The Management of COVID-19-Related Coagulopathy: A Focus on the Challenges of Metabolic and Vascular Diseases

Int J Mol Sci. 2023 Aug 14;24(16):12782. doi: 10.3390/ijms241612782.

Abstract

The course of COVID-19 is highly dependent on the associated cardiometabolic comorbidities of the patient, which worsen the prognosis of coronavirus infection, mainly due to systemic inflammation, endothelium dysfunction, and thrombosis. A search on the recent medical literature was performed in five languages, using the PubMed, Embase, Cochrane, and Google Scholar databases, for the review of data regarding the management of patients with a high risk for severe COVID-19, focusing on the associated coagulopathy. Special features of COVID-19 management are presented, based on the underlying conditions (obesity, diabetes mellitus, and cardiovascular diseases), emphasizing the necessity of a modern, holistic approach to thromboembolic states. The latest findings regarding the most efficient therapeutic approaches are included in the article, offering guidance for medical professionals in severe, complicated cases of SARS-CoV-2 infection. We can conclude that severe COVID-19 is closely related to vascular inflammation and intense cytokine release leading to hemostasis disorders. Overweight, hyperglycemia, cardiovascular diseases, and old age are important risk factors for severe outcomes of coronavirus infection, involving a hypercoagulable state. Early diagnosis and proper therapy in complicated SARS-CoV-2-infected cases could reduce mortality and the need for intensive care during hospitalization in patients with cardiometabolic comorbidities.

Keywords: COVID-19; cardiovascular diseases; coagulopathy; diabetes mellitus; hypercoagulable state; obesity; stroke; thrombosis; venous thromboembolism; viscoelastometry.

Publication types

  • Review

MeSH terms

  • Blood Coagulation Disorders* / etiology
  • Blood Coagulation Disorders* / therapy
  • COVID-19* / complications
  • Cardiovascular Diseases* / etiology
  • Cardiovascular Diseases* / therapy
  • Humans
  • Inflammation / therapy
  • SARS-CoV-2
  • Vascular Diseases*

Grants and funding

This research received no external funding.