COVID-19的凝血功能障碍和抗凝临床试验

IF 2.2 4区 医学 Q3 HEMATOLOGY Best Practice & Research Clinical Haematology Pub Date : 2022-09-01 DOI:10.1016/j.beha.2022.101377
Heng Zhang , Qifang Lao , Jue Zhang , Jieqing Zhu
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引用次数: 3

摘要

2019年12月,严重急性呼吸道疾病冠状病毒2型(SARS-COV-2)首次在中国武汉出现,并引发了现代前所未有的全球大流行。感染SARS-CoV-2的人可以无症状、有中度症状或发展为严重的COVID-19。除了典型的急性呼吸窘迫综合征(ARDS)外,中度或重度COVID-19患者还会出现独特的全身性凝血功能障碍,即COVID-19相关凝血功能障碍(CAC),这与败血症相关的弥散性血管内凝血(DIC)不同。内皮病变或内皮炎是CAC的其他独特特征。内皮细胞扰动可进一步增加COVID-19患者血栓形成事件的风险。在这篇综述中,我们将总结目前关于COVID-19凝血功能障碍的知识及其可能的机制。我们还讨论了缓解COVID-19患者血栓事件的临床试验结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Coagulopathy in COVID-19 and anticoagulation clinical trials

Severe acute respiratory disease coronavirus 2 (SARS-COV-2) first emerged in Wuhan, China, in December 2019 and has caused a global pandemic of a scale unprecedented in the modern era. People infected with SARS-CoV-2 can be asymptomatic, moderate symptomatic or develop severe COVID-19. Other than the typical acute respiratory distress syndrome (ARDS), patients with moderate or severe COVID-19 also develop a distinctive systemic coagulopathy, known as COVID-19-associated coagulopathy (CAC), which is different from sepsis-related forms of disseminated intravascular coagulation (DIC). Endotheliopathy or endotheliitis are other unique features of CAC. The endothelial cell perturbation can further increase the risk of thrombotic events in COVID-19 patients. In this review, we will summarize the current knowledge on COVID-19 coagulopathy and the possible mechanisms for the condition. We also discuss the results of clinical trials testing methods for mitigating thrombosis events in COVID-19 patients.

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来源期刊
CiteScore
4.20
自引率
0.00%
发文量
42
审稿时长
35 days
期刊介绍: Best Practice & Research Clinical Haematology publishes review articles integrating the results from the latest original research articles into practical, evidence-based review articles. These articles seek to address the key clinical issues of diagnosis, treatment and patient management. Each issue follows a problem-orientated approach which focuses on the key questions to be addressed, clearly defining what is known and not known, covering the spectrum of clinical and laboratory haematological practice and research. Although most reviews are invited, the Editor welcomes suggestions from potential authors.
期刊最新文献
Erratum to “Special issue 37.2 and 37.3 Genetics and Function of HLA and immune-related genes in transplantation and cellular immunotherapy” [Best Pract Res Clin Haematol (2024) 101588] Editorial Board From clones to immunopeptidomes: New developments in the characterization of permissive HLA-DP mismatches in hematopoietic cell transplantation Relevance of donor-specific HLA antibodies in hematopoietic cell transplantation HLA structure and function in hematopoietic-cell transplantation
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