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Hereditary Thrombophilia in the Era of COVID-19.

Oana-Viola BadulescuPaul Dan SirbuNina FilipGabriela BordeianuElena CojocaruCristian Constantin BudacuMinerva Codruţa BădescuIris Bararu-BojanBogdan VeliceasaManuela Ciocoiu
Published in: Healthcare (Basel, Switzerland) (2022)
Thrombophilia, also called hypercoagulability or prothrombotic condition, usually reflects a certain imbalance that occurs either in the coagulation cascade or in the anticoagulation/fibrinolytic system. A similar imbalance may be induced by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Thrombotic complications are associated with multiorgan failure and increased mortality. In this context, activation of coagulation and thrombocytopenia appeared as prognostic markers in COVID-19. Our work provides a structured and updated analysis of inherited thrombophilia and its involvement in COVID-19, emphasizing the importance of diagnosing and initiating thromboprophylaxis. Since the state of hypercoagulation is directly correlated with COVID-19, we consider that studies on the genetic profiles of proteins involved in thrombophilia in patients who have had COVID-19 and thrombotic events are of great importance, both in treating and in preventing deaths due to COVID-19.
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