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Updated: May 5, 2026

Rapid Point-of-Care Assay of Enoxaparin Anticoagulant Efficacy in Whole Blood
Published on: October 12, 2012
Percutaneous coronary intervention after subcutaneous enoxaparin pretreatment in patients with unstable angina
J P Collet1, G Montalescot, L Lison
1Department of Cardiology, Pitié-Salpêtrière University Hospital, Paris, France.
Insights
Subcutaneous low-molecular-weight heparin (LMWH) is safe and effective for patients undergoing cardiac catheterization for unstable angina. This strategy avoids additional anticoagulation and monitoring, with low rates of adverse events.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Subcutaneous low-molecular-weight heparins (LMWH) are alternatives to unfractionated heparin for unstable angina.
- Optimal anticoagulation during cardiac catheterization for these patients remains unclear.
Purpose of the Study:
- To evaluate a simple anticoagulation strategy using subcutaneous LMWH in patients with unstable angina/non-Q-wave myocardial infarction requiring cardiac catheterization.
Main Methods:
- 451 patients received enoxaparin (1 mg/kg every 12 hours).
- 293 patients underwent coronary angiography within 8 hours of the last LMWH dose.
- 132 patients proceeded to percutaneous coronary intervention (PCI) without additional heparin or monitoring.
Main Results:
- Anti-Xa activity was consistently high (0.98 IU/mL) at catheterization.
- No in-hospital abrupt closures or urgent revascularizations occurred post-PCI.
- 30-day death/myocardial infarction rates were 3.0% (PCI group) and 6.2% (all patients).
- Major bleeding rates were low (0.8% PCI group, 1.3% non-PCI group).
Conclusions:
- PCI within 8 hours of subcutaneous enoxaparin appears safe and effective.
- Further research is needed on LMWH combined with glycoprotein IIb/IIIa inhibitors.
Background:
Subcutaneous low-molecular-weight (LMW) heparins can effectively replace unfractionated heparin in patients with unstable angina or non-Q-wave myocardial infarction. However, the optimal anticoagulation strategy for these patients when they require cardiac catheterization is still unclear. Therefore, we evaluated a new and simple strategy of anticoagulation in these patients.
Methods And Results:
A total of 451 consecutive patients with unstable angina/non-Q-wave myocardial infarction were treated for at least 48 hours with subcutaneous injections of enoxaparin (1 mg [100 IU]/kg every 12 hours, cycled at 6 AM and 6 PM). Of this unselected population, 293 patients (65%) underwent a coronary angiography within 8 hours of the morning LMW heparin injection, followed by immediate percutaneous coronary intervention (PCI) in 132 patients (28%). PCI was performed without any additional bolus of unfractionated/LMW heparin and without coagulation monitoring. Anti-Xa activity at the time of catheterization was 0.98+/-0.03 IU/mL, was >0.5 IU/mL in 97.6% of patients, and did not relate to the LMW heparin injection-to-catheterization time. There were no in-hospital abrupt closures or urgent revascularizations after PCI. The death/myocardial infarction rate at 30 days was 3.0% in the PCI group (n=132) but 6.2% in the whole population (n=451) and 10.8% in the patients not undergoing catheterization (n=158). The 30-day major bleeding rate was 0.8% in the PCI group, which was comparable to that of patients without catheterization (1.3%).
Conclusions:
PCI within 8 hours of the last enoxaparin subcutaneous injection seems to be safe and effective. The safety of subcutaneous LMW heparin in combination with platelet glycoprotein IIb/IIIa blockade awaits further study.
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