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Initial Experience of the Use of 3-Factor Prothrombin Complex Concentrate and Thromboembolic Complications After
India Zweng1, Sean Galvin2, Ray Robbins3
1Department of Surgery, Austin Hospital, Melbourne, Vic, Australia.
Insights
Three-factor prothrombin complex concentrate (3F-PCC) use in cardiac surgery patients did not show an increased risk of thromboembolic events compared to conventional therapy. This study suggests 3F-PCC is a safe option for managing coagulopathy.
Area of Science:
- Cardiology
- Hematology
- Anesthesiology
Background:
- 3-factor prothrombin complex concentrate (3F-PCC) is a potential treatment for coagulopathy in cardiac surgery.
- Concerns exist regarding 3F-PCC's potential to increase thromboembolic events.
Purpose of the Study:
- To compare the incidence of thromboembolic events in cardiac surgery patients treated with 3F-PCC versus conventional therapy.
Main Methods:
- Retrospective cohort study comparing patients who received 3F-PCC with a control group.
- Propensity-score matching was used for risk adjustment.
- Demographic, operative, and postoperative data were analyzed.
Main Results:
- Patients receiving 3F-PCC were younger and had fewer comorbidities but underwent more complex surgeries.
- Unadjusted and adjusted 30-day mortality and readmission rates were similar between groups.
- The incidence of thromboembolic events was comparable between the 3F-PCC and control groups (9.2% vs. 6.8%, p=0.40), with adjusted odds ratio of 1.512 (p=0.541).
Conclusions:
- 3-factor prothrombin complex concentrate was administered to patients at higher risk for bleeding complications.
- Initial findings suggest that 3F-PCC use does not elevate thromboembolic risks compared to conventional treatments in cardiac surgery.
Background:
3-factor prothrombin complex concentrate (3F-PCC) may provide a valuable treatment option for coagulopathy in cardiac surgery patients. However, it may expose patients to increased risk of thromboembolic events. Accordingly, we compared the incidence of thromboembolic events between patients exposed to 3F-PCC and those receiving conventional therapy.
Methods:
Demographic, operative and postoperative data was obtained in a cohort of consecutive patients exposed to 3F-PCC and a contemporaneous control population. Propensity-score matching was performed for risk adjustment. Unadjusted and adjusted patient demographics and incidence of thromboembolism were compared.
Results:
Patients receiving 3F-PCC (PCC) were younger (mean age PCC: 64±14.2 vs. No PCC: 67.6±11.6, p=0.022), and less likely to have diabetes or previous myocardial infarction. PCC patients experienced more prolonged aortic cross clamp times (mean time in minutes PCC: 119.9±58.8 vs. No PCC: 92.3±54), more complex cardiac surgeries and were more likely to have received more fresh frozen plasma (FFP), cryoprecipitate and red blood cells. Despite this, both unadjusted and adjusted 30-day mortality and readmission rates were similar between groups. There were 9 (9.2%) and 34 (6.8%) (p=0.40) thromboembolic events in the unadjusted PCC and control groups respectively. Adjusted risk for thromboembolic event rates was also comparable (Odds ratio: 1.512, 95% Confidence Interval 0.401-5.7, p=0.541).
Conclusions:
3-factor prothrombin complex concentrate was administered to patients at greater risk of complications including bleeding. Our initial experience suggests that the use of PCC does not appear to increase thromboembolic risks compared to conventional treatment.
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