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March 10, 2005New England Journal of Medicine1,930 citations

Addition of Clopidogrel to Aspirin and Fibrinolytic Therapy for Myocardial Infarction with ST-Segment Elevation

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MSMarc S. SabatineCCChristopher P. CannonCGC. Michael Gibson

Structured PICO

Does the addition of clopidogrel to aspirin and fibrinolytic therapy reduce the composite of an occluded infarct-related artery, death, or recurrent myocardial infarction in patients 18 to 75 years of age with ST-elevation myocardial infarction?

P
Population
n=3491 patients, 18 to 75 years of age, who presented within 12 hours after the onset of an ST-elevation myocardial infarction.
I
Intervention
Clopidogrel (300-mg loading dose, followed by 75 mg once daily) added to a fibrinolytic agent, aspirin, and when appropriate, heparin (dispensed according to body weight).
C
Comparator
Placebo added to a fibrinolytic agent, aspirin, and when appropriate, heparin (dispensed according to body weight).
O
Outcome
Composite of an occluded infarct-related artery (defined by a Thrombolysis in Myocardial Infarction flow grade of 0 or 1) on angiography or death or recurrent myocardial infarction before angiography (scheduled 48 to 192 hours after the start of study medication).composite

In patients 75 years of age or younger with STEMI receiving standard fibrinolytic therapy, the addition of clopidogrel significantly improves infarct-related artery patency and reduces ischemic complications without increasing major bleeding.

Abstract

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. METHODS: We enrolled 3491 patients, 18 to 75 years of age, who presented within 12 hours after the onset of an ST-elevation myocardial infarction and randomly assigned them to receive clopidogrel (300-mg loading dose, followed by 75 mg once daily) or placebo. Patients received a fibrinolytic agent, aspirin, and when appropriate, heparin (dispensed according to body weight) and were scheduled to undergo angiography 48 to 192 hours after the start of study medication. The primary efficacy end point was a composite of an occluded infarct-related artery (defined by a Thrombolysis in Myocardial Infarction flow grade of 0 or 1) on angiography or death or recurrent myocardial infarction before angiography. RESULTS: The rates of the primary efficacy end point were 21.7 percent in the placebo group and 15.0 percent in the clopidogrel group, representing an absolute reduction of 6.7 percentage points in the rate and a 36 percent reduction in the odds of the end point with clopidogrel therapy (95 percent confidence interval, 24 to 47 percent; P<0.001). By 30 days, clopidogrel therapy reduced the odds of the composite end point of death from cardiovascular causes, recurrent myocardial infarction, or recurrent ischemia leading to the need for urgent revascularization by 20 percent (from 14.1 to 11.6 percent, P=0.03). The rates of major bleeding and intracranial hemorrhage were similar in the two groups. CONCLUSIONS: In patients 75 years of age or younger who have myocardial infarction with ST-segment elevation and who receive aspirin and a standard fibrinolytic regimen, the addition of clopidogrel improves the patency rate of the infarct-related artery and reduces ischemic complications.

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Cite This Study

Sabatine et al. (2005) studied this question.

synapsesocial.com/papers/69f41d04f3e494ed2b7d0394https://doi.org/10.1056/nejmoa050522
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