4.6 Article

The CoVID-TE risk assessment model for venous thromboembolism in hospitalized patients with cancer and COVID-19

期刊

JOURNAL OF THROMBOSIS AND HAEMOSTASIS
卷 19, 期 10, 页码 2522-2532

出版社

WILEY
DOI: 10.1111/jth.15463

关键词

clinical decision rules; COVID-19; SARS-CoV-2; thrombosis; venous thromboembolism

资金

  1. Texas Cancer Prevention and Research Institute of Texas [RR190104]
  2. Hemostasis and Thrombosis Research Society (Mentored Research Award) - Shire
  3. National Hemophilia Foundation Shire Clinical Fellowship Award
  4. National Cancer Institute [P30 CA068485]

向作者/读者索取更多资源

Hospitalized patients with cancer and COVID-19 are at increased risk of VTE and ATE. A simplified RAM model named CoVID-TE was developed to predict VTE in this vulnerable population, showing good performance in stratifying patients into low-risk and high-risk cohorts based on clinical risk factors. The CoVID-TE RAM may aid in real-time data-driven decisions for thrombosis prevention in this population.
Background Hospitalized patients with COVID-19 have increased risks of venous (VTE) and arterial thromboembolism (ATE). Active cancer diagnosis and treatment are well-known risk factors; however, a risk assessment model (RAM) for VTE in patients with both cancer and COVID-19 is lacking. Objectives To assess the incidence of and risk factors for thrombosis in hospitalized patients with cancer and COVID-19. Methods Among patients with cancer in the COVID-19 and Cancer Consortium registry (CCC19) cohort study, we assessed the incidence of VTE and ATE within 90 days of COVID-19-associated hospitalization. A multivariable logistic regression model specifically for VTE was built using a priori determined clinical risk factors. A simplified RAM was derived and internally validated using bootstrap. Results From March 17, 2020 to November 30, 2020, 2804 hospitalized patients were analyzed. The incidence of VTE and ATE was 7.6% and 3.9%, respectively. The incidence of VTE, but not ATE, was higher in patients receiving recent anti-cancer therapy. A simplified RAM for VTE was derived and named CoVID-TE (Cancer subtype high to very-high risk by original Khorana score +1, VTE history +2, ICU admission +2, D-dimer elevation +1, recent systemic anti-cancer Therapy +1, and non-Hispanic Ethnicity +1). The RAM stratified patients into two cohorts (low-risk, 0-2 points, n = 1423 vs. high-risk, 3+ points, n = 1034) where VTE occurred in 4.1% low-risk and 11.3% high-risk patients (c statistic 0.67, 95% confidence interval 0.63-0.71). The RAM performed similarly well in subgroups of patients not on anticoagulant prior to admission and moderately ill patients not requiring direct ICU admission. Conclusions Hospitalized patients with cancer and COVID-19 have elevated thrombotic risks. The CoVID-TE RAM for VTE prediction may help real-time data-driven decisions in this vulnerable population.

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