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Updated: Jul 14, 2026

Catheter Ablation in Combination With Left Atrial Appendage Closure for Atrial Fibrillation
Published on: February 26, 2013
Probable right atrial thrombus immediately after recombinant activated factor VII administration.
1Department of Anaesthesia and Perioperative Medicine, Royal Brisbane and Women's Hospital, Butterfield Street, Herston, Brisbane, Queensland 4006, Australia. georgepang@hotmail.com
A probable right atrial thrombus was found in a trauma patient after receiving recombinant activated factor VII (rFVIIa). This case highlights a potential immediate adverse event associated with rFVIIa use in critical care settings.
Area of Science:
- Cardiology
- Hematology
- Trauma Surgery
Background:
- Severe trauma often leads to coagulopathy and hemodynamic instability.
- Recombinant activated factor VII (rFVIIa) is used to manage bleeding in such critical conditions.
- Continuous transesophageal echocardiography is a valuable tool for real-time cardiac assessment.
Observation:
- A 33-year-old male with severe multi-system trauma presented with refractory coagulopathy and hemodynamic instability.
- Following administration of recombinant activated factor VII (rFVIIa), a probable right atrial thrombus was visualized.
- The thrombus partially occluded the right ventricular inflow tract, appearing immediately post-rFVIIa infusion.
Findings:
- This is the first reported case demonstrating an immediate temporal association between rFVIIa administration and the formation of a space-occupying lesion consistent with localized thrombosis.
- The event occurred despite the patient's ongoing severe systemic coagulopathy.
- Echocardiography confirmed the presence and location of the suspected thrombus.
Implications:
- The findings suggest a potential risk of localized thrombosis formation secondary to rFVIIa administration, even in the context of systemic coagulopathy.
- Further investigation into the mechanisms and risk factors for rFVIIa-associated thrombosis is warranted.
- This case underscores the importance of vigilant monitoring for thrombotic events in critically ill patients receiving hemostatic agents.
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