The coronavirus disease 2019 , first identified in December 2019 in Wuhan, China, is a major public health crisis with new infections increasing exponentially worldwide. 1 COVID-19 is an acute infectious disease caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV2) and has contributed to significant morbidity and mortality, including the development of coagulopathy. 2 Similar thrombotic and thromboembolic events have occurred during other viral outbreaks, including severe acute respiratory syndrome (SARS), Middle Eastern respiratory syndrome, and influenza A H1N1. [3][4][5][6][7] Venous thromboembolism (VTE) (ie, deep vein thrombosis or pulmonary embolism [PE]) is a common complication of acute infectious diseases, which increase VTE risk 2-fold to 32-fold. 8-10 Survival among patients with incident and recurrent VTE is significantly reduced, especially after PE. 11 Hospitalized patients with acute medical illness, including infections such as pneumonia, are at increased risk of VTE, both in-hospital and for an extended period of time (up to 45 days) after hospital discharge. 8,9,[12][13][14][15][16] Despite this well-established association, 8-10 there are few data specifically addressing VTE in patients recently hospitalized with COVID-19 infections. 17,18 Indeed, infection-associated VTE might account for a substantial burden of incident or recurrent VTE among those with COVID-19.In addition, small-vessel hyaline thrombus formation has been described in autopsies of patients with COVID pneumonia. 19 There is increasing concern that mortality seen across all age groups may be secondary to PE, as 31% incidence of thrombotic complications in ICU patients with COVID-19 infections is recently reported. PE was the most frequent thrombotic complication and contributed to 81% of thrombotic complications. 20 To improve outcomes, targeted prophylaxis efforts to improve coagulopathy and reduce incident VTE in patients with acute infectious diseases, specifically COVID-19, may be advantageous.Currently, VTE prophylaxis duration is mainly limited to the period of hospitalization, 21 but most VTE events occur within the first month following hospital discharge. 22 Recent data support the finding that an elevated D-dimer (>2Ă upper limit of normal [ULN]) is anThis is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.