Chen Wenjing, Pan Jing Ye
School of the First Clinical Medical Sciences, Wenzhou Medical University, Wenzhou, China.
Department of Intensive Care Unit, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Biol Proced Online. 2021 Jan 20;23(1):4. doi: 10.1186/s12575-021-00142-y.
The spread of the coronavirus (SARS-CoV-2, COVID-19 for short) has caused a large number of deaths around the world. We summarized the data reported in the past few months and emphasized that the main causes of death of COVID-19 patients are DAD (Diffuse Alveolar Damage) and DIC (Disseminated intravascular coagulation). Microthrombosis is a prominent clinical feature of COVID-19, and 91.3% of dead patients had microthrombosis.Endothelial damage caused by SARS-CoV-2 cell invasion and subsequent host response disorders involving inflammation and coagulation pathways play a key role in the progression of severe COVID-19. Microvascular thrombosis may lead to microcirculation disorders and multiple organ failure lead to death.The characteristic pathological changes of DAD include alveolar epithelial and vascular endothelial injury, increased alveolar membrane permeability, large numbers of neutrophil infiltration, alveolar hyaline membrane formation, and hypoxemia and respiratory distress as the main clinical manifestations. DAD leads to ARDS in COVID-19 patients. DIC is a syndrome characterized by the activation of systemic intravascular coagulation, which leads to extensive fibrin deposition in the blood. Its occurrence and development begin with the expression of tissue factor and interact with physiological anticoagulation pathways. The down-regulation of fibrin and the impaired fibrinolysis together lead to extensive fibrin deposition.DIC is described as a decrease in the number of platelets and an increase in fibrin degradation products, such as D-dimer and low fibrinogen. The formation of microthrombus leads to the disturbance of microcirculation, which in turn leads to the death of the patient. However, the best prevention and treatment of COVID-19 microthrombosis is still uncertain.This review discusses the latest findings of basic and clinical research on COVID-19-related microthrombosis, and then we proposed the theory of microcirculation perfusion bundle therapy to explore effective methods for preventing and treating COVID-19-related microthrombosis. Further research is urgently needed to clarify how SARS-CoV-2 infection causes thrombotic complications, and how it affects the course and severity of the disease. To cultivate a more comprehensive understanding of the underlying mechanism of this disease. Raise awareness of the importance of preventing and treating microthrombosis in patients with COVID-19.
新型冠状病毒(严重急性呼吸综合征冠状病毒2,简称SARS-CoV-2,新冠病毒)的传播已在全球导致大量死亡。我们总结了过去几个月报告的数据,并强调新冠病毒疾病(COVID-19)患者的主要死亡原因是弥漫性肺泡损伤(DAD)和弥散性血管内凝血(DIC)。微血栓形成是COVID-19的一个突出临床特征,91.3%的死亡患者存在微血栓形成。严重急性呼吸综合征冠状病毒2侵袭细胞导致内皮损伤,随后宿主反应紊乱,涉及炎症和凝血途径,在重症COVID-19的进展中起关键作用。微血管血栓形成可能导致微循环障碍和多器官功能衰竭,进而导致死亡。弥漫性肺泡损伤的特征性病理变化包括肺泡上皮和血管内皮损伤、肺泡膜通透性增加、大量中性粒细胞浸润、肺泡透明膜形成,以及以低氧血症和呼吸窘迫为主要临床表现。弥漫性肺泡损伤导致COVID-19患者发生急性呼吸窘迫综合征(ARDS)。弥散性血管内凝血是一种以全身血管内凝血激活为特征的综合征,导致血液中广泛的纤维蛋白沉积。其发生和发展始于组织因子的表达,并与生理性抗凝途径相互作用。纤维蛋白减少和纤维蛋白溶解受损共同导致广泛的纤维蛋白沉积。弥散性血管内凝血表现为血小板数量减少以及纤维蛋白降解产物增加,如D-二聚体和纤维蛋白原降低。微血栓的形成导致微循环障碍,进而导致患者死亡。然而,针对COVID-19微血栓形成的最佳预防和治疗方法仍不确定。本综述讨论了COVID-19相关微血栓形成的基础和临床研究的最新发现,然后我们提出了微循环灌注束疗法理论,以探索预防和治疗COVID-19相关微血栓形成的有效方法。迫切需要进一步研究以阐明严重急性呼吸综合征冠状病毒2感染如何导致血栓形成并发症,以及它如何影响疾病的进程和严重程度。从而培养对这种疾病潜在机制更全面的理解。提高对COVID-19患者预防和治疗微血栓形成重要性的认识。