Therapeutic versus Prophylactic Bemiparin in Hospitalized Patients with Nonsevere COVID-19 Pneumonia (BEMICOP Study): An Open-Label, Multicenter, Randomized, Controlled Trial

Author:

Marcos-Jubilar María1,Carmona-Torre Francisco2,Vidal Rosa3,Ruiz-Artacho Pedro45ORCID,Filella David6,Carbonell Cristina7,Jiménez-Yuste Víctor8,Schwartz Juana9,Llamas Pilar3,Alegre Félix10,Sádaba Belén9,Núñez-Córdoba Jorge9,Yuste José R.2,Fernández-García Javier9,Lecumberri Ramón111,

Affiliation:

1. Hematology Service, Clínica Universidad de Navarra, Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain

2. Divison of Infectious Diseases, Clínica Universidad de Navarra, Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain

3. Hematology Service, Hospital Universitario Fundación Jiménez-Díaz, Madrid, Spain

4. Internal Medicine Department, Clínica Universidad de Navarra, Madrid, Spain

5. CIBER Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, Madrid, Spain

6. Internal Medicine Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain

7. Internal Medicine Department, Hospital Universitario de Salamanca-IBSAL, Universidad de Salamanca, Salamanca, Spain

8. Hematology Service, Hospital Universitario La Paz, Madrid, Spain

9. Clinical Trials Unit, Clínica Universidad de Navarra, Pamplona, Spain

10. Internal Medicine Department, Clínica Universidad de Navarra, Pamplona, Spain

11. CIBER Cardiovascular (CIBERCV), Instituto de Salud Carlos III, Madrid, Spain

Abstract

AbstractThromboprophylaxis with low molecular weight heparin in hospitalized patients with COVID-19 is mandatory, unless contraindicated. Given the links between inflammation and thrombosis, the use of higher doses of anticoagulants could improve outcomes. We conducted an open-label, multicenter, randomized, controlled trial in adult patients hospitalized with nonsevere COVID-19 pneumonia and elevated D-dimer. Patients were randomized to therapeutic-dose bemiparin (115 IU/kg daily) versus standard prophylaxis (bemiparin 3,500 IU daily), for 10 days. The primary efficacy outcome was a composite of death, intensive care unit admission, need of mechanical ventilation support, development of moderate/severe acute respiratory distress, and venous or arterial thrombosis within 10 days of enrollment. The primary safety outcome was major bleeding (International Society on Thrombosis and Haemostasis criteria). A prespecified interim analysis was performed when 40% of the planned study population was reached. From October 2020 to May 2021, 70 patients were randomized at 5 sites and 65 were included in the primary analysis; 32 patients allocated to therapeutic dose and 33 to standard prophylactic dose. The primary efficacy outcome occurred in 7 patients (22%) in the therapeutic-dose group and 6 patients (18%) in the prophylactic-dose (absolute risk difference 3.6% [95% confidence interval [CI], –16% –24%]; odds ratio 1.26 [95% CI, 0.37–4.26]; p = 0.95). Discharge in the first 10 days was possible in 66 and 79% of patients, respectively. No major bleeding event was registered. Therefore, in patients with COVID-19 hospitalized with nonsevere pneumonia but elevated D-dimer, the use of a short course of therapeutic-dose bemiparin does not appear to improve clinical outcomes compared with standard prophylactic doses. Trial Registration: ClinicalTrials.gov NCT04604327.

Publisher

Georg Thieme Verlag KG

Subject

Hematology

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