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Randomized Trial of Anticoagulation Strategies for Noncritically Ill Patients Hospitalized With COVID-19

BACKGROUND: Prior studies of therapeutic-dose anticoagulation in patients with COVID-19 have reported conflicting results. OBJECTIVES: We sought to determine the safety and effectiveness of therapeutic-dose anticoagulation in noncritically ill patients with COVID-19. METHODS: Patients hospitalized w...

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Autores principales: Stone, Gregg W., Farkouh, Michael E., Lala, Anuradha, Tinuoye, Elizabeth, Dressler, Ovidiu, Moreno, Pedro R., Palacios, Igor F., Goodman, Shaun G., Esper, Rodrigo B., Abizaid, Alexandre, Varade, Deepak, Betancur, Juan F., Ricalde, Alejandro, Payro, Gerardo, Castellano, José María, Hung, Ivan F.N., Nadkarni, Girish N., Giustino, Gennaro, Godoy, Lucas C., Feinman, Jason, Camaj, Anton, Bienstock, Solomon W., Furtado, Remo H.M., Granada, Carlos, Bustamante, Jessica, Peyra, Carlos, Contreras, Johanna, Owen, Ruth, Bhatt, Deepak L., Pocock, Stuart J., Fuster, Valentin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: by the American College of Cardiology Foundation. Published by Elsevier. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9987252/
https://www.ncbi.nlm.nih.gov/pubmed/36889611
http://dx.doi.org/10.1016/j.jacc.2023.02.041
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author Stone, Gregg W.
Farkouh, Michael E.
Lala, Anuradha
Tinuoye, Elizabeth
Dressler, Ovidiu
Moreno, Pedro R.
Palacios, Igor F.
Goodman, Shaun G.
Esper, Rodrigo B.
Abizaid, Alexandre
Varade, Deepak
Betancur, Juan F.
Ricalde, Alejandro
Payro, Gerardo
Castellano, José María
Hung, Ivan F.N.
Nadkarni, Girish N.
Giustino, Gennaro
Godoy, Lucas C.
Feinman, Jason
Camaj, Anton
Bienstock, Solomon W.
Furtado, Remo H.M.
Granada, Carlos
Bustamante, Jessica
Peyra, Carlos
Contreras, Johanna
Owen, Ruth
Bhatt, Deepak L.
Pocock, Stuart J.
Fuster, Valentin
author_facet Stone, Gregg W.
Farkouh, Michael E.
Lala, Anuradha
Tinuoye, Elizabeth
Dressler, Ovidiu
Moreno, Pedro R.
Palacios, Igor F.
Goodman, Shaun G.
Esper, Rodrigo B.
Abizaid, Alexandre
Varade, Deepak
Betancur, Juan F.
Ricalde, Alejandro
Payro, Gerardo
Castellano, José María
Hung, Ivan F.N.
Nadkarni, Girish N.
Giustino, Gennaro
Godoy, Lucas C.
Feinman, Jason
Camaj, Anton
Bienstock, Solomon W.
Furtado, Remo H.M.
Granada, Carlos
Bustamante, Jessica
Peyra, Carlos
Contreras, Johanna
Owen, Ruth
Bhatt, Deepak L.
Pocock, Stuart J.
Fuster, Valentin
author_sort Stone, Gregg W.
collection PubMed
description BACKGROUND: Prior studies of therapeutic-dose anticoagulation in patients with COVID-19 have reported conflicting results. OBJECTIVES: We sought to determine the safety and effectiveness of therapeutic-dose anticoagulation in noncritically ill patients with COVID-19. METHODS: Patients hospitalized with COVID-19 not requiring intensive care unit treatment were randomized to prophylactic-dose enoxaparin, therapeutic-dose enoxaparin, or therapeutic-dose apixaban. The primary outcome was the 30-day composite of all-cause mortality, requirement for intensive care unit–level of care, systemic thromboembolism, or ischemic stroke assessed in the combined therapeutic-dose groups compared with the prophylactic-dose group. RESULTS: Between August 26, 2020, and September 19, 2022, 3,398 noncritically ill patients hospitalized with COVID-19 were randomized to prophylactic-dose enoxaparin (n = 1,141), therapeutic-dose enoxaparin (n = 1,136), or therapeutic-dose apixaban (n = 1,121) at 76 centers in 10 countries. The 30-day primary outcome occurred in 13.2% of patients in the prophylactic-dose group and 11.3% of patients in the combined therapeutic-dose groups (HR: 0.85; 95% CI: 0.69-1.04; P = 0.11). All-cause mortality occurred in 7.0% of patients treated with prophylactic-dose enoxaparin and 4.9% of patients treated with therapeutic-dose anticoagulation (HR: 0.70; 95% CI: 0.52-0.93; P = 0.01), and intubation was required in 8.4% vs 6.4% of patients, respectively (HR: 0.75; 95% CI: 0.58-0.98; P = 0.03). Results were similar in the 2 therapeutic-dose groups, and major bleeding in all 3 groups was infrequent. CONCLUSIONS: Among noncritically ill patients hospitalized with COVID-19, the 30-day primary composite outcome was not significantly reduced with therapeutic-dose anticoagulation compared with prophylactic-dose anticoagulation. However, fewer patients who were treated with therapeutic-dose anticoagulation required intubation and fewer died (FREEDOM COVID [FREEDOM COVID Anticoagulation Strategy]; NCT04512079)
