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Upstream anticoagulation for patients with ST-elevation myocardial infarction undergoing primary percutaneous
Warren J Cantor1, Shahar Lavi2, Vladimír Džavík3
1Division of Cardiology, Southlake Regional Health Centre, University of Toronto, Toronto, Ontario, Canada.
Insights
Preprocedural anticoagulation in ST-elevation myocardial infarction (STEMI) patients undergoing percutaneous coronary intervention (PCI) improved blood flow and reduced complications. However, it did not significantly impact major adverse events like death or heart failure at one year.
Area of Science:
- Cardiology
- Interventional Cardiology
- Clinical Trials
Background:
- Optimal timing of anticoagulant administration in ST-elevation myocardial infarction (STEMI) patients undergoing primary percutaneous coronary intervention (PCI) is not well-defined.
- Understanding the impact of preprocedural anticoagulation on clinical and angiographic outcomes is crucial for STEMI management.
Purpose of the Study:
- To assess the relationship between preprocedural anticoagulation use and clinical and angiographic outcomes in STEMI patients undergoing primary PCI.
- To evaluate the impact of preprocedural anticoagulation on procedural success and one-year clinical outcomes.
Main Methods:
- Analysis of data from the TOTAL trial, stratifying 10,064 patients based on preprocedural parenteral anticoagulant use before PCI.
- Comparison of baseline and procedural characteristics between groups.
- Use of Cox proportional modeling and logistic regression, adjusted for propensity scores, to analyze one-year clinical and angiographic outcomes.
Main Results:
- Preprocedural anticoagulation was administered to 63% of patients, most commonly intravenous unfractionated heparin.
- Patients receiving preprocedural anticoagulation showed improved TIMI flow and reduced thrombus burden before PCI.
- Associated with decreased use of bailout thrombectomy, GP IIb/IIIa inhibitors, and intra-aortic balloon pump, as well as lower rates of CABG and minor bleeding at one year.
Conclusions:
- Preprocedural anticoagulation improves angiographic outcomes, including blood flow and thrombus reduction, prior to PCI in STEMI patients.
- Associated with reduced need for bailout procedures during PCI.
- No significant difference in major adverse cardiovascular events such as death, recurrent infarction, or heart failure at one year was observed.
Objectives:
To assess the relationship between preprocedural anticoagulation use and clinical and angiographic outcomes.
Background:
For patients with ST-elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PCI), the optimal timing of anticoagulant administration remains uncertain.
Methods:
Patients enrolled in the TOTAL trial were stratified based on whether or not they had received any parenteral anticoagulant prior to randomization and PCI. Baseline and procedural characteristics were compared. For one-year clinical outcomes, Cox proportional modeling adjusted on a propensity score was used to analyze differences between groups. Angiographic endpoints were analyzed by logistic regression models adjusted for propensity scores.
Results:
In the trial, 10,064 patients were enrolled and underwent PCI. Preprocedural anticoagulation was used in 6,381 patients (63%).The most common anticoagulant was intravenous unfractionated heparin (5,188, 81%). Patients who received preprocedural anticoagulation had higher rates of TIMI-2-3 or TIMI-3 flow and lower grades of thrombus prior to PCI. Pretreatment with anticoagulation was associated with lower use of bailout thrombectomy, GP IIb/IIIa inhibitors, and intra-aortic balloon pump. After adjustment, preprocedural anticoagulation was associated with lower rates of CABG and minor bleeding at 1 year but there were no significant differences in death, stroke, recurrent MI, cardiogenic shock, or congestive heart failure.
Conclusions:
Preprocedural anticoagulation is associated with improved flow and reduced thrombus in the IRA prior to PCI, less bailout thrombectomy during PCI but no difference in death, recurrent infarction, or heart failure at 1 year.
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