Complement activation and coagulopathy - an ominous duo in COVID19

Sojit Tomo1, Kiran Pvsn Kumar1, Dipayan Roy1

  • 1Department of Biochemistry, AIIMS Jodhpur, Jodhpur, Rajasthan, India.

Insights

COVID-19 coagulopathy presents diagnostic challenges due to mixed complement-mediated and consumption features. Tailored anticoagulant therapy, considering D-dimer levels, is recommended over uniform approaches for better patient outcomes.

Area of Science:

  • * Infectious Diseases
  • * Hematology
  • * Immunology

Background:

  • * COVID-19 shares similarities with SARS and MERS, with severe cases exhibiting abnormal coagulation.
  • * Immune-mediated pathology is significant in COVID-19, necessitating assessment of the complement system's role.
  • * The complement system and coagulation cascade are intricately linked, influencing disease pathophysiology.

Purpose of the Study:

  • * To discuss the pathophysiology of coagulopathy in COVID-19 patients.
  • * To analyze the role of D-dimer in predicting COVID-19 severity.
  • * To provide expert opinion on anticoagulant therapy for COVID-19.

Main Methods:

  • * A comprehensive literature search was conducted on PubMed up to May 30, 2020.
  • * Keywords included 'COVID-19', 'SARS-CoV-2', 'Coronavirus', 'Coagulopathy', and 'D-dimer'.
  • * Twenty-two studies were included for a weighted pooled analysis of D-dimer.

Main Results:

  • * Coagulopathy in COVID-19 shows mixed features of complement-mediated and consumption coagulopathy.
  • * D-dimer levels are discussed in relation to predicting COVID-19 severity.
  • * Atypical manifestations and varying D-dimer levels complicate uniform treatment recommendations.

Conclusions:

  • * A tailored anticoagulant regimen, potentially intensifying standard prophylaxis with low-molecular-weight heparin, is advisable.
  • * Uniform recommendations for anticoagulant therapy are insufficient due to atypical presentations and variable D-dimer levels.
  • * Consideration of direct thrombin and platelet inhibitors on a patient-specific basis is recommended.
Abstract

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