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spelling pubmed-99872522023-03-06 Randomized Trial of Anticoagulation Strategies for Noncritically Ill Patients Hospitalized With COVID-19 Stone, Gregg W. Farkouh, Michael E. Lala, Anuradha Tinuoye, Elizabeth Dressler, Ovidiu Moreno, Pedro R. Palacios, Igor F. Goodman, Shaun G. Esper, Rodrigo B. Abizaid, Alexandre Varade, Deepak Betancur, Juan F. Ricalde, Alejandro Payro, Gerardo Castellano, José María Hung, Ivan F.N. Nadkarni, Girish N. Giustino, Gennaro Godoy, Lucas C. Feinman, Jason Camaj, Anton Bienstock, Solomon W. Furtado, Remo H.M. Granada, Carlos Bustamante, Jessica Peyra, Carlos Contreras, Johanna Owen, Ruth Bhatt, Deepak L. Pocock, Stuart J. Fuster, Valentin J Am Coll Cardiol Original Investigation BACKGROUND: Prior studies of therapeutic-dose anticoagulation in patients with COVID-19 have reported conflicting results. OBJECTIVES: We sought to determine the safety and effectiveness of therapeutic-dose anticoagulation in noncritically ill patients with COVID-19. METHODS: Patients hospitalized with COVID-19 not requiring intensive care unit treatment were randomized to prophylactic-dose enoxaparin, therapeutic-dose enoxaparin, or therapeutic-dose apixaban. The primary outcome was the 30-day composite of all-cause mortality, requirement for intensive care unit–level of care, systemic thromboembolism, or ischemic stroke assessed in the combined therapeutic-dose groups compared with the prophylactic-dose group. RESULTS: Between August 26, 2020, and September 19, 2022, 3,398 noncritically ill patients hospitalized with COVID-19 were randomized to prophylactic-dose enoxaparin (n = 1,141), therapeutic-dose enoxaparin (n = 1,136), or therapeutic-dose apixaban (n = 1,121) at 76 centers in 10 countries. The 30-day primary outcome occurred in 13.2% of patients in the prophylactic-dose group and 11.3% of patients in the combined therapeutic-dose groups (HR: 0.85; 95% CI: 0.69-1.04; P = 0.11). All-cause mortality occurred in 7.0% of patients treated with prophylactic-dose enoxaparin and 4.9% of patients treated with therapeutic-dose anticoagulation (HR: 0.70; 95% CI: 0.52-0.93; P = 0.01), and intubation was required in 8.4% vs 6.4% of patients, respectively (HR: 0.75; 95% CI: 0.58-0.98; P = 0.03). Results were similar in the 2 therapeutic-dose groups, and major bleeding in all 3 groups was infrequent. CONCLUSIONS: Among noncritically ill patients hospitalized with COVID-19, the 30-day primary composite outcome was not significantly reduced with therapeutic-dose anticoagulation compared with prophylactic-dose anticoagulation. However, fewer patients who were treated with therapeutic-dose anticoagulation required intubation and fewer died (FREEDOM COVID [FREEDOM COVID Anticoagulation Strategy]; NCT04512079) by the American College of Cardiology Foundation. Published by Elsevier. 2023-05-09 2023-03-06 /pmc/articles/PMC9987252/ /pubmed/36889611 http://dx.doi.org/10.1016/j.jacc.2023.02.041 Text en © 2023 by the American College of Cardiology Foundation. Published by Elsevier. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Original Investigation
Stone, Gregg W.
Farkouh, Michael E.
Lala, Anuradha
Tinuoye, Elizabeth
Dressler, Ovidiu
Moreno, Pedro R.
Palacios, Igor F.
Goodman, Shaun G.
Esper, Rodrigo B.
Abizaid, Alexandre
Varade, Deepak
Betancur, Juan F.
Ricalde, Alejandro
Payro, Gerardo
Castellano, José María
Hung, Ivan F.N.
Nadkarni, Girish N.
Giustino, Gennaro
Godoy, Lucas C.
Feinman, Jason
Camaj, Anton
Bienstock, Solomon W.
Furtado, Remo H.M.
Granada, Carlos
Bustamante, Jessica
Peyra, Carlos
Contreras, Johanna
Owen, Ruth
Bhatt, Deepak L.
Pocock, Stuart J.
Fuster, Valentin
Randomized Trial of Anticoagulation Strategies for Noncritically Ill Patients Hospitalized With COVID-19
title Randomized Trial of Anticoagulation Strategies for Noncritically Ill Patients Hospitalized With COVID-19
title_full Randomized Trial of Anticoagulation Strategies for Noncritically Ill Patients Hospitalized With COVID-19
title_fullStr Randomized Trial of Anticoagulation Strategies for Noncritically Ill Patients Hospitalized With COVID-19
title_full_unstemmed Randomized Trial of Anticoagulation Strategies for Noncritically Ill Patients Hospitalized With COVID-19
title_short Randomized Trial of Anticoagulation Strategies for Noncritically Ill Patients Hospitalized With COVID-19
title_sort randomized trial of anticoagulation strategies for noncritically ill patients hospitalized with covid-19
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9987252/
https://www.ncbi.nlm.nih.gov/pubmed/36889611
http://dx.doi.org/10.1016/j.jacc.2023.02.041
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