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COVID-19 carries excess risk for venous and arterial thrombotic complications driven by a hyperactive platelet-neutrophil interaction, endothelial cell dysfunction, and activation of the coagulation cascade. Despite the known benefits of anticoagulation in critically ill patients with COVID-19, optimal dosing remains uncertain. In the COVID-PACT study (an open-label trial in patients with COVID-19 receiving intensive care unit [ICU] care), Bohula and colleagues randomized 390 patients at 34 U.S. centers to full-dose anticoagulation or prophylactic doses of anticoagulation therapy; 292 patients with no contraindications to antiplatelet therapy were additionally randomized to clopidogrel or no clopidogrel.
At randomization, 99% of patients were on advanced respiratory therapy, including 15% on mechanical ventilation; 40% required invasive mechanical ventilation at some point during hospitalization. Full-dose anticoagulation substantially reduced venous or arterial thrombotic events compared with prophylactic anticoagulation (9.9% vs. 15.2%). No additional benefit was conferred by clopidogrel. Fatal or life-threatening bleeding occurred in four patients in the full-dose anticoagulated group versus one in the prophylactic-dose group (2.1% vs. 0.5%), but all-cause mortality did not differ between groups.
Bohula EA et al. Anticoagulation and antiplatelet therapy for prevention of venous and arterial thrombotic events in critically ill patients with COVID-19: COVID-PACT. Circulation 2022 Aug 29; [e-pub]. (https://doi.org/10.1161/CIRCULATIONAHA.122.061533)
Comment
Current NIH guidelines recommend prophylactic doses of anticoagulation in treating moderate to severe COVID-19. The results of this study indicate that, in critically ill patients with COVID-19, the benefit of full-dose anticoagulation may outweigh risk. However, the trial was terminated early because of decreasing ICU admission rates. In addition, patients' vaccination status was not accounted for, and the differential impact of evolving waves of SARS-CoV-2 variants over the course of the study was not considered. Unless reductions in mortality can be demonstrated with full-dose anticoagulation, the added risk for bleeding must be further evaluated.