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Practical guideline for major hereditary thrombophilia.

作者信息

Tang Liang V, Morange Pierre-Emmanuel, Corral Javier, Ntaios Georgios, Spyropoulos Alex C, Lip Gregory Y H, Douketis James D

机构信息

Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.

Service d'hématologie, La Timone Hospital, Aix-Marseille University, INSERM, INRAE, C2VN, 13385 Marseille, France.

出版信息

Innovation (Camb). 2025 Apr 1;6(6):100890. doi: 10.1016/j.xinn.2025.100890. eCollection 2025 Jun 2.

DOI:10.1016/j.xinn.2025.100890
PMID:40528894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12169261/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0328/12169261/00e51e443fff/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0328/12169261/00e51e443fff/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0328/12169261/00e51e443fff/gr1.jpg

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Practical guideline for major hereditary thrombophilia.主要遗传性血栓形成倾向实用指南。
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本文引用的文献

1
The use of direct oral anticoagulants in the secondary prevention of venous thromboembolism in patients with severe thrombophilia: communication from the ISTH SSC Subcommittee on Physiological Anticoagulants and Thrombophilia.直接口服抗凝剂在严重血栓形成倾向患者中用于静脉血栓栓塞症二级预防的应用：ISTH SSC 生理抗凝剂和血栓形成倾向小组委员会的交流。
J Thromb Haemost. 2024 Nov;22(11):3322-3329. doi: 10.1016/j.jtha.2024.08.006. Epub 2024 Sep 2.
2
Heterozygous Prothrombin Mutation-Associated Thrombophilia.杂合子凝血酶原突变相关血栓形成倾向
Thromb Haemost. 2025 Jan;125(1):69-81. doi: 10.1055/a-2350-8338. Epub 2024 Jun 24.
3
Defining heparin resistance: communication from the ISTH SSC Subcommittee of Perioperative and Critical Care Thrombosis and Hemostasis.
定义肝素抵抗：国际血栓与止血学会围手术期及危重症血栓形成与止血学分会发布的资讯
J Thromb Haemost. 2023 Dec;21(12):3649-3657. doi: 10.1016/j.jtha.2023.08.013. Epub 2023 Aug 22.
4
American Society of Hematology 2023 guidelines for management of venous thromboembolism: thrombophilia testing.美国血液学会 2023 年静脉血栓栓塞症管理指南：血栓形成倾向检测。
Blood Adv. 2023 Nov 28;7(22):7101-7138. doi: 10.1182/bloodadvances.2023010177.
5
Gene editing of human iPSCs rescues thrombophilia in hereditary antithrombin deficiency in mice.对人类诱导多能干细胞进行基因编辑可挽救小鼠遗传性抗凝血酶缺乏症中的血栓形成倾向。
Sci Transl Med. 2022 Nov 30;14(673):eabq3202. doi: 10.1126/scitranslmed.abq3202.