Use of Oral Anti-Xa Inhibitor in Prosthetic Mechanical Aortic Valve with Warfarin Hypersensitivity Due to the FIX p.(Ala37Thr) Propeptide Variant: Case Report and Literature Review.

IF 3.6 2区 医学 Q2 HEMATOLOGY
Antonella Tufano, Carmine Fierarossa, Ferdinando Cirillo, Ciro Miele, Filomena Capasso, Cristina Mazzaccara, Lucia Micale, Gennaro Vecchione, Marco Castori, Ignazio Frangipane, Luca Mocerino, Ernesto Cimino, Matteo Di Minno
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引用次数: 0

Abstract

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.

口服抗xa抑制剂在FIX p.(Ala37Thr)前肽变异致华法林过敏的人工机械主动脉瓣中的应用:病例报告及文献复习
出血是维生素K拮抗剂(VKAs)治疗期间最常见的副作用。有时,由于因子IX (FIX)前肽的罕见变异改变了FIX前肽与γ-谷氨酰羧化酶结合的亲和力,VKA的使用导致出血发作。我们报告了一位51岁的患者,他在使用华法林(VKA)治疗假体机械主动脉瓣时出现复发性自发性和严重的肌肉和皮肤出血。实验室评估显示INR在治疗范围内,aPTT明显延长,FIX水平大幅降低。当华法林与低分子量肝素切换时,实验室参数显著改善。下一代测序分析揭示了F9基因中的变异p.(Ala37Thr),该基因先前与VKA敏感性相关。作为华法林的替代品,阿哌沙班5mg,每日2次,阿司匹林100mg,每日2次,随访12个月,无血栓形成或出血复发,INR, aPTT和FIX水平正常化。我们还对PubMed和Scopus进行了文献检索,直到2025年1月。分析证实了5个病例报告和2个病例系列。这种罕见的VKA超敏反应的机制也进行了综述。总之,虽然VKA超敏反应是一种罕见的现象,但对这种并发症的认识以及目前分子检测的可及性使得识别有风险的患者变得重要。直接使用凝血酶或Xa因子抑制剂治疗f9p (Ala37Thr)变异引起的机械心脏瓣膜和VKA过敏患者的疗效/安全性值得进一步关注和研究。
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来源期刊
Seminars in thrombosis and hemostasis
Seminars in thrombosis and hemostasis 医学-外周血管病
CiteScore
8.80
自引率
21.10%
发文量
132
审稿时长
6-12 weeks
期刊介绍: Seminars in Thrombosis and Hemostasis is a topic driven review journal that focuses on all issues relating to hemostatic and thrombotic disorders. As one of the premiere review journals in the field, Seminars in Thrombosis and Hemostasis serves as a comprehensive forum for important advances in clinical and laboratory diagnosis and therapeutic interventions. The journal also publishes peer reviewed original research papers. Seminars offers an informed perspective on today''s pivotal issues, including hemophilia A & B, thrombophilia, gene therapy, venous and arterial thrombosis, von Willebrand disease, vascular disorders and thromboembolic diseases. Attention is also given to the latest developments in pharmaceutical drugs along with treatment and current management techniques. The journal also frequently publishes sponsored supplements to further highlight emerging trends in the field.
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