CLARITY-TIMI 28 (Clopidogrel as Adjunctive Reperfusion Therapy- Thrombolysis In Myocardial Infarction 28)

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18 Mar, 14

Background

A substantial proportion of patients receiving fibrinolytic therapy for myocardial infarction with ST-segment elevation have inadequate reperfusion or reocclusion of the infarct-related artery, leading to an increased risk of complications and death.

Prior clopidogrel studies such as CREDO and CURE have been conducted in patients with non-ST elevation acute coronary syndromes.

However, benefits of addition of clopidogrel in patients of MI with ST-segment elevation and receiving fibrinolytic therapy, including aspirin, has not been evaluated.

Aim

To evaluate whether the addition of clopidogrel to standard fibrinolytic therapy, including aspirin, would improve infarct-related artery patency and decrease ischemic complications in patients with ST-segment elevation MI (STEMI).

Study Design

Multicenter, randomized, double-blind, placebo controlled study.

Patient Characteristics

3491 patients, aged 18-75 years, presenting with ischemic discomfort at rest within 12 hours before randomization and which lasted more than 20 minutes; ST-segment elevation of at least 0.1 mV in at least two contiguous limb leads, ST-segment elevation of at least 0.2 mV in at least two contiguous precordial leads, or left bundle-branch block that was not known to be old; and if they were scheduled to receive a fibrinolytic agent, an anticoagulant (if a fibrin-specific lytic agent was prescribed) and aspirin.

Exclusion Criteria

  • Clopidogrel treatment within 7 days before enrollment or planned treatment with clopidogrel or glycoprotein (GP) IIb/IIIa inhibitors before coronary angiography
  • Contraindication to thrombolytic therapy
  • Cardiogenic shock
  • Prior coronary artery bypass grafting
  • Intention of angiography with 48 hours in absence of new indication
  • Received excessive doses of heparin

Study Groups

  1. Group 1: N=1752, randomized to 300-mg loading dose of clopidogrel followed by 75 mg/day
  2. Group 2: N=1739, placebo

Primary Endpoint

Composite of death or recurrent MI or an occluded infarct-related artery (TIMI flow 0 or 1) on angiography.

Results

  • Clopidogrel significantly reduced the primary composite endpoint by 36%, as compared to placebo

  • Rate of an occluded infarct-related artery was reduced by 41% with clopidogrel, as compared to placebo

  • Rate of recurrent MI was reduced by 30% with clopidogrel

  • Clopidogrel improved all angiographic measurements, including optimal epicardial flow (defined by TIMI flow grade of 3) by 36%, and the odds of achieving optimal myocardial reperfusion (defined by a TIMI myocardial-reperfusion grade of 3) by 21%. The odds of intracoronary thrombus was reduced by 27% with clopidogrel. Clopidogrel also resulted in less severe stenosis and a larger minimal luminal diameter of the infarct-related artery
  • Clopidogrel reduced the cumulative incidence of the end point of death from cardiovascular causes, recurrent MI, or recurrent ischemia leading to the need for urgent revascularization, by 20%
  • Major and minor bleeding complication rates were similar in both groups

Conclusion

Addition of clopidogrel to aspirin and a standard fibrinolytic regimen improves the patency rate of the infarct-related artery and reduces ischemic complications in STEMI patients aged 75 years or younger.

Presented at ACC Scientific Sessions, 2005