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Therapeutic Anticoagulation Delays Death in COVID-19 Patients: Cross-Sectional Analysis of a Prospective Cohort

A hypercoagulable state has been described in coronavirus disease 2019 (COVID-19) patients. Others have reported a survival advantage with prophylactic anticoagulation (pAC) and therapeutic anticoagulation (tAC), but these retrospective analyses have important limitations such as confounding by indi...

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Detalles Bibliográficos
Autores principales: Ionescu, Filip, Grasso-Knight, Giovi, Castillo, Edward, Naeem, Ehsun, Petrescu, Ioana, Imam, Zaid, Patel, Vishal K., Narasimhan, Mangala, Nair, Girish B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519875/
https://www.ncbi.nlm.nih.gov/pubmed/32995704
http://dx.doi.org/10.1055/s-0040-1716721
Descripción
Sumario:A hypercoagulable state has been described in coronavirus disease 2019 (COVID-19) patients. Others have reported a survival advantage with prophylactic anticoagulation (pAC) and therapeutic anticoagulation (tAC), but these retrospective analyses have important limitations such as confounding by indication. We studied the impact of tAC and pAC compared with no anticoagulation (AC) on time to death in COVID-19. We performed a cross-sectional analysis of 127 deceased COVID-19 patients and compared time to death in those who received tAC ( n  = 67), pAC ( n  = 47), and no AC ( n  = 13). Median time to death was longer with higher doses of AC (11 days for tAC, 8 days for pAC, and 4 days for no AC, p  < 0.001). In multivariate analysis, AC was associated with longer time to death, both at prophylactic (hazard ratio [HR] = 0.29; 95% confidence interval [CI]: 0.15 to 0.58; p  < 0.001) and therapeutic doses (HR = 0.15; 95% CI: 0.07 to 0.32; p  < 0.001) compared with no AC. Bleeding rates were similar among tAC and remaining patients (19 vs. 18%; p  = 0.877). In deceased COVID-19 patients, AC was associated with a delay in death in a dose-dependent manner. Randomized trials are required to prospectively investigate the benefit and safety of higher doses of AC in this population.