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Inherited antithrombin deficiency (ATD) is associated with a high risk of venous thromboembolic complications. Association of ATD with other conditions such as pregnancy obviously increases thromboembolic risk and may require anticoagulant therapy for prevention. Although there are several/heterogenous international guidelines regarding thromboprophylaxis in pregnant patients with ATD, data on anticoagulant prophylaxis in this context are scarce in the literature. Thus, this situation remains a challenge both in the antepartum period and during delivery. Physicians from the French Society of Thrombosis and Haemostasis (SFTH) performed a review of the literature to suggest propositions regarding the management of thrombosis prevention based on anticoagulation and antithrombin substitution in ATD pregnant women. In this review, after reporting the thrombotic risk associated with ATD, the indication of anticoagulant therapy, its dosing regimen and monitoring, and the indication of antithrombin concentrates during pregnancy and the postpartum period are discussed as well as peripartum management. Finally, this work confirms the complex management of thrombotic prevention in pregnant patients with ATD. Indeed, it requires to take into account a multiplicity of features cited in our propositions that will hopefully provide some help in this field. This work also highlights the importance of multidisciplinary discussions for pregnant women with ATD who should be counseled in an expert center including hematologist, obstetrician, and anesthetist to optimize their management.
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http://dx.doi.org/10.1055/a-2650-7959 | DOI Listing |
Res Pract Thromb Haemost
July 2025
Department of Neurology, Bishan Hospital of Chongqing Medical University, Chongqing, China.
Background: Inherited thrombophilia (IT) is a genetically determined predisposition to thromboembolic events. Beyond the well-known G20210A mutation, there has been limited research on other prothrombin mutations in the Chinese population.
Objectives: This study aimed to identify and characterize a novel prothrombin mutation in a Han Chinese family with IT.
J Thromb Haemost
August 2025
Centre for Thrombosis and Haemostasis, Guy's & St Thomas' National Health Service (NHS) Foundation Trust, London, United Kingdom. Electronic address:
Background: Inherited antithrombin deficiency (ATD) is associated with a high risk of venous thromboembolism (VTE), particularly during risk periods, including pregnancy. Guidelines vary regarding thromboprophylaxis with low-molecular-weight heparin (LMWH). LMWH use in women with inherited ATD is hampered by the fact that antithrombin is the substrate for its anticoagulant effect, and therefore, larger doses of LMWH are needed.
View Article and Find Full Text PDFThromb Haemost
July 2025
Hematology Department, CHU de Poitiers, Poitiers, France.
Inherited antithrombin deficiency (ATD) is associated with a high risk of venous thromboembolic complications. Association of ATD with other conditions such as pregnancy obviously increases thromboembolic risk and may require anticoagulant therapy for prevention. Although there are several/heterogenous international guidelines regarding thromboprophylaxis in pregnant patients with ATD, data on anticoagulant prophylaxis in this context are scarce in the literature.
View Article and Find Full Text PDFRinsho Ketsueki
July 2025
Department of Clinical Laboratory Science, Division of Health Sciences, Graduate School of Medical Science, Kanazawa University.
Inherited thrombophilia is a rare disorder that increases risk of thrombotic events. The risk of venous thromboembolism (VTE) increases during pregnancy and the postpartum period. Type I antithrombin (AT) deficiency in particular confers a higher risk compared to protein C (PC) or protein S (PS) deficiency.
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