Effects of pretreatment with clopidogrel and aspirin followed by long-term therapy in patients undergoing percutaneous coronary intervention: the PCI-CURE study

被引:2428
作者
Mehta, SR
Yusuf, S
Peters, RJG
Bertrand, ME
Lewis, BS
Natarajan, MK
Maimberg, K
Rupprecht, HJ
Zhao, F
Chrolavicius, S
Copland, I
Fox, KAA
机构
[1] McMaster Univ, Med Ctr, Populat Hlth Res Inst, Div Cardiol, Hamilton, ON L8N 3Z5, Canada
[2] McMaster Univ, Canadian Cardiovasc Collaborat Project Off, Hamilton, ON L8N 3Z5, Canada
[3] Univ Amsterdam, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
[4] Hop Cardiol, Dept Cardiol, F-59037 Lille, France
[5] Lady Davies Carmel Hosp, Haifa, Israel
[6] Karolinska Hosp, S-10401 Stockholm, Sweden
[7] Univ Mainz Klinikum, Mainz, Germany
[8] Royal Edinburgh Infirm, Edinburgh, Midlothian, Scotland
关键词
D O I
10.1016/S0140-6736(01)05701-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Despite the use of aspirin, there is still a risk of ischaemic events after percutaneous coronary intervention (PCI). We aimed to find out whether, in addition to aspirin, pretreatment with clopidogrel followed by long-term therapy after PCI is superior to a strategy of no pretreatment and short-term therapy for only 4 weeks after PCI. Methods 2658 patients with non-ST-elevation acute coronary syndrome undergoing PCI in the CURE study had been randomly assigned double-blind treatment with clopidogrel (n=1313) or placebo (n=1345). Patients were pretreated with aspirin and study drug for a median of 6 days before PCI during the initial hospital admission, and for a median of 10 days overall. After PCI, most patients (>80%) in both groups received open-label thienopyridine for about 4 weeks, after which study drug was restarted for a mean of 8 months. The primary endpoint was a composite of cardiovascular death, myocardial infarction, or urgent target-vessel revascularisation within 30 days of PCI The main analysis was by intention to treat. Findings There were no drop-outs. 59 (4.5%) patients in the clopidogrel group had the primary endpoint, compared with 86 (6.4%) in the placebo group (relative risk 0.70 [95% CI 0.50-0.97], p=0.03). Long-term administration of clopidogrel after PCI was associated with a lower rate of cardiovascular death, myocardial infarction, or any revascularisation (p=0.03), and of cardiovascular death or myocardial infarction (p=0.047). Overall (including events before and after PCI) there was a 31% reduction cardiovascular death or myocardial infarction (p=0.002). There was less use of glycoprotein IIb/IIIa inhibitor in the clopidogrel group (P=0.001). At follow-up, there was no significant difference in major bleeding between the groups (p=0.64). Interpretation In patients with acute coronary syndrome receiving aspirin, a strategy of clopidogrel pretreatment followed by long-term therapy is beneficial in reducing major cardiovascular events, compared with placebo.
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页码:527 / 533
页数:7
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