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10.1177/1076029620938149

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32677459!7370334!32677459
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suck abstract from ncbi


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pmid32677459      Clin+Appl+Thromb+Hemost 2020 ; 26 (ä): 1076029620938149
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  • COVID-19: Coagulopathy, Risk of Thrombosis, and the Rationale for Anticoagulation #MMPMID32677459
  • Miesbach W; Makris M
  • Clin Appl Thromb Hemost 2020[Jan]; 26 (ä): 1076029620938149 PMID32677459show ga
  • The novel coronavirus infection (COVID-19) is caused by the new coronavirus SARS-CoV-2 and is characterized by an exaggerated inflammatory response that can lead to severe manifestations such as adult respiratory syndrome, sepsis, coagulopathy, and death in a proportion of patients. Among other factors and direct viral effects, the increase in the vasoconstrictor angiotensin II, the decrease in the vasodilator angiotensin, and the sepsis-induced release of cytokines can trigger a coagulopathy in COVID-19. A coagulopathy has been reported in up to 50% of patients with severe COVID-19 manifestations. An increase in d-dimer is the most significant change in coagulation parameters in severe COVID-19 patients, and progressively increasing values can be used as a prognostic parameter indicating a worse outcome. Limited data suggest a high incidence of deep vein thrombosis and pulmonary embolism in up to 40% of patients, despite the use of a standard dose of low-molecular-weight heparin (LMWH) in most cases. In addition, pulmonary microvascular thrombosis has been reported and may play a role in progressive lung failure. Prophylactic LMWH has been recommended by the International Society on Thrombosis and Haemostasis (ISTH) and the American Society of Hematology (ASH), but the best effective dosage is uncertain. Adapted to the individual risk of thrombosis and the d-dimer value, higher doses can be considered, especially since bleeding events in COVID-19 are rare. Besides the anticoagulant effect of LMWH, nonanticoagulant properties such as the reduction in interleukin 6 release have been shown to improve the complex picture of coagulopathy in patients with COVID-19.
  • |*Betacoronavirus[MESH]
  • |*Pandemics[MESH]
  • |Angiotensin II/metabolism[MESH]
  • |Anticoagulants/*therapeutic use[MESH]
  • |Arterial Occlusive Diseases/blood/epidemiology/etiology[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/blood/*complications/epidemiology[MESH]
  • |Cytokine Release Syndrome/blood/etiology[MESH]
  • |Disease Outbreaks[MESH]
  • |Disseminated Intravascular Coagulation/etiology/prevention & control[MESH]
  • |Fibrin Fibrinogen Degradation Products/analysis[MESH]
  • |Fibrinolytic Agents/therapeutic use[MESH]
  • |Heparin, Low-Molecular-Weight/therapeutic use[MESH]
  • |Humans[MESH]
  • |Incidence[MESH]
  • |Inflammation[MESH]
  • |Pneumonia, Viral/blood/*complications/epidemiology[MESH]
  • |Prognosis[MESH]
  • |Pulmonary Embolism/etiology/prevention & control[MESH]
  • |Risk[MESH]
  • |SARS-CoV-2[MESH]
  • |Sepsis/blood/complications[MESH]
  • |Severe Acute Respiratory Syndrome/blood/complications/epidemiology[MESH]
  • |Thrombophilia/blood/drug therapy/*etiology[MESH]
  • |Thrombosis/blood/epidemiology/etiology/*prevention & control[MESH]
  • |Thrombotic Microangiopathies/etiology/prevention & control[MESH]


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