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J Thromb Haemost ; 19(6): 1533-1545, 2021 06.
Article in English | MEDLINE | ID: covidwho-1153569

ABSTRACT

BACKGROUND: Studies report hypercoagulability in coronavirus disease 2019 (COVID-19), leading many institutions to escalate anticoagulation intensity for thrombosis prophylaxis. OBJECTIVE: To determine the bleeding risk with various intensities of anticoagulation in critically ill patients with COVID-19 compared with other respiratory viral illnesses (ORVI). PATIENTS/METHODS: This retrospective cohort study compared the incidence of major bleeding in patients admitted to an intensive care unit (ICU) within a single health system with COVID-19 versus ORVI. In the COVID-19 cohort, we assessed the effect of anticoagulation intensity received on ICU admission on bleeding risk. We performed a secondary analysis with anticoagulation intensity as a time-varying covariate to reflect dose changes after ICU admission. RESULTS: Four hundred and forty-three and 387 patients were included in the COVID-19 and ORVI cohorts, respectively. The hazard ratio of major bleeding for the COVID-19 cohort relative to the ORVI cohort was 1.26 (95% confidence interval [CI]: 0.86-1.86). In COVID-19 patients, an inverse-probability treatment weighted model found therapeutic-intensity anticoagulation on ICU admission had an adjusted hazard ratio of bleeding of 1.55 (95% CI: 0.88-2.73) compared with standard prophylactic-intensity anticoagulation. However, when anticoagulation was assessed as a time-varying covariate and adjusted for other risk factors for bleeding, the adjusted hazard ratio for bleeding on therapeutic-intensity anticoagulation compared with standard thromboprophylaxis was 2.59 (95% CI: 1.20-5.57). CONCLUSIONS: Critically ill patients with COVID-19 had a similar bleeding risk as ORVI patients. When accounting for changes in anticoagulation that occurred in COVID-19 patients, therapeutic-intensity anticoagulation was associated with a greater risk of major bleeding compared with standard thromboprophylaxis.


Subject(s)
COVID-19 , Venous Thromboembolism , Anticoagulants/adverse effects , Critical Illness , Humans , Retrospective Studies , SARS-CoV-2
2.
Thromb Res ; 196: 355-358, 2020 12.
Article in English | MEDLINE | ID: covidwho-796186

ABSTRACT

As the Coronavirus disease 2019 (COVID-19) pandemic spread to the US, so too did descriptions of an associated coagulopathy and thrombotic complications. Hospitals created institutional protocols for inpatient management of COVID-19 coagulopathy and thrombosis in response to this developing data. We collected and analyzed protocols from 21 US academic medical centers developed between January and May 2020. We found greatest consensus on recommendations for heparin-based pharmacologic venous thromboembolism (VTE) prophylaxis in COVID-19 patients without contraindications. Protocols differed regarding incorporation of D-dimer tests, dosing of VTE prophylaxis, indications for post-discharge pharmacologic VTE prophylaxis, how to evaluate for VTE, and the use of empiric therapeutic anticoagulation. These findings support ongoing efforts to establish international, evidence-based guidelines.


Subject(s)
Anticoagulants/administration & dosage , Blood Coagulation/drug effects , COVID-19 Drug Treatment , Clinical Protocols , Pulmonary Embolism/prevention & control , Thrombophilia/prevention & control , Venous Thromboembolism/prevention & control , Venous Thrombosis/prevention & control , Academic Medical Centers , Anticoagulants/adverse effects , COVID-19/blood , COVID-19/complications , COVID-19/diagnosis , Consensus , Healthcare Disparities/trends , Humans , Practice Patterns, Physicians'/trends , Pulmonary Embolism/blood , Pulmonary Embolism/diagnosis , Pulmonary Embolism/etiology , Risk Assessment , Risk Factors , Thrombophilia/blood , Thrombophilia/diagnosis , Thrombophilia/etiology , Treatment Outcome , United States , Venous Thromboembolism/blood , Venous Thromboembolism/diagnosis , Venous Thromboembolism/etiology , Venous Thrombosis/blood , Venous Thrombosis/diagnosis , Venous Thrombosis/etiology
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