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直接口服抗凝剂在抗磷脂综合征血栓预防中的作用。

Role of Direct Oral Anticoagulation Agents as Thromboprophylaxis in Antiphospholipid Syndrome.

作者信息

Arora Shreya, Nair Shaalina, Prabhu Rishab, Avanthika Chaithanya, Jhaveri Sharan, Samayam Shilpa, Katta Maanya R, Agarwal Pahel

机构信息

Internal Medicine, Government Medical College and Hospital, Chandigarh, Chandigarh, IND.

Internal Medicine, California Institute of Behavioral Neurosciences and Psychology, Fairfield, USA.

出版信息

Cureus. 2021 Oct 24;13(10):e19009. doi: 10.7759/cureus.19009. eCollection 2021 Oct.

Abstract

Antiphospholipid syndrome (APS) is an autoimmune disorder that causes venous, arterial and small-vessel thrombosis, pregnancy loss, and premature birth. Cardiac valvular disease, renal thrombotic microangiopathy, thrombocytopenia, hemolytic anemia, and cognitive impairment are some of its other clinical symptoms. Antiphospholipid antibodies cause endothelial cells, monocytes, and platelets to become activated, as well as an increase in tissue factor and thromboxane A2. Complement activation might play a key function in pathogenesis. Long-term oral anticoagulation is used to treat thrombosis, and individuals having arterial episodes should be treated quickly. Patients with systemic lupus erythematosus (SLE), as well as those with solely obstetric antiphospholipid syndrome, should get primary thromboprophylaxis. Obstetric care is based on a combination of medical and obstetric high-risk management, as well as aspirin and heparin therapy. Possible supplementary therapy for this condition is hydroxychloroquine. Statins, rituximab, and novel anticoagulant medicines are all potential future treatments for non-pregnant individuals with antiphospholipid syndrome. We aim to review the role of direct-acting oral anticoagulants (DOACs) as thromboprophylactic drugs in the treatment of APS in this article. The treatment of venous thromboembolism has been transformed by a new class of DOACs. These drugs, such as rivaroxaban, function by inhibiting factor Xa directly. Not only do they have known anticoagulant actions, but they also obviate the need for dosage monitoring and modification, in contrast to warfarin. We conducted an exhaustive literature search of PubMed/MEDLINE and Google Scholar Indexes using the keywords "Antiphospholipid syndrome," "thromboprophylaxis," and "oral anticoagulants" up to September 2021. We found that DOACs have been shown to be non-inferior to warfarin in a variety of anticoagulation situations in a number of high-powered clinical studies. In many hypercoagulable conditions such as APS, DOACs are quickly establishing themselves as first-line therapy. This article is focused on comprehensively reviewing the mechanism of action of DOACs, their role as thromboprophylactic drugs, risks and complications of DOACs, and comparing their efficacy with the standard treatment protocol and warfarin.

摘要

抗磷脂综合征(APS)是一种自身免疫性疾病,可导致静脉、动脉和小血管血栓形成、流产和早产。心脏瓣膜病、肾血栓性微血管病、血小板减少、溶血性贫血和认知障碍是其其他一些临床症状。抗磷脂抗体可使内皮细胞、单核细胞和血小板活化,还会使组织因子和血栓素A2增加。补体激活可能在发病机制中起关键作用。长期口服抗凝药用于治疗血栓形成,发生动脉事件的个体应迅速接受治疗。系统性红斑狼疮(SLE)患者以及仅患有产科抗磷脂综合征的患者应进行一级血栓预防。产科护理基于医学和产科高危管理以及阿司匹林和肝素治疗的联合应用。羟氯喹可能是针对这种情况的辅助治疗方法。他汀类药物、利妥昔单抗和新型抗凝药物都是未来抗磷脂综合征非妊娠个体可能的治疗方法。我们旨在在本文中综述直接作用口服抗凝药(DOACs)作为血栓预防药物在抗磷脂综合征治疗中的作用。一类新型DOACs改变了静脉血栓栓塞的治疗方式。这些药物,如利伐沙班,通过直接抑制因子Xa发挥作用。与华法林相比,它们不仅具有已知的抗凝作用,而且无需进行剂量监测和调整。我们使用关键词“抗磷脂综合征”“血栓预防”和“口服抗凝药”对截至2021年9月的PubMed/MEDLINE和谷歌学术索引进行了详尽的文献检索。我们发现,在多项大型临床研究中,DOACs在多种抗凝情况下已被证明不劣于华法林。在许多高凝状态如抗磷脂综合征中,DOACs正迅速确立其作为一线治疗的地位。本文重点全面综述DOACs的作用机制、它们作为血栓预防药物的作用、DOACs的风险和并发症,并将其疗效与标准治疗方案和华法林进行比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/571b/8610415/eaca1e4602b7/cureus-0013-00000019009-i01.jpg

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