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本文引用的文献

1
Omicron overpowers key COVID antibody treatments in early tests.在早期测试中,奥密克戎毒株使主要的新冠病毒抗体疗法失效。
Nature. 2021 Dec 21. doi: 10.1038/d41586-021-03829-0.
2
The REMDACTA trial: do interleukin receptor antagonists provide additional benefit in COVID-19?REMDACTA试验:白细胞介素受体拮抗剂在新冠病毒病中是否能带来额外益处?
Intensive Care Med. 2021 Nov;47(11):1315-1318. doi: 10.1007/s00134-021-06540-w. Epub 2021 Oct 7.
3
Tocilizumab and remdesivir in hospitalized patients with severe COVID-19 pneumonia: a randomized clinical trial.托珠单抗联合瑞德西韦治疗重症 COVID-19 肺炎住院患者:一项随机临床试验。
Intensive Care Med. 2021 Nov;47(11):1258-1270. doi: 10.1007/s00134-021-06507-x. Epub 2021 Oct 5.
4
SARS-CoV-2-neutralising monoclonal antibodies for treatment of COVID-19.用于治疗 COVID-19 的 SARS-CoV-2 中和单克隆抗体。
Cochrane Database Syst Rev. 2021 Sep 2;9(9):CD013825. doi: 10.1002/14651858.CD013825.pub2.
5
Mechanism of molnupiravir-induced SARS-CoV-2 mutagenesis.莫努匹拉韦诱导的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)诱变机制。
Nat Struct Mol Biol. 2021 Sep;28(9):740-746. doi: 10.1038/s41594-021-00651-0. Epub 2021 Aug 11.
6
Ongoing global and regional adaptive evolution of SARS-CoV-2.SARS-CoV-2 在全球和区域范围内持续的适应性进化。
Proc Natl Acad Sci U S A. 2021 Jul 20;118(29). doi: 10.1073/pnas.2104241118. Epub 2021 Jul 2.
7
COVID-19-related laboratory coagulation findings.与 COVID-19 相关的实验室凝血发现。
Int J Lab Hematol. 2021 Jul;43 Suppl 1(Suppl 1):36-42. doi: 10.1111/ijlh.13547.
8
Tocilizumab in Hospitalized Patients with Severe Covid-19 Pneumonia.托珠单抗治疗重症 COVID-19 肺炎住院患者。
N Engl J Med. 2021 Apr 22;384(16):1503-1516. doi: 10.1056/NEJMoa2028700. Epub 2021 Feb 25.
9
Tocilizumab in Patients Hospitalized with Covid-19 Pneumonia.托珠单抗治疗新冠肺炎合并肺炎住院患者的疗效。
N Engl J Med. 2021 Jan 7;384(1):20-30. doi: 10.1056/NEJMoa2030340. Epub 2020 Dec 17.
10
COVID-19-associated coagulopathy and disseminated intravascular coagulation.COVID-19 相关凝血功能障碍和弥散性血管内凝血。
Int J Hematol. 2021 Jan;113(1):45-57. doi: 10.1007/s12185-020-03029-y. Epub 2020 Nov 7.

COVID-19 感染期间的凝血功能障碍:简要综述。

Coagulopathy during COVID-19 infection: a brief review.

机构信息

Medical Laboratory Sciences Program, Department of Diagnostic and Health Sciences, University of Tennessee Health Science Center, 930 Madison Avenue, Suite 676, Memphis, TN, 38163, USA.

Office of Research, University of Tennessee Health Science Center, Memphis, TN, USA.

出版信息

Clin Exp Med. 2023 Jul;23(3):655-666. doi: 10.1007/s10238-022-00891-4. Epub 2022 Sep 19.

DOI:10.1007/s10238-022-00891-4
PMID:36121504
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9483403/
Abstract

The COVID-19 pandemic caused by SARS-CoV-2 continues to spread rapidly due to its virulence and ability to be transmitted by asymptomatic infected persons. If they are present, the symptoms of COVID-19 may include rhinorrhea (runny nose), headache, cough, and fever. Up to 5% of affected persons may experience more severe COVID-19 illness, including severe coagulopathy, acute respiratory distress syndrome (ARDS) characterized by respiratory failure that requires supplementary oxygen and mechanical ventilation, and multi-organ failure. Interestingly, clinical evidence has highlighted the distinction between COVID-19-associated coagulopathy (CAC) and disseminated intravascular coagulation (DIC). Patients with CAC exhibit different laboratory values than DIC patients for activated partial thromboplastin time (aPTT) and prothrombin time (PT) which may be normal or shortened, varying platelet counts, altered red blood cell morphology, unique bleeding complications, a lack of schistocytes in the peripheral blood, and no decrease in fibrinogen levels. In this review, we consider the search for 1) laboratory results that can diagnose or predict development of CAC, including serum levels of D-dimers, fibrinogen, interleukin-6 (IL-6) and the growth factor angiopoietin-2 (Ang-2), 2) mechanisms of CAC induction, and 3) novel therapeutic regimens that will successfully treat COVID-19 before development of CAC.

摘要

由 SARS-CoV-2 引起的 COVID-19 大流行由于其毒力和无症状感染者的传播能力而迅速传播。如果存在,COVID-19 的症状可能包括流鼻涕(流鼻水)、头痛、咳嗽和发烧。多达 5%的受感染者可能会经历更严重的 COVID-19 疾病,包括严重的凝血功能障碍、急性呼吸窘迫综合征(ARDS),其特征是呼吸衰竭需要补充氧气和机械通气,以及多器官衰竭。有趣的是,临床证据强调了 COVID-19 相关凝血功能障碍(CAC)和弥散性血管内凝血(DIC)之间的区别。与 DIC 患者相比,CAC 患者的活化部分凝血活酶时间(aPTT)和凝血酶原时间(PT)的实验室值不同,可能正常或缩短,血小板计数不同,红细胞形态改变,独特的出血并发症,外周血中无裂体细胞,纤维蛋白原水平无降低。在这篇综述中,我们考虑了 1)可以诊断或预测 CAC 发展的实验室结果,包括血清 D-二聚体、纤维蛋白原、白细胞介素-6(IL-6)和生长因子血管生成素-2(Ang-2)的水平,2)CAC 诱导的机制,以及 3)在 CAC 发生之前成功治疗 COVID-19 的新型治疗方案。