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Published on: September 9, 2012
Thrombosis risk assessment in patients with congenital thrombophilia during COVID - 19 infection
Mirjana Kovac1, Gorana Mitic2, Marija Milenkovic3
1Faculty of Medicine, University of Belgrade, Serbia; Blood Transfusion Institute of Serbia, Hemostasis Department, Belgrade, Serbia.
Insights
Congenital thrombophilia did not increase COVID-19 thrombosis risk in this study. However, patients with thrombophilia may still benefit from tailored anticoagulant prophylaxis due to potential risks.
Area of Science:
- Cardiology
- Hematology
- Infectious Diseases
Background:
- COVID-19 infection can cause coagulation dysfunction and severe thrombotic complications.
- Comorbidities and age are known risk factors for thrombosis in COVID-19 patients.
- Limited data exists on the association between congenital thrombophilia and COVID-19-related thrombotic events.
Purpose of the Study:
- To investigate the risk of COVID-19-associated thrombosis in patients with congenital thrombophilia.
- To evaluate if congenital thrombophilia influences the occurrence or characteristics of thrombotic events post-COVID-19.
Main Methods:
- Prospective case-control study of 90 COVID-19 patients (30 with congenital thrombophilia, 60 without).
- Follow-up for 6 months post-COVID-19 diagnosis, monitoring for symptomatic thrombotic events.
- Assessment of hemostatic parameters, including Factor VIII (FVIII) activity and D-dimer levels, at 1, 3, and 6 months.
Main Results:
- Symptomatic thrombotic events occurred in 23% of patients with thrombophilia and 20% without (P=0.715).
- No significant differences were observed in thrombotic event localization, timing, or response to antithrombotic treatment between groups.
- D-dimer levels were significantly higher in patients without thrombophilia.
Conclusions:
- Congenital thrombophilia did not appear to elevate the risk of symptomatic thrombotic events in COVID-19 patients in this cohort.
- Despite similar event rates, individualized anticoagulant prophylaxis is recommended for patients with congenital thrombophilia, tailored to their specific genetic defect.
Background:
Coagulation dysfunction represents a serious complication in patients during the COVID-19 infection, while fulminant thrombotic complications emerge as critical issues in individuals with severe COVID-19. In addition to a severe clinical presentation, comorbidities and age significantly contribute to the development of thrombotic complications in this disease. However, there is very little data on association of congenital thrombophilia and thrombotic events in the setting of COVID-19. Our study aimed to evaluate the risk of COVID-19 associated thrombosis in patients with congenital thrombophilia.
Methods:
This prospective, case-control study included patients with confirmed COVID-19 infection, followed 6 months post-confirmation. The final outcome was a symptomatic thrombotic event. In total, 90 COVID-19 patients, 30 with known congenital thrombophilia and 60 patients without thrombophilia within the period July 2020-November 2021, were included in the study. Evaluation of hemostatic parameters including FVIII activity and D-dimer was performed for all patients at 1 month, 3 months and 6 months post-COVID-19 diagnosis.
Results:
Symptomatic thrombotic events were observed in 7 out of 30 (23 %) COVID-19 patients with thrombophilia, and 12 out of 60 (20 %) without thrombophilia, P = 0.715. In addition, the two patient groups had comparable localization of thrombotic events, time to thrombotic event, effect of antithrombotic treatment and changes in FVIII activity, while D-dimer level were significantly increased in patients without thrombophilia.
Conclusion:
Our findings suggest that patients with congenital thrombophilia, irrespective of their age, a mild clinical picture and absence of comorbidities, should receive anticoagulant prophylaxis, adjusted based on the specific genetic defect.
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