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Updated: May 28, 2026

Postconditioning with Lactate-enriched Blood for Cardioprotection in ST-segment Elevation Myocardial Infarction
Published on: May 28, 2019
Use of early clopidogrel by reperfusion strategy among patients presenting with ST-segment elevation myocardial
Chiara Melloni1, Matthew T Roe, Anita Y Chen
1Division of Cardiology and Duke Clinical Research Institute, Duke University Medical Center, 2400 Pratt St, Durham, NC 27705, USA. mello004@mc.duke.edu
Insights
Early clopidogrel use in ST-elevation myocardial infarction (STEMI) patients is inconsistent, particularly in those not receiving reperfusion therapy. Despite guidelines, uptake remains low, though associated with reduced in-hospital death across strategies.
Area of Science:
- Cardiology
- Clinical Medicine
- Pharmacology
Background:
- The 2007 ACC/AHA guidelines recommended clopidogrel with aspirin for STEMI patients, irrespective of reperfusion strategy.
- A bolus dose of clopidogrel was specifically recommended for patients under 75 years old.
Purpose of the Study:
- To evaluate the utilization and dosing of early clopidogrel therapy in STEMI patients across different reperfusion strategies.
- To assess the association of clopidogrel use with in-hospital outcomes, including bleeding and mortality.
Main Methods:
- Analysis of 52,140 STEMI patients from January 2007 to September 2009 in the ACTION Registry®--Get with the Guidelines (GWTG™).
- Patients were stratified by reperfusion strategy: primary percutaneous coronary intervention (PCI), fibrinolysis, or no reperfusion, and by age (<75 or ≥75 years).
- Adjusted odds ratios for in-hospital outcomes were calculated based on early clopidogrel use.
Main Results:
- Early clopidogrel administration was high in primary PCI (97%) but low in fibrinolysis (18%) and no-reperfusion (6%) groups.
- Loading doses were frequently used in PCI (91%) but less so in fibrinolysis (83%) and no-reperfusion (74%) patients.
- Clopidogrel use was linked to significantly lower in-hospital death across all reperfusion strategies, but increased major bleeding in older patients not receiving reperfusion.
Conclusions:
- Early clopidogrel use has not been widely adopted in routine care for STEMI patients undergoing fibrinolysis or not receiving reperfusion.
- Adherence to guideline recommendations for clopidogrel in STEMI management remains suboptimal in specific patient subgroups.
Background:
The 2007 update of the ACC/AHA guidelines for STEMI patients recommended addition of clopidogrel to aspirin regardless of reperfusion strategy, with a bolus dose in patients <75 years of age.
Methods And Results:
We evaluated use and dose of early clopidogrel among 52,140 STEMI patients enrolled in 368 hospitals participating in NCDR's ACTION Registry®--Get with the Guidelines (GWTG™) from January 2007-September 2009. Patients were stratified by reperfusion strategy: primary percutaneous coronary intervention (PCI, n=37,108), fibrinolysis (n=5805), or no-reperfusion (n=9227), and by age (<75 or ≥75 years). Adjusted odds for in-hospital outcomes are reported by clopidogrel use across reperfusion strategies. Clopidogrel was administered early to 97% of primary PCI, 18% of fibrinolytic, and 6% of non-reperfused patients. Among patients receiving clopidogrel, a loading dose (≥300 mg) was often used in primary PCI (91%) but less frequently among fibrinolysis-treated (83%) and non-reperfused patients (74%). A positive time trend from Q1 2007-Q3 2009 in overall clopidogrel use was observed only in fibrinolytic patients (15-20%) Use of clopidogrel was associated with a significant increase in major bleeding only among older patients in the no-reperfusion group (21.9% vs. 13.2%; OR 2.19; 95% CI 1.47-3.27). A significantly lower risk of in-hospital death was associated with clopidogrel use across all reperfusion strategies (OR [95% CI], primary PCI: 0.15 [0.13-0.19]; fibrinolysis: 0.26 [0.12-0.57]; no reperfusion: 0.42 [0.27-0.65]).
Conclusion:
Early clopidogrel use has not yet extended to the routine care of STEMI patients treated with fibrinolysis or those not receiving reperfusion as recommended in the guideline update.
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