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Comparison of Low Dose Recombinant Factor VIIa and 4-Factor Prothrombin Complex Concentrate for Treatment of Bleeding
Lauren Caldwell1, Rima Bhakta1, Neha Naik1
1Erlanger Health System, Chattanooga, TN, USA.
Insights
Recombinant factor VIIa (rFVIIa) and prothrombin concentrate complex (PCC) showed similar packed red blood cell transfusion needs in cardiac surgery bleeding. However, PCC use was linked to more adverse events and longer ICU stays.
Area of Science:
- Cardiology
- Hematology
- Anesthesiology
Background:
- Uncontrolled bleeding in cardiac surgery (CS) is managed with recombinant factor VIIa (rFVIIa) and prothrombin concentrate complex (PCC).
- Direct comparative studies on rFVIIa and PCC efficacy and safety in CS are limited.
Purpose of the Study:
- To compare the efficacy and safety of low-dose rFVIIa and 4-factor PCC in managing bleeding during cardiac surgery.
- To evaluate transfusion requirements, adverse events, and mortality associated with rFVIIa versus PCC use.
Main Methods:
- Retrospective study of 179 adult CS patients receiving either low-dose rFVIIa (<30 mcg/kg) or 4-factor PCC.
- Primary outcome: packed red blood cell (pRBC) transfusion within 6 hours.
- Secondary outcomes: 0-18 hour transfusion, additional factor use, thrombotic events, acute kidney injury (AKI), ICU length of stay, and mortality.
Main Results:
- No significant difference in pRBC transfusion requirements within 6 or 18 hours between rFVIIa and PCC groups.
- PCC group showed higher rates of requiring additional factor products (47.5% vs 24.4%).
- PCC group had increased incidence of AKI (25.7% vs 12.8%), longer ICU stays, and higher in-hospital mortality (10.9% vs 2.6%).
Conclusions:
- While both agents had similar pRBC transfusion needs, PCC was associated with more adverse events and poorer outcomes in CS patients.
- Further direct comparative studies are needed to fully elucidate the risks and benefits of PCC versus rFVIIa in cardiac surgery.
Abstract:
Background: Recombinant factor VIIa (rFVIIa) and prothrombin concentrate complex (PCC) are used for uncontrolled bleeding in cardiac surgery (CS), however, there are limited direct comparisons of these agents. Objective: To evaluate the efficacy and safety of rFVIIa and PCC in CS related bleeding. Methods: This retrospective study included adult CS patients who received either low dose rFVIIa (<30 mcg/kg) or 4-factor PCC. The primary outcome was transfusion requirements of packed red blood cells (pRBC) within 6 hours of factor administration. Secondary efficacy outcomes included transfusion requirements 0-18 hours, doses of additional factor product, thrombotic events, and acute kidney injury (AKI). Results: A total of 179 patients were included (n = 78 rFVIIa; n = 101 PCC). Of patients who received blood products, there was no difference in the requirement of pRBCs within 6 hours (73.8 vs 68.9%, P = .5359) or in the median amount of pRBC transfused (500 mL vs 640 mL, P = .0723) in the rFVIIa and PCC groups respectively. Patients in the PCC group were more likely to require additional factor products (24.4% vs 47.5%, P = .0015), develop AKI (12.8% vs 25.7%, P = .0325), have longer ICU lengths of stay [2 (IQR 1-5) vs 4 (IQR 2-6), P = .0487] and greater in-hospital mortality (2.6% vs 10.9%, P = .033). There was no difference in thrombotic events. Conclusion: Although, there was no difference in pRBC transfusion requirements between PCC and rFVIIa, more patients in the PCC group required additional factor products and had increased adverse effects. Further comparisons of PCC and rFVIIa are warranted.
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