Why the study?
Vitamin K antagonist use can cause bleeding due to rare factor IX propeptide variants modifying binding affinity to gamma-glutamyl carboxylase, requiring management alternatives in patients with mechanical heart valves.
Does apixaban combined with aspirin prevent thrombosis and hemorrhage in a patient with a mechanical aortic valve and severe warfarin hypersensitivity?
Does apixaban combined with aspirin prevent thrombosis and hemorrhage in a patient with a mechanical aortic valve and severe warfarin hypersensitivity?
This case suggests that apixaban may be a safe and effective alternative to warfarin in patients with mechanical heart valves who have severe warfarin hypersensitivity due to the F9 p.(Ala37Thr) variant, despite general contraindications for DOACs in this population.
Answers are grounded in this paper and cite their sources.
Rare FIX propeptide variants may underlie refractory VKA bleeding; leaves open need for validation before targeted testing.
Bleeding is the most common side effect during treatment with vitamin K antagonists (VKAs). Sometimes, VKA use causes bleeding episodes due to rare variants in the factor IX (FIX) propeptide that modify the affinity of FIX propeptide to the binding of γ-glutamyl carboxylase. We report on a 51-year-old patient who presented with recurrent spontaneous and severe intramuscular and cutaneous bleedings during VKA (warfarin) treatment for the presence of a prosthetic mechanical aortic valve. Laboratory evaluation revealed INR within the therapeutic range with markedly prolonged aPTT and a large reduction of FIX levels. Laboratory parameters significantly improved when warfarin was switched with low-molecular-weight heparin. Next-generation sequencing analysis revealed the variant p.(Ala37Thr) in the F9 gene, which has been previously associated with VKA sensitivity. As an alternative to warfarin, apixaban 5 mg twice daily and aspirin 100 mg daily were started, with no thrombosis or recurrence of hemorrhage and normalization of INR, aPTT, and FIX levels, at 12-month follow-up. We also performed a literature search across PubMed and Scopus, until January 2025. The analysis evidenced five case reports and two case series. The mechanisms of this rare VKA hypersensitivity have also been reviewed. In conclusion, while VKA hypersensitivity is a rare phenomenon, awareness of this complication and the current accessibility to molecular testing make it important to identify patients at risk. The efficacy/safety of direct thrombin or factor Xa inhibitors in patients with a mechanical heart valve and VKA hypersensitivity due to the F9 p.(Ala37Thr) variant deserves more attention and further investigation.
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Tufano et al. (2025) studied this question.
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