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2120 Risk Stratification for Acute Arterial and Venous Thromboembolism using CHA2DS2-VASc Score in Hospitalized COVID-19 Patients: A Multicenter Study

Program: Oral and Poster Abstracts
Session: 331. Thrombosis: Poster II
Hematology Disease Topics & Pathways:
Bleeding and Clotting, Adults, Lymphomas, non-Hodgkin lymphoma, Workforce, thromboembolism, Diseases, SARS-CoV-2/COVID-19, Infectious Diseases, Real World Evidence
Sunday, December 12, 2021, 6:00 PM-8:00 PM

Yi Lee, MD1, Qasim Jehangir, MD2*, Pin Li, PhD3*, Chun-Hui Lin, MS3*, Anupam A Sule, MD, PhD2,4*, Geetha Krishnamoorthy, MD2*, Judie R Goodman, DO5, Abdul R. Halabi, MD6*, Kiritkumar Patel, MD6*, Dee Dee Wang, MD7*, Laila Poisson, PhD3* and Girish B Nair, MD, MS8*

1Department of Medicine, St Joseph Mercy Oakland Hospital, Pontiac, MI
2Department of Medicine, St. Joseph Mercy Oakland Hospital, Pontiac, MI
3Department of Public Health Sciences, Henry Ford Health System, Detroit, MI
4Department of Informatics, St. Joseph Mercy Oakland Hospital, Pontiac, MI
5Division of Hematology/Oncology, St. Joseph Mercy Oakland Hospital, Pontiac, MI
6Division of Cardiology, St. Joseph Mercy Oakland Hospital, Pontiac, MI
7Division of Cardiology, Henry Ford Hospital, Detroit, MI
8Division of Pulmonary and Critical Care Medicine, William Beaumont Hospital, Royal Oak, MI

Introduction: Arterial and venous thromboembolism are common complications in COVID-19. Micro-macro thrombosis-related organ dysfunction can confer an increased risk for mortality. The optimal dosage of anticoagulation (AC) in COVID-19 patients remains unclear. Interim data from adaptive randomized control trials (ATTACC, REMAP-CAP, and ACTIV-4a) showed divergent results of therapeutic AC (TAC) versus usual care AC for the primary outcome of organ support free days in hospitalized COVID-19 patients. Components of CHA2DS2-VASc, a model originally built for predicting ischemic stroke in atrial fibrillation, are consistent with independent risk factors for COVID-19 severity and mortality. Herein, we analyzed the performance of the CHA2DS2-VASc model in hospitalized COVID-19 patients for predicting arterial and venous thromboembolic events, which could potentially aid in risk stratification of hospitalized patients and guide AC dosing.

Methods: This is a large, retrospective, multicenter cohort study that included all adult patients from one tertiary care and five community hospitals with PCR-proven SARS-CoV-2 infection between 3/1/2020 and 12/1/2020. The primary composite outcome was acute arterial thromboembolism (ATE) and venous thromboembolism (VTE). We identified patients with ATE [cerebrovascular accident (CVA), myocardial infarction (MI) including both ST-segment elevation MI and non-ST-segment elevation MI], and VTE [deep vein thrombosis (DVT) and pulmonary embolism (PE)] using ICD -10 codes. Mean and standard deviation were reported for continuous variables; proportions were reported for categorical variables. To compare the groups, the Chi-square test was used for categorical variables, and the t-test was used for continuous variables. CHA2DS2-VASc scores were calculated on admission and were used as a measure of the predictive accuracy of the scoring system. Sensitivity and specificity with different cut-offs of CHA2DS2-VASc scores were calculated. All statistical tests were 2-sided with an α (significance) level of 0.05. All data were analyzed using R version 4.0.5.

Results: Among 3526 patients, a total of 619 patients had thromboembolic events: 383 had ATE and 236 had VTE. Of 383 patients who had ATE, 350 patients were found to have acute MI, 48 had CVA, and 15 had both MI and CVA. In patients with VTE, 134 had DVT, 168 had PE, and 66 had both DVT and PE (Figure 1). We analyzed the primary composite outcome of ATE and VTE (group 1) vs no ATE and VTE (group 2). Baseline characteristics are included in Table 1. The in-patient all-cause mortality rate was 28.4% in group 1 vs 12.6% in group 2 (p<0.001). The mean hospital length of stay was 12.3 days in group 1 vs 8.8 days in group 2 (p<0.001). Group 1 had a mean CHA2DS2-VASc score of 3.3 ±1.6. vs 2.7±1.7 in group 2 (p<0.001) (Figure 2). At CHA2DS2-VASc scores of 3 and 4, the model had a specificity of 46% and 67% and sensitivity of 68% and 42% respectively for predicting ATE/VTE. The CHA2DS2-VASc score of 5 had a specificity of 86% and sensitivity of 25%. The score of 7 had 98% specificity but 3% sensitivity (Table 2).

Conclusion: Our results suggest that the CHA2DS2-VASc model for arterial and venous thromboembolism has a moderate performance. The CHA2DS2-VASc score of 5 has a high specificity, though low sensitivity, for predicting thromboembolism. The CHA2DS2-VASc score can be used as an adjunct risk stratification tool to initiate TAC.

Disclosures: No relevant conflicts of interest to declare.

*signifies non-member of ASH