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Predictors of venous thromboembolic events in hospitalized patients with COVID-19
Giovanni Scimeca1,2, Darsiya Krishnathasan1,3, Sina Rashedi1,3
1Thrombosis Research Group, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Insights
COVID-19 patients face higher venous thromboembolism (VTE) risks. Prior VTE, corticosteroid use, and thrombophilia increase VTE risk, while anticoagulation and statins decrease it.
Area of Science:
- Cardiology
- Pulmonology
- Hematology
Background:
- Hospitalized COVID-19 patients have an elevated risk of venous thromboembolism (VTE).
- Previous studies identifying VTE predictors were limited by small sample sizes and administrative data.
- The CORONA-VTE Network provides a robust dataset for investigating VTE risk factors in COVID-19.
Purpose of the Study:
- To identify predictors of VTE in hospitalized patients with confirmed COVID-19.
- To analyze the association between various clinical factors and the risk of VTE.
- To inform risk assessment strategies for COVID-19 patients.
Main Methods:
- Utilized data from 3,844 adult patients in the multicenter CORONA-VTE Network registry.
- Primary outcome: time-to-first adjudicated pulmonary embolism or deep vein thrombosis within 90 days.
- Employed cause-specific Cox regression analysis with pooled hazard ratios (HRs).
Main Results:
- The cumulative incidence of VTE was 5.3% at 90 days.
- Increased VTE risk associated with prior VTE (HR: 1.71), corticosteroid therapy (HR: 1.76), and thrombophilia (HR: 3.56).
- Reduced VTE risk associated with therapeutic anticoagulation (HR: 0.42), statin use (HR: 0.67), and prophylactic anticoagulation (HR: 0.52).
Conclusions:
- Identified key clinical factors associated with VTE risk in COVID-19 patients.
- Prior VTE, corticosteroids, and thrombophilia are risk factors.
- Anticoagulation and statins demonstrate protective effects against VTE.
Abstract:
COVID-19 is associated with an increased risk of venous thromboembolism (VTE) in hospitalized patients. Although prior studies have attempted to identify predictors of VTE, restricted sample size and use of administrative claims data have limited such analyses. We utilized data from hospitalized patients in the CORONA-VTE Network, a United States multicenter registry of adult patients with PCR-confirmed COVID-19 (N = 3,844). The primary outcome was time-to-first event for a composite of adjudicated pulmonary embolism or deep vein thrombosis during 90-day follow-up. The candidate variables were selected by a priori clinical consensus. We conducted cause-specific Cox regression analysis adjusted for the selected variables for each imputed dataset and pooled the estimated HRs for reporting (p < 0.05 for significance). VTE occurred in 206 patients, with a cumulative incidence of 5.3% at 90 days. The covariates associated with increased risk of VTE were history of VTE (HR: 1.71; 95% CI: 1.11-2.63), corticosteroid therapy (HR: 1.76; 95% CI: 1.32-2.33) and known thrombophilia (HR: 3.56; 95% CI: 1.54-8.21) while therapeutic anticoagulation at baseline (HR: 0.42; 95% CI: 0.26-0.69), antecedent use of statins (HR: 0.67; 95% CI: 0.50-0.90), and prophylactic anticoagulation during hospitalization (HR: 0.52; 95% CI: 0.38-0.71) were associated with reduced risk of VTE. While prior VTE, corticosteroid therapy, and known thrombophilia were associated with an increased risk of VTE, prescriptions of prophylactic and therapeutic anticoagulation, and statins were associated with a decreased risk. Once externally validated, these findings may inform risk assessment in hospitalized patients with COVID-19.
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