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Published on: September 30, 2021
Recombinant activated factor VII for refractory bleeding after acute aortic dissection surgery: a propensity score
Luigi Tritapepe1, Vincenzo De Santis, Domenico Vitale
1Department of Anesthesiology and Intensive Care, University of Rome La Sapienza, Rome, Italy.
Recombinant activated factor VII (rFVIIa) effectively reduced bleeding and transfusion needs in complex aortic dissection surgery. This study suggests rFVIIa is a safe additional therapy for refractory bleeding, though further randomized trials are needed.
Area of Science:
- Cardiovascular Surgery
- Hematology
- Anesthesiology
Background:
- Refractory bleeding is a significant complication in acute aortic dissection surgery.
- Deep hypothermic circulatory arrest (DHCA) increases surgical complexity and bleeding risk.
- Conventional methods may be insufficient for managing severe hemorrhage in these patients.
Purpose of the Study:
- To evaluate the safety and effectiveness of recombinant activated factor VII (rFVIIa) as an adjunct therapy.
- To assess rFVIIa's impact on blood loss and transfusion requirements.
- To determine the incidence of adverse events associated with rFVIIa use in this specific patient population.
Main Methods:
- A propensity score-matched analysis was conducted.
- Twenty-three cardiac surgery patients receiving rFVIIa were compared to 23 matched controls.
- rFVIIa was administered as an intravenous bolus (70 microg/kg) post-transfusion protocol.
Main Results:
- rFVIIa administration significantly reduced blood loss and transfusion requirements.
- Hourly blood loss showed significant decreases post-rFVIIa administration (p < .001).
- Significant improvements were observed in coagulation parameters (INR, PTT, platelet count, fibrinogen, antithrombin) with no difference in adverse events between groups.
Conclusions:
- rFVIIa demonstrated successful use as an additional therapy for refractory bleeding during and after acute aortic dissection surgery with DHCA.
- rFVIIa can be a valuable option when conventional hemostatic methods are inadequate.
- Randomized studies are warranted to definitively confirm the safety and efficacy of rFVIIa in this context.
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