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Short-Term Heparin Kinetics during Catheter Ablation of Atrial Fibrillation
Vincent Gabus1, Anne Rollin2, Philippe Maury2
1Service of Cardiology, Department of Medicine, Lausanne University Hospital, Lausanne, Switzerland.
Insights
Unfractionated heparin (UFH) shows slow anticoagulation kinetics in many patients undergoing catheter ablation for atrial fibrillation (AF), highlighting the need for early monitoring and administration before procedures.
Area of Science:
- Cardiology
- Interventional Cardiology
- Pharmacokinetics
Background:
- Catheter ablation for atrial fibrillation (CA-AF) is a treatment for drug-refractory AF.
- Thromboembolic complications during CA-AF are reduced by unfractionated heparin (UFH).
- Optimal UFH administration and kinetics require precise determination.
Purpose of the Study:
- To investigate the kinetics of unfractionated heparin (UFH) during percutaneous catheter ablation for atrial fibrillation (CA-AF).
- To assess the time course of anticoagulation and identify factors influencing UFH efficacy.
Main Methods:
- 102 patients undergoing CA-AF received weight-adjusted UFH bolus (100 U/kg).
- Activated clotting time (ACT) was measured at baseline, 10 minutes (T10), and 20 minutes (T20).
- Patient characteristics and preprocedural medications were analyzed.
Main Results:
- ACT significantly increased from baseline (100 ± 27s) to T10 (355 ± 94s) and T20 (375 ± 90s).
- 24 patients did not reach the target ACT (≥300s) at T10, with many remaining subtherapeutic at T20.
- Patients with delayed UFH kinetics were more likely to have received preprocedural vitamin K1.
Conclusions:
- UFH demonstrates unexpectedly slow anticoagulation kinetics in a significant portion of patients up to 20 minutes post-infusion.
- Infusing UFH before transseptal puncture and early ACT monitoring are recommended to identify patients with delayed kinetics.
- Findings align with guidelines advocating therapeutic anticoagulation during CA-AF.
Background:
Percutaneous catheter ablation of atrial fibrillation (CA-AF) is a treatment option for symptomatic drug-refractory atrial fibrillation (AF). CA-AF carries a risk for thromboembolic complications that has been minimized by the use of intraprocedural intravenous unfractionated heparin (UFH). The optimal administration of UFH as well as its kinetics are not well established and need to be precisely determined.
Methods And Results:
A total 102 of consecutive patients suffering from symptomatic drug-refractory AF underwent CA-AF. The mean age was 61 ± 10 years old. After transseptal puncture of the fossa ovalis, weight-adjusted UFH bolus (100 U/kg) was infused. A significant increase in activated clotting time (ACT) was observed from an average value of 100 ± 27 seconds at baseline, to 355 ± 94 seconds at 10 min (T10), to 375 ± 90 seconds at 20 min (T20). Twenty-four patients failed to reach the targeted ACT value of ≥300 seconds at T10 and more than half of these remained with subtherapeutic ACT values at T20. This subset of patients showed similar clinical characteristics and amount of UFH but were more frequently prescribed preprocedural vitamin K1 than the rest of the study population.
Conclusions:
In a typical intervention setting, UFH displays unexpected slow anticoagulation kinetics in a significant proportion of procedures up to 20 minutes after infusion. These findings support the infusion of UFH before transseptal puncture or any left-sided catheterization with early ACT measurements to identify patients with delayed kinetics. They are in line with recent guidelines to perform CA-AF under therapeutic anticoagulation.
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