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Updated: Jun 19, 2025

Author Spotlight: Deciphering Coagulation Disorders in Traumatic Brain Injury Patients
Published on: August 4, 2023
Anti-Xa activity below range is related to thrombosis in patients with severe COVID-19
Pilar Marcos-Neira1, Cristian Morales-Indiano2, Mariana Fernández-Caballero3
1Intensive Care Unit, Germans Trias i Pujol University Hospital, Badalona, Barcelona, Spain.
Objective:
We aimed to anlayse the relationship between anti-Xa activity below range and thomboembolic events.
Design:
Single center prospective observational longitudinal cohort study (February-November 2021).
Setting:
Patients admitted to the ICU of a University Hospital.
Participants:
Patients with severe COVID-19 pneumoniae.
Interventions:
Enoxaparin was used for prophylactic and therapeutic anticoagulation. Enoxaparin dosing and dose adjustment were based on anti-Xa activity according to the hospital protocol.
Main Variables Of Interest:
Target: thomboembolic events.
Predictors:
demographics, pharmacotherapy, anti-Xa measurements, clinical data, and laboratory results. Logistic regression was used to identify independent risk factors for thomboembolic events.
Results:
Data were available for 896 serum anti-Xa measurements from 228 subjects. Overall, 71.9% were male, with a median age of 62. Most patients needed invasive mechanical ventilation (87.7%) and mortality was 24.1%. A total of 28.9% new thomboembolic events were diagnosed. There were 27.1% anti-Xa measesurements below range. When multivariable logistic regression analysis was performed anti-Xa activity below range (RR, 4.2; p = 0.000), C-reactive protein (25 mg/L increase) (RR, 1.14; p = 0.005) and D-dimer (1000 ng/L increase) (RR, 1.06; p = 0.002) were the independent factors related to new thomboembolic events in patients with severe COVID-19.
Conclusions:
Anti-Xa activity below range, C-reactive protein and D-dimer were the independent factors related to thomboembolic events in patients with severe COVID-19. Purposely designed clinical trials should be carried out to confirm the benefit of an anti-Xa monitoring.
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