients with coronary artery disease [J].
Chen, Wai-Hong ;
Cheng, Xi ;
Lee, Pui-Yin ;
Ng, William ;
Kwok, Jeanette Yat-Yin ;
Tse, Hung-Fat ;
Lau, Chu-Pak .
AMERICAN JOURNAL OF MEDICINE, 2007, 120 (07) :631-635
[7]   Aspirin resistance is associated with a high incidence of myonecrosis after non-urgent percutaneous coronary intervention despite clopidogrel pretreatment [J].
Chen, WH ;
Lee, PY ;
Ng, W ;
Tse, HF ;
Lau, CP .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2004, 43 (06) :1122-1126
[8]   Predictors of subacute stent thrombosis - Results of a systematic intravascular ultrasound study [J].
Cheneau, E ;
Leborgne, L ;
Mintz, GS ;
Kotani, J ;
Pichard, AD ;
Satler, LF ;
Canos, D ;
Castagna, M ;
Weissman, NJ ;
Waksman, R .
CIRCULATION, 2003, 108 (01) :43-47
[9]   High post-treatment platelet reactivity identified low-responders to dual antiplatelet therapy at increased risk of recurrent cardiovascular events after stenting for acute coronary syndrome [J].
Cuisset, T ;
Frere, C ;
Quilici, J ;
Barbou, F ;
Morange, PE ;
Hovasse, T ;
Bonnet, JL ;
Alessi, MC .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2006, 4 (03) :542-549
[10]   Benefit of a 600-mg loading dose of clopidogrel on platelet reactivity and clinical outcomes in patients with non-ST-segment elevation acute coronary syndrome undergoing coronary stenting [J].
Cuisset, Thomas ;
Frere, Corinne ;
Quilici, Jacques ;
Morange, Pierre-Emmanuel ;
Nait-Saidi, Lyassine ;
Carvajal, Joseph ;
Lehmann, Agnes ;
Lambert, Marc ;
Bonnet, Jean-Louis ;
Alessi, Marie-Christine .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2006, 48 (07) :1339-1